BEGIN:VCALENDAR
VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
METHOD:PUBLISH
BEGIN:VTIMEZONE
TZID:Europe/Vienna
BEGIN:DAYLIGHT
DTSTART:20260329T030000
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
RRULE:FREQ=YEARLY;BYDAY=-1SU;BYMONTH=3
TZNAME:CEST
END:DAYLIGHT
BEGIN:STANDARD
DTSTART:20261025T020000
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
RRULE:FREQ=YEARLY;BYDAY=-1SU;BYMONTH=10
TZNAME:CET
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1784278800@ist.ac.at
DTSTART:20260717T110000
DTEND:20260717T120000
DESCRIPTION:Speaker: Christine Fiedler\nhosted by Edouard Hannezo\nAbstract
 : Thermoelectric materials can directly convert between heat and electrici
 ty\, offering a route toward sustainable energy generation. However\, thei
 r use remains limited to niche applications due to high fabrication costs 
 and relatively low efficiencies compared to competing energy technologies.
  Tin chalcogenides such as SnSe and SnS are promising candidates and\, whe
 n processed via solution-based routes\, provide a scalable and lower-cost 
 alternative to conventional solid-state synthesis\, opening pathways towar
 d broader adoption. However\, realizing their full potential in polycrysta
 lline form requires a deeper understanding of how defects\, dopants\, and 
 microstructure govern charge and heat transport.This thesis demonstrates t
 hat\, in solution-processed materials\, dopants including those introduced
  unintentionally through precursor chemistry\, are not just confined to sp
 ecific lattice sites. Instead\, they distribute across the microstructure\
 , partitioning within grain interiors\, grain boundaries\, and segregated 
 regions\, where they govern grain growth\, carrier concentration\, and cha
 rge transport. Through a systematic study of alkali metals and lead halide
 s in SnSe and SnS\, this work links synthesis\, defect partitioning\, micr
 ostructure evolution\, and thermoelectric performance reshaping how high-p
 erformance p- and n-type thermoelectric materials are designed.
LOCATION:Sunstone Bldg / Ground floor / Big Seminar Room B (I23.EG.102) and
  Zoom\, ISTA
ORGANIZER:
SUMMARY:Christine Fiedler: Thesis Defense: Mechanistic Insight into Solutio
 n-Processed P-type Tin Chalcogenides as a Basis for Designing their N-type
  Analogs
URL:https://talks-calendar.ista.ac.at/events/6530
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1785229200@ist.ac.at
DTSTART:20260728T110000
DTEND:20260728T120000
DESCRIPTION:Speaker: Miguel Cueto Noval\nhosted by Carrie Bernecky\nAbstrac
 t: The widespread adoption of apps like Whatsapp and Signal has translated
  into billions of people all around the world communicating on a regular b
 asis by making use of services that offer end-to-end encryption and even p
 rovide security guarantees when a user's device is compromised.This was ma
 de possible by the introduction of the Double Ratchet Algorithm\, which wa
 s designed for a setting where communication takes place between two parti
 es. However\, in practice\, many apps offer the possibility of creating gr
 oups. The protocols they use to secure communication are inefficient for l
 arge group which has the undesirable consequence that the aforementioned a
 pps have established limits on the group size of roughly 1000 users. This 
 has motivated the introduction of the Messaging Layer Security (MLS) stand
 ard by the IETF which is based on a primitive called Continuous Group Key 
 Agreement (CGKA).This primitive allows a group of users to maintain a shar
 ed secret key that is frequently rotated by the group members in order to 
 change group membership\, achieve forward secrecy (FS) and post compromise
  security (PCS). Most protocols are based on binary trees where the nodes 
 are associated to a pair formed by public key and a secret key. Each leaf 
 corresponds to one of the group members and a user knows the secret keys a
 ssociated to nodes along the path from their leaf to the root. When a user
  wants to update their key material they have to change $ \\log(N) $ many 
 keys. This requires uploading $ \\log(N) $ many ciphertexts to communicate
  the new keys to the rest of the group members in a way that respects the 
 tree structure.In this thesis we study how much communication between grou
 p members is required in order to add and remove users from a group as wel
 l as in order to provide PCS when we consider CGKAs built using standard c
 ryptographic primitives like pseudo-random functions and public-key encryp
 tion. Furthermore\, we also consider the case of MLS and provide the first
  lower bound showing that its communication complexity is much worse than 
 previously believed\, i.e.\, it is very far from $ \\log(N) $. Finally\, w
 e also propose a variant of MLS which provably achieves the same security 
 properties with a much lower communication cost.
LOCATION:Moonstone Bldg / Ground floor / Seminar Room F (I24.EG.030f ) and 
 Zoom\, ISTA
ORGANIZER:
SUMMARY:Miguel Cueto Noval: Thesis Defense: Towards Efficient Secure Group 
 Messaging
URL:https://talks-calendar.ista.ac.at/events/6544
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1785744000@ist.ac.at
DTSTART:20260803T100000
DTEND:20260803T110000
DESCRIPTION:Speaker: Felix Pertl\nhosted by Georgios Katsaros\nAbstract: Co
 ntact electrification (CE) is a simple yet elusive phenomenon that occurs 
 when two materials come into contact and separate\, leaving behind net ele
 ctrical charge. Despite its ubiquity\, the microscopic origin of CE remain
 s unclear. In this thesis\, we investigate CE from three complementary per
 spectives: developing a quantitative method to measure charge at the nanos
 cale\, exploring the dynamic behavior of charge on insulating surfaces\, a
 nd uncovering the role of mechanical history in forming a triboelectric se
 ries.In the first part\, we establish a rigorous framework for converting 
 qualitative Kelvin probe force microscopy (KPFM) voltage maps into quantit
 ative charge density distributions. Using finite element method (FEM) simu
 lations\, we determine the point-spread function of the KPFM tip–sample 
 geometry and demonstrate that the true surface charge can be reconstructed
  by numerical deconvolution. This procedure enables the recovery of both t
 he magnitude and sign of charge density with high fidelity\, resolving nan
 oscale features that are otherwise obscured. Applying the method to contac
 t-charged SiO$_2$ surfaces\, we show that existing analytical approximatio
 ns\, such as parallel plate or spherical models\, can miscalculate charge 
 magnitude by orders of magnitude. Our hybrid FEM/KPFM approach therefore p
 rovides a fast and general method to convert qualitative KPFM signals into
  quantitative charge data\, enabling nanoscale charge mapping under realis
 tic experimental conditions.In the second part\, we study the temporal sta
 bility of CE-induced charges and identify the key material factors that de
 termine whether KPFM can capture meaningful charge patterns. Through time-
 resolved experiments combining a custom-built transfer system with both mi
 croscopic and macroscopic measurements\, we demonstrate that only the best
  insulators\, such as SiO$_2$\, preserve CE charge long enough for station
 ary imaging. For less conductive polymers\, such as PDMS\, charge decays w
 ithin the duration of a single KPFM scan due to bulk conduction. Using a s
 imple capacitor-based model\, we reproduce the observed decay dynamics and
  confirm that the transferred charge decays characteristic to the sample's
  bulk conductivity. Further\, we always observe homogeneous charge transfe
 r.In the third part\, we address the question: can we form a triboelectric
  series with identical materials? Using controlled repetitive contact expe
 riments\, we show that nominally identical materials can progressively ord
 er themselves into a triboelectric series\, where surfaces with more conta
 ct history charge negatively relative to fresher ones. By constructing a m
 inimal model based on this contact bias''\, we replicate the evolution fro
 m random to ordered charging observed in experiments. Supporting surface a
 nalyses\, including atomic force microscopy\, reveal that repeated contact
  induces nanoscale morphological changes\, suggesting a mechanism tightly 
 coupled to mechanical strain. These results highlight the crucial role of 
 surface history and nanoscale mechanics in dictating charge transfer\, mot
 ivating further exploration of mechanisms such as mechanochemical bond cle
 avage and flexoelectric polarization.
