Results 11 to 20 of about 4,166 (227)

Chalcogen‐Bonding Catalysis with Telluronium Cations [PDF]

open access: yesAngewandte Chemie, 2021
AbstractChalcogen bonding results from non‐covalent interactions occurring between electrodeficient chalcogen atoms and Lewis bases. Among the chalcogens, tellurium is the strongest Lewis acid, but Te‐based compounds are scarcely used as organocatalysts.
Weiss, Robin   +3 more
openaire   +3 more sources

Bifurcated Chalcogen Bonds Based on One σ-Hole

open access: yesOrganic Materials, 2022
Chalcogen bonds are noncovalent interactions and are increasingly coming into focus for the design of complex structures in research areas such as crystal engineering, molecular recognition and catalysis. Conceptionally, chalcogen bonds can be considered
Saber Mehrparvar   +3 more
doaj   +1 more source

Assessing the Possibility and Properties of Types I and II Chalcogen Bonds

open access: yesCrystals, 2023
Type I and II halogen bonds are well-recognized motifs that commonly occur within crystals. Quantum calculations are applied to examine whether such geometries might occur in their closely related chalcogen bond cousins. Homodimers are constructed of the
Steve Scheiner
doaj   +1 more source

Halogen bonding and chalcogen bonding mediated sensing

open access: yesChemical Science, 2022
Sigma–hole mediated detection of anions is rapidly emerging as a new paradigm in supramolecular sensor chemistry. Herein, we provide an overview of this field including halogen bonding and chalcogen bonding optical, electrochemical and other sensors.
Hein, R, Beer, PD
openaire   +2 more sources

Ability of Lewis Acids with Shallow σ-Holes to Engage in Chalcogen Bonds in Different Environments

open access: yesMolecules, 2021
Molecules of the type XYT = Ch (T = C, Si, Ge; Ch = S, Se; X,Y = H, CH3, Cl, Br, I) contain a σ-hole along the T = Ch bond extension. This hole can engage with the N lone pair of NCH and NCCH3 so as to form a chalcogen bond.
Rafał Wysokiński   +3 more
doaj   +1 more source

Chalcogen bonding in crystal engineering [PDF]

open access: yesActa Crystallographica Section A Foundations and Advances, 2019
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Resnati, G, Scilabra, P, Terraneo, G
openaire   +2 more sources

Tuning of the Electrostatic Potentials on the Surface of the Sulfur Atom in Organic Molecules: Theoretical Design and Experimental Assessment

open access: yesMolecules, 2023
Noncovalent sulfur interactions are ubiquitous and play important roles in medicinal chemistry and organic optoelectronic materials. Quantum chemical calculations predicted that the electrostatic potentials on the surface of the sulfur atom in organic ...
Ziyu Wang, Weizhou Wang, Hai-Bei Li
doaj   +1 more source

A Structural Approach to the Strength Evaluation of Linear Chalcogen Bonds

open access: yesMolecules, 2023
The experimental structural features of chalcogen bonding (ChB) interactions in over 34,000 linear fragments R–Ch⋯A (Ch = S, Se, Te; R = C, N, O, S, Se, Te; A = N, O, S, Se, Te, F, Cl, Br, I) were analyzed.
Maria Carla Aragoni   +5 more
doaj   +1 more source

The Origin of Chalcogen-Bonding Interactions [PDF]

open access: yesJournal of the American Chemical Society, 2017
Favorable molecular interactions between group 16 elements have been implicated in catalysis, biological processes, and materials and medicinal chemistry. Such interactions have since become known as chalcogen bonds by analogy to hydrogen and halogen bonds. Although the prevalence and applications of chalcogen-bonding interactions continues to develop,
Dominic J. Pascoe   +2 more
openaire   +2 more sources

Activating Chalcogen Bonding (ChB) in Alkylseleno/Alkyltelluroacetylenes toward Chalcogen Bonding Directionality Control [PDF]

open access: yesAngewandte Chemie International Edition, 2020
AbstractActivation of a deep electron‐deficient area on chalcogen atoms (Ch=Se, Te) is demonstrated in alkynyl chalcogen derivatives, in the prolongation of the (C≡)C−Ch bond. The solid‐state structures of 1,4‐bis(methylselenoethynyl)perfluorobenzene (1Se) show the formation of recurrent chalcogen‐bonded (ChB) motifs.
Arun Dhaka   +5 more
openaire   +2 more sources

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