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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2010-3-10
pubmed:abstractText
Cyclopolymerization of isopropylidene diallylmalonate (1) in CH(2)Cl(2) using as the initiator a crystallographically defined alpha-diimine Pd(II) complex with a trans-azobenzene strap (trans-3) proceeds stereospecifically to give a cycloolefinic polymer that is rich in threo-disyndiotactic sequences (st(rich)-2; syndiotactic tetrad content = 60% at -10 to 0 degrees C). Polymer 2, when perfectly threo-disyndiotactic, adopts a "barb"-shaped geometry with its cyclic malonate pendants sticking out alternately up and down along the rigid main chain. Under appropriate conditions, st(rich)-2 regularly self-assembles, not only in the solid state but also in solution, into nanofibers that eventually give rise to physical gelation of halogenated solvents such as CH(2)Cl(2). In sharp contrast, a reference polymer 2 that is rich in threo-diisotactic sequences (it(rich)-2), which likely adopts a helical geometry, has poor self-assembly capability in solution and neither forms nanofibers nor induces physical gelation of CH(2)Cl(2).
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Mar
pubmed:issn
1520-5126
pubmed:author
pubmed:issnType
Electronic
pubmed:day
17
pubmed:volume
132
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3292-4
pubmed:year
2010
pubmed:articleTitle
Shape-directed assembly of a "macromolecular barb" into nanofibers: stereospecific cyclopolymerization of isopropylidene diallylmalonate.
pubmed:affiliation
Department of Chemistry and Biotechnology, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
pubmed:publicationType
Journal Article