LOCATION:Sunstone Bldg / Ground floor / Big Seminar Room B (I23.EG.102)\, I
 STA
ORGANIZER:
SUMMARY:Felix Pertl: Thesis Defense: Experimental probing of nanoscale char
 ge features and surface morphology changes during tribocharging
URL:https://talks-calendar.ista.ac.at/events/6537
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1785744000@ist.ac.at
DTSTART:20260803T100000
DTEND:20260803T110000
DESCRIPTION:Speaker: Marek Randuch\nhosted by Michael Sixt\nAbstract: Root 
 growth inhibition (RG) by auxin and other cues (e.g. eATP\, RALF peptide) 
 involves rapid\, non-transcriptional pathways. Specific steps leading to g
 rowth inhibition are unclear. Notably\, the RG inhibition is associated wi
 th increases in cytosolic Ca2+\, plasma membrane depolarization and apopla
 st alkalization. However\, the causal relationship between them is unclear
 . To untangle these processes\, we utilized multiplexed reporter imaging 
 to observe pairwise the real-time dynamics of these three processes. Furth
 ermore\, we tested causal relationships. We employed microfluidics for rap
 id medium exchange and leveraged new optogenetically regulated channels. 
 Our comprehensive approach uncovered a network with tight feedback loops. 
 Results indicate that cytosolic Ca2+ serves as the universal initial signa
 l\, triggering both plasma membrane depolarization and subsequent apoplast
  alkalization following auxin perception. his conclusion provides a basis 
 for the fundamental regulatory mechanism governing growth but also opens q
 uestions about the molecular mechanisms behind it.
LOCATION:Office Bldg West / Ground floor / Heinzel Seminar Room (I21.EG.101
 ) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Marek Randuch: Thesis Defense: Fast growth responses in plants: Pho
 spho‐proteomic and growth regulation
URL:https://talks-calendar.ista.ac.at/events/6553
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1785934800@ist.ac.at
DTSTART:20260805T150000
DTEND:20260805T160000
DESCRIPTION:Speaker: Silvia Jamrichova\nhosted by Maria Ibáñez\nAbstract:
  A fundamental question in neuroscience is how the biophysical properties 
 of synapses shape higher network computations. The mossy fiber synapse is 
 a key synapse of the trisynaptic circuit of the hippocampus\, a brain regi
 on central to the encoding and retrieval of declarative memory. Its unique
  size\, large vesicle pool\, wide range of plasticity\, striking "detonato
 r" properties\, and involvement in several higher-order computations\, nam
 ely pattern separation and pattern completion\, make it an ideal model for
  studying synaptic mechanisms with direct relevance to memory and its impa
 irments.Despite extensive study over the years\, however\, key questions r
 emain unresolved: the molecular identity of the Ca² sensors driving its d
 istinct modes of release and plasticity\, and whether its fundamental prop
 erties are preserved in the human brain.Thanks to newly generated transgen
 ic mice and a method of direct presynaptic patch-clamp recordings from mos
 sy fiber boutons\, we used a combination of electrophysiological\, imaging
  and behavioral methods to investigate the role of synaptotagmins in timin
 g of transmission and plasticity at this synapse.We found that Syt1 is the
  primary Ca² sensor for synchronous release\, with a major trigger and mi
 nor clamping function of neurotransmitter release. Syt1 deletion led to an
  increase in asynchronous release converting the teacher synapse from a te
 mporally precise conditional detonator to an asynchronous one. Moreover\, 
 at the behavioral level\, desynchronized release selectively impaired patt
 ern completion\, while pattern separation remained intact\, demonstrating 
 that disruption of its precise timing and strength leads to selective impa
 irments in behaviorally relevant hippocampal computations in mice. Interes
 tingly\, our data did not support a proposed role for Syt7 in either async
 hronous release\, or facilitation or pool refilling\, leaving its function
  at this synapse enigmatic.Furthermore\, utilizing non-sclerotic tissue ob
 tained from temporal lobe epilepsy patients undergoing brain surgery\, we 
 discovered several notable species differences: human mossy fiber boutons 
 display larger vesicle pools and amplitude responses\, and — strikingly 
 — exhibit full detonator properties in CA3. Furthermore\, mossy fiber sy
 napses targeting CA4 neurons lack such properties\, suggesting a distinct 
 functional role at this projection.Together\, the findings presented in th
 is thesis shed light on the molecular mechanisms underlying information pr
 ocessing at the hippocampal mossy fiber synapse\, with implications for ou
 r understanding of memory\, and reveal both conserved and distinct synapti
 c properties between mice and humans\, suggesting that human mossy fibers 
 are not a simple scaled version of their rodent counterpart.
