Catalytic properties of novel chiral polyoxomolybdate(VI) salts: The ring-opening metathesis polymerization (ROMP) of norbornene
β Scribed by Malachy McCann; Andrew J. Beaumont
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 584 KB
- Volume
- 108
- Category
- Article
- ISSN
- 1381-1169
No coin nor oath required. For personal study only.
β¦ Synopsis
Each of the chiral polyoxomolybdate(VI1 salts (R,N 0,02&R jN>,] and (Na),(R ,N )2[Mo,0,,] (R,N = (-I-)cinchonine, t +)-hydroquinidine or (-kquinine).
in the presence of the cocatalyst EtAICl,, catalyses the ring-opening metathesis polymerization of norbomene at room temperature. Thr, polynorbomene produced in these reactions was found to be mostly insoluble. Inclusion of a chain transfer agent, I-hexene, in the reactions leads to greatly improved yields of polynorbomene which is freely soluble in chloroform, and the quantity of polymer formed is highly sensitive to the amount of I -hexene added.
π SIMILAR VOLUMES
## Abstract Amino acidβderived novel norbornene monomers were synthesized and polymerized with ruthenium catalysts. The polymerization rates were affected by the stereo structure of the monomers; __exo,exo__βNBL underwent ROMP faster to give the polymers in higher yields than the __endo,exo__βcount
## Abstract A series of pentavalent tantalum and niobium complexes with aryloxy ligands was prepared, and their catalytic behavior for the ROMP of norbornene was studied in the presence of an alkylaluminum cocatalyst. Tantalum complexes **1**β**4** showed very high activity for the ROMP of NBE in c