scispace - formally typeset
A

Andrey Solovyev

Researcher at University of Pittsburgh

Publications -  19
Citations -  1388

Andrey Solovyev is an academic researcher from University of Pittsburgh. The author has contributed to research in topics: Carbene & Boranes. The author has an hindex of 13, co-authored 19 publications receiving 1250 citations. Previous affiliations of Andrey Solovyev include University of St Andrews & University of Illinois at Chicago.

Papers
More filters
Journal ArticleDOI

Synthesis and reactions of N-heterocyclic carbene boranes.

TL;DR: This Review provides comprehensive coverage of the synthesis, characterization, and reactions of NHC-boranes.
Journal ArticleDOI

N-Heterocyclic Carbene Boryl Radicals: A New Class of Boron-Centered Radical

TL;DR: These are the first NHC-boranes with boron-sulfur bonds, and their structures have been secured by spectroscopic and crystallographic means and Spectral analysis suggests that it is a pi-radical analogous to the benzyl radical.
Journal ArticleDOI

EPR Studies of the Generation, Structure, and Reactivity of N-Heterocyclic Carbene Borane Radicals

TL;DR: Spectroscopic data and DFT computations demonstrated that the NHC-BH(2)* radicals are planar pi-delocalized species, which is well suited for their reactivity to be tuned by inclusion of different NHC ring units and by appropriate placement of diverse substituents.
Journal ArticleDOI

Generation and Reactions of an Unsubstituted N-Heterocyclic Carbene Boryl Anion†

TL;DR: A lithiated unsubstituted N-heterocyclic carbene (NHC) boryl anion can be generated by reduction, and trapped by electrophiles to provide new substituted NHC boranes, thereby extending the scope of N HC borane chemistry.
Journal ArticleDOI

Substitution reactions at tetracoordinate boron: synthesis of N-heterocyclic carbene boranes with boron-heteroatom bonds.

TL;DR: Boryl halide, carboxylate and sulfonate complexes of 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene, which have been prepared from the parent borane dipp-Imd-BH(3) are remarkably stable, and many have been characterized by X-ray crystallography.