By exerting control over two populations of coexisting cyclopentadienyl, amidinate (CPAM) group 4 metal active species that possess different stereoselectivities for chain growth propagation during the living coordinative chain transfer polymerization (LCCTP) of 4-methyl-1-pentene, controlled production of grades for poly(4-methyl-1-pentene) (PMP) materials that display a tunable range of viscoelastic properties can be achieved in “one-pot” fashion. Analytical and spectroscopic investigations reveal that these differences in viscoelastic properties are associated with formation of atactic/isotactic PMP stereoblends, rather than a stereoblock chain architecture. These results serve to establish the ability of low molar mass atactic PMP to fu...
Sequential cyclic/linear/cyclic living coordination polymerization of 1,6-heptadiene (HPD), propene,...
ConspectusSome of the most readily available and inexpensive monomers for ring-opening metathesis po...
External control over the rate of dynamic methyl group exchange between configurationally stable act...
A novel polymerization method, living coordinative chain transfer polymerization (CCTP), was recentl...
Olefin coordinative chain-transfer polymerization (CCTP) under concurrent tandem catalysis condition...
Olefin coordinative chain-transfer polymerization (CCTP) under concurrent tandem catalysis condition...
The research presented herein, addresses key issues of homogeneous Group 4 single-site coordination ...
The living polymerization of ethene, propene, higher carbon-number linear and branched chain α-olefi...
The living, isoselective polymerization of 4-methyl- 1,3-pentadiene, 4-methylstyrene, and 4-tert-but...
Several papers have claimed the amenability for binary metallocene systems to undergo coordinative c...
New synthetic methods in polymer chemistry developed over the last twenty years and advances in mate...
New synthetic methods in polymer chemistry developed over the last twenty years and advances in mate...
C1-symmetric, cationic group 4 metal (Zr and Hf) mono-methyl complexes, {(η5-C5Me5)M[N(tBu)C(Me...
Current studies on novel, metallocenebased catalysts for the polymerization of α-olefins have far-re...
International audienceIsoprene chain shuttling polymerisation between the 1,4-trans regulating Cp*La...
Sequential cyclic/linear/cyclic living coordination polymerization of 1,6-heptadiene (HPD), propene,...
ConspectusSome of the most readily available and inexpensive monomers for ring-opening metathesis po...
External control over the rate of dynamic methyl group exchange between configurationally stable act...
A novel polymerization method, living coordinative chain transfer polymerization (CCTP), was recentl...
Olefin coordinative chain-transfer polymerization (CCTP) under concurrent tandem catalysis condition...
Olefin coordinative chain-transfer polymerization (CCTP) under concurrent tandem catalysis condition...
The research presented herein, addresses key issues of homogeneous Group 4 single-site coordination ...
The living polymerization of ethene, propene, higher carbon-number linear and branched chain α-olefi...
The living, isoselective polymerization of 4-methyl- 1,3-pentadiene, 4-methylstyrene, and 4-tert-but...
Several papers have claimed the amenability for binary metallocene systems to undergo coordinative c...
New synthetic methods in polymer chemistry developed over the last twenty years and advances in mate...
New synthetic methods in polymer chemistry developed over the last twenty years and advances in mate...
C1-symmetric, cationic group 4 metal (Zr and Hf) mono-methyl complexes, {(η5-C5Me5)M[N(tBu)C(Me...
Current studies on novel, metallocenebased catalysts for the polymerization of α-olefins have far-re...
International audienceIsoprene chain shuttling polymerisation between the 1,4-trans regulating Cp*La...
Sequential cyclic/linear/cyclic living coordination polymerization of 1,6-heptadiene (HPD), propene,...
ConspectusSome of the most readily available and inexpensive monomers for ring-opening metathesis po...
External control over the rate of dynamic methyl group exchange between configurationally stable act...