The Best Chemistry compound: 14694-95-2

In addition to the literature in the link below, there is a lot of literature about this compound(Tris(triphenylphosphine)chlororhodium)SDS of cas: 14694-95-2, illustrating the importance and wide applicability of this compound(14694-95-2).

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: Tris(triphenylphosphine)chlororhodium, is researched, Molecular C54H45ClP3Rh, CAS is 14694-95-2, about Amphiphilic Triblock Copolymers Containing Polypropylene as the Middle Block, the main research direction is amphiphilic triblock polypropylene isotactic middle block polylactone polyester; copolymerization; homogeneous catalysis; polyolefin; postpolymerization modification; telechelic polypropylene.SDS of cas: 14694-95-2.

The synthesis of stereoregular telechelic polypropylene (PP) and their use to access triblock amphiphilic copolymers with the PP block located in the center is described. The strategy consists of selectively copolymerizing propylene and a bi-functional comonomer (1,3-diisopropenylbenzene) to yield a α,ω-substituted polypropylene. Initiation of the copolymerization favors insertion of DIB over propylene; propagation steps favor insertion of propylene. Termination via a chain-transfer reaction yields the terminal unsaturation of the polymer. The telechelic polypropylene is then converted into α,ω-hydroxyl-terminated polypropylene and used as a macroinitiator for the synthesis of triblock copolymers. Water-soluble amphiphilic triblock polymers are also synthesized. The use of catalytic reactions simultaneously provides the stereocontrol of the polypropylene and high productivity (multiple chains of block copolymer per metal center).

In addition to the literature in the link below, there is a lot of literature about this compound(Tris(triphenylphosphine)chlororhodium)SDS of cas: 14694-95-2, illustrating the importance and wide applicability of this compound(14694-95-2).

Reference:
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate