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Synthesis and reactions of new diphosphenes bearing extremely bulky substituents
Author(s) -
Sasamori Takahiro,
Takeda Nobuhiro,
Tokitoh Norihiro
Publication year - 2003
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/poc.608
Subject(s) - trimethylsilyl , chemistry , steric effects , tris , sulfur , medicinal chemistry , computational chemistry , selenium , solid state , stereochemistry , organic chemistry , biochemistry
In this paper, we present the synthesis of new diphosphenes TbtPPTbt and BbtPPBbt having extremely bulky substituents, 2,4,6‐tris[bis(trimethylsilyl)methyl]phenyl (Tbt) and 2,6‐bis[bis(trimethylsilyl)methyl]‐4‐[tris(trimethylsilyl)methyl]phenyl groups (Bbt). Their x‐ray crystallographic analysis revealed their unique structures in the solid state. Furthermore, the configurations of these extremely overcrowded diphosphenes, TbtPPTbt and BbtPPBbt, are twisted in different ways in spite of the close structural similarity between Tbt and Bbt groups. DFT calculations were performed to estimate the energy difference between the two configurations of diphosphenes. In addition, their structures and physical properties were compared with those of their heavier congeners, distibenes (ArSbSbAr, Ar = Tbt and Bbt) and dibismuthenes (ArBiBiAr, Ar = Tbt and Bbt) having the same substituents. Although the reactivities of the extremely hindered diphosphenes might be considerably suppressed owing to the severe steric congestion, it was found that they can react with elemental sulfur and selenium to give the corresponding thia‐ and selenadiphosphirane derivatives, respectively, in addition to the previously reported diphosphenes. Copyright © 2003 John Wiley & Sons, Ltd.