RUTHENIUM CARBENE INITIATED RING-OPEN METATHESIS POLYMERIZATION OF ENDO-BICYCLO[3.2.0]HEPT-6-EN-3-YL BENZOATES WITH TACTICITY STUDIES

Ze Zhang a b Qing-ping Song a Guan-wu Wang b

Citation:  Ze Zhang a, b, Qing-ping Song a, Guan-wu Wang b. RUTHENIUM CARBENE INITIATED RING-OPEN METATHESIS POLYMERIZATION OF ENDO-BICYCLO[3.2.0]HEPT-6-EN-3-YL BENZOATES WITH TACTICITY STUDIES[J]. Chinese Journal of Polymer Science, 2010, 28(2): 181-189. doi: 10.1007/s10118-010-8245-4 shu

RUTHENIUM CARBENE INITIATED RING-OPEN METATHESIS POLYMERIZATION OF ENDO-BICYCLO[3.2.0]HEPT-6-EN-3-YL BENZOATES WITH TACTICITY STUDIES

摘要: After tentative ring-opening cross metathesis (ROCM) of endo-bicyclo[3.2.0]hept-6-en-3-yl 4-bromobenzoate with PhCH=CH2 initiated by (Cy3P)2Cl2Ru=CHPh in CH2Cl2, ring-opening metathesis polymerization (ROMP) of a series of endo-bicyclo[3.2.0]hept-6-en-3-yl benzoates was achieved under the same conditions, furnishing a variety of the corresponding polymers. Then some of them were selected to hydrogenate the C=C double bonds in their backbone with p-tosylhydrazide, affording saturated and thus more flexible polymers. All of these polymers were well characterized by spectroscopic means including GPC, UV-Vis, NMR and IR, based on which the tacticity of these polymers was investigated together with nonlinear optical (electric-field-induced second-harmonic generation, EFISH)) analysis.

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  • 发布日期:  2010-03-20
  • 收稿日期:  2008-12-30
  • 修回日期:  2009-02-17
通讯作者: 陈斌, bchen63@163.com
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