Formation of benzodiazaborolanes from borazine

Benjamin L. Davis; Andrew D. Sutton; John C. Gordon; Daniel E. Schwarz; Brian L. Scott; David L. Thorn

doi:10.3233/MGC-2010-0010

Formation of benzodiazaborolanes from borazine

Benjamin L. Davis
, Andrew D. Sutton
, John C. Gordon
, Daniel E. Schwarz
, Brian L. Scott
, David L. Thorn

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

Phenylenediamines are shown to form benzodiazaborolanes upon reaction with borazine, essentially extracting the B-H bonds. This surrogate for partially dehydrogenated ammonia borane provides useful insight into potential regeneration strategies for ammonia borane spent fuel.

Original language	English
Pages (from-to)	135-139
Number of pages	5
Journal	Main Group Chemistry
Volume	9
Issue number	1-2
DOIs	https://doi.org/10.3233/MGC-2010-0010
State	Published - 2010
Externally published	Yes

Keywords

Ammonia borane
aryldiamine
borazine

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10.3233/MGC-2010-0010

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@article{1a1efe5893434ca0a5483773f743415e,

title = "Formation of benzodiazaborolanes from borazine",

abstract = "Phenylenediamines are shown to form benzodiazaborolanes upon reaction with borazine, essentially extracting the B-H bonds. This surrogate for partially dehydrogenated ammonia borane provides useful insight into potential regeneration strategies for ammonia borane spent fuel.",

keywords = "Ammonia borane, aryldiamine, borazine",

author = "Davis, \{Benjamin L.\} and Sutton, \{Andrew D.\} and Gordon, \{John C.\} and Schwarz, \{Daniel E.\} and Scott, \{Brian L.\} and Thorn, \{David L.\}",

year = "2010",

doi = "10.3233/MGC-2010-0010",

language = "English",

volume = "9",

pages = "135--139",

journal = "Main Group Chemistry",

issn = "1024-1221",

publisher = "IOS Press",

number = "1-2",

}

TY - JOUR

T1 - Formation of benzodiazaborolanes from borazine

AU - Davis, Benjamin L.

AU - Sutton, Andrew D.

AU - Gordon, John C.

AU - Schwarz, Daniel E.

AU - Scott, Brian L.

AU - Thorn, David L.

PY - 2010

Y1 - 2010

N2 - Phenylenediamines are shown to form benzodiazaborolanes upon reaction with borazine, essentially extracting the B-H bonds. This surrogate for partially dehydrogenated ammonia borane provides useful insight into potential regeneration strategies for ammonia borane spent fuel.

AB - Phenylenediamines are shown to form benzodiazaborolanes upon reaction with borazine, essentially extracting the B-H bonds. This surrogate for partially dehydrogenated ammonia borane provides useful insight into potential regeneration strategies for ammonia borane spent fuel.

KW - Ammonia borane

KW - aryldiamine

KW - borazine

UR - https://www.scopus.com/pages/publications/77954928053

U2 - 10.3233/MGC-2010-0010

DO - 10.3233/MGC-2010-0010

M3 - Article

AN - SCOPUS:77954928053

SN - 1024-1221

VL - 9

SP - 135

EP - 139

JO - Main Group Chemistry

JF - Main Group Chemistry

IS - 1-2

ER -

Formation of benzodiazaborolanes from borazine

Abstract

Keywords

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