Crystallography Open Database
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Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 52
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1542543 | CIF | C9 H6.2 N6 O0.1 | R -3 m :H | 12.657; 12.657; 9.296 90; 90; 120 | 1289.7 | Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation. Chemical communications (Cambridge, England), 2016, 52, 4991-4994 |
| 1542544 | CIF | C12 H17 F9 N6 O7 | P b c n | 12.335; 21.047; 7.89 90; 90; 90 | 2048.4 | Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation. Chemical communications (Cambridge, England), 2016, 52, 4991-4994 |
| 1542545 | CIF | C14 H3.5 F10.5 N7 | P 41 3 2 | 15.8427; 15.8427; 15.8427 90; 90; 90 | 3976.4 | Zhou, Dong-Dong; Xu, Yan-Tong; Lin, Rui-Biao; Mo, Zong-Wen; Zhang, Wei-Xiong; Zhang, Jie-Peng High-symmetry hydrogen-bonded organic frameworks: air separation and crystal-to-crystal structural transformation. Chemical communications (Cambridge, England), 2016, 52, 4991-4994 |
| 7118161 | CIF | C9 H15 Dy N2 O14 | P 1 21/n 1 | 10.1045; 15.4994; 10.4754 90; 102.207; 90 | 1603.5 | Liang Qin; Li-Xian Lin; Zhi-Ping Fang; Shui-Ping Yang; Gui-Hua Qiu; Jin-Xiang Chen; Wen-Hua Chen A water-stable metal-organic framework of a zwitterionic carboxylate with dysprosium: a sensing platform for Ebolavirus RNA sequences Chem.Commun., 2016, 52, 132 |
| 7118162 | CIF | C12 H16 N2 O4 | P 1 21 1 | 5.1412; 26.4969; 9.2776 90; 105.207; 90 | 1219.59 | Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed Gelation by supramolecular dimerization of mono(urea)s Chem.Commun., 2016, 52, 198 |
| 7118163 | CIF | C11 H14 N2 O4 | P -1 | 4.6214; 8.2787; 14.248 92.962; 94.351; 95.33 | 540.25 | Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed Gelation by supramolecular dimerization of mono(urea)s Chem.Commun., 2016, 52, 198 |
| 7118164 | CIF | C12 H16 N2 O4 | P -1 | 4.529; 9.009; 15.234 101.869; 93.598; 101.742 | 592 | Abigail E. Hooper; Stuart R. Kennedy; Christopher D. Jones; Jonathan W. Steed Gelation by supramolecular dimerization of mono(urea)s Chem.Commun., 2016, 52, 198 |
| 7118165 | CIF | C93 H14 N O2 S2 Sc3 | P n a 21 | 19.9441; 15.7417; 14.9924 90; 90; 90 | 4706.9 | Maira R. Ceron; Marta Izquierdo; Nuria Alegret; Juan A. Valdez; Antonio Rodriguez-Fortea; Marilyn M. Olmstead; Alan L. Balch; Josep M. Poblet; Luis Echegoyen Reactivity differences of Sc3N at C2n (2n = 68 and 80). Synthesis of the first methanofullerene derivatives of Sc3N at D5h-C80 Chem.Commun., 2016, 52, 64 |
| 7118166 | CIF | C30 H49 B Fe N4 O2 Si2 | P 1 21/n 1 | 16.807; 12.849; 17.795 90; 114.07; 90 | 3509 | Holger Braunschweig; Rian D. Dewhurst; Katharina Ferkinghoff Carbene-induced synthesis of the first borironium cations using the [(eta^5^-C5Me5)Fe(CO)2]^-^ anion as an unlikely leaving group Chem.Commun., 2016, 52, 183 |
| 7118167 | CIF | C34 H57 B Fe N4 O2 Si2 | P 1 21/c 1 | 10.5605; 17.2867; 20.8645 90; 99.455; 90 | 3757.2 | Holger Braunschweig; Rian D. Dewhurst; Katharina Ferkinghoff Carbene-induced synthesis of the first borironium cations using the [(eta^5^-C5Me5)Fe(CO)2]^-^ anion as an unlikely leaving group Chem.Commun., 2016, 52, 183 |
| 7118168 | CIF | C71 H58 Cl4 N2 S2 | P 21 21 21 | 13.4055; 15.0828; 29.1775 90; 90; 90 | 5899.5 | Ping Chen; Sheng-mei Lu; Wengang Guo; Yan Liu; Can Li A highly enantioselective thiolation of sulfonyl indoles to access 3-sec-sulfur-substituted indoles in water Chem.Commun., 2016, 52, 96 |