LOCATION:Central Bldg / O1 / Lecture Hall (I02.O1.014) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Silvia Jamrichova: Thesis Defense: Timing and strength of synaptic 
 transmission at hippocampal mossy fiber synapses in mice and humans
URL:https://talks-calendar.ista.ac.at/events/6570
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1786021200@ist.ac.at
DTSTART:20260806T150000
DTEND:20260806T160000
DESCRIPTION:Speaker: Peipeng Lin\nhosted by Charles Roques-Carmes\nAbstract
 : The hippocampal mossy fiber (MF) to CA3 pyramidal neuron synapse plays a
  key role in hippocampal information processing\, acting as a teacher syna
 pse that can conditionally drive postsynaptic firing and instruct informat
 ion storage in the downstream CA3 network. How the detonation properties o
 f this synapse are kept in check remains unclear. Our study demonstrates t
 hat CA3 stratum lucidum interneurons inhibit MF synaptic transmission via 
 presynaptic GABAB receptors. Pharmacological activation of these receptors
  by baclofen markedly reduced MF synaptic transmission\, switching the syn
 apse from a reliable conditional detonator into a coincidence-detecting su
 bdetonator. We identified a dual mechanism underlying this presynaptic inh
 ibition: a reduction in Ca² influx and\, more substantially\, a decrease 
 in the readily releasable pool of synaptic vesicles. Synaptically released
  GABA\, evoked by optogenetic stimulation of stratum lucidum interneurons 
 at in vivo-like frequencies\, produced comparable effects and further inte
 rfered with the stability of the short-term plasticity-associated vesicle 
 pool engram\, pointing to a physiological role for presynaptic inhibition.
  Expansion microscopy showed that interneuron terminals are positioned in 
 close proximity to MF boutons\, providing a structural basis for GABA spil
 lover onto presynaptic receptors. Together\, our findings reveal how inter
 neuron activity calibrates synaptic efficacy and plasticity at MF synapses
  through presynaptic inhibition\, with implications for memory encoding in
  the hippocampal trisynaptic circuit.
LOCATION:Central Bldg / O1 / Lecture Hall (I02.O1.014) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Peipeng Lin: Thesis Defense:  	Calibrating the Teacher Synapse: Mec
 hanisms and Functional Significance of Presynaptic Inhibition at Hippocamp
 al Mossy Fiber Synapses
URL:https://talks-calendar.ista.ac.at/events/6569
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1786606200@ist.ac.at
DTSTART:20260813T093000
DTEND:20260813T103000
DESCRIPTION:Speaker: Manjunath Javoor\nhosted by Rafal Klajn\nAbstract: Cel
 l motility depends on the protrusive force generated by the actin cytoskel
 eton at the leading edge of cells. In lamellipodia\, thin protrusions at t
 he front of migrating cells\, actin forms higher-order networks with versa
 tile physical properties. Previous studies have hinted at the presence of 
 different sub-populations of filaments and their spatial organization with
 in actin filament networks at the leading edge of migrating cells. Due to 
 limitations of existing experimental methods\, it has not been possible to
  fully describe the complexity of the actin filament populations involved 
 in protrusions at the leading edge.Cryo-electron tomography (cryo-ET) has 
 been used to describe the actin networks in cellular protrusions at single
  filament resolution in 3D. However\, these descriptions have been limited
  to 1-2 μm2 area of the protrusions\, providing merely snapshots of much 
 larger assemblies that span serval tens to hundreds of square microns area
 . Consequently\, they have not provided a holistic overview of the existin
 g variability within actin networks. We therefore lack a comprehensive und
 erstanding of how actin network geometries orchestrate cell migration.To a
 ddress these challenges\, I developed a montage cryo-electron tomography w
 orkflow to obtain three-dimensional views of lamellipodial regions coverin
 g areas of up to 100 μm2 at single-filament resolution. Seamless three-di
 mensional tomogram stitching is achieved by combining neural-network-based
  denoising strategies with novel optical-flow-based algorithms\, thereby p
 reserving filament continuity across large reconstructed volumes. Our comp
 utational analysis pipeline enabled us to vectorize all filaments within t
 hese volumes\, including filaments reaching lengths of up to 4 μm. The da
 ta generated here represent a valuable resource for the actin community\, 
 as they provide one of the most detailed and extensive three-dimensional d
 escriptions of actin filament architecture in the lamellipodium. Specifica
 lly\, they reveal accurate F-actin concentrations\, filament length distri
 butions\, connectivity\, and the spatial organization of filament sub-popu
 lations. These datasets can be used to support and constrain biophysical a
 nd theoretical models of actin network organization\, dynamics\, and force
  generation.
LOCATION:Sunstone Bldg / Ground floor / Big Seminar Room B / 63 seats (I23.
 EG.102) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Manjunath Javoor: Thesis Defense: Large-scale imaging of cellular a
 ctin networks at single-filament resolution using montage cryo-electron to
 mography
URL:https://talks-calendar.ista.ac.at/events/6576
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1786623300@ist.ac.at
DTSTART:20260813T141500
DTEND:20260813T151500
DESCRIPTION:Speaker: Vicente Luis Diaz Melian\nhosted by Kimberly Modic \nA
 bstract: When a Leidenfrost droplet floats on its own vapor layer\, the in
 terplay between vapor pressure\, surface tension\, and gravity determines 
 its shape\, and in the stable regime the underside of the droplet exhibits
  curvature inversion. Using interferometric imaging\, we observe a differe
 nt behavior for a levitated hydrogel sphere. Curvature inversion appears b
 riefly after deposition\, but the continuous vaporization process removes 
 this feature\, leading first to an oscillatory regime and eventually to a 
 steady state without curvature inversion. We demonstrate the essential rol
 e of vaporization in shaping the hydrogel underbelly\, where direct mass l
 oss has a stronger influence than the balance between vapor pressure and e
 lastic forces.
