Results 21 to 30 of about 10,808 (271)

NHC-Boranes: Air- and Water-tolerant Co-initiators for Type II Photopolymerizations

open access: yesCHIMIA, 2012
N-Hetereocyclic carbene (NHC) complexes of boranes are stable compounds that can be used as co-initiators for the type II photopolymerization of acrylates.
Emmanuel Lacôte   +2 more
doaj   +1 more source

DFT Investigation of Hydrogen Atom Abstraction from NHC-Boranes by Methyl, Ethyl and Cyanomethyl Radicals—Composition and Correlation Analysis of Kinetic Barriers

open access: yesMolecules, 2020
Understanding the hydrogen atom abstraction (HAA) reactions of N-heterocyclic carbene (NHC)-boranes is essential for extending the practical applications of boron chemistry.
Hong-jie Qu   +4 more
doaj   +1 more source

Construction of boron-stereogenic compounds via enantioselective Cu-catalyzed desymmetric B–H bond insertion reaction

open access: yesNature Communications, 2022
Enantioselective catalytic methods for the construction of boron-stereogenic compounds are elusive. In this article, the authors describe a route to these compounds via a copper-catalysed desymmetric B-H insertion on 2-arylpyridine-boranes with carbenes.
Guan Zhang   +6 more
doaj   +1 more source

Redox Targets for Phosphine–Boranes

open access: yesInorganics, 2023
Understanding the complex mechanisms underlying redox-mediated biological processes is a fundamental pillar of cellular biology. We describe the identification and quantification of disulfide formation and reduction in response to phosphine–borane ...
Yonatan Morocz   +2 more
doaj   +1 more source

Photolysis of Diborane at 1849 Å [PDF]

open access: yes, 1962
The photolysis of diborane at 1849 Å has been studied in a specially constructed, internal‐type mercury‐vapor lamp. The products have been found to be H_2, B_(4)H_(10), B_(5)H_(11), and, at low pressures, a —BH— polymer.
Kreye, W. C., Marcus, R. A.
core   +1 more source

Could humans recognize odor by phonon assisted tunneling? [PDF]

open access: yes, 2006
Our sense of smell relies on sensitive, selective atomic-scale processes that are initiated when a scent molecule meets specific receptors in the nose. However, the physical mechanisms of detection are not clear.
A. M. Stoneham   +16 more
core   +2 more sources

A frustrated-Lewis-pair approach to catalytic reduction of alkynes to cis-alkenes [PDF]

open access: yes, 2013
Frustrated Lewis pairs are compounds containing both Lewis acidic and Lewis basic moieties, where the formation of an adduct is prevented by steric hindrance.
Chernichenko, K.   +2 more
core   +1 more source

Ambiphilic boron in 1,4,2,5-diazadiborinine

open access: yesNature Communications, 2016
Boranes are archetypal Lewis acids owing to an empty p-orbital on the boron, although Lewis basic tricoordinate boranes have been developed too. Here, the authors report an annulated 1,4,2,5-diazadiborinine derivative with boron atoms that exhibit both ...
Baolin Wang   +4 more
doaj   +1 more source

A combined "electrochemical-frustrated Lewis pair" approach to hydrogen activation: surface catalytic effects at platinum electrodes [PDF]

open access: yes, 2014
Herein, we extend our “combined electrochemical–frustrated Lewis pair” approach to include Pt electrode surfaces for the first time. We found that the voltammetric response of an electrochemical–frustrated Lewis pair (FLP) system involving the B(C6F5)3 ...
Ashley   +48 more
core   +2 more sources

Pairing and unpairing electron densities in organic systems: Two-electron three center through space and through bonds interactions [PDF]

open access: yes, 2014
Two-electron three-center bonding interactions in organic ions like methonium (CH + 5 ), ethonium (C2H + 7 ), and protonated alkanes n−C4H + 11 isomers (butonium cations) are described and characterized within the theoretical framework of the ...
Bochicchio, Roberto Carlos   +1 more
core   +1 more source

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