scholarly journals Oxanorbornenes: Promising New Single Addition Monomers for the Metathesis Polymerization

2021 ◽  
Author(s):  
Subhajit Pal ◽  
Mahshid Alizadeh ◽  
Phally Kong ◽  
Andreas F.M. Kilbinger

Higher ring-opening metathesis propagation rates of exo-norbornene derivatives over endo derivatives are well established in the literature. Here, we report for the first time that endo-isomers of oxanorbornene derivatives show...

2021 ◽  
Author(s):  
Taichi Sotani ◽  
Toshiko Mizokuro ◽  
Tatsuo Yajima ◽  
Hiromitsu Sogawa ◽  
Fumio Sanda

Ring-opening metathesis polymerization (ROMP) of norbornene derivatives is useful for preparing thermally stable and transparent polymeric materials with good moldability. This study deals with ROMP of norbornene monomer 1 bearing...


2021 ◽  
Author(s):  
Janis V. Musso ◽  
Mathis Benedikter ◽  
Paul Gebel ◽  
Vincent Gramm ◽  
Dongren Wang ◽  
...  

Cationic W alkylidene N-heterocyclic carbene complexes allow for the stereospecific ring-opening metathesis polymerization of norbornenes with high trans-iso- and high cis-syndiospecificity, respectively.


2001 ◽  
Vol 704 ◽  
Author(s):  
James H. Wynne ◽  
Christopher T. Lloyd ◽  
Steven E. Bullock ◽  
Robert F. Cozzens

AbstractWe report the synthesis of a series of highly functional metal chelated silyl- and tert-butyl-protected 2, 3-diaminomethyl norbornene derivatives. Subsequent alterations to the previously synthesized norbornene adducts afford many other derivatives containing such functionalities as alkyl, cyano, esters, and ethers. These derivatives are then subjected to ring-opening metathesis polymerization (ROMP) employing a ruthenium homogeneous catalyst to afford phase separated block polymers. The block polymers formed serve as unique templates for the formation of size controlled metal nanoclusters having a narrow dispersion. These metal nanoclusters containing diblock polymers are evaluated as unique electrical and optical materials.


2019 ◽  
Vol 15 ◽  
pp. 44-51 ◽  
Author(s):  
Yuan-Zhen Ke ◽  
Shou-Ling Huang ◽  
Guoqiao Lai ◽  
Tien-Yau Luh

At 0 °C in THF in the presence of Grubbs first generation catalyst, cyclobutene derivatives undergo ROMP readily, whereas norbornene derivatives remain intact. When the substrate contains both cyclobutene and norbornene moieties, the conditions using THF as the solvent at 0 °C offer a useful protocol for the selective ROMP of cyclobutene to give norbornene-appended polycyclobutene. Unsymmetrical ladderphane having polycyclobutene and polynorbornene as two strands is obtained by further ROMP of the norbornene appended polycyclobutene in the presence of Grubbs first generation catalyst in DCM at ambient temperature. Methanolysis of this unsymmetrical ladderphane gives polycyclobutene methyl ester and insoluble polynorbornene-amide-alcohol. The latter is converted into the corresponding soluble acetate. Both polymers are well characterized by spectroscopic means. No norbornene moiety is found to be incorporated into polycyclobutene strand at all. The double bonds in the polycyclobutene strand are mainly in cis configuration (ca 70%), whereas the E/Z ratio for polynorbornene strand is 8:1.


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