Crystallography Open Database

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Searching journal of publication like 'Polym. Chem.' volume of publication is 8

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COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1544903 CIFC29 H31 N3 O3 PdP 41 21 29.1556; 9.1556; 66.051
90; 90; 90
5536.7Huang, Yingda; He, Jianyun; Liu, Zhanxiong; Cai, Guilong; Zhang, Shaowen; Li, Xiaofang
A highly active chiral (S,S)-bis(oxazoline) Pd(ii) alkyl complex/activator catalytic system for vinyl polymerization of norbornene in air and water
Polym. Chem., 2017, 8, 1217
1545167 CIFC25 H22.5 N6 O6.25P 1 21/n 114.144; 12.445; 14.545
90; 91.32; 90
2559.6Li, Wenfang; Zhang, Chenyang; Qi, Shuaiwei; Deng, Xiaoli; Wang, Wei; Yang, Bing; Liu, Junqiu; Dong, Zeyuan
A folding-directed catalytic microenvironment in helical dynamic covalent polymers formed by spontaneous configuration control
Polym. Chem., 2017, 8, 1294
1545270 CIFC18 H22 N2 O7 SP 1 21 16.4419; 14.7348; 10.7176
90; 106.31; 90
976.38Gregory, Georgina L.; Hierons, Elizabeth M.; Kociok-Köhn, Gabriele; Sharma, Ram I.; Buchard, Antoine
CO2-Driven stereochemical inversion of sugars to create thymidine-based polycarbonates by ring-opening polymerisation
Polym. Chem., 2017, 8, 1714
1545271 CIFC12 H14 N2 O6P 1 21 17.0627; 9.6573; 10.032
90; 110.448; 90
641.13Gregory, Georgina L.; Hierons, Elizabeth M.; Kociok-Köhn, Gabriele; Sharma, Ram I.; Buchard, Antoine
CO2-Driven stereochemical inversion of sugars to create thymidine-based polycarbonates by ring-opening polymerisation
Polym. Chem., 2017, 8, 1714
1545283 CIFC15 H18 O11C 1 2 128.835; 6.5931; 9.909
90; 105.373; 90
1816.4Su, Lu; Khan, Sarosh; Fan, Jingwei; Lin, Yen-Nan; Wang, Hai; Gustafson, Tiffany P.; Zhang, Fuwu; Wooley, Karen L.
Functional sugar-based polymers and nanostructures comprised of degradable poly(d-glucose carbonate)s
Polym. Chem., 2017, 8, 1699

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