LOCATION:Central Bldg / O1 / Lecture Hall (I02.O1.014) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Vicente Luis Diaz Melian: Thesis Defense: The morphology underneath
  a levitated hydrogel sphere
URL:https://talks-calendar.ista.ac.at/events/6561
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1786975200@ist.ac.at
DTSTART:20260817T160000
DTEND:20260817T170000
DESCRIPTION:Speaker: Kevin Kögler\nhosted by Krzysztof Pietrzak\nAbstract:
  Modern datasets often contain as many variables as observations\, or many
  more\, making classical statistical tools difficult to apply and standard
  machine-learning models hard to understand. To address this problem\, thi
 s thesis develops methods for inference and compression in this high-dimen
 sional regime\, centered on approximate message passing (AMP)\, a family o
 f iterative inference algorithms which are conjecture to be optimal for ma
 ny of these problems.First\, we introduce rotationally invariant generaliz
 ed AMP (RI-GAMP)\, extending AMP beyond independent Gaussian design matric
 es to a broad class of matrices with complex correlations and arbitrary li
 miting spectra. We characterize its performance rigorously through state e
 volution and show that it approaches the performance of Vector AMP while a
 voiding its computationally expensive singular-value decomposition.We then
  study nonlinear autoencoders when the input and compressed dimensions gro
 w proportionally. For Gaussian data\, we derive fundamental limits for one
 -bit compression by shallow two-layer autoencoders\, characterize their op
 timal solutions\, and prove that gradient methods reach them. For structur
 ed data\, however\, a shallow linear decoder may ignore information such a
 s sparsity and behave exactly as it does for Gaussian inputs. Adding nonli
 nearities or depth overcomes this limitation: deeper decoders can learn co
 mputations closely related to AMP and approach optimal reconstruction for 
 a fixed encoder.Finally\, we apply these ideas to predict plasma-protein a
 bundance from UK Biobank individual-level genetic data\, using approximate
 ly 8.4 million genetic variants from roughly 40\,000 individuals. A two-st
 age genetic Vector AMP pipeline first selects a small set of predictive ge
 nomic regions and then fits more detailed linear or tree-based models. Com
 bined with a one-hot representation of the genotype data\, this procedure 
 closes the previously reported average gap between linear and deep-learnin
 g prediction and improves prediction for many proteins in a proteome-wide 
 comparison. 
LOCATION:Office Bldg West / Ground floor / Heinzel Seminar Room (I21.EG.101
 ) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Kevin Kögler: Thesis Defense: Compression and Inference in High Di
 mensions: An Approximate Message Passing Perspective
URL:https://talks-calendar.ista.ac.at/events/6577
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1788163200@ist.ac.at
DTSTART:20260831T100000
DTEND:20260831T110000
DESCRIPTION:Speaker: Anastasiia Teplova\nhosted by Martin Loose\nAbstract: 
 This thesis comprises two parts addressing distinct questions in plant sig
 nalling. Part I examines the proposed nucleotide-cyclase activities of pro
 teins involved in plant hormone signalling. Part II investigates how plant
 s sense gravity and how this information is translated into a directional 
 growth response.In this thesis defense talk\, I will focus on the second p
 art and present my research on the molecular mechanisms underlying root gr
 avitropism. Gravity is perceived in specialized cells called statocytes\, 
 where starch-filled amyloplasts sediment according to the direction of gra
 vity. This leads to auxin redistribution\, which drives differential growt
 h and allows the root to bend towards gravity. LZY proteins provide an imp
 ortant molecular link between statolith sedimentation and the establishmen
 t of cell polarity. However\, how LZY polarity is connected to the downstr
 eam regulation of auxin transport remains incompletely understood.My work 
 investigates this connection\, focusing on the dynamic localization and po
 larization of proteins in root statocytes following root reorientation. In
  particular\, I examine the relationship between LZY proteins and two pote
 ntially interconnected systems: AGC kinases involved in regulating PIN aux
 in transporter activity\, and the RLD–GNOM machinery involved in membran
 e trafficking and PIN polarity. I show that components of both systems dyn
 amically redistribute during the gravitropic response and investigate thei
 r connections with LZY proteins and with each other. Together\, these resu
 lts contribute to understanding how gravity-induced cell polarity is conne
 cted to the regulation of auxin transport during root gravitropism.
LOCATION:Sunstone Bldg / Ground floor / Big Seminar Room B (I23.EG.102) and
  Zoom\, ISTA
ORGANIZER:
SUMMARY:Anastasiia Teplova: Thesis Defense: Chasing the elusive: Investigat
 ing nucleotide cyclase activity in gibberellin and strigolactone signallin
 g\; Cellular mechanisms of gravity sensing and response in roots
URL:https://talks-calendar.ista.ac.at/events/6593
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1788253200@ist.ac.at
DTSTART:20260901T110000
DTEND:20260901T120000
DESCRIPTION:Speaker: Stepan Ovchinnikov\nhosted by Johannes Fink\nAbstract:
  Bacterial adaptation depends not only on the selective environment but al
 so on the genetic background that determines which variants can arise and 
 how they affect fitness. This thesis investigates how genetic background a
 ffects bacterial adaptive capacity by experimentally examining the effect 
 of insertion sequence (IS) elements activity and establishing a strain sys
 tem for future experiments to reveal the role of natural competence.The ma
 in experimental study compared Escherichia coli MG1655 with a derivative l
 acking all 45 chromosomal IS elements\, together with additional strains d
 esigned to separate the effects of IS removal from restoration of the IS-d
 isrupted gene wbbL. Replicate populations were adapted to increasing conce
 ntrations of a five-antibiotic mixture and to each antibiotic individually
 \, and their adaptive responses and evolutionary routes were compared. Und
 er mixture selection\, IS-containing and IS-free populations reached simil
 ar endpoint resistance and acquired similar numbers of mutations\, althoug
 h their mutation spectra differed significantly. IS-driven mutations were 
 rare\, indicating that IS activity contributed little to adaptation under 
 this condition. Adaptation to individual antibiotics produced larger treat
 ment-specific resistance gains and more recurrent mutations in the same lo
 ci across independently evolved populations than adaptation to the antibio
 tic mixture. The contribution of IS-driven mutations varied among antibiot
 ics and was highest under tetracycline selection. Under tetracycline treat
 ment\, IS-containing populations adapted faster and reached higher selecti
 on concentrations than IS-free populations. Inactivation of wbbL partially
  restored the adaptive capacity of the IS-free strain but did not fully el
 iminate the difference\, while IS-containing populations repeatedly access
 ed IS-mediated mutations unavailable to the IS-free strains.Earlier experi
 ments examining adaptation to ethanol\, sodium chloride\, and butanol did 
 not provide reliable evidence for differences between the IS backgrounds. 
