1967
DOI: 10.1071/ch9670503
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Proton magnetic resonance spectra of some organodiphosphorus compounds

Abstract: The principal characteristics of the p.m.r, spectra of 21 previously unreported diphosphorus compounds and related substances are described, discussed, and compared with results already in the literature. A simple synthesis of unsymmetrical ethane-1,2-diphosphorus compounds is reported.

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Cited by 14 publications
(4 citation statements)
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“…Cyclic bis(CDP) 5 was synthesized over three steps from the literature-known propane-1,3-bis(methyldiphenylphosphonium) diiodide 2 [25] in 13 % overall yield (Scheme 1). The structure of 5 was determined by X-ray crystallography to reveal the two CDP moieties exist independently and have similar CÀ P bond distances and PÀ CÀ P bond angles compared to the reported monodentate CDP, hexaphenylcarbodiphosphorane (Figure 3).…”
Section: Resultsmentioning
confidence: 99%
“…Cyclic bis(CDP) 5 was synthesized over three steps from the literature-known propane-1,3-bis(methyldiphenylphosphonium) diiodide 2 [25] in 13 % overall yield (Scheme 1). The structure of 5 was determined by X-ray crystallography to reveal the two CDP moieties exist independently and have similar CÀ P bond distances and PÀ CÀ P bond angles compared to the reported monodentate CDP, hexaphenylcarbodiphosphorane (Figure 3).…”
Section: Resultsmentioning
confidence: 99%
“…Some sulfur-containing compounds related to long-chain fatty acids are described (1679) ; and qpectra analyzed for 1,2-dithiol-3-ones and 3-thiones (287) and thiophenes (2003,2000,1105). A variety of organophosphorous compounds have been reported (1489,1549,278) including dialkylamino derivatives (458) , alkynylamino derivatives (363) and acetylenic phosphorous compounds (552). Azoles have received a great deal of attention ( N H proton shifts are included in tabulations of hydrazone and acid hydrazide spectra (1860), various amine salts and hydrazines (96) , and urethanes (207).…”
Section: Effects Of K-0 and C=noh Onmentioning
confidence: 99%
“…Building blocks 1 and 4 are commercially available but at relatively high costs, and therefore a more economical synthetic process is highly desirable. Limited syntheses of 4 have been reported based on the use of carbon disulphide [23] and diazomethane [24]; however, these reagents require special precautions for their use and have severe restrictions due to being toxic, highly flammable, and suspected carcinogens.…”
mentioning
confidence: 99%