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An open chain product in the reaction of benzil with thiocarbohydrazide 被引量:1

An open chain product in the reaction of benzil with thiocarbohydrazide
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摘要 An open chain compound was obtained by reaction of benzil with thiocarbohy-drazide in acidic condition. Its derivative, namely, benzil bis-(5-isopropylidene-3-thiocarbohydrazone) has been structurally characterized by X-ray single crystal diffraction method. Crystallographic data: C22H26N8S2, Mr=466.62, monoclinic, space group C2/c, a=12.215(3), b=11.473(2), c=17.032 (3)A, B=98.96(2)0, V=2357.7(9)A3, Z=4, Dc=1.32 g/cm3, F(000)=1040, u(Mo Ka)=2.43 cm-1. Final R=0.050, Rw=0.061 for 1103 unique and observed reflections with I> 3o(I). The effect of the structures on the formation of the open-chain intermediates during the cyclization of (2:2) Schiff base macrocyclic compound has been discussed and a possible mechanism for the ring closure has been suggested. An open chain compound was obtained by reaction of benzil with thiocarbohy-drazide in acidic condition. Its derivative, namely, benzil bis-(5-isopropylidene-3-thiocarbohydrazone) has been structurally characterized by X-ray single crystal diffraction method. Crystallographic data: C22H26N8S2, Mr=466.62, monoclinic, space group C2/c, a=12.215(3), b=11.473(2), c=17.032 (3)A, B=98.96(2)0, V=2357.7(9)A3, Z=4, Dc=1.32 g/cm3, F(000)=1040, u(Mo Ka)=2.43 cm-1. Final R=0.050, Rw=0.061 for 1103 unique and observed reflections with I> 3o(I). The effect of the structures on the formation of the open-chain intermediates during the cyclization of (2:2) Schiff base macrocyclic compound has been discussed and a possible mechanism for the ring closure has been suggested.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1994年第3期270-276,共7页 中国化学(英文版)
关键词 THIOCARBOHYDRAZIDE Schiff base open-chain intermediate. Thiocarbohydrazide, Schiff base, open-chain intermediate.
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  • 1Gang Zheng, Mohammad Aoadia, David Lee, et al..Chlorin-based symmetrical and unsymmetrical dimmers with amide linkages: effect of the substituents of photodynamic andphotophysical properties[J]. J. Chem. Soc., Perkin Trans, 2000, 1:3113.
  • 2Hughes M N. The Inorganic Chemistry of Biological Processes[M].New York:Wiley, N. Y.,1981.
  • 3Lindoy L F.The Chemistry of Macrocyclic Ligand Complexes[M]. Cambridge: Cambridge University Press, 1989.21.
  • 4Pandey UK,Pandey O P,Sengupta S K,et al..Syntheses and spectroscopic studies on tetraaza macrocyclic complexes of LanthaNum(Ⅲ)[J].Synth. Inorg. Met.-Org. Chem., 1987, 17: 567.
  • 5Burns G R. Metal compiexes of thiocarbohydrazide[J]. Inorg. Chem., 1968,7:277.
  • 6Freddrick G, Bord Well, Guo-Zhen J. Effects of structural changes on acidities and hemolytic bond dissociation energies of the H-N bonds in amidines, carboxmides, thiocarboxamides[J]. J. Am. Chem. Soc., 1991, 113(22):8399.

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