 Growth observed at high sodium chloride and butanol concentrations during 
 selection was not retained after stress-free recovery\, whereas turbidosta
 t-based ethanol experiments revealed technical limitations of using the de
 vice for parallel long-term evolution. These results motivated the more ro
 bust antibiotic-selection design. Finally\, an experimental framework was 
 developed to test whether natural competence contributes to the adaptive c
 apacity of Bacillus subtilis. As a first step toward the proposed experime
 nts\, a genotypically verified ΔcomEC strain and characterized fluorescen
 t strains were constructed\, but the evolution experiments remain to be in
 itiated.Together\, these results show that IS elements can expand the repe
 rtoire of accessible mutations without conferring a universal adaptive adv
 antage. Whether IS activity improves adaptation depends on the selective e
 nvironment\, the wider genetic background\, and whether IS-mediated mutati
 ons provide particularly beneficial adaptive routes.
LOCATION:Central Bldg / O1 / Ballroom (I01.O1.006) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Stepan Ovchinnikov: Thesis Defense: The Role of Genetic Background 
 in Bacterial Adaptation
URL:https://talks-calendar.ista.ac.at/events/6601
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1788267600@ist.ac.at
DTSTART:20260901T150000
DTEND:20260901T160000
DESCRIPTION:Speaker: Jonas Ingmanns\nhosted by Monika Henzinger\nAbstract: 
 Precise microscopic models of physical processes are often too complex to 
 be useful for understanding or simulating phenomena on a macroscopic scale
 . The complexity can be drastically reduced if there is a suitable approxi
 mation which still accurately captures the effective large-scale behavior 
 of the underlying model. This thesis contains contributions to the rigorou
 s justification of such large-scale approximations  or three different mo
 dels. Chapter 2 presents joint work with Federico Cornalba\, Julian Fisch
 er\, and Claudia Raithel. We consider a large system of weakly interacting
  particles\, driven by independent Brownian motions. The physicists Dean a
 nd Kawasaki proposed a strongly singular SPDE to describe fluctuations of 
 the particle density. However\, without a suitable regularization\, the De
 an–Kawasaki equation has been shown to be ill-posed in the sense that it
  does not admit martingale solutions for any continuous initial data. We s
 how that a structure-preserving discretization of the Dean–Kawasaki equa
 tion – acting as a suitable regularization – captures the density fluc
 tuations of the particle system up to arbitrary order in the inverse numbe
 r of particles and a discretization error. Chapter 3 presents joint work 
 with Elisa Davoli and Lorenza D’Elia. We consider a magnetic body consis
 ting of a composite material with a random microstructure. The oscillating
  magnetic properties are encoded in the micromagnetic energy functional wh
 ich is restricted to functions taking values on the sphere\, governing the
  observable states of magnetization. We obtain a qualitative stochastic ho
 mogenization result in the form of Γ-convergence. The Γ-limit is a micro
 magnetic energy functional with constant\, deterministic coefficients\, me
 aning that the magnetic body can be treated as if consisting of a single m
 aterial when the microstructure is small enough. On a technical level\, we
 obtain an analogous result replacing the sphere with other sufficiently re
 gular manifolds.Chapter 4 and Chapter 5 present joint work with Julian Fis
 cher. We consider interface motions driven by curvature and a uniform forc
 ing through a stationary field of possibly impenetrable random obstacles s
 atisfying a finite range of dependence assumption. This process models\, e
 .g.\, the motion of dislocation lines or magnetic domain boundaries in mat
 erials with inhibiting impurities. In Chapter 5\, for dimension  = 2\, we 
 introduce an easy-to-check criterion for general obstacle fields which imp
 lies ballistic behavior. More precisely\, this criterion yields an almost 
 guaranteed effective minimum speed on large scales for the interface motio
 n \, with ‘effective’ meaning that enclosures left behind a main front
  can be ignored. In Chapter 4\, for any dimension  ≥ 2\, assuming such a
 n almost guaranteed effective minimum speed\, we obtain a quantitative sto
 chastic homogenization result in any dimension\, proving that the main fro
 nt can be approximated with a constant-speed motion on large scales.
LOCATION:Office Bldg West / Ground floor / Heinzel Seminar Room (I21.EG.101
 ) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Jonas Ingmanns: Thesis Defense: On the large-scale behavior of inte
 racting particle systems\, composite magnetic materials\, and interface mo
 tions through random obstacle fields
URL:https://talks-calendar.ista.ac.at/events/6560
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1788433200@ist.ac.at
DTSTART:20260903T130000
DTEND:20260903T140000
DESCRIPTION:Speaker: Nathalie Gruber\nhosted by Jérémie Palacci\nAbstract
 : Bacteria inhabit an extraordinary range of environments\, each shaped by
  its own selective pressures that can fluctuate within seconds to seasons.
  A persistent selective pressure across these environments is imposed by v
 iruses that infect bacteria\, called phages. This ongoing coevolution betw
 een bacteria and phages has led to multiple defense strategies on both sid
 es. Bacteria have defense strategies at multiple levels: at the cell surfa
 ce\, physical barriers such as capsules\, exopolysaccharides\, and recepto
 r modifications limit phage adsorption\, while intracellularly\, molecular
  defense systems degrade or restrict invading genomes. However\, how these
  spatially distinct layers are coordinated during infection remains largel
 y unexplored.To address this\, we investigated the genome-clustered anti-p
 hage defense island of Escherichia coli K-12\, which encodes four anti-pha
 ge systems. We found that a single system dominated intracellular defense 
 across diverse phages. Strikingly\, under sustained phage pressure\, a sec
 ond extracellular layer of defense emerges: phage-induced mucoidy. This is
  a regulator of capsule synthesis (Rcs)-dependent and quorum-sensing-indep
 endent response that generates protective extracellular matrix. This mucoi
 d matrix confers broad resistance\, protecting against 29 of the 31 phages
  tested. Critically\, the two layers are not independent\; the strength of
  the defense system-mediated restriction directly sets the phage dose thre
 shold at which mucoidy is induced. Therefore\, intracellular and extracell
 ular defenses do not operate in isolation but as a single\, quantitatively
  coupled immune response.By revealing a direct mechanistic link between in
 tracellular anti-phage systems and phenotypic switching to mucoidy\, this 
 work reframes bacterial immunity as an integrated\, multi-layered process\
 , with broad implications for phage–host coevolution and for the design 
 of phage therapies against mucoid variants\, which are associated with inc
 reased patient mortality.