| 7118169 | CIF | C17 H19 Cl O5 | C 1 2 1 | 21.41; 9.115; 8.678 90; 90.827; 90 | 1693.4 | Qiang Sha; Hadi Arman; Michael P. Doyle Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement Chem.Commun., 2016, 52, 108 |
| 7118170 | CIF | C23 H22 Cl N O3 | P 21 21 21 | 9.258; 9.554; 22.789 90; 90; 90 | 2015.7 | Qiang Sha; Hadi Arman; Michael P. Doyle Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement Chem.Commun., 2016, 52, 108 |
| 7118171 | CIF | C96 H104 N7 O Re | P -1 | 15.7923; 16.6247; 21.4456 70.8548; 70.4554; 71.4233 | 4872.6 | Jan Paulo T. Zaragoza; Maxime A. Siegler; David P. Goldberg Rhenium(V)-oxo corrolazines: isolating redox-active ligand reactivity Chem.Commun., 2016, 52, 167 |
| 7118172 | CIF | C18 H26 N3 Ni O2 | P 21 21 21 | 5.79; 10.095; 29.897 90; 90; 90 | 1747.5 | Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism Chem.Commun., 2016, 52, 202 |
| 7118173 | CIF | C24 H23 F2 N3 Ni O2 | P 21 21 21 | 10.148; 11.913; 17.409 90; 90; 90 | 2104.6 | Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism Chem.Commun., 2016, 52, 202 |
| 7118174 | CIF | C21.5 H31 F N3 Ni O2.5 | P 21 21 21 | 10.777; 10.97; 36.58 90; 90; 90 | 4325 | Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism Chem.Commun., 2016, 52, 202 |
| 7118175 | CIF | C15 H12 F2 | C 1 2/c 1 | 24.87; 5.944; 16.266 90; 107.995; 90 | 2287 | Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism Chem.Commun., 2016, 52, 202 |
| 7118176 | CIF | C15 H13 F | C 1 c 1 | 7.74284; 17.2689; 8.39473 90; 91.1751; 90 | 1122.23 | Jan Wenz; Christoph A. Rettenmeier; Hubert Wadepohl; Lutz H. Gade Catalytic C-F bond activation of geminal difluorocyclopropanes by nickel(I) complexes via a radical mechanism Chem.Commun., 2016, 52, 202 |
| 7118177 | CIF | C20 H26 N2 O6 S | P 21 21 2 | 14.0216; 21.3117; 6.4976 90; 90; 90 | 1941.64 | Pedras, M. S. C.; To, Q. H.; Schatte, G. Divergent reactivity of an indole glucosinolate yields Lossen or Neber rearrangement products: the phytoalexin rapalexin A or a unique β-d-glucopyranose fused heterocycle. Chemical communications (Cambridge, England), 2016, 52, 2505-2508 |
| 7118178 | CIF | C60 H90 Li2 O12 Th | R -3 :H | 14.8737; 14.8737; 24.3175 90; 90; 120 | 4658.9 | Pedrick, Elizabeth A.; Hrobárik, Peter; Seaman, Lani A.; Wu, Guang; Hayton, Trevor W. Synthesis, structure and bonding of hexaphenyl thorium(iv): observation of a non-octahedral structure. Chemical communications (Cambridge, England), 2015, 52, 689-692 |
| 7118179 | CIF | C60 H78 Li2 O10 Th | P 1 21/n 1 | 16.5641; 16.7043; 21.3854 90; 108.682; 90 | 5605.4 | Pedrick, Elizabeth A.; Hrobárik, Peter; Seaman, Lani A.; Wu, Guang; Hayton, Trevor W. Synthesis, structure and bonding of hexaphenyl thorium(iv): observation of a non-octahedral structure. Chemical communications (Cambridge, England), 2015, 52, 689-692 |
| 7118185 | CIF | C29 H21 N O | P 21 21 21 | 9.002; 13.225; 17.293 90; 90; 90 | 2058.8 | Barsu, Nagaraju; Sen, Malay; Premkumar, J. Richard; Sundararaju, Basker Cobalt(iii) catalyzed C-8 selective C-H and C-O coupling of quinoline N-oxide with internal alkynes via C-H activation and oxygen atom transfer. Chemical communications (Cambridge, England), 2016, 52, 1338-1341 |
