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Chalcogen bonding in synthesis, catalysis and design of materialsChalcogen bonding is a type of noncovalent interaction in which a covalently bonded chalcogen atom

Se⋯π Chalcogen Bonding in 1,2,4-Selenodiazolium Tetraphenylborate Complexes of assemblies exhibiting selenium–π interactions. The chalcogen bonding (ChB) interactions involving the π

Robust Supramolecular Dimers Derived from Benzylic-Substituted 1,2,4-Selenodiazolium Salts Featuring Selenium⋯π Chalcogen Bonding chalcogen bonding and two antiparallel selenium⋯π interactions. Chalcogen bonding interactions were studied

2-Pyridylselenenyl versus 2-Pyridyltellurenyl Halides: Symmetrical Chalcogen Bonding in the Solid State and Reactivity towards Nitriles that the Te atom of 2-pyridyltellurenyl bromide was involved in four different noncovalent contacts: Te

Chalcogen bonding in coordination chemistry deficient region (so-called as σ or π hole) of a covalently bonded chalcogen atom and a nucleophilic (Nu

Donor-acceptor coordination of anions by chalcogen atoms of 1,2,5-chalcogenadiazoles-acceptor coordination of anions (A–) by chalcogen atoms (E) of 1,2,5-chalcogenadiazoles, are considered. According

Exploring Supramolecular Assembly Space of Cationic 1,2,4-Selenodiazoles: Effect of the Substituent at the Carbon Atom and Anions of cationic 1,2,4-selenodiazoles via chalcogen bonding. © 2022 by the authors. Licensee MDPI, Basel

Novel Chalcogen Bond Donors Derived from [3+2] Cycloaddition Reaction between 2-Pyridylselenyl Reagents and Isocyanates: Synthesis, Structures and Theoretical Studies to be structurally easily tunable donors of the chalcogen bonding (ChB). Noncovalent interactions in the solid state

Sulfonium and Selenonium Salts as Noncovalent Organocatalysts for the Multicomponent Groebke-Blackburn-Bienaymé Reaction effect is induced by the ligation of the reaction substrates to the σ-holes on the S or Se atom

Влияние вакансионных дефектов и примесей на электронную структуру двумерных кристаллов MoS2, MoSе2, WS2 и WSe2 impurity atoms are considered to substitute chalcogen atoms or to adsorb at the surface of the crystal

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