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Volumn 63, Issue 8, 2010, Pages 1159-1163

Synthesis and solution-state assembly or bulk state thiol-ene crosslinking of pyrrolidinone- and alkene-functionalized amphiphilic block fluorocopolymers: From functional nanoparticles to anti-fouling coatings

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYL GROUPS; AMPHIPHILIC DIBLOCK COPOLYMERS; AMPHIPHILIC NETWORK; AMPHIPHILICS; ANTIFOULING; ANTIFOULING MATERIAL; BIFUNCTIONAL MONOMERS; BULK STATE; COMPLEX BUILDINGS; CROSS-LINKED NETWORKS; FLUORINATED POLYMERS; FLUORO-COPOLYMERS; FUNCTIONAL NANOPARTICLES; FUNCTIONALIZED; FUNCTIONALIZED NANOPARTICLES; PYRROLIDINONE; RAFT POLYMERIZATION; REVERSIBLE ADDITION-FRAGMENTATION CHAIN TRANSFER POLYMERIZATION; SIDE-CHAIN FUNCTIONALITIES; SYNTHETIC METHODOLOGY; THIOL-ENE REACTIONS; THIOL-ENES;

EID: 77955675577     PISSN: 00049425     EISSN: None     Source Type: Journal    
DOI: 10.1071/CH10011     Document Type: Conference Paper
Times cited : (17)

References (33)
  • 14
    • 0035834259 scopus 로고    scopus 로고
    • doi:10.1016/ S0168-3659(01
    • J. J. Kim, K. Park, J. Control. Release 2001, 77, 39. doi:10.1016/ S0168-3659(01)00447-453
    • (2001) J. Control. Release , vol.77 , pp. 00447-453
    • Kim, J.J.1    Park, K.2
  • 27
    • 77955694698 scopus 로고    scopus 로고
    • Slight shoulders in the high molecular weight side of the GPC curves of 6a and 6b were observed (Fig. S1 in the Accessory Publication), which were presumably caused by the side reactions of the pendant alkene groups of the block copolymers at the late stage of RAFT polymerization. See ref. [9]
    • Slight shoulders in the high molecular weight side of the GPC curves of 6a and 6b were observed (Fig. S1 in the Accessory Publication), which were presumably caused by the side reactions of the pendant alkene groups of the block copolymers at the late stage of RAFT polymerization. See ref. [9].
  • 32
    • 77955680517 scopus 로고    scopus 로고
    • The cross-linking percentages are obtained by the [alkene]/[thiol] feed ratios, with the assumption of quantitative efficiency of the thiol-ene reaction
    • The cross-linking percentages are obtained by the [alkene]/[thiol] feed ratios, with the assumption of quantitative efficiency of the thiol-ene reaction.
  • 33
    • 77955673284 scopus 로고    scopus 로고
    • The increase of the contact angles of networks after cross-linking may be caused by enhanced roughness of the films, and the additional hydrophobicity from the incorporated aliphatic 1,10-decanedithiol
    • The increase of the contact angles of networks after cross-linking may be caused by enhanced roughness of the films, and the additional hydrophobicity from the incorporated aliphatic 1,10-decanedithiol.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.