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Volumn 42, Issue 5, 2009, Pages 1439-1442

Polymethylenes containing [2.2]paracyclophane in the side chain

Author keywords

[No Author keywords available]

Indexed keywords

[2.2]PARACYCLOPHANE; CATALYZED POLYMERIZATION; COTTON EFFECTS; FE CATALYST; HIGH YIELD; NMR SPECTRUM; OPTICALLY ACTIVE; POLYMETHYLENE; SIDE CHAINS;

EID: 66549099633     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma8022876     Document Type: Article
Times cited : (18)

References (74)
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    • p)-5 are shown in Figure S1 in Supporting Information.
    • p)-5 are shown in Figure S1 in Supporting Information.
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    • 13C NMR spectra of polymer (rac)-6are shown in Figures S6 and S7 in Supporting Information.
    • 13C NMR spectra of polymer (rac)-6are shown in Figures S6 and S7 in Supporting Information.
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    • The absorption spectrum of (rac)-6was identical to those of optically active polymers (Rp)-6and (Sp)-6, as shown in Figure S9.
    • The absorption spectrum of (rac)-6was identical to those of optically active polymers (Rp)-6and (Sp)-6, as shown in Figure S9.
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    • In the present system, aromatic rings are not layered due to interaction each other, but they interact each other because they are layered. The polymerization of monomers with electron-rich and -poor aromatic rings would proceed more smoothly; for example, see:Pugh, C.; Tang, C. N.; Paz-Pazos, M.; Samtani, O.; Dao, A. H. Macromolecules 2007, 40, 8178-8188.
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    • For (Sp)-4-methyl[2.2]paracyclophane: Weigner, O. E., Jr.; Nugent, M. J. J. Am. Chem. Soc. 1969, 91, 4556-4558.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.