Crystallography Open Database
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Searching journal of publication like 'Chemical science' volume of publication is 9
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1548292 | CIF | C164.05 H143.07 Cu2 F36 N29.98 O2.48 P6 Ru2 | P -1 | 12.383; 18.49; 19.983 69.381; 79.742; 88.826 | 4209 | Hayes, Dugan; Kohler, Lars; Hadt, Ryan G.; Zhang, Xiaoyi; Liu, Cunming; Mulfort, Karen L.; Chen, Lin X. Excited state electron and energy relays in supramolecular dinuclear complexes revealed by ultrafast optical and X-ray transient absorption spectroscopy. Chemical science, 2018, 9, 860-875 |
| 1548293 | CIF | C53 H45 B3 F20 N4 O2 | P 1 21/c 1 | 8.281; 27.653; 23.173 90; 91.817; 90 | 5304 | Zheng, Junhao; Li, Zhen Hua; Wang, Huadong Addition of dihydrogen to a borylborenium center. Chemical science, 2018, 9, 1433-1438 |
| 1548345 | CIF | C39 H38 N2 O3 S | P 1 21/c 1 | 16.5942; 8.7199; 21.4742 90; 93.516; 90 | 3101.5 | Yamamoto, Y.; Murayama, T.; Jiang, J.; Yasui, T.; Shibuya, M. The vinylogous Catellani reaction: a combined computational and experimental study. Chemical science, 2018, 9, 1191-1199 |
| 1548346 | CIF | C204 H158 B8 F32 N40 O7 Zn4 | C 1 2/c 1 | 47.6161; 31.7486; 56.289 90; 111.305; 90 | 79279 | Yang, Linlin; Jing, Xu; An, Bowen; He, Cheng; Yang, Yang; Duan, Chunying Binding of anions in triply interlocked coordination catenanes and dynamic allostery for dehalogenation reactions. Chemical science, 2018, 9, 1050-1057 |
| 1548347 | CIF | C206 H163 B3.5 F14 I4.5 N41 O8 Zn4 | C 1 2/c 1 | 47.061; 32.0425; 55.568 90; 110.406; 90 | 78535 | Yang, Linlin; Jing, Xu; An, Bowen; He, Cheng; Yang, Yang; Duan, Chunying Binding of anions in triply interlocked coordination catenanes and dynamic allostery for dehalogenation reactions. Chemical science, 2018, 9, 1050-1057 |
| 1548380 | CIF | C58 H48 Ag5 F6 N17 O6 S2 | C m c m | 12.842; 21.083; 25.145 90; 90; 90 | 6808 | He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization. Chemical science, 2018, 9, 1481-1487 |
| 1548381 | CIF | C59 H55 Ag5 F6 N17 O6 S2 | P -1 | 14.3867; 15.4794; 18.9913 101.197; 93.2; 94.368 | 4125.97 | He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization. Chemical science, 2018, 9, 1481-1487 |
| 1548382 | CIF | C64 H58 Ag4 F9 N17 O10 S2 | C 1 2/c 1 | 32.1129; 12.1233; 24.0913 90; 130.309; 90 | 7152.2 | He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization. Chemical science, 2018, 9, 1481-1487 |
| 1548383 | CIF | C73.5 H68 Ag5 F9 N18 O12.5 S3 | P -1 | 14.8347; 15.7643; 18.6915 96.459; 93.928; 95.369 | 4310.55 | He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization. Chemical science, 2018, 9, 1481-1487 |
| 1548384 | CIF | C63 H55 Ag5 Cl4.5 F12 N17 O13.25 S4 | P -1 | 13.189; 13.561; 28.427 103.51; 90.23; 118.57 | 4302 | He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization. Chemical science, 2018, 9, 1481-1487 |
| 1548385 | CIF | C67 H57 Ag5 F9 N17 O9 S3 | P 1 21/c 1 | 14.3943; 31.0527; 22.6971 90; 125.685; 90 | 8240.3 | He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization. Chemical science, 2018, 9, 1481-1487 |
| 1548386 | CIF | C58 H53 Ag5 F6 N17 O6 S2 | P 1 | 12.278; 25.145; 12.408 90; 117.31; 90 | 3403.7 | He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization. Chemical science, 2018, 9, 1481-1487 |
