期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 31, 页码 10822-10831出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b05464
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资金
- National Science Foundation (NSF) [CHE-1362118]
- Spanish Ministry of Economy and Competitiveness (MINE CO) [CTQ2016-80600-P]
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1362118] Funding Source: National Science Foundation
Dibenzo-7-phosphanorbornadiene compounds, RPA (A=C14H10 or anthracene), are investigated as phosphinidene sources upon thermally induced (70-90 degrees C). anthracene elimination. Analysis of substituent effects reveals that pi-donating dialkylamide groups are paramount to successful phosphinidene transfer; poorer pi-donors give reduced or no transfer. Substituent steric bulk is also implicated in successful transfer. Molecular beam mass spectrometry (MBMS) studies of each derivative reveal dialkylamide derivatives to be promising precursors for further gas-phase spectroscopic studies of phosphinidenes; in particular, we present evidence of direct-detection of the-dimethylamide derivative, [Me2N=P]. Kinetic investigations of (i)Pr(2)NPA thermolysis in 1,3-cyclohexadiene and/or benzene-d(6) are consistent with a model of unimolecular fragmentation to yield free phosphinidene [(Pr2N)-Pr-i=P] as a transient reactive intermediate. This conclusion is probed by density functional theory (DFT) calculations, which favored a mechanistic model featuring free singlet aminophosphinidenes. The breadth of phosphinidene acceptors is expanded to unsaturated substrates beyond 1,3-dienes to include olefins and alkynes; this provides a new synthetic route to valuable amino-substituted phosphiranes and phosphirenes, respectively. Stereoselective phosphinidene transfer to. olefins is consistent with singlet phosphinidene reactivity by analogy with the Skell hypothesis for singlet carbene addition to olefins.
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