| 7118186 | CIF | C12 H14 N6 O6 | P 1 21/n 1 | 9.22642; 9.71725; 18.0546 90; 101.605; 90 | 1585.6 | Erhardt, Hellmuth; Mohr, Fabian; Kirsch, Stefan F. Synthesis of geminal bis- and tristriazoles: exploration of unconventional azide chemistry. Chemical communications (Cambridge, England), 2016, 52, 545-548 |
| 7118187 | CIF | C31 H25 N9 O6 | P 1 21/n 1 | 14.6712; 12.489; 17.0137 90; 106.677; 90 | 2986.3 | Erhardt, Hellmuth; Mohr, Fabian; Kirsch, Stefan F. Synthesis of geminal bis- and tristriazoles: exploration of unconventional azide chemistry. Chemical communications (Cambridge, England), 2016, 52, 545-548 |
| 7118188 | CIF | C33 H35 Cl2 I N4 O Pd | P -1 | 10.7622; 12.8238; 13.4282 114.432; 100.558; 93.044 | 1641.4 | Vicente-Hernández, Inmaculada; Chicote, María-Teresa; Vicente, José; Bautista, Delia A new type of oxidative addition of an iodoarene to a Pd(ii) complex. Chemical communications (Cambridge, England), 2016, 52, 594-596 |
| 7118189 | CIF | C40 H38 Cu2 N9 O12 S2 | P 4/n c c | 11.4766; 11.4766; 30.5554 90; 90; 90 | 4024.5 | Abrahams, C. T.; Abrahams, B. F.; Hudson, T. A.; Robson, R. Templation of a square grid copper(ii) 4,4'-bipyridine network by a 3D PtS-related Cu(i)-Cu(ii) 4,4'-bipyridine crystal. Chemical communications (Cambridge, England), 2016, 52, 609-612 |
| 7118190 | CIF | C20 H20 Cu N4 O8 S2 | P 4/n c c | 11.5095; 11.5095; 15.4286 90; 90; 90 | 2043.8 | Abrahams, C. T.; Abrahams, B. F.; Hudson, T. A.; Robson, R. Templation of a square grid copper(ii) 4,4'-bipyridine network by a 3D PtS-related Cu(i)-Cu(ii) 4,4'-bipyridine crystal. Chemical communications (Cambridge, England), 2016, 52, 609-612 |
| 7118196 | CIF | C77 H100 N4 O10 Pd Si | P 1 21/c 1 | 24.3213; 10.002; 32.0407 90; 111.912; 90 | 7231.2 | Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André Catenane-based mechanically-linked block copolymers. Chemical communications (Cambridge, England), 2016, 52, 2149-2152 |
| 7118197 | CIF | C75 H96 N4 O10 Pd Si | C 1 2/c 1 | 39.473; 12.053; 35.42 90; 114.26; 90 | 15364 | Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André Catenane-based mechanically-linked block copolymers. Chemical communications (Cambridge, England), 2016, 52, 2149-2152 |
| 7118198 | CIF | C75 H93 N4 O13 Pd | I 1 2/a 1 | 37.2375; 11.7434; 32.5955 90; 101.666; 90 | 13959.4 | Nisar Ahamed, B.; Duchêne, Roland; Robeyns, Koen; Fustin, Charles-André Catenane-based mechanically-linked block copolymers. Chemical communications (Cambridge, England), 2016, 52, 2149-2152 |
| 7118199 | CIF | C22 H29 O P | P 1 21/c 1 | 15.6981; 7.4997; 16.6619 90; 93.155; 90 | 1958.65 | Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard Cyclopropane formation under frustrated Lewis pair conditions. Chemical communications (Cambridge, England), 2016, 52, 2695-2697 |
| 7118200 | CIF | C22 H29 P | P -1 | 8.3322; 8.5865; 13.0867 87.833; 85.945; 86.322 | 931.49 | Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard Cyclopropane formation under frustrated Lewis pair conditions. Chemical communications (Cambridge, England), 2016, 52, 2695-2697 |
| 7118201 | CIF | C43 H37 B F15 O P Si | P 1 21/c 1 | 10.8091; 25.3584; 16.9567 90; 96.133; 90 | 4621.25 | Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard Cyclopropane formation under frustrated Lewis pair conditions. Chemical communications (Cambridge, England), 2016, 52, 2695-2697 |