LOCATION:Central Bldg / O1 / Ballroom (I01.O1.006) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Nathalie Gruber: Thesis Defense: Genetic Strategies Enabling Bacter
 ial Adaptation to Selective Pressures
URL:https://talks-calendar.ista.ac.at/events/6591
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1788508800@ist.ac.at
DTSTART:20260904T100000
DTEND:20260904T110000
DESCRIPTION:Speaker: Andreas Ehrmann\nhosted by Paul Schanda\nAbstract: Bio
 logy is overwhelmingly good at designing building blocks that are orchestr
 ated in remarkable processes to enable the functioning of complex organism
 s. Is it possible to achieve similar complexity in nanotechnology? The fie
 ld of self-assembly offers a promising route towards bio-inspired function
 ality. While significant progress has been made in the inverse design of c
 omplex structures\, little is currently known about embedding these struct
 ures with dynamics and functional behavior at levels found in biology. Unl
 ike biology\, we do not have million years of evolution to result in optim
 al behavior. We aspire to discover fundamental design principles in simple
  physical systems by taking an optimization approach that builds up on met
 hods developed by the Machine Learning community to achieve a desired func
 tion. Many future nanotechnologies will need to do more than hold a desig
 ned shape: they will need to move\, switch states\, and interact with othe
 r objects in controlled ways. Is it possible to replicate the precise\, ta
 rgeted energy delivery of ATP hydrolysis in synthetic systems\, where we c
 annot rely on biochemical interactions\, to power synthetic nanomachines? 
 In this thesis\, we develop a mechanical model for a controlled energy-del
 ivery mechanism between bistable nanostructures\, and discover key design 
 features necessary to generate a pathway for efficient energy transduction
 . Inspired by the universality of ATP hydrolysis\, this achievement could 
 serve as a scheme for powering more and more complex tasks. We show how bi
 stable nanostructures can be designed so that their conformational changes
  produce a prescribed behavior. By separating the energetic control of a n
 anoscale switch from the geometric placement of its binding sites\, we ide
 ntify which aspects of its energy landscape can be programmed under realis
 tic constraints. The results provide design principles for turning synthet
 ic nanostructures into functional\, machine-like objects. By demonstrating
  how we can translate the scheme for energy delivery to three-state molecu
 lar machines walking along a track at a very basic level\, we take a first
  step towards performing a task. We reveal a fundamental speed-efficiency 
 tradeoff and important design considerations. This research contributes to
 wards designing nanomachines that might eventually be able to contest with
  the levels of complexity and functionality found in biology.
LOCATION:Central Bldg / O1 / Mondi 2a (I01.O1.008)\, ISTA
ORGANIZER:
SUMMARY:Andreas Ehrmann: Thesis Defense: Biological functionality without b
 iochemistry: designing nanomachines for target behavior 
URL:https://talks-calendar.ista.ac.at/events/6578
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1788951600@ist.ac.at
DTSTART:20260909T130000
DTEND:20260909T140000
DESCRIPTION:Speaker: Andrea Stöllner\nhosted by Jorryt Matthee\nAbstract: 
 Charge accumulation on aerosol particles plays an important role in a vari
 ety of natural and industrial processes. An example is cloud electrificati
 on\, in which collisions between ice crystals and graupel cause large amou
 nts of charge to be exchanged between airborne particles. Optical tweezers
  are a highly specialized tool that can hold a single micrometer-sized air
 borne particle stably in the same position over weeks while measuring its 
 electric charge with elementary-charge resolution. In this work\, we show 
 that the trapping laser can also be used to give charge to the micropartic
 le. Via a two-photon process the particle acquires more and more positive 
 charge\, enabling us to study its electrical behavior from uncharged up to
  multiple hundred elementary charges. By studying the dynamics of such hig
 hly charged particles over days and weeks we find that they spontaneously 
 undergo microdischarges which range from just a few to several hundred ele
 mentary charges. We show that these discharges are triggered by cosmic-ray
  muons which pass through the air close to the particle and supply the ion
 s needed to cause charge loss. Our findings highlight the potential of aer
 osol optical tweezers to provide new insights into microscale charging and
  discharging phenomena\, with implications for both fundamental studies an
 d atmospheric electrification processes.
LOCATION:Central Bldg / O1 / Mondi 3 (I01.O1.010)\, ISTA
ORGANIZER:
SUMMARY:Andrea Stöllner: Thesis Defense: Microscale Electrical Behavior of
  Highly Charged Individual Aerosol Particles Using Optical Tweezers
URL:https://talks-calendar.ista.ac.at/events/6572
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1790074800@ist.ac.at
DTSTART:20260922T130000
DTEND:20260922T180000
DESCRIPTION:Abstract: We are excited to announce the 2nd annual Neuroscienc
 e Faculty Symposium organized by your student neuroscience track represent
 atives!Every neuroscience PI will hold a brief talk discussing their lab'
 s current research. The symposium will include catered breaks! Please als
 o join us for the Pizza Reception following the talks.We look forward to 
 seeing you all there!
