Lewis and Bronsted basicity of phosphine-diazomethane derivatives

被引:12
|
作者
Schneider, Carolin [1 ]
LaFortune, James H. W. [1 ]
Melen, Rebecca L. [2 ]
Stephan, Douglas W. [1 ]
机构
[1] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada
[2] Cardiff Univ, Sch Chem, Main Bldg,Pk Pl, Cradiff CF10 3AT, Wales
基金
英国工程与自然科学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
FREE HYDROGEN ACTIVATION; ETHYL DIAZOACETATE; CARBONYL-COMPOUNDS; PAIR CHEMISTRY; NITROUS-OXIDE; BORANE ADDUCT; BASIS-SETS; DINITROGEN; REDUCTION; PHOSPHAZINE;
D O I
10.1039/c8dt02420k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The compounds EtOC(=O)CHNNPR3(R = Ph 1, Cy 2, tBu 3) were prepared via the reactions of the diazomethane and a phosphine. In subsequent reactions with B(C6F5)(3), the compounds 2 and 3 are shown to exhibit Lewis basicity at the carbonyl oxygen affording EtOC(=O(B(C6F5)(3)))CHNNPR3(R = Cy 5, tBu 6). Reactions of 5 and 6 with water or phenol illustrated the Bronsted basicity at the nitrogen atom adjacent phosphorus, affording the compounds, [EtOC(=O)CHNNHPR3][HOB(C6F5)(3)] (R = Cy 7, tBu 8) and [EtOC(=O)CHNNHPR3][PhOB(C6F5)(3)] (R = Cy 9, tBu 10), respectively. The formulation of these products is confirmed via spectroscopic and crystallographic studies, and insight is garnered from computations.
引用
收藏
页码:12742 / 12749
页数:8
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