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 |
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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 |
7118218 | CIF | C36 H26 Br2 O4 | P 21 21 21 | 5.6288; 12.578; 41.669 90; 90; 90 | 2950.1 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
7118219 | CIF | C36 H28 O4 | P 21 21 21 | 9.263; 12.8186; 22.369 90; 90; 90 | 2656.1 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
7118220 | CIF | C36 H26 Br2 O4 | P 21 21 21 | 5.5911; 13.004; 40.623 90; 90; 90 | 2953.6 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
7118221 | CIF | C13 H11 F N2 | P -1 | 10.0641; 11.0425; 12.1824 114.924; 95.055; 111.476 | 1094.39 | Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak 'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks. Chemical communications (Cambridge, England), 2016, 52, 2141-2144 |
7118222 | CIF | C13 H10 F2 N2 | P 1 21/c 1 | 12.7028; 8.3775; 11.5509 90; 117.017; 90 | 1095.1 | Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak 'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks. Chemical communications (Cambridge, England), 2016, 52, 2141-2144 |
7118223 | CIF | C41 H33 N3 O6 | P 1 21/c 1 | 11.1829; 11.5006; 26.2259 90; 92.219; 90 | 3370.4 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118224 | CIF | C41 H33 Cd Cl0 I2 N3 O6 | R -3 :H | 54.6374; 54.6374; 8.9458 90; 90; 120 | 23127.6 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118225 | CIF | C42.17 H36 Br Cd I2 N3 O6.33 | R -3 :H | 54.5811; 54.5811; 8.9081 90; 90; 120 | 22982.7 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118226 | CIF | C42 H35 Cd I4 N3 O6 | R -3 :H | 54.772; 54.772; 8.8733 90; 90; 120 | 23053.3 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118227 | CIF | C41 H33 Cd I2 N3 O6 | R -3 :H | 54.8819; 54.8819; 8.8759 90; 90; 120 | 23152.7 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118230 | CIF | C26 H18 Br Cl4 N2 O4 | P 1 21 1 | 13.0622; 8.2259; 13.1485 90; 106.33; 90 | 1355.79 | Cao, Zhong-Yan; Zhao, Yu-Lei; Zhou, Jian Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles. Chemical communications (Cambridge, England), 2016, 52, 2537-2540 |
7118231 | CIF | C27 H21 Br Cl2 N2 O5 | P 21 21 21 | 12.315; 13.9146; 15.2049 90; 90; 90 | 2605.49 | Cao, Zhong-Yan; Zhao, Yu-Lei; Zhou, Jian Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles. Chemical communications (Cambridge, England), 2016, 52, 2537-2540 |
7118232 | CIF | C31 H30 Br N3 O5 | I 1 2 1 | 14.6406; 9.57209; 19.5953 90; 97.003; 90 | 2725.62 | Zhao, Kun; Zhi, Ying; Li, Xinyi; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter Asymmetric synthesis of 3,3'-pyrrolidinyl-dispirooxindoles via a one-pot organocatalytic Mannich/deprotection/aza-Michael sequence. Chemical communications (Cambridge, England), 2016, 52, 2249-2252 |
7118241 | CIF | C40 H24 In N2 O8 | C 1 2/c 1 | 28.286; 20.9422; 27.5862 90; 120.798; 90 | 14037 | Li, Xingjun; Chen, Xueyuan; Jiang, Feilong; Chen, Lian; Lu, Shan; Chen, Qihui; Wu, Mingyan; Yuan, Daqiang; Hong, Maochun The dynamic response of a flexible indium based metal-organic framework to gas sorption. Chemical communications (Cambridge, England), 2016, 52, 2277-2280 |
7118242 | CIF | C40 H24 In N2 O8 | I 1 2/c 1 | 26.9793; 21.3293; 26.4721 90; 97.001; 90 | 15119.8 | Li, Xingjun; Chen, Xueyuan; Jiang, Feilong; Chen, Lian; Lu, Shan; Chen, Qihui; Wu, Mingyan; Yuan, Daqiang; Hong, Maochun The dynamic response of a flexible indium based metal-organic framework to gas sorption. Chemical communications (Cambridge, England), 2016, 52, 2277-2280 |
7118243 | CIF | C25 H32 B F6 I2 N8 O P W | P 1 21/n 1 | 8.352; 22.5729; 18.2914 90; 100.772; 90 | 3387.69 | Helmdach, Kai; Rüger, Julia; Villinger, Alexander; Seidel, Wolfram W. Dual nucleophilic substitution at a W(ii) η(2)-coordinated diiodo acetylene leading to an amidinium carbyne complex. Chemical communications (Cambridge, England), 2016, 52, 2616-2619 |
