Abstract

Several sterically protected, low-coordinate organophosphorus compounds with P=P, P=C, and C≡P bond are described in this study. Molecules such as diphosphenes, phosphaalkenes, 1-phosphaallenes, 1,3-diphosphaallenes, 3,4-diphosphinidenecyclobutenes, and phosphaalkynes are stabilized with an extremely bulky 2,4,6-tri-t-butylphenyl (Mes*) group. The synthesis, structures, physical, and chemical properties of these molecules are discussed, together with some successful applications in catalytic organic reactions.

Highlights

  • Low-coordinate organophosphorus compounds with coordination numbers of 1 or 2 compounds with coordination numbers of 1 or 2

  • By introducing a sterically bulky group such as 2,4,6-tri-t-butylphenyl into a molecule, various kinds of unusual bulky group such as 2,4,6-tri-t-butylphenyl into a molecule, various kinds of unusual phosphorus compounds have been isolated as kinetically stable species since 1981

  • In this phosphorus compounds have been isolated as kinetically stable species since 1981

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Summary

Introduction

By introducing a sterically were once believed to only exist as unstable species. By introducing a sterically bulky group such as 2,4,6-tri-t-butylphenyl into a molecule, various kinds of unusual bulky group such as 2,4,6-tri-t-butylphenyl into a molecule, various kinds of unusual phosphorus compounds have been isolated as kinetically stable species since 1981. In this phosphorus compounds have been isolated as kinetically stable species since 1981. Including the preparation, structural, physical, theoretical and chemical aspects, as well including the preparation, structural, physical, theoretical and chemical aspects, as well as as some catalytic applications to organic reactions—are described.

Steric
31 Psingle
17. The irradiation of 17ofwith
Temperatureandand wavelength-dependent photolysis of diphosphene
Chemical
Reaction
Stable
10. Preparation
11. Preparation
12. Preparation of phosphaalkene phosphaalkene 33
13. Photoisomerization
17. Preparation
19. Preparation
21. Preparation
22. Preparation
Singlet
Preparation
76 Scheme followed oxidative coupling reaction with76
27. Preparation
30. Rotational
Transition
Synthetic Application to Catalytic Reactions of DPCB–Transition Metal Complexes
Synthetic
Closing
Arduengo, IIIIII (Tuscaloosa, chemistry
Findings
Structure of phosphobenzene
Full Text
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