LOCATION:Raiffeisen Lecture Hall\, ISTA
ORGANIZER:
SUMMARY:Neuroscience Faculty Symposium
URL:https://talks-calendar.ista.ac.at/events/6589
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1792396800@ist.ac.at
DTSTART:20261019T100000
DTEND:20261019T110000
DESCRIPTION:Speaker: Adrijana Smoljan\nhosted by Andela Saric\nAbstract: Th
 e successful colonization of terrestrial environments by plants required t
 he evolution of developmental and signalling mechanisms that enabled adapt
 ation to increasingly heterogeneous environments. Among these innovations\
 , environmental sensing and directional transport of the plant hormone aux
 in have played central roles in shaping plant morphology and adaptation to
  external cues. However\, the evolutionary origins of these regulatory sys
 tems remain incompletely understood. This thesis investigates two fundamen
 tal evolutionary questions: when auxin transport mediated by PIN auxin tra
 nsporters emerged during plant evolution and how MIZ1 proteins acquired th
 eir role in root hydrotropism.The first part of the thesis examines the ev
 olution of PIN-FORMED (PIN) auxin transporters using chlorophyte algae and
  other early-diverging eukaryotic lineages. Physiological analyses demonst
 rated that chlorophyte algae exhibit concentration-dependent responses to 
 exogenous auxin and possess both passive and energy-dependent auxin transp
 ort systems\, indicating that fundamental aspects of auxin biology predate
  the emergence of land plants. Phylogenetic\, structural\, and functional 
 analyses revealed that PIN homologs are broadly distributed across diverse
  eukaryotic lineages and retain the characteristic PIN protein fold and pr
 edicted auxin-binding residues. However\, heterologous expression assays i
 n Xenopus laevis oocytes\, tobacco BY-2 cells\, and Arabidopsis thaliana d
 emonstrated that these ancestral PIN homologs lack the directional auxin e
 xport activity characteristic of canonical land plant PIN proteins. Instea
 d\, they predominantly localize to the endoplasmic reticulum and display l
 imited or no auxin transport activity\, suggesting that ancestral PIN prot
 eins primarily functioned in intracellular auxin homeostasis before being 
 recruited for polar auxin transport during land plant evolution.The second
  part of the thesis investigates the evolutionary diversification of MIZ1 
 proteins\, key regulators of root hydrotropism in Arabidopsis thaliana. Ph
 ylogenetic analyses showed that MIZ1 proteins are conserved throughout lan
 d plants but absent from green algae\, indicating that the protein family 
 originated early during terrestrialization. Although MIZ1 homologs from Ma
 rchantia polymorpha\, Physcomitrium patens\, Selaginella moellendorffii\, 
 and Amborella trichopoda displayed highly conserved predicted structures a
 nd endoplasmic reticulum localization\, none were able to complement the h
 ydrotropic or cytokinin-response defects of the Arabidopsis miz1 mutant. F
 unctional characterization of Marchantia revealed that MpMIZ1a regulates t
 hallus development\, cytokinin-dependent growth responses\, expression of 
 cytokinin biosynthetic genes\, and normal sporophyte development\, indicat
 ing an ancestral role in cytokinin homeostasis and developmental regulatio
 n rather than hydrotropism. Furthermore\, protein docking predicted an int
 eraction between MpMIZ1a and its native cytokinin receptor MpCHK\, which w
 as supported experimentally by bimolecular fluorescence complementation (B
 iFC). BiFC revealed interactions between the cognate protein pairs MpMIZ1a
 –MpCHK and AtMIZ1–AtAHK4\, whereas little or no interaction was detect
 ed for the reciprocal cross-species combinations MpMIZ1a–AtAHK4 and AtMI
 Z1–MpCHK. This species-specific interaction compatibility provides a pot
 ential mechanistic explanation for the inability of MpMIZ1a to functionall
 y complement the Arabidopsis miz1 mutant. Together\, the findings present
 ed in this thesis demonstrate that both auxin transport and MIZ1 protein f
 unction evolved through the progressive modification and recruitment of an
 cestral molecular components. The results support a model in which early P
 IN proteins primarily regulated intracellular auxin homeostasis before evo
 lving into specialized plasma membrane auxin exporters\, while MIZ1 protei
 ns originated as endoplasmic reticulum-associated regulators of cytokinin-
 dependent development and were subsequently recruited into the hydrotropic
  signalling pathway of seed plants. By integrating comparative genomics\, 
 structural biology\, molecular genetics\, live-cell imaging\, and physiolo
 gical analyses across diverse evolutionary lineages\, this work provides n
 ew insights into the molecular innovations that contributed to the success
 ful colonization of terrestrial environments and the evolution of developm
 ental plasticity in land plants.
LOCATION:Central Bldg / O1 / Mondi 2a (I01.O1.008)\, ISTA
ORGANIZER:
SUMMARY:Adrijana Smoljan: Thesis Defense: Evolution of auxin transport and 
 MIZ1-mediated developmental responses during plant adaptation to terrestri
 al environments
URL:https://talks-calendar.ista.ac.at/events/6666
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1792494000@ist.ac.at
DTSTART:20261020T130000
DTEND:20261020T140000
DESCRIPTION:Speaker: Yuri Ignatyev\nhosted by Beatriz Vicoso\nAbstract: The
  spinal cord plays a central role in sensorimotor behavior\, integrating s
 ensory input and descending commands from the brain to generate movement. 
 Like the brain\, it is composed of diverse populations of excitatory and i
 nhibitory neurons. Over the course of evolution\, vertebrates have adapted
  to new environments and evolved distinct body plans\, yet it remains uncl
 ear how the neuronal architecture of the spinal cord has changed to suppor
 t these adaptations. Advances in single-cell genomics have made it possibl
 e to characterize neuronal diversity at single-cell resolution\, but in th
 e spinal cord such data are largely limited to mammals. To address this ga
 p and understand how spinal neuronal diversity has evolved\, this thesis c
 ompares spinal cell types across vertebrates\, including zebrafish\, frog\
 , lizard\, mouse and human.First\, we generate a single-cell transcriptomi
 c atlas of the developing spinal cord of the amphibian Xenopus laevis and 
 compare it with mouse developmental data. This reveals a highly conserved 
 developmental framework across tetrapods\, including conservation of the m
 ajor cardinal classes\, their spatial distributions and temporal subdivisi
 ons.Second\, we extend this comparison to the adult spinal cord by generat
 ing a single-cell and spatial transcriptomic atlas of the frog spinal cord
  and comparing it with mouse and human data. In contrast to development\, 
 we find marked divergence between amphibians and mammals\, largely restric
 ted to dorsal excitatory interneurons of the superficial dorsal horn\, inc
 luding several mammalian-specific populations. Adding zebrafish further su
 pports the dorsal excitatory compartment as a major site of species-specif
 ic diversification.Finally\, we characterize the adult spinal cord of the 
 lizard Pogona vitticeps to test whether these populations are specific to 
 mammals or shared across amniotes. This analysis further supports their ma
 mmalian specificity and links them to late-born dorsal lineages.Together\,
  these findings suggest that the spinal cord is built on a largely conserv
 ed developmental framework\, whereas adult neuronal diversity has diverged
  selectively in the dorsal spinal cord. The superficial dorsal spinal cord
  thus emerges as a recently evolved hub for sensory integration in mammals
 .
