Vijayanand Chandrasekaran

ORCID: 0000-0002-8314-8611
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Research Areas
  • Advanced Chemical Physics Studies
  • Astrophysics and Star Formation Studies
  • Photochromic and Fluorescence Chemistry
  • Astro and Planetary Science
  • Atomic and Molecular Physics
  • Click Chemistry and Applications
  • Molecular Spectroscopy and Structure
  • Photoreceptor and optogenetics research
  • Carbohydrate Chemistry and Synthesis
  • Atmospheric Ozone and Climate
  • Chemical Synthesis and Analysis
  • Mass Spectrometry Techniques and Applications
  • Advanced Combustion Engine Technologies
  • Inorganic Fluorides and Related Compounds
  • Glycosylation and Glycoproteins Research
  • Spectroscopy and Quantum Chemical Studies
  • Biochemical and Structural Characterization
  • Ion-surface interactions and analysis
  • Fullerene Chemistry and Applications
  • Origins and Evolution of Life
  • Bone health and treatments
  • Synthetic Organic Chemistry Methods
  • Bacteriophages and microbial interactions
  • Combustion and flame dynamics
  • Laser-Matter Interactions and Applications

Vellore Institute of Technology University
2019-2025

Centre National de la Recherche Scientifique
2009-2020

Institut des Sciences Moléculaires
2011-2020

Institut de Physique de Rennes
2008-2020

Université de Rennes
2009-2020

Weizmann Institute of Science
2013-2018

Kiel University
2011-2016

Hebrew University of Jerusalem
2015-2016

Clinical Research Center Kiel
2015

Université de Bordeaux
2011-2012

We present a novel chemical database for gas-phase astrochemistry. Named the KInetic Database Astrochemistry (KIDA), this consists of reactions with rate coefficients and uncertainties that will be vetted to greatest extent possible. Submissions measured calculated are welcome, studied by experts before inclusion into database. Besides providing kinetic information interstellar medium, KIDA is planned contain such data planetary atmospheres circumstellar envelopes. Each year, subset in...

10.1088/0067-0049/199/1/21 article EN The Astrophysical Journal Supplement Series 2012-03-01

Abstract The surface recognition in many biological systems is guided by the interaction of carbohydrate‐specific proteins (lectins) with carbohydrate epitopes (ligands) located within unordered glycoconjugate layer (glycocalyx) cells. Thus, for recognition, respective ligand has to reorient a successful matching event. Herein, we present first time model system, which only orientation altered controlled manner without changing quality itself. key this orientational control embedding into an...

10.1002/anie.201409808 article EN Angewandte Chemie International Edition 2014-11-27

We determined absolute rate coefficients for the recurrent fluorescence (RF) process in C6– anions at excitation energies above adiabatic electron attachment energy of 4.18 eV. The experiment was performed by extracting ions from a sputter ion source and storing them bent electrostatic beam trap. After 1 s storage, during which cooled down to temperatures close room temperature, they were excited short laser pulse neutralization due vibrational autodetachment (VAD) measured as function time...

10.1021/jz502100z article EN The Journal of Physical Chemistry Letters 2014-11-10

Bacterial adhesion to glycosylated surfaces is a key issue in human health and disease. Inhibition of bacterial by suitable carbohydrates could lead an anti‐adhesion therapy as novel approach against infections. A selection five α‐mannosides has been evaluated inhibitors the polysaccharide mannan, well surface live HT‐29 cells. Cell toxicity studies were performed identify therapeutic window for potential vivo‐application tested carbohydrates. previously published mannosidic squaric acid...

10.1016/j.febslet.2012.03.059 article EN FEBS Letters 2012-04-10

Azobenzene glycoconjugates can be switched between two isomeric states, E and Z, to change the spatial orientation of conjugated carbohydrate ligands. Mono-, di- trivalent azobenzene were synthesized using click chemistry their photochromic properties determined. Multivalency effects observed in photoisomerisation.

10.1039/c2cc33542e article EN Chemical Communications 2012-01-01

Abstract Unique black coatings were observed in the inner wall of pottery shreds excavated from Keeladi, Tamilnadu, India. Raman spectroscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy used to understand nature coating. The analysis revealed presence single, multi-walled carbon nanotubes layered sheets average diameter single-walled nanotube found be about 0.6 ± 0.05 nm. This is lowest among reported artefacts so far close theoretically predicted value (0.4 nm)....

