T. Brent Gunnoe

Prof. T. Brent Gunnoe

Department of Chemistry, University of Virginia, Charlottesville, VA 22904-4319, USA

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 July 2017 in ACS Catalysis
Verified
Journal Article
Closed access
ZHZachary B. Hoffman
Zachary B. Hoffman
TGTristan S. Gray
Tristan S. Gray
KMKasey B. Moraveck
Kasey B. Moraveck
T. Brent GunnoeT. Brent Gunnoe
T. Brent Gunnoe
GZGiovanni Zangari
Giovanni Zangari

24 April 2015 in Science
Verified
Journal Article
Closed access
PDF file
BVBenjamin A. Vaughan
Benjamin A. Vaughan
MWMichael S. Webster-Gardiner
Michael S. Webster-Gardiner
TCThomas R. Cundari
Thomas R. Cundari
T. Brent GunnoeT. Brent Gunnoe
T. Brent Gunnoe
A more direct way to synthesize styrene: Foam cups, foam pellets, plastic cutlery: All are made of polystyrene, which in turn is made of styrene. The massive manufacturing scale of this commodity chemical places a premium on the efficiency of its synthesis. The current industrial route requires three steps to make styrene from benzene and ethylene. Vaughan et al. present a rhodium catalyst that achieves the coupling in a single step by using a recyclable copper salt as an oxidant. Although the catalyst is slow for industrial application, it demonstrates the viability of a more direct process. Science , this issue p. 421

1 December 2010 in ChemSusChem
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Journal Article
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JWJoanna R. Webb
Joanna R. Webb
TBTamara Bolaño
Tamara Bolaño
T. Brent GunnoeT. Brent Gunnoe
T. Brent Gunnoe

19 September 2019 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
ZZZhiyong Zhang
Zhiyong Zhang
QWQiyuan Wu
Qiyuan Wu
GJGrayson Johnson
Grayson Johnson
YYYifan Ye
Yifan Ye
XLXing Li
Xing Li
SZSen Zhang
Sen Zhang

26 April 2019 in ACS Catalysis
Verified
Journal Article
Closed access
GBGordon Brezicki
Gordon Brezicki
JKJames D. Kammert
James D. Kammert
T. Brent GunnoeT. Brent Gunnoe
T. Brent Gunnoe
CPChristopher Paolucci
Christopher Paolucci
RDRobert J. Davis
Robert J. Davis

25 September 2013 in Dalton Transactions
Verified
Journal Article
Closed access
PDF file
JWJoanna R. Webb
Joanna R. Webb
SBSamantha A. Burgess
Samantha A. Burgess
TCThomas R. Cundari
Thomas R. Cundari
T. Brent GunnoeT. Brent Gunnoe
T. Brent Gunnoe
The controlled conversion of hydrocarbons to functionalized products requires selective C–H bond cleavage. This perspective provides an overview of 1,2-CH-addition of hydrocarbons across d0 transition metal imido complexes and compares and contrasts these to examples of analogous reactions that involve later transition metal amide, hydroxide and alkoxide complexes with d6 and d8 metals.