Andrei S. Batsanov mostly deals with Photochemistry, Crystallography, Crystal structure, Stereochemistry and Molecule. His Photochemistry research integrates issues from Fluorescence, Phosphorescence, Excited state, Intramolecular force and Iridium. His research in Crystallography intersects with topics in Cobalt, Adduct, van der Waals force and Sonogashira coupling.
Crystal structure is a subfield of Organic chemistry that Andrei S. Batsanov studies. The Stereochemistry study which covers Crystal engineering that intersects with Ab initio. His work deals with themes such as Inorganic chemistry, Optoelectronics, Moiety and Carbazole, which intersect with Molecule.
Andrei S. Batsanov mainly investigates Crystal structure, Crystallography, Stereochemistry, Medicinal chemistry and Molecule. His Crystal structure research is multidisciplinary, incorporating elements of Yield, X-ray, Polymer chemistry, Photochemistry and Tetrathiafulvalene. In his research on the topic of Photochemistry, Iridium is strongly related with Phosphorescence.
The Crystallography study combines topics in areas such as Ligand, Intramolecular force, Moiety and Hydrogen bond. His work carried out in the field of Stereochemistry brings together such families of science as Adduct and Ring. His Medicinal chemistry research incorporates elements of Coupling reaction, Palladium, Derivative, Organic chemistry and Aryl.
His primary scientific interests are in Photochemistry, Molecule, Fluorescence, Phosphorescence and Crystallography. His Photochemistry research is multidisciplinary, relying on both Excited state, Intersystem crossing and Acceptor. His Molecule study integrates concerns from other disciplines, such as Conductance and Steric effects.
His study in Fluorescence is interdisciplinary in nature, drawing from both Donor acceptor, Carbazole, Electron acceptor and Chromophore. Andrei S. Batsanov has researched Phosphorescence in several fields, including Luminescence, Intramolecular force, Iridium and Density functional theory. His work on Crystal structure as part of general Crystallography study is frequently connected to Pnictogen, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
His scientific interests lie mostly in Photochemistry, Fluorescence, Phosphorescence, Molecule and Excited state. Andrei S. Batsanov interconnects Luminescence, Acceptor and Molecular geometry in the investigation of issues within Photochemistry. His Phosphorescence study also includes
His research on Molecule frequently links to adjacent areas such as Crystallography. His Crystallography study combines topics from a wide range of disciplines, such as Decomposition, Triple bond, X-ray crystallography, Stereochemistry and Break junction. His studies in Excited state integrate themes in fields like Conformational isomerism, Quantum yield and Crystal structure.
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Formation of Aryl‐ and Benzylboronate Esters by Rhodium‐Catalyzed C−H Bond Functionalization with Pinacolborane
Shigeru Shimada;Andrei S. Batsanov;Judith A. K. Howard;Todd B. Marder.
Angewandte Chemie (2001)
Precision control of single-molecule electrical junctions.
Wolfgang Haiss;Changsheng Wang;Iain Grace;Andrei S. Batsanov.
Nature Materials (2006)
The Role of Local Triplet Excited States and D-A Relative Orientation in Thermally Activated Delayed Fluorescence: Photophysics and Devices.
Fernando B. Dias;Jose Santos;Jose Santos;David R. Graves;Przemyslaw Data;Przemyslaw Data.
Advanced Science (2016)
Structural, Luminescence, and NMR Studies of the Reversible Binding of Acetate, Lactate, Citrate, and Selected Amino Acids to Chiral Diaqua Ytterbium, Gadolinium, and Europium Complexes
Rachel S. Dickins;Silvio Aime;Andrei S. Batsanov;Andrew Beeby.
Journal of the American Chemical Society (2002)
Selective Ir-catalysed borylation of polycyclic aromatic hydrocarbons: structures of naphthalene-2,6-bis(boronate), pyrene-2,7-bis(boronate) and perylene-2,5,8,11-tetra(boronate) esters.
David N. Coventry;Andrei S. Batsanov;Andrés E. Goeta;Judith A. K. Howard.
Chemical Communications (2005)
Synthesis, Crystal Structures, Linear and Nonlinear Optical Properties, and Theoretical Studies of (p‐R‐Phenyl)‐, (p‐R‐Phenylethynyl)‐, and (E)‐[2‐(p‐R‐Phenyl)ethenyl]dimesitylboranes and Related Compounds
Zheng Yuan;Christopher D. Entwistle;Jonathan C. Collings;David Albesa-Jové.
Chemistry: A European Journal (2006)
General method of diastereo- and enantioselective synthesis of β-hydroxy-α-amino acids by condensation of aldehydes and ketones with glycine
Y. N. Belokon;A. G. Bulychev;S. V. Vitt;Y. T. Struchkov.
Journal of the American Chemical Society (1985)
Single-molecule conductance of functionalized oligoynes:length dependence and junction evolution
Pavel Moreno-García;Murat Gulcur;David Zsolt Manrique;Thomas Pope.
Journal of the American Chemical Society (2013)
Requirement for an Oxidant in Pd/Cu Co-Catalyzed Terminal Alkyne Homocoupling To Give Symmetrical 1,4-Disubstituted 1,3-Diynes
Andrei S. Batsanov;Jonathan C. Collings;Ian J.S. Fairlamb;Jason P. Holland.
Journal of Organic Chemistry (2005)
Ir-catalyzed borylation of C-H bonds in N-containing heterocycles : regioselectivity in the synthesis of heteroaryl boronate esters.
Ibraheem A. I. Mkhalid;David N. Coventry;David Albesa‐Jove;Andrei S. Batsanov.
Angewandte Chemie (2006)
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