10.1038/s41598-020-76720-z article EN cc-by Scientific Reports 2020-11-13

<title>Abstract</title> Organic Residue Analysis (ORA) has emerged as a pivotal technique in archaeology, offering direct molecular insights into past societies' dietary practices and culinary traditions. By analyzing the lipids, proteins, other organic compounds preserved within porous matrix of ancient pottery, researchers can reconstruct types foods consumed, processing methods employed, even gain glimpses early agricultural animal husbandry practices. Here, we present groundbreaking...

10.21203/rs.3.rs-6604909/v1 preprint EN Research Square (Research Square) 2025-05-12

The direct infrared (IR) absorption spectrum of benzene dimer formed in a free-jet expansion was recorded the 3.3 μm region for first time. This has led to observation C–H stretching fundamental mode ν13 (B1u), which is both IR and Raman forbidden monomer. Moreover, allowed ν7 (E2g) been observed as well. These two modes were found be red-shifted along with ν20 (E1u) mode, previously reported by Erlekam et al. [Erlekam; Frankowski; Meijer; Gert von Helden J. Chem. Phys.2006, 124, 171101],...

10.1021/jp204628g article EN The Journal of Physical Chemistry A 2011-09-20

Abstract The study of bacterial adhesion is crucial to our understanding infection processes as well for the development antiadhesives. Here we have investigated new nanodiamond glycoconjugates intended inhibit type 1 fimbriated E. coli bacteria. For conjugation saccharides and nanodiamond, thiourea‐bridging was employed, a method that has not been used before in derivatization. Amino‐prefunctionalized diamond nanoparticles were prepared employing aromatic diazonium salts reacted with...

10.1002/ejoc.201500532 article EN European Journal of Organic Chemistry 2015-06-29

Abstract Azobenzene linker molecules can be utilized to control peptide/protein function when they are ligated appropriately spaced amino acid side chains of the peptide. This is because photochemical E / Z isomerization azobenzene NN double bond allows switch peptide conformation between folded and unfolded. In this context, we have introduced carbohydrate‐functionalized derivatives in order advance biocompatible properties linkers. Chloroacetamide‐functionalized O ‐allylated carbohydrate...

10.1002/chem.201501571 article EN Chemistry - A European Journal 2015-08-06

The building blocks of life, amino acids, are believed to have been synthesized in the extreme conditions that prevail space, starting from simple molecules containing hydrogen, carbon, oxygen and nitrogen. However, fate role acids when they subjected similar processes largely remain unexplored. Here we report, for first time, shock processed tend form complex agglomerate structures. Such structures formed on timescales about 2 ms due impact induced heating subsequent cooling. This discovery...

10.3390/molecules25235634 article EN cc-by Molecules 2020-11-30

In order to allow spatial and temporal control of carbohydrate-specific bacterial adhesion, it has become our goal synthesise azobenzene mannosides as photoswitchable inhibitors type 1 fimbriae-mediated adhesion E. coli. An mannobioside 2 was prepared its photochromic properties were investigated. The E→Z isomerisation found be highly effective, yielding a long-lived (Z)-isomer. Both isomers, E Z, show excellent water solubility tested mannoside-specific in solution. Their inhibitory potency...

10.3762/bjoc.9.26 article EN cc-by Beilstein Journal of Organic Chemistry 2013-02-01

Abstract Photoisomerizable glyco‐SAMs (self‐assembled monolayers), utilizing synthetic azobenzene glycoside derivatives were fabricated. The ultimate goal of this project is to assay the influence 3D arrangement sugar ligands on cell adhesion, and eventually make adhesion photoswitchable. However, it a prerequisite for any biological study spatial conditions carbohydrate recognition, that photoisomerization surface molecules can be verified. Here, we employed IRRAS XPS spectroscopically...

10.1002/chem.201402075 article EN Chemistry - A European Journal 2014-06-20

Isomers of CAl4Mg and CAl4Mg− have been theoretically characterized for the first time. The most stable isomer both neutral anion contain a planar tetracoordinate carbon (ptC) atom. Unlike isovalent CAl4Be case, which contains pentacoordinate atom as global minimum geometry, replacing beryllium with magnesium makes ptC due to increased ionic radii magnesium. However, it is relatively easier conduct experimental studies CAl4Mg0/− toxic. While molecule containing follows 18 valence electron...

10.3390/atoms9020024 article EN cc-by Atoms 2021-04-09

Abstract Spatial orientation of carbohydrates is a meaningful parameter in carbohydrate recognition processes. To vary sugars with temporal and spatial resolution, photosensitive glycoconjugates favorable photochromic properties appear to be opportune. Here, series azobenzene glycosides were synthesized, employing glycoside synthesis Mills reaction, allow “switching” by reversible E / Z isomerization the N=N double bond. Their tested effects substitution as well effect anomeric configuration...

