TL;DR: A review of low coordinate phosphorus ligands featuring P=C double bonds can be found in this article, where the most significant developments are presented and discussed for each class of ligands.
TL;DR: In this article, the authors present a survey of the use of P-compounds in a variety of applications, including the following: 1) Reaction Bond Strengths and Bond Lengths Phosphides of Non-Metals The Element Oxides Sulphides Hydrides Nitrides Halides Borides Carbides Silicides Oxyphosphorus Compounds
Abstract: Introduction and Historical Background General Overview Historical Survey Classification and Nomenclature of P Compounds Literature of Phosphorus Chemistry Distribution and Environment General Occurrence Phosphate Mineral Deposits Environmental Phosphorus Atomic and Molecular Properties Atomic Properties Equilibria and Stereochemistry Types of Reaction Bond Strengths and Bond Lengths Phosphides of Non-Metals The Element Oxides Sulphides Hydrides Nitrides Halides Borides Carbides Silicides Oxyphosphorus Compounds Introduction Phosphoric and Polyphosphoric Acids Orthophosphates Condensed Phosphates Substituted Phosphates Phosphate Esters Complex Phosphates and Space-Containing Structures References Carbophosphorus Compounds Introduction and Nomenclature Phosphines Phosphine Oxides Phosphonous and Phosphinous Halides Phosphonic and Phosphinic Halides Phosphonous and Phosphinous Acids Phosphonic and Phosphinic Acids Phosphites Phosphonium Salts Phosphonium Ylides Carbenes and Carbanions Phosphoranes Phosphorides Compounds with one- and Two-Connected P Atoms Compounds with Three-Connected P Atoms Cyaphides and Cyanides Polyphosphines Polyphosphonates and Polyphosphinates Diphosphenes and Related PV-PIII Compounds Saturated Rings with Phosphorus and Carbon Unsaturated Rings with Phosphorus and Carbon Condensed Rings and Cages with Phosphorus and Carbon Rings and Cages with Phosphorus, Carbon and Oxygen Azaphosphorus Compounds Nomenclature Compounds of Phosphorus, Nitrogen and Hydrogen Phosphazanes with P-NH Linkages Phosphazanes with P-N-C Linkages Phosphazanes with P-N and P-C Linkages Hydrazides and Azides Polymeric Phosphazanes and Cyclic Compounds Cyclic Phosphazenes Linear Phosphazenes Monophosphazenes Two- and Three-Connected Phosphazenes Phosphazynes Chapter 8 Metallophosphorus Compounds Metal Phosphides: Introduction Metal-Rich Phosphides MXPYX > Y Ionic Phosphides Phosphides with Complex Anions Monophosphides Phosphorus-Rich Phosphides Miscellaneous Phosphides Metallophosphines and Metallophosphites Metallophosphorus Coordination Complexes Complexes with M-P-C Bonds Complexes with M-P-H Bonds Complexes with M-P-Halogen Bonds Complexes with P-M, P-O and P-C Bonds Bonding Effects in Metal Complexes Complexes with P-P Bonds Complexes with Pn Units Bonded To M Atoms Diphosphene and Phosphaalkene Complexes Metallophosphene and Metallophosphyne Complexes Metal Complexes of Cyclic P and C Compounds Metal Complexes OF P-N and P/N Compounds Polymers with Metal-Phosphorus Linkages Miscellaneous Complexes Containing P and M Atoms Compounds with p-Block Elements Phosphorus and Boron Phosphorus and Aluminium1,2 Phosphorus and Gallium Phosphorus and Indium Phosphorus and Silicon Phosphorus and Germanium Phosphorus and Tin Phosphorus and Lead Phosphorus and Arsenic, Antimony or Bismuth Phosphorus and Sulphur Phosphorus and Selenium or Tellurium Biopolymers and Phospho-Bioassemblies Polysaccharides Proteins Lipids Nucleic Acids and Nucleotides Biophosphorus Chemistry Body Composition and General Biochemical Background Nutritional Aspects of Phosphorus Energy Carriers Enzymes Essential Bio Processes Polynucleotide Functions Phosphonate Metabolism Applications of Phosphorus Compounds Phosphoric Acid Fertilisers Animal Foodstuffs Food Technology Detergents Water Treatment Metal Surface Treatment Pigments and Dyestuffs Glasses Phosphoceramic Constructional Materials Industrial Phosphate Esters Pesticides Medicinal Compounds and Toxic Esters Dental and Medical Materials Synthetic Polymers and Fire Retardants Pyrotechnics Natural Products Catalysts and Synthetic Reagents Metallurgy and Metal Phosphides Electronic, Electrical and Related Materials Special Topics Hydrogen Bonding Stereochemistry and Isomerism Pseudorotation and the Trigonal Bipyramid Free Radicals and Short-Lived Species Radioactivity and Radiochemistry Migrations, Rearrangements and other Reactions Analysis and Characterisation Chemical Methods Physical Methods Biopolymer Analysis Appendices Atomic Data for the Elements Hazards of Phosphorus Compounds Properties of White Phosphorus P4 Properties of 'Red' Phosphorus Pn Properties of Phosphine PH3 Properties of Orthophosphoric Acid, H3PO4 Abbreviations and Symbols Conversion Factors Shortened Journal Nomenclature
TL;DR: One-electron oxidation of a readily available phosphaalkene derived from a cyclic (alkyl)(amino)carbene affords a phosphorus-centered radical cation that is indefinitely stable both in solution and in the solid state, allowing a single X-ray diffraction study to be performed.
Abstract: One-electron oxidation of a readily available phosphaalkene derived from a cyclic (alkyl)(amino)carbene affords a phosphorus-centered radical cation that is indefinitely stable both in solution and in the solid state, allowing a single X-ray diffraction study to be performed. This species can be regarded as a phosphinyl radical bearing a cationic substituent or, alternatively, as a carbene-stabilized phospheniumyl radical (carbene−RP+•).
TL;DR: In this paper, the major developments in the phospha-Wittig reaction are highlighted and divided into these three methodologies, and the complementary nature and the differences between the three approaches are also discussed.
TL;DR: Remarkably, selective Z-isomer formation (i.e., trans arylene moieties) is observed for PPPs when bulky P-substituents are employed while E/Z-mixtures are otherwise obtained.
Abstract: A new class of π-conjugated macromolecule, poly(p-phenylenephosphaalkene) (PPP), is reported. PPPs are phosphorus analogues of the important electronic material poly(p-phenylenevinylene) (PPV) wher...