메뉴 건너뛰기




Volumn 34, Issue 4, 2001, Pages 727-733

Polyaddition of bis(cyclic thiocarbonate) with diamines. Novel efficient synthetic method of polyhydroxythiourethanes

Author keywords

[No Author keywords available]

Indexed keywords

POLYHYDROXYTHIOURETHANES;

EID: 0035251007     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma001353l     Document Type: Article
Times cited : (19)

References (49)
  • 5
    • 4243221340 scopus 로고
    • Mikheev, V. V.; Svetlakov, N. V.; Sysoev, V. A.; Brus'ko, N. V. Deposited Doc., SPSTL 41 Khp-D82, 1982; Chem. Abstr. 1983, 98, 127745a.
    • (1983) Chem. Abstr. , vol.98
  • 7
    • 84889118382 scopus 로고    scopus 로고
    • note
    • The water absorption percentages of the polyhydroxyurethane films were more than 30%, while those of commercial polyurethanes were less than 2%. The thermal decomposition temperatures of the polyhydroxyurethane films were 32-88 °C higher than that of commercial polyurethane (259°C: CRISVON 9004 [hard type polyurethane (Dainippon Ink and Chemicals, Inc.)]).
  • 9
    • 84889162070 scopus 로고    scopus 로고
    • note
    • The calculated ring-strain energy of six-membered cyclic carbonate was larger than that of the five-membered one. (ring-strain energy difference: 2.86 kcal/mol).
  • 12
    • 84889165406 scopus 로고
    • Sharkey, W. H. Chem. Sulfides, Conf. 1966 1968, 205; Chem. Abstr. 1969, 70, 12393.
    • (1969) Chem. Abstr. , vol.70 , pp. 12393
  • 15
    • 84889140658 scopus 로고
    • Woodhams, R. T. Rep. Prog. Appl. Chem. 1965, 50, 480; Chem. Abstr. 1967, 67, 32935.
    • (1967) Chem. Abstr. , vol.67 , pp. 32935
  • 18
    • 0040555980 scopus 로고
    • Interscience Publishers: New York, London, and Sydney, Australia
    • Janssen, M. J. Organosulfur Chemistry; Interscience Publishers: New York, London, and Sydney, Australia, 1967; p 219.
    • (1967) Organosulfur Chemistry , pp. 219
    • Janssen, M.J.1
  • 28
    • 0013513113 scopus 로고
    • Patai, S., Ed.; Interscience Publishers: New York, London, and Sydney, Australia
    • Janssen, M. J. In Thiolo, Thiono, and Dithio acids and Esters; Patai, S., Ed.; Interscience Publishers: New York, London, and Sydney, Australia, 1969; p 705.
    • (1969) Thiolo, Thiono, and Dithio Acids and Esters , pp. 705
    • Janssen, M.J.1
  • 31
    • 14344275086 scopus 로고
    • Ger. 1 270 552, 1967
    • Becke, F.; Hagen, H. Ger. 1 270 552, 1967; Chem. Abstr. 1969, 70, 3573.
    • (1969) Chem. Abstr. , vol.70 , pp. 3573
    • Becke, F.1    Hagen, H.2
  • 35
    • 0016348601 scopus 로고
    • Auzzi, G.; Papini, P.; Vettori, L. P. Boll. Chim. Farm. 1974, 113, 633; Chem. Abstr. 1975, 82, 170785.
    • (1975) Chem. Abstr. , vol.82 , pp. 170785
  • 37
    • 84889125936 scopus 로고
    • Sannicolo, F. Ann. Chim. (Roma) 1973, 63, 825; Chem. Abstr. 1975, 83, 9861.
    • (1975) Chem. Abstr. , vol.83 , pp. 9861
  • 40
    • 84889152520 scopus 로고    scopus 로고
    • European Patent Application 408459 A1, 1990
    • Yean, L.; Bochu, C. European Patent Application 408459 A1, 1990.
    • Yean, L.1    Bochu, C.2
  • 46
    • 0000840877 scopus 로고
    • Jones, N., Ed.; Pergamon Press: Oxford, England, New York, Toronto, Canada, Sydney, Australia, Paris, and Frankfurt, Germany
    • Duus, F. In Comprehensive Organic Chemistry; Jones, N., Ed.; Pergamon Press: Oxford, England, New York, Toronto, Canada, Sydney, Australia, Paris, and Frankfurt, Germany, 1979; Vol 3, p 373.
    • (1979) Comprehensive Organic Chemistry , vol.3 , pp. 373
    • Duus, F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.