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

被引:15
作者
Li, Maxwell W. [1 ]
Pendleton, Ian M. [1 ]
Nett, Alex J. [1 ]
Zimmerman, Paul M. [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
OXYGEN-REDUCTION REACTION; AMMONIA-BORANE DEHYDROGENATION; NITROGEN-DOPED GRAPHENE; GROWING STRING METHOD; METAL-FREE ELECTROCATALYSTS; TRANSITION-STATE SEARCHES; CHEMISTRY PROGRAM PACKAGE; CHEMICAL HYDROGEN STORAGE; CARBON-DIOXIDE; QUANTUM-CHEMISTRY;
D O I
10.1021/acs.jpca.5b11156
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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).
引用
收藏
页码:1135 / 1144
页数:10
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