| 1548387 | CIF | C92 H118 As4 Co3 N16 O24 | P 4 21 2 | 20.6668; 20.6668; 16.8568 90; 90; 90 | 7199.8 | Srinivasan, Anandi; Cortijo, Miguel; Bulicanu, Vladimir; Naim, Ahmad; Clérac, Rodolphe; Sainctavit, Philippe; Rogalev, Andrei; Wilhelm, Fabrice; Rosa, Patrick; Hillard, Elizabeth A. Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain. Chemical science, 2018, 9, 1136-1143 |
| 1548388 | CIF | C56 H48 As2 Co3 N16 O12 | C 1 2/c 1 | 17.794; 19.121; 19.042 90; 116.941; 90 | 5776 | Srinivasan, Anandi; Cortijo, Miguel; Bulicanu, Vladimir; Naim, Ahmad; Clérac, Rodolphe; Sainctavit, Philippe; Rogalev, Andrei; Wilhelm, Fabrice; Rosa, Patrick; Hillard, Elizabeth A. Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain. Chemical science, 2018, 9, 1136-1143 |
| 1548389 | CIF | C50 H51 Co3 F12 N15 O P2 | P 1 21 1 | 11.7226; 21.8073; 12.0149 90; 112.115; 90 | 2845.5 | Srinivasan, Anandi; Cortijo, Miguel; Bulicanu, Vladimir; Naim, Ahmad; Clérac, Rodolphe; Sainctavit, Philippe; Rogalev, Andrei; Wilhelm, Fabrice; Rosa, Patrick; Hillard, Elizabeth A. Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain. Chemical science, 2018, 9, 1136-1143 |
| 1548390 | CIF | C92 H118 As4 Co3 N16 O24 | P 4 21 2 | 20.6481; 20.6481; 16.8896 90; 90; 90 | 7200.8 | Srinivasan, Anandi; Cortijo, Miguel; Bulicanu, Vladimir; Naim, Ahmad; Clérac, Rodolphe; Sainctavit, Philippe; Rogalev, Andrei; Wilhelm, Fabrice; Rosa, Patrick; Hillard, Elizabeth A. Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain. Chemical science, 2018, 9, 1136-1143 |
| 1548396 | CIF | C28 H30 N4 Ni2 O15 S | I a -3 | 39.7584; 39.7584; 39.7584 90; 90; 90 | 62847.3 | Feng, Rui; Jia, Yan-Yuan; Li, Zhao-Yang; Chang, Ze; Bu, Xian-He Enhancing the stability and porosity of penetrated metal-organic frameworks through the insertion of coordination sites. Chemical science, 2018, 9, 950-955 |
| 1548397 | CIF | C36 H20 Co2 N6 O15 | F d -3 m :2 | 46.6983; 46.6983; 46.6983 90; 90; 90 | 101836 | Feng, Rui; Jia, Yan-Yuan; Li, Zhao-Yang; Chang, Ze; Bu, Xian-He Enhancing the stability and porosity of penetrated metal-organic frameworks through the insertion of coordination sites. Chemical science, 2018, 9, 950-955 |
| 1548407 | CIF | C44 H44 B4 Cl6 Dy2 N24 O4 | P 1 21/n 1 | 13.932; 15.014; 14.827 90; 107.69; 90 | 2954.8 | Zhang, Peng; Perfetti, Mauro; Kern, Michal; Hallmen, Philipp P.; Ungur, Liviu; Lenz, Samuel; Ringenberg, Mark R.; Frey, Wolfgang; Stoll, Hermann; Rauhut, Guntram; van Slageren, Joris Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes. Chemical science, 2018, 9, 1221-1230 |
| 1548408 | CIF | C44 H44 B4 Cl6 N24 O4 Y2 | P 1 21/n 1 | 13.937; 15.046; 14.786 90; 107.46; 90 | 2957.7 | Zhang, Peng; Perfetti, Mauro; Kern, Michal; Hallmen, Philipp P.; Ungur, Liviu; Lenz, Samuel; Ringenberg, Mark R.; Frey, Wolfgang; Stoll, Hermann; Rauhut, Guntram; van Slageren, Joris Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes. Chemical science, 2018, 9, 1221-1230 |
| 1548409 | CIF | C44 H44 B4 Cl6 Gd2 N24 O4 | P 1 21/n 1 | 14.15; 15.225; 14.969 90; 107.75; 90 | 3071.3 | Zhang, Peng; Perfetti, Mauro; Kern, Michal; Hallmen, Philipp P.; Ungur, Liviu; Lenz, Samuel; Ringenberg, Mark R.; Frey, Wolfgang; Stoll, Hermann; Rauhut, Guntram; van Slageren, Joris Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes. Chemical science, 2018, 9, 1221-1230 |
| 1548410 | CIF | C44 H44 B4 Cl6 N24 O4 Tb2 | P 1 21/n 1 | 14.003; 15.079; 14.825 90; 107.59; 90 | 2984 | Zhang, Peng; Perfetti, Mauro; Kern, Michal; Hallmen, Philipp