7118244 | CIF | C33 H38 B F6 N8 O2 P W | P 1 21/n 1 | 25.7178; 11.6201; 25.7435 90; 97.686; 90 | 7624.2 | Helmdach, Kai; Rüger, Julia; Villinger, Alexander; Seidel, Wolfram W. Dual nucleophilic substitution at a W(ii) η(2)-coordinated diiodo acetylene leading to an amidinium carbyne complex. Chemical communications (Cambridge, England), 2016, 52, 2616-2619 |
7118245 | CIF | C20 H21 Br O5 | P 1 21/c 1 | 12.3928; 8.3243; 18.5364 90; 95.888; 90 | 1902.15 | Yu, Zhunzhun; Qiu, Haile; Liu, Lu; Zhang, Junliang Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C-H functionalization and aldol annulation. Chemical communications (Cambridge, England), 2016, 52, 2257-2260 |
7118246 | CIF | C21 H23 Br O5 | P 1 21/c 1 | 9.2166; 9.0685; 23.2491 90; 99.08; 90 | 1918.83 | Yu, Zhunzhun; Qiu, Haile; Liu, Lu; Zhang, Junliang Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C-H functionalization and aldol annulation. Chemical communications (Cambridge, England), 2016, 52, 2257-2260 |
7118247 | CIF | C27 H24 N2 O3 | P -1 | 10.9476; 11.03; 11.0714 86.1003; 64.8281; 60.6087 | 1037.28 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118249 | CIF | C31 H24 N2 O2 | P -1 | 9.365; 11.4265; 11.9971 74.104; 80.112; 71.016 | 1162.72 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118250 | CIF | C25 H20 N3 O | P 1 21/c 1 | 18.817; 10.53; 9.5207 90; 96.996; 90 | 1872.4 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118251 | CIF | C28 H28 Cl N O3 | P -1 | 9.469; 10.0316; 13.1967 83.975; 70.468; 85.668 | 1173.8 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118252 | CIF | C19 H15 N O4 | P 1 21/c 1 | 8.3566; 17.7311; 10.5304 90; 101.637; 90 | 1528.24 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118253 | CIF | C27 H26 N2 O3 | P -1 | 8.2128; 12.0722; 12.1473 80.826; 73.356; 74.316 | 1106.54 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118254 | CIF | C18 H19 N O3 | P n m a | 15.9415; 14.8517; 6.2573 90; 90; 90 | 1481.5 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118255 | CIF | C14 H15 N O5 | P 1 21/c 1 | 9.5866; 19.5978; 7.6285 90; 111.316; 90 | 1335.17 | Baumann, A. N.; Music, A.; Karaghiosoff, K.; Didier, D. Highly diastereoselective approach to methylenecyclopropanes via boron-homologation/allylboration sequences. Chemical communications (Cambridge, England), 2016, 52, 2529-2532 |
7118256 | CIF | C45 H37 Cl N5 O P Ru | P 1 21/n 1 | 13.9666; 12.6444; 21.018 90; 95.457; 90 | 3694.9 | Tseng, Kuei-Nin T; Lin, Steve; Kampf, Jeff W.; Szymczak, Nathaniel K. Upgrading ethanol to 1-butanol with a homogeneous air-stable ruthenium catalyst. Chemical communications (Cambridge, England), 2016, 52, 2901-2904 |
7118257 | CIF | C39 H31 Cl N5 O3 P Ru | P 1 21/c 1 | 16.1333; 12.495; 16.9891 90; 98.709; 90 | 3385.27 | Tseng, Kuei-Nin T; Lin, Steve; Kampf, Jeff W.; Szymczak, Nathaniel K. Upgrading ethanol to 1-butanol with a homogeneous air-stable ruthenium catalyst. Chemical communications (Cambridge, England), 2016, 52, 2901-2904 |
7118258 | CIF | C38 H42 Cl6 Cu2 N6 | P -1 | 8.2153; 11.1662; 11.5343 85.272; 84.43; 77.543 | 1026.24 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118259 | CIF | C38 H42 Cl6 Cu2 N6 | P -1 | 8.1887; 10.9691; 11.3579 85.0163; 85.1738; 77.5551 | 990.21 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118260 | CIF | C40 H46 Cl6 Cu2 N6 | P -1 | 8.3056; 11.1055; 11.873 86.315; 89.284; 77.72 | 1067.9 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118261 | CIF | C40 H46 Cl6 Cu2 N6 | P -1 | 8.3293; 10.9929; 11.7343 86.079; 89.732; 77.869 | 1047.9 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118262 | CIF | C38 H40 Cl8 Cu2 N6 | P -1 | 8.253; 10.948; 11.802 85.792; 89.721; 78.477 | 1042 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118263 | CIF | C40 H46 Cl6 Cu2 N6 O2 | P -1 | 8.292; 10.995; 12.277 84.743; 86.68; 78.394 | 1090.9 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118264 | CIF | C18 H18 Cl Cu N4 O2 | P 21 21 21 | 9.0636; 9.6375; 20.925 90; 90; 90 | 1827.8 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118265 | CIF | C21 H25 Cl Cu N3 | P 1 21/c 1 | 9.5545; 8.8034; 23.9329 90; 96.6239; 90 | 1999.61 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118266 | CIF | C36 H38 Cl2 Cu2 N6 | P 1 21/n 1 | 10.0169; 15.969; 10.7209 90; 95.056; 90 | 1708.24 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118267 | CIF | C43.5 H37 Al Au Cl F36 N2 O4 P4 | P 1 21/n 1 | 10.7137; 38.3822; 14.7478 90; 90.909; 90 | 6063.8 | Borger, Jaap E.; Bakker, Martijn S.; Ehlers, Andreas W.; Lutz, Martin; Chris Slootweg, J.; Lammertsma, Koop Functionalization of P4 in the coordination sphere of coinage metal cations. Chemical communications (Cambridge, England), 2016, 52, 3284-3287 |
