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Mechanism for Forming B,C,N,O Rings from NH3BH3 and CO2 via Reaction Discovery Computations.

作者信息

Li Maxwell W, Pendleton Ian M, Nett Alex J, Zimmerman Paul M

机构信息

Department of Chemistry, University of Michigan , Ann Arbor, Michigan 48109, United States.

出版信息

J Phys Chem A. 2016 Mar 3;120(8):1135-44. doi: 10.1021/acs.jpca.5b11156. Epub 2016 Feb 18.

DOI:10.1021/acs.jpca.5b11156
PMID:26844585
Abstract

This study employs computational reaction finding tools to probe the unique biphilic reactivity between ammonia-borane (AB) and CO2. The results show that sequential reactions involving multiple equivalents of AB and CO2 can lead to the formation of stable nonplanar B,C,N,O-heterocycles (Cy-BCN). Cy-BCN is shown to emerge through boron-oxygen bond formation, hydroboration, dative bond formation, and single- or double-hydrogen transfers. The most kinetically facile reactions (computed at the coupled cluster singles and doubles with perturbative triples (CCSD(T)) level of theory) result from polarized nitrogen-boron double bonds whereas thermodynamic stability results from formation of covalent boron-oxygen bonds. An important structure, HCOOBHNH2 (DHFAB), contains both of these features and is the key intermediate involved in generation of Cy-BCN. Crucially, it is shown that favorable boron-oxygen bond formation results in production of Cy-BCN species that are more stable than polyaminoboranes. These types of reaction intermediates could serve as building blocks in the formation of B,N-codoped graphene oxide (BCN).

摘要

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