13C and 15N NMR shieldings of 1,2,4-diazaphospholes in the solid state and in solution

The solid state 13C and 15N CPMAS NMR spectra of 3,5-di-tert-butyl-1,2,4-diazaphosphole 4 and 3,5-diphenyl-1,2,4-diazaphosphole 5 have been recorded. The X-ray structure of the first compound was already known (it is a cyclic dimer with localized N-H protons) while the structure of the second cannot be determined due to the difficulty to grow suitable single crystals. NMR results pointed out that 4 is a >classical> compound while 5 is probably a tetramer showing Intermolecular Solid-State Proton Transfer (ISSPT). GIAO/ab initio calculations have been carried out to estimate the absolute 1H, 13C and 15N shieldings. The agreement with the experimental chemical shifts is good enough to assign the signals of carbons C-3 and C-5.This work has been financially supported by the Spanish DGI/MCT (project numbers PB96-0001-C03 and BQU 2000-0252) and to the “Comunidad de Madrid” (project number 07N/0001/1999) of Spain.Peer Reviewe

C and 15 N NMR shieldings of 1,2,4-diazaphospholes in the solid state and in solution

Abstract. The solid state 13 C and 15 N CPMAS NMR spectra of 3,5-di-tert-butyl-1,2,4-diazaphosphole 4 and 3,5-diphenyl-1,2,4-diazaphosphole 5 have been recorded. The X-ray structure of the first compound was already known (it is a cyclic dimer with localized N-H protons) while the structure of the second cannot be determined due to the difficulty to grow suitable single crystals. NMR results pointed out that 4 is a "classical" compound while 5 is probably a tetramer showing Intermolecular Solid-State Proton Transfer (ISSPT). GIAO/ab initio calculations have been carried out to estimate the absolute 1 H, 13 C and 15 N shieldings. The agreement with the experimental chemical shifts is good enough to assign the signals of carbons C-3 and C-5