Results 191 to 200 of about 5,131 (236)
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Chalcogen bonding catalysis

Chemical Society Reviews
This tutorial review will focus on the recently evolved chalcogen bonding catalysis. Emphasis will be given to the basics of non-covalent bonding, chiral chalcogen bonding catalysis, chiral separation, and chalcogen bonding in biomolecules.
Govindasamy Sekar   +2 more
openaire   +2 more sources

From Noncovalent Chalcogen–Chalcogen Interactions to Supramolecular Aggregates: Experiments and Calculations

Chemical Reviews, 2018
This review considers noncovalent bonds between divalent chalcogen centers. In the first part we present X-ray data taken from the solid state structures of dimethyl- and diphenyl-dichalcogenides as well as oligoalkynes kept by alkyl-sulfur, -selenium, and -tellurium groups.
Rolf Gleiter   +4 more
openaire   +2 more sources

A World Beyond Hydrogen Bonds?—Chalcogen–Chalcogen Interactions Yielding Tubular Structures

Chemistry – A European Journal, 2003
AbstractIt is shown that tubular structures arise in the solid state through close chalcogen–chalcogen (X⋅⋅⋅X) contacts. As examples a variety of cyclic systems containing sulfur and selenium centers is presented. Common to all of them are close contacts between the chalcogen centers of neighboring stacks giving rise to a zigzag or ladder‐type ...
Rolf, Gleiter   +2 more
openaire   +2 more sources

Chalcogen-Centered Radicals

Sulfur reports, 1995
Abstract The main types of radicals formed in initiated reactions of organic compounds of selenium and tellurium, detection methods, and their physico-chemical properties and reactivity are presented in this review.
E. N. Deryagina, M. G. Voronkov
openaire   +1 more source

Chalcogen-based Probes

2023
Recently, selenium and tellurium atoms have been incorporated in various fluorophores such as rhodamine, cyanine, fluorescein, BODIPY, coumarin, and BOPHY for the detection and quantification of different analytes of biochemical and environmental interest by fluorescence measurements.
Gauri S. Malankar   +7 more
openaire   +1 more source

Carbon–chalcogen wires: alkynyltellurolatocarbynes

Chemical Communications
The reactions of [W(CBr)(CO)2(Tp*)] with LiTeCCR (R = SiMe3, SiiPr3, iPr, nBu, tBu, Ph, C6H4Me-4, methylimidazol-2-yl) afford the first alkynyltellurolatocarbynes [W(CTeCCR)(CO)2(Tp*)] feauring an unsaturated carbon–tellurium spine.
Chee S. Onn, Anthony F. Hill
openaire   +2 more sources

Electrochemical Fluoro-Chalcogenation

Phosphorus, Sulfur, and Silicon and the Related Elements, 1997
Electrochemical fluoro-chalcogenation (S, Se) of alkenes and alkynes, and recycle use of in situ generated PhSeF for allylic fluorination are discussed.
Kenji Uneyama   +3 more
openaire   +1 more source

Chalcogen-Based Organocatalysis

2011
Most current organocatalysts are based on nitrogen (or phosphorus) as reactive atom, including also most processes depending on proton acidity and/or Lewis basicity. Only few organocatalytic systems use organochalcogens, although such reactions are of great importance in nature, especially evident in hydrolases with serine or cysteine as catalytic ...
Ludger A. Wessjohann   +2 more
openaire   +1 more source

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