Organophosphorus(0), (I), and (II) Compounds
Compounds where phosphorus exists in a formal oxidation state of less than III are uncommon, but examples are known for each class. Organophosphorus(0) species are illustrated by the carbene adducts, 2, where NHC is an N-heterocyclic carbene. With the formulae (RP)n and (R2P)2, respectively, compounds of phosphorus(I) and (II) are generated by reduction of the related organophosphorus(III) chlorides:
- 5 PhPCl2 + 5 Mg → (PhP)5 + 5 MgCl2
- 2 Ph2PCl + Mg → Ph2P-PPh2 + MgCl2
Diphosphenes, with the formula R2P2, formally contain phosphorus-phosphorus double bonds. These phosphorus(I) species are rare but are stable provided that the organic substituents are large enough to prevent catenation. Many mixed-valence compounds are known, e.g. the cage P7(CH3)3.
CH | He | ||||||||||||||||
CLi | CBe | CB | CC | CN | CO | CF | Ne | ||||||||||
CNa | CMg | CAl | CSi | CP | CS | CCl | CAr | ||||||||||
CK | CCa | CSc | CTi | CV | CCr | CMn | CFe | CCo | CNi | CCu | CZn | CGa | CGe | CAs | CSe | CBr | CKr |
CRb | CSr | CY | CZr | CNb | CMo | CTc | CRu | CRh | CPd | CAg | CCd | CIn | CSn | CSb | CTe | CI | CXe |
CCs | CBa | CHf | CTa | CW | CRe | COs | CIr | CPt | CAu | CHg | CTl | CPb | CBi | CPo | CAt | Rn | |
Fr | Ra | Rf | Db | Sg | Bh | Hs | Mt | Ds | Rg | Cn | Uut | Fl | Uup | Lv | Uus | Uuo | |
↓ | |||||||||||||||||
CLa | CCe | CPr | CNd | Pm | CSm | CEu | CGd | CTb | CDy | CHo | CEr | CTm | CYb | CLu | |||
Ac | CTh | CPa | CU | CNp | CPu | CAm | CCm | CBk | Cf | CEs | Fm | Md | No | Lr |
Core organic chemistry | Many uses in chemistry |
Academic research, but no widespread use | Bond unknown |
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