M. A. Veksler

ORCID: 0000-0001-7100-1439
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About
Contact & Profiles
Research Areas
  • Analytical Chemistry and Chromatography
  • Field-Flow Fractionation Techniques
  • Constraint Satisfaction and Optimization
  • Chromatography in Natural Products
  • Computational Drug Discovery Methods
  • Statistical and Computational Modeling
  • Process Optimization and Integration
  • Engineering Technology and Methodologies
  • Surface Chemistry and Catalysis
  • Crystallization and Solubility Studies
  • Logic, Reasoning, and Knowledge
  • Advanced Data Processing Techniques
  • Advanced biosensing and bioanalysis techniques
  • AI-based Problem Solving and Planning
  • Veterinary medicine and infectious diseases
  • Metamaterials and Metasurfaces Applications
  • Engineering Diagnostics and Reliability
  • Supramolecular Self-Assembly in Materials
  • Advanced Statistical Process Monitoring
  • Polymer Synthesis and Characterization
  • Chemical Synthesis and Analysis
  • Optimal Experimental Design Methods
  • Electrostatics and Colloid Interactions
  • Pigment Synthesis and Properties
  • Parallel Computing and Optimization Techniques

University of Michigan
2020-2023

BioSurfaces (United States)
2020-2023

Technion – Israel Institute of Technology
2010-2016

IBM Research - Haifa
2005

Chemical Pharmaceutical Research Institute
1968-1975

N.D. Zelinsky Institute of Organic Chemistry
1974

Moscow Technological Institute
1973

Planta
1972

Novokuznetsk State Institute of Advanced Medical Education
1971

Complex chiral particles Synthetic colloids are usually smooth, but nature can produce micrometer-scale with intricate structure and shape, such as the coccoliths produced by algae. Jiang et al. controlled self-assembly of gold–cysteine nanoplatelets into a variety chiral, hierarchically organized colloidal changing fraction cysteine nucleation temperature. Organic cations created electrostatic repulsions that favored edge assembly nanoplatelets, which in turn could create surfaces bearing...

10.1126/science.aaz7949 article EN Science 2020-04-09

Chiral nanostructures have been extensively studied for bioanalysis and optoelectronics because of their high rotatory optical activity but not enantioselective catalysis the chirality mismatch geometric scales. Here, we investigate whether catalytic supraparticles (SPs) made from ZnS NPs could provide a general pathway to reconcile difficulties. SPs synthesized by two different pathways enantioselectively oxidize tyrosine (Tyr). Upon illumination with 300–450 nm photons, convert Tyr into...

10.1021/acsenergylett.0c02537 article EN ACS Energy Letters 2021-03-22

Nanoscale chirality is an actively growing research field spurred by the giant chiroptical activity, enantioselective biological and asymmetric catalytic activity of chiral nanostructures. Compared to molecules, handedness nano- microstructures can be directly established via electron microscopy, which utilized for automatic analysis nanostructures prediction their properties. However, in complex materials may have multiple geometric forms scales. Computational identification from microscopy...

10.1021/acsnano.2c12056 article EN ACS Nano 2023-04-14

10.1016/j.artint.2016.06.002 article EN publisher-specific-oa Artificial Intelligence 2016-06-17

PCS is a CSP solver that can produce machine-checkable deductive proof in case it decides the input problem unsatisfiable. The roots of may be nonclausal constraints, whereas rest based on resolution signed clauses, ending with empty clause. uses parameterized, constraint-specific inference rules order to bridge between and clausal parts proof. consequent each such rule clause 1) logically implied by premise, 2) strong enough premise consecutive steps. process itself integrated learning...

10.1609/aaai.v24i1.7543 article EN Proceedings of the AAAI Conference on Artificial Intelligence 2010-07-03

Chirality of helical objects, exemplified by nanostructured inorganic particles, has unifying importance for many scientific fields. Their handedness can be determined visually, but its identification analysis electron microscopy images is fundamentally difficult because (1) image features differentiating left- and right-handed particles ambiguous ancillary, (2) three-dimensional particle structure essential chirality 'flattened' into two-dimensional projections. Here we show that deep...

10.26434/chemrxiv-2022-4pv1z preprint EN cc-by-nc 2022-07-19

Abstract Nicodin (II) wird durch Umsetzung von Nicotinamid (I) mit Formaldehyd her gestellt.

10.1002/chin.197135328 article DE Chemischer Informationsdienst Organische Chemie 1971-08-31
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