7118268 | CIF | C94 H97 Al Au2 F36 N4 O4 P4 | C 1 2/c 1 | 39.9091; 25.1072; 22.5843 90; 100.38; 90 | 22259.3 | Borger, Jaap E.; Bakker, Martijn S.; Ehlers, Andreas W.; Lutz, Martin; Chris Slootweg, J.; Lammertsma, Koop Functionalization of P4 in the coordination sphere of coinage metal cations. Chemical communications (Cambridge, England), 2016, 52, 3284-3287 |
7118269 | CIF | C27 H24 Br N O3 | P 21 21 21 | 8.8669; 14.7074; 17.9059 90; 90; 90 | 2335.1 | Li, Mingfeng; Guo, Xin; Jin, Weifeng; Zheng, Qing; Liu, Shunying; Hu, Wenhao An enantioselective three-component reaction of diazoacetates with indoles and enals by iridium/iminium co-catalysis. Chemical communications (Cambridge, England), 2016, 52, 2736-2739 |
7118270 | CIF | C18 H32 O3 Si | C 1 2/c 1 | 29.017; 11.4978; 12.6967 90; 111.472; 90 | 3942 | Stepherson, Jacob R.; Fronczek, Frank R.; Kartika, Rendy An expedient synthesis of functionalized 1,4-diketone-derived compounds via silyloxyallyl cation intermediates. Chemical communications (Cambridge, England), 2016, 52, 2300-2303 |
7118271 | CIF | C52 H44 N2 O20 Zn3 | P -1 | 9.4533; 18.614; 19.976 68.27; 82.61; 82.18 | 3223.2 | Chakraborty, Anindita; Bhattacharyya, Sohini; Hazra, Arpan; Ghosh, Ashta Chandra; Maji, Tapas Kumar Post-synthetic metalation in an anionic MOF for efficient catalytic activity and removal of heavy metal ions from aqueous solution. Chemical communications (Cambridge, England), 2016, 52, 2831-2834 |
7118272 | CIF | C15 H26 Cl N W | P n a 21 | 13.1669; 12.7572; 20.0394 90; 90; 90 | 3366.07 | Wright, Christopher M. R.; Turner, Zoë R; Buffet, Jean-Charles; O'Hare, Dermot Tungsten imido catalysts for selective ethylene dimerisation. Chemical communications (Cambridge, England), 2016, 52, 2850-2853 |
7118273 | CIF | C16 H25 Cl4 N O W | P -1 | 8.5941; 14.1186; 17.4478 95.806; 98.562; 97.484 | 2059.88 | Wright, Christopher M. R.; Turner, Zoë R; Buffet, Jean-Charles; O'Hare, Dermot Tungsten imido catalysts for selective ethylene dimerisation. Chemical communications (Cambridge, England), 2016, 52, 2850-2853 |
7118274 | CIF | C22 H21 N O4 | P -1 | 11.0068; 18.8343; 19.829 72.08; 89.811; 77.711 | 3813.1 | Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine. Chemical communications (Cambridge, England), 2016, 52, 2177-2180 |
7118275 | CIF | C22 H21 N O4 | P -1 | 9.035; 13.258; 16.686 90.402; 103.495; 105.139 | 1871.2 | Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine. Chemical communications (Cambridge, England), 2016, 52, 2177-2180 |
7118276 | CIF | C24 H27 N O3 | C 1 2/c 1 | 44.225; 11.0988; 15.9916 90; 99.538; 90 | 7740.9 | Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine. Chemical communications (Cambridge, England), 2016, 52, 2177-2180 |
7118277 | CIF | C90 H187 O100 | P 1 21 1 | 15.517; 9.825; 21.953 90; 90.05; 90 | 3346.8 | Rutenberg, R.; Leitus, G.; Fallik, E.; Poverenov, E. Discovery of a non classic host guest complexation mode in a β-cyclodextrin/propionic acid model. Chemical communications (Cambridge, England), 2016, 52, 2565-2568 |
7118278 | CIF | C30 H25 F N2 O3 S | P 1 21 1 | 5.552; 17.133; 13.413 90; 93.446; 90 | 1273.6 | Sun, Xiao-Xue; Zhang, Hong-Hao; Li, Guo-Hao; Meng, Li; Shi, Feng Diastereo- and enantioselective construction of an indole-based 2,3-dihydrobenzofuran scaffold via catalytic asymmetric [3+2] cyclizations of quinone monoimides with 3-vinylindoles. Chemical communications (Cambridge, England), 2016, 52, 2968-2971 |
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