10.1002/open.201402010 article EN cc-by-nc-nd ChemistryOpen 2014-06-01

Dissociation pathways of the global minimum geometry Si2C5H2 with a planar tetracoordinate carbon (ptC) atom, 2,7-disilatricyclo[4.1.0.01,3]hept-2,4,6-trien-2,7-diyl (1), have been theoretically investigated using density functional theory and coupled-cluster (CC) methods. Si-C bond connected to ptC atom leads formation 4,7-disilabicyclo[4.1.0]hept-1(6),4(5)-dien-2-yn-7-ylidene (4) through single transition state. C-C an intermediate two identical states back 1 itself. Simultaneous breaking...

10.3390/chemistry3010002 article EN cc-by Chemistry 2020-12-31

Fullerene C 60 is one of the most iconic forms carbon found in interstellar medium (ISM). The chemistry carbon-rich components, including fullerenes, driven by a variety energetic processes UV and X-ray irradiation, cosmic-ray (CR) bombardment, electron impact, shock waves. These violent events strongly alter particle phase lead to release new molecular species gas phase. Only few experimental studies on processing cosmic analogs have been conducted so far. We explored laboratory destruction...

10.1051/0004-6361/202347035 article EN cc-by Astronomy and Astrophysics 2024-01-01

Abstract In vielen biologischen Systemen wird die Erkennung von Oberflächen durch Wechselwirkung Kohlenhydrat‐spezifischen Proteinen (Lektinen) mit den Kohlenhydratepitopen (Liganden) der ungeordneten Glycokonjugatschicht (Glycokalyx) Zellen gesteuert. Damit es zu einer erfolgreichen Anbindung kommt, müssen sich diese Liganden geeignet im Raum orientieren. Wir stellen zum ersten Mal ein Modellsystem vor, in dem Orientierung auf Oberfläche kontrolliert variiert wird, ohne dabei ihre...

10.1002/ange.201409808 article DE Angewandte Chemie 2014-11-27

Absolute photoabsorption cross sections of negatively charged tetra-atomic aluminum clusters have been measured for photon energies between 1.8 and 2.7 eV. The experiment used the depletion technique in combination with an electrostatic ion-beam trap, which ${{\mathrm{Al}}_{4}}^{\ensuremath{-}}$ ions produced a sputter ion source were stored 90 ms before being subjected to short laser pulse. Moreover, competition one-atom fragmentation electron emission laser-excited has measured. These...

10.1103/physreva.92.052503 article EN Physical Review A 2015-11-02

The interaction of intense ultrafast laser pulses with atomic ${\mathrm{F}}^{\ensuremath{-}}$ and molecular $\mathrm{S}{{\mathrm{F}}_{6}}^{\ensuremath{-}}$ anions is directly compared. double-detachment mechanism investigated by a systematic variation peak intensity, polarization ellipticity, pulse shape. For both systems, the observed weak ellipticity dependence not consistent rescattering-based mechanism. A saturation intensity...

10.1103/physreva.92.061401 article EN Physical Review A 2015-12-01

Abstract More than 70 molecules of varied nature have been identified in the envelopes carbon‐rich stars through their spectral fingerprints microwave or far infrared regions. Many them are carbon chain and radicals, a significant number unique to circumstellar medium. The determination relevant laboratory kinetics data is critical keep up with development high spatial resolution observations refinement chemical models. Neutral–neutral reactions CN radical unsaturated hydrocarbons could be...

10.1002/kin.20730 article EN International Journal of Chemical Kinetics 2012-08-06

Isomerization and carbon chemistry in the gas phase are key processes many scientific studies. Here we report on isomerization process from linear [Formula: see text] to its monocyclic isomer. ions were trapped an electrostatic ion beam trap then excited with a laser pulse of precise energy. The neutral products formed upon photoexcitation measured as function time after pulse. It was found using statistical model that, although system is above barrier energy, actual conformation takes place...

10.1038/s41467-018-03197-w article EN cc-by Nature Communications 2018-02-26

Abstract The Mitsunobu reaction has been revisited to join hydroxyazobenzene and mannose derivatives supply photoswitchable glycoconjugates. These are suited modulating controlling carbohydrate‐lectin interactions, as well switching bacterial adhesion surfaces. Employing in a protocol, free led mixture of azobenzene pyranosides furanosides. Protected reducing can give good yields β‐ D ‐mannopyranoside, unprotected alkyl α‐ ‐mannosides be converted 6‐ O ‐azobenzene‐modified glycosides single...

10.1002/ijch.201400211 article EN Israel Journal of Chemistry 2015-03-27
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