| 7118202 | CIF | C25 H6 B F15 O | P -1 | 9.4516; 12.1427; 12.2399 110.414; 100.07; 97.111 | 1269.99 | Krupski, Sergei; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard Cyclopropane formation under frustrated Lewis pair conditions. Chemical communications (Cambridge, England), 2016, 52, 2695-2697 |
| 7118203 | CIF | C96 H110 F12 N8 O18 P2 | P -1 | 12.01; 13.437; 16.32 106.161; 102.667; 98.007 | 2411 | Han, Ying; Meng, Zheng; Chen, Chuan-Feng Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts. Chemical communications (Cambridge, England), 2016, 52, 590-593 |
| 7118204 | CIF | C90 H96 F12 N2 O16 P2 | P -1 | 13.799; 15.7; 22.416 104.6; 96.36; 107.93 | 4377 | Han, Ying; Meng, Zheng; Chen, Chuan-Feng Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts. Chemical communications (Cambridge, England), 2016, 52, 590-593 |
| 7118205 | CIF | C80 H88 Cl6 F12 N2 O16 P2 | C 1 2/c 1 | 20.956; 17.451; 24.943 90; 109.498; 90 | 8599 | Han, Ying; Meng, Zheng; Chen, Chuan-Feng Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts. Chemical communications (Cambridge, England), 2016, 52, 590-593 |
| 7118206 | CIF | C92 H104 F12 N2 O20 P2 | P -1 | 12.778; 12.983; 14.022 108.815; 93.025; 100.752 | 2147 | Han, Ying; Meng, Zheng; Chen, Chuan-Feng Acid/base controllable complexation of a triptycene-derived macrotricyclic host and protonated 4,4'-bipyridinium/pyridinium salts. Chemical communications (Cambridge, England), 2016, 52, 590-593 |
| 7118207 | CIF | C32 H29 N O2 S | P 1 21/c 1 | 11.62; 11.0673; 21.125 90; 98.311; 90 | 2688.2 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118208 | CIF | C26 H25 N O2 S | P 1 21/n 1 | 13.926; 10.6835; 14.955 90; 92.243; 90 | 2223.3 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118209 | CIF | C26 H27 N O3 S | P 1 21/n 1 | 10.4657; 19.751; 12.477 90; 114.712; 90 | 2342.9 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118210 | CIF | C24 H21 N O2 S | P 1 21/c 1 | 10.6663; 10.8826; 18.121 90; 103.78; 90 | 2042.9 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118211 | CIF | C24 H21 N O2 S | P 1 21/c 1 | 14.001; 12.335; 11.587 90; 95.497; 90 | 1991.9 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118212 | CIF | C24 H21 N O2 S | P 1 21/c 1 | 8.9249; 9.9995; 22.944 90; 107.13; 90 | 1956.8 | Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s. Chemical communications (Cambridge, England), 2016, 52, 2811-2814 |
| 7118213 | CIF | C54 H58 N3 P2 Rh | P 1 21/n 1 | 13.58; 21.768; 17.29 90; 111.548; 90 | 4754 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118214 | CIF | C48 H48 N3 P2 Rh | P 1 21/c 1 | 16.185; 18.144; 15.477 90; 118.406; 90 | 3998 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118215 | CIF | C72 H66 N3 P2 Rh | P 1 21/n 1 | 13.567; 28.198; 16.293 90; 109.213; 90 | 5886 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118216 | CIF | C98 H96 N6 P4 Rh2 | C 1 2/c 1 | 42.986; 17.237; 27.577 90; 119.527; 90 | 17779 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
| 7118217 | CIF | C60 H56 N3 P2 Rh | P 1 21/n 1 | 13.907; 27.103; 16.593 90; 112.133; 90 | 5793 | Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G. Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift. Chemical communications (Cambridge, England), 2016, 52, 586-589 |
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