Results 181 to 190 of about 8,987 (212)

A Chalcogen-Bonding Cascade Switch for Planarizable Push-Pull Probes. [PDF]

open access: yesAngew Chem Int Ed Engl, 2019
Macchione M   +7 more
europepmc   +1 more source

Chalcogen⋅⋅⋅π Bonding Catalysis

Angewandte Chemie, 2021
AbstractWhile the presence of sulfur⋅⋅⋅π bonding interaction is a general phenomenon in the biological systems, the exploitation of this noncovalent force in a chemical process yet remains elusive. Herein, we describe the concept of chalcogen⋅⋅⋅π bonding catalysis that activates molecules of π systems through the interaction between chalcogen and π ...
Xiangjin Kong, Pan‐Pan Zhou, Yao Wang
openaire   +4 more sources

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   +4 more sources

Chalcogen bonding in materials chemistry

Coordination Chemistry Reviews, 2020
Abstract This review examines recent literature in search for evidence of the influence that chalcogen bonding has on the structure and properties of functional materials. Key examples from research on charge transfer salts, neutral heterocyclic free radicals, and paramagnetic coordination compounds are highlighted as intermolecular interactions are ...
Peter C. Ho   +3 more
openaire   +3 more sources

Chalcogen Bonding Catalysis with Phosphonium Chalcogenide (PCH)

Accounts of Chemical Research, 2023
ConspectusThe exploration of new catalysis concepts and strategies to drive chemical reactions is of vital importance for the sustainable development of organic synthesis. Recently, chalcogen bonding catalysis has emerged as a new concept for organic synthesis and has been demonstrated to be an important synthetic tool capable of addressing elusive ...
Zhiguo Zhao, Yao Wang
openaire   +4 more sources

Supramolecular Capsules: Strong versus Weak Chalcogen Bonding

Angewandte Chemie International Edition, 2018
AbstractResorcin[4]arene cavitands containing either 2,1,3‐benzotelluradiazole or 2,1,3‐benzothiadiazole motifs were dimerized to supramolecular capsules by chalcogen bonding. Their respective behavior varied depending on the interaction strength of the chalcogen bonds with Te forming strong interactions and S weak interactions. The tremendous strength
Leslie‐Joana Riwar   +4 more
openaire   +4 more sources

Dual Chalcogen–Chalcogen Bonding Catalysis

Journal of the American Chemical Society, 2020
The noncovalent S···O bonding interaction is an evolutionary force that has been smartly exploited by nature to modulate the conformational preferences of proteins. The employment of this type of weak noncovalent force to drive chemical reactions is promising yet remains largely elusive.
Wei Wang   +6 more
openaire   +2 more sources

Chalcogen-Bonding Supramolecular Polymers

The Journal of Organic Chemistry, 2020
Exploring unknown supramolecular interacting forces to create novel supramolecular materials is an eternal theme of supramolecular science. Here, we first report a new family of supramolecular polymers formed by unconventional chalcogen-bonding interactions. A class of chalcogen-containing macrocyclic receptors, termed as chalcogena[4]arene (ChA[4], Ch
Rongjin Zeng, Zehao Gong, Qiang Yan
openaire   +2 more sources

A Porous Chalcogen-Bonded Organic Framework

Journal of the American Chemical Society, 2021
The manner of bonding between constituent atoms or molecules invariably influences the properties of materials. Perhaps no material family is more emblematic of this than porous frameworks, wherein the namesake modes of connectivity give rise to discrete subclasses with unique collections of properties.
Brian J. Eckstein   +5 more
openaire   +2 more sources

Chalcogen Bonding: An Overview

Angewandte Chemie International Edition, 2018
AbstractIn the last few decades, “unusual” noncovalent interactions like anion‐π and halogen bonding have emerged as interesting alternatives to the ubiquitous hydrogen bonding in many research areas. This is also true, to a somewhat lesser extent, for chalcogen bonding, the noncovalent interaction involving Lewis acidic chalcogen centers.
Lukas Vogel   +2 more
openaire   +2 more sources

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