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2,3-Bis(hydroxymethyl)-2,3-dinitro-1,4-butanediol(C6H12N2O8) was synthesized by condensation,cyclization,oxidative dimerization and deketalization of nitromethane with a total yield of 42.4%.The structure of the title compound was characterized by 1H NMR,13C NMR,FT-IR,elementary analysis,and X-ray single-crystal diffraction analysis,which reveals that the title compound crystallizes in triclinic,space group P with a = 0.6324(2),b = 0.6454(3),c = 0.7062(3) nm,α= 111.550(4),β= 95.505(4),γ= 113.395(4)°,V = 0.23595(16) nm3,Z = 1,Mr = 240.18,Dc = 1.690 g·cm-3,μ = 0.159 mm-1,F(000) = 126,R = 0.0304 and wR = 0.0907.
Synthesis of 2,3-Bis (hydroxymethyl) -2,3-dinitro-1,4-butanediol (C6H12N2O8) was synthesized by condensation, cyclization, oxidative dimerization and deketalization of nitromethane with a total yield of 42.4%. The structure of the title compound was characterized by 1H NMR, 13C NMR, FT-IR, elementary analysis, and X-ray single-crystal diffraction analysis, which reveals that the title compound crystallizes in triclinic, space group P with a = 0.6324 (2), b = Α = 111.550 (4), β = 95.505 (4), γ = 113.395 (4) °, V = 0.23595 (16) nm3, Z = 1, Mr = 240.18, Dc = 1.690 g-cm-3, μ = 0.159 mm-1, F (000) = 126, R = 0.0304 and wR = 0.0907.