Direct synthesis of functional novolacs and their polymer reactions

Polymer Journal

Volumn 42, Issue 6, 2010, Pages 443-449

  Konishi, Gen Ichi ^a   Tajima, Takatsugu ^a,b   Kimura, Tsuyoshi ^a,b   Tojo, Yusuke ^a   Mizuno, Kazuhiko ^c   Nakamoto, Yoshiaki ^b  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b KANAZAWA UNIVERSITY   (Japan)

^c Osaka Prefecture University   (Japan)

Author keywords

Allyl phenyl ether; Claisen condensation; Graft polymerization; Novolac; Phenolic resin; Polycondensation; Polymer reaction

Indexed keywords

2-METHYL-2-OXAZOLINE; ADDITION-CONDENSATION; ALLYL ETHERS; ALLYL PHENYL ETHER; ALLYLATED NOVOLAC; AMPHIPHILICS; CLAISEN REARRANGEMENT; CURING SYSTEM; DIRECT SYNTHESIS; FOURIER TRANSFORM INFRARED; GRAFT POLYMERIZATION; KEY REACTIONS; NMR SPECTRUM; NOVOLAC; NUMBER-AVERAGE; PHENOL MOIETY; PHENOL-FORMALDEHYDE; PHENOLIC HYDROXYL GROUP; POLYCONDENSATION POLYMERS; POLYMER REACTION; REACTIVE POLYMERS; SIDE CHAINS; THERMAL STIMULI; VINYL ETHERS;

ALLYL RESINS; CURING; ETHERS; FORMALDEHYDE; FOURIER TRANSFORMS; FUNCTIONAL GROUPS; GRAFTING (CHEMICAL); HYDRATES; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHENOLIC RESINS; PHENOLS; POLYCONDENSATION; POLYMERS; RESINS; RING OPENING POLYMERIZATION; SULFURIC ACID; SYNTHESIS (CHEMICAL); WAVELET TRANSFORMS;

FUNCTIONAL POLYMERS;

EID: 77953645840     PISSN: 00323896     EISSN: 13490540     Source Type: Journal    
DOI: 10.1038/pj.2010.26     Document Type: Article

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