Phosphorus heterocycles four-membered rings

A fascinating feature of the chemistry of boron-phosphorus heterocycles is the existence of stable singlet biradicals, e.g. fBuBP Pr2)2 (for a discussion of the electronic structure, see Section 5.4.2.2). The synthesis of this four-membered ring is illustrated in Scheme 5.2. Related derivatives of the type (RBPR 2)2 are also prepared by a salt-elimination reaction of the appropriate lithium phosphide with a 1,2-dichlorodiborane or, in the case of the perphenylated derivative (PhBPPh2)2, by reduction of the cyclic dimer [Ph(Cl)BPPh2]2 with lithium naphthalenide (Scheme 9.11). ... 

In conformity with the calculations the yicrz-fused heterocycles with a phosphorus atom proved to be quite stable. For instance, treating 1,8-dilithionaphthalene (18) with (A, A -diisopropylamino)dichlorophosphine afforded in a 75% yield a P-substituted naphtho[l,8-Z)c]phosphete (19) that took up tungsten pentacarbonyl to form a complex compound 20 (02AG(E)3897). The latter on further reaction with platinum tetratriphenylphosphinate and carbon monoxide suffers a recyclization of the four-membered ring into a five-membered one (20—>21). The reaction of... 

Four-membered Rings containing Sulphur, Nitrogen, and Phosphorus.— The compound (160) results from the reaction of (155 R=p-anisyl) and (McjSOjNMe. Heterocycle (161) is obtained from isocyanates and (162). Thionyl chloride reacts with (163) to give (164). ... 

Ti -Cyclopentadienyl(triphenylphosphine)cobalt reacts with phosphites and forms complexes of 1-alkoxyphosphole oxides 251 (R = Me, Et, Ph) through a step involving (ri -cyclopentadienyl)(phosphite)cobalt (80JA4363). (ri -Cp)Co(PF3)2 reacts with hexafluorobut-2-yne and 252 is formed, which hydrolyzes into 253 (X = OH) [73JCS(CC)583 75JCS(D)197]. The five-member ring has the envelope conformation, in which the carbon atoms are coplanar, and the phosphorus atom deviates from this plane in the direction opposite to the cobalt atom. The heterocycle is a four-electron donor relative to the metal center. 

Diathiadiphosphetane disulfides are probably the most studied and the most thermally and hydrolytically stable of all the phosphorus-chalcogen heterocycles. They contain a central four membered P2S2 ring and can be prepared from heating phosphorus pentasulfide with aromatic compounds. The most well-known of these is Lawesson s reagent (43), which is made from anisole and phosphorus pentasulfide,92 and is used extensively in organic synthesis procedures (see Section 5.4.1). Other dithiadiphosphetane disulfides of note are 44 and 45, formed from the reaction of phosphorus pentasulfide with ferrocene or 1 -bromonaphthalene respectively.93... 

Vacuum thermolysis (160°C) of the hemiaminal 11 generates the azaphos-phetane 65 in 85% yield.32 This product clearly results from the intramolecular insertion of the transient (amino) (phosphino)carbene 2h into the C-H bond of a diisopropylamino group bonded to phosphorus. Note that the four-membered heterocycle 65 is formed exclusively in spite of the ratio of six methyl-CH bonds to one methine-CH bond, and that only one of the two possible diastereomers is detected. The same regio- and diastereo-selectivity have already been observed with the di(phosphino)carbene 2g,74 but is in marked contrast to the exclusive formation of five-membered rings... 

Chapter 2 by Laszlo Nyulaszi and Zoltan Benko deals with the chemistry and physical organic chemistry of aromatic phosphorus heterocycles and is divided into four subchapters dealing with three-, four-, five-, and six-membered rings, in which there may be more than one phosphorus atom. The chapter begins with a clear presentation of the electronic structure that phosphorus may achieve in molecules with CP bonds. For cyclopentadiene and phosphole eight aromaticity indices are collected. Almost all of them indicate that phosphole is more aromatic than cyclopentadiene. It is also shown that even small structural effects (substituent, bonding modes) can have a substantial impact on the chemistry of the reported systems. 

The compounds with five-membered rings containing three or four heteroatoms including at least one phosphorus were first systematically reviewed in Chapter 4.22 of CHEC-II(1996) by Schmidpeter <1996CHEC-II(4)771>. In CHEC(1984), only few examples of 2//4,2,3-diazaphospholcs were mentioned in the general chapter on phosphorus heterocycles <1984CHEC(1)493>. 

Initially, ring expansion by tellurium leads to a four-membered heterocycle (n = 1) intermolecular rearrangements produce additional tellurium-phosphorus hctcrocycles, which are ultimately converted by extrusion of tellurium to tetra-/-butylcyclotetra-phosphane1. 

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