LOCATION:Office Bldg West / Ground floor / Heinzel Seminar Room (I21.EG.101
 ) and Zoom\, ISTA
ORGANIZER:
SUMMARY:Yuri Ignatyev: Thesis Defense: Deciphering spinal interneuron heter
 ogeneity across vertebrate evolution
URL:https://talks-calendar.ista.ac.at/events/6691
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1794216600@ist.ac.at
DTSTART:20261109T103000
DTEND:20261109T113000
DESCRIPTION:Speaker: Chao Shen\nhosted by Maximilian Jösch\nAbstract: It i
 s a basic property of electromagnetic waves that they propagate. Yet the i
 mplications of this fact are often glossed over when it comes to nonlinear
  terahertz (THz) spectroscopy of bulk dielectrics\, with propagation effec
 ts being given marginal attention. In thick samples\, the THz fields\, opt
 ical probe\, and nonlinear polarization all propagate with different veloc
 ities\, experiencing different dispersion\, absorption and birefringence. 
 This gives rise to complicated nonlinear optical interactions prone to mis
 interpretation in the absence of a comprehensive theoretical framework. Th
 is thesis combines two-dimensional THz Kerr-effect spectroscopy (2D-TKE)\,
  two-dimensional THz-field-induced second-harmonic generation (2D-TFISH)\,
  and propagation-resolved numerical modeling to interpret time-resolved TH
 z-pump/optical-probe spectroscopies and track nonlinear THz polariton tran
 sport in bulk dielectrics.In birefringent LaAlO$_3$\, we use 2D-TKE data a
 nd four-wave-mixing simulations to separate propagation-induced electronic
  features from the intrinsic Raman-mediated Kerr response. We unambiguousl
 y identify the $0.86~\\mathrm{THz}$ and $0.36~\\mathrm{THz}$ oscillations 
 in TKE as arising from phase-matched co- and counter-propagating THz-pump/
 optical-probe coupling\, whereas the $1.1~\\mathrm{THz}$ oscillation arise
 s from the $E_g$ Raman phonon in LaAlO$_3$ excited through THz two-photon 
 absorption.In KTaO$_3$\, we identify the origin of the non-oscillatory par
 t of the TFISH signal by combining single-pulse and 2D-TFISH measurements 
 with simulations based on a Maxwell--Duffing model. We show that propagati
 ng soft-mode polaritons produce non-local transient polarization inside th
 e sample. Spatial integration of the TFISH response at different locations
  acts to single out a polariton mode with a wavevector corresponding to th
 e phase mismatch between the probe and its second harmonic. A Maxwell--Duf
 fing model reproduces the temperature and field-strength dependence of bot
 h the single-pulse and 2D-TFISH signals\, showing that the non-oscillatory
  component arises purely from nonlinear polariton propagation effects with
 out invoking transient ferroelectricity. The 2D data also rule out the pro
 posed mechanisms based on relaxational polar nanoregions or hot phonons.Fi
 nally\, we develop a spatiotemporal method for tracking soft-mode phonon-p
 olariton transport in bulk SrTiO$_3$ using 2D-TKE. The nonlinear Kerr sign
 al is shown to probe the spatial overlap between two independent polariton
 ic wave packets. Then\, using the less anharmonic $A_{2u}$ polariton as a 
 moving reference\, we track the field-dependent evolution of $E_u$ polarit
 ons. We observe that anharmonic effects lead to the formation of additiona
 l polarization accumulation near the sample entrance and an approximately 
 30\\% increase in the effective velocity of the leading peak of the $E_u$ 
 polariton. A minimal Maxwell--Duffing model captures many qualitative feat
 ures of the 2D-TKE signal\, including the entrance-layer response\, but pr
 edicts a substantially weaker velocity renormalization than observed exper
 imentally. These results establish 2D-TKE as a protocol to trace field-tun
 able polariton transport in an anharmonic medium\, while revealing behavio
 r beyond the Maxwell--Duffing description.Together\, these results establi
 sh propagation as a crucial part of understanding nonlinear THz spectrosco
 py of bulk dielectrics. Propagation effects can mimic intrinsic material r
 esponse but\, when identified\, become a sensitive probe of nonlinear latt
 ice dynamics and transport in quantum materials.
LOCATION:Sunstone Bldg / Ground floor / Big Seminar Room A (I23.EG.102) \, 
 ISTA
ORGANIZER:
SUMMARY:Chao Shen: Propagation-Resolved Nonlinear Terahertz Spectroscopy of
  Bulk Dielectrics
URL:https://talks-calendar.ista.ac.at/events/6683
END:VEVENT
BEGIN:VEVENT
DTSTAMP:20261012T171652Z
UID:1796374800@ist.ac.at
DTSTART:20261204T100000
DTEND:20261204T110000
DESCRIPTION:Speaker: Aleksander Bena\nhosted by Calin Guet\nAbstract: Trans
 ition-metal catalysis has transformed modern organic synthesis\, enabling 
 the efficient and selective formation of chemical bonds. The success of th
 is field largely depended on the development of tailored ligands that can 
 tune the reactivity of the metal center. Nickel catalysis has emerged as a
  particularly versatile platform for cross-coupling reactions\, thanks to 
 its ability to access multiple oxidation states. However\, the instability
  of paramagnetic nickel species can make these reactions difficult to cont
 rol. Despite the central role of ligands in transition-metal catalysis\, t
 heir use in tuning the reactivity of such nickel intermediates remains com
 paratively underexplored. Modular amino-functionalized bipyridine ligands
  were developed to control the reactivity of Ni(I) intermediates and facil
 itate challenging elementary steps in cross-coupling catalysis. This appro
 ach facilitated carbon-carbon and carbon-heteroatom bond formation via Ni(
 I)/Ni(III) catalytic pathways. Notably\, a new ligand-design facilitated v
 isible-light induced C(sp²)-heteroatom cross-coupling reactions\, elimina
 ting the need for an additional photocatalyst and enabling the coupling of
  a broad range of nitrogen-\, oxygen-\, sulfur- and phosphorus-based nucle
 ophiles with challenging aryl electrophiles\, using unprecedented low cata
 lyst loadings.
LOCATION:Sunstone Bldg / Ground floor / Lab Meeting room (I23.EG.005)\, IST
 A
ORGANIZER:
SUMMARY:Aleksander Bena: Tuning the Catalytic Reactivity of Ni(I) through L
 igand Design
URL:https://talks-calendar.ista.ac.at/events/6689
END:VEVENT
END:VCALENDAR
