Synthesis and Structure of Two Isomers of Di(indenyl)phenylphosphine Sulfide
Cornelis Lensink and Graeme J. Gainsford
Australian Journal of Chemistry 51(8) 667 - 672
Abstract
Dichlorophenylphosphine reacts with indenyllithium in tetrahydrofuran followed
by sulfur to yield di(1H-inden-3-yl)phenylphosphine
sulfide (2). The same reaction sequence in toluene yields
di(1H-inden-1-yl)phenylphosphine sulfide (3) as a
mixture of (±) and two meso isomers. The
structures of (2) and (±)-(3) were determined [(2):
C24H19PS, Mr
370·42, monoclinic,
P21/n, a
14·329(4), b 7·0936(10),
c 19·405(5) Å, β 99·18(2)°,
Z 4, R 0·060 for 2422
observed reflections; (3):
C24H19PS, Mr
370·42, monoclinic,
P21/n,
a 9·521(5), b
16·223(8), c 12·930(6) Å, β
107·41(3)°, Z 4, R
0·105 for 923 reflections].
Full text doi:10.1071/C97210
© CSIRO 1998





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