Stereoregular polymerization of phenylacetylene using alkynyl and methyl rhodium(I) complexes with functionalized phosphine ligands: linear vs. branched poly(phenylacetylene)s
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F24%3A39921803" target="_blank" >RIV/00216275:25310/24:39921803 - isvavai.cz</a>
Result on the web
<a href="https://pubs.rsc.org/en/Content/ArticleLanding/2024/PY/D4PY00497C" target="_blank" >https://pubs.rsc.org/en/Content/ArticleLanding/2024/PY/D4PY00497C</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/d4py00497c" target="_blank" >10.1039/d4py00497c</a>
Alternative languages
Result language
angličtina
Original language name
Stereoregular polymerization of phenylacetylene using alkynyl and methyl rhodium(I) complexes with functionalized phosphine ligands: linear vs. branched poly(phenylacetylene)s
Original language description
The alkynyl [Rh(C equivalent to C-Ph)(nbd){Ph2P(CH2)(3)Z}(2)] and [Rh(C equivalent to C-Ph)(cod){Ph2P(CH2)(3)Z}] (cod = 1,5-cyclooctadiene, nbd = 2,5-norbornadiene) and methyl complexes [Rh(CH3)(cod){Ph2P(CH2)(3)Z}] featuring functionalized phosphine ligands (Z = NMe2, OEt) have been prepared. These complexes efficiently catalyze the polymerization of phenylacetylene in the absence of a base to afford stereoregular poly(phenylacetylene)s with high molar masses. Polymer characterization by SEC-MALS and A4F-MALS revealed a bimodal molar mass distribution due to the presence of a high molar mass polymer fraction. The diene ligand in the alkynyl complexes influences the morphology of the polymers. The poly(phenylacetylene)s prepared with the square-planar alkynyl complexes [Rh(C equivalent to C-Ph)(cod){Ph2P(CH2)(3)Z}] having cod as the diene are linear, whereas the catalysts [Rh(C equivalent to C-Ph)(nbd){Ph2P(CH2)(3)Z}(2)] with nbd as the diene afford PPAs with a fraction of high molar mass branched polymer. However, neither the catalytic performance nor the PPA morphology is affected by the donor function of the functionalized phosphine ligand (-NMe2 or -OEt). The alkynyl complexes having nbd as the diene ligand, [Rh(C equivalent to C-Ph)(nbd){Ph2P(CH2)(3)Z}(2)], are much more active than the square-planar alkynyl and methyl complexes having cod as the diene. These catalysts polymerize phenylacetylene at a faster rate than the catalyst [Rh(C equivalent to C-Ph)(nbd)(PPh3)(2)] bearing a non-functionalized phosphine ligand and afford polymers with a much higher molecular weight.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10404 - Polymer science
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2024
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Polymer Chemistry
ISSN
1759-9954
e-ISSN
1759-9962
Volume of the periodical
15
Issue of the periodical within the volume
30
Country of publishing house
GB - UNITED KINGDOM
Number of pages
14
Pages from-to
3086-3099
UT code for WoS article
001267511900001
EID of the result in the Scopus database
2-s2.0-85198969880