Metal-Catalyzed Synthesis of Cyclic Carbonates from Carbon Dioxide and Oxiranes
β Scribed by Dr. Michael Ratzenhofer; Priv.-Doz. Dr. Horst Kisch
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 216 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
β¦ Synopsis
Table 1. Iy5Pt-NMR data for some platinum-tin complexes [a].
1runs-[PtC1(SnC1~)(PEt~)~] [c] 28954 -4780 -864 Irun~-[Pt(SnCl~)~(PEt,)~] [d] 20410 -5152 -618 [el trans-[PtH(SnCla)(PEt,)2J [fl 9 067 -5302 -426 truns-[PtH(SnCb)(PPh2CH2Ph)2] [fl 10955 -5322 -428 I~u~~-[P~(C(CO,E~)==CHCOZE~)(S~C~~)(PP~~)Z] [g] 11 320 -4771 -469 [a] Chemical shifts (6 values rel. to external Na,PtCI,) and coupling constants (in Hz). [b] A8=6[PtX(SnC13)(PR3)2]-6[PtX(CI)(PR3)2]. [c] In CD2C12 at -40Β°C. [d] In (CD3),CO at -50Β°C. [el 6[PtC12(PEt3)2] -6[Pt(SnC13)2(PEt3)2] divided by 2. [fl In CD2C12 at -70 "C. [g] In CD2Cl2 at room temperature. tmns-[PtH(SnCI3)(PPh,)2l [fl 11512 -5195 -354
π SIMILAR VOLUMES
## Abstract A series of easily prepared Lewis basic ionic liquids were developed for cyclic carbonate synthesis from epoxide and carbon dioxide at low pressure without utilization of any organic solvents or additives. Notably, quantitative yields together with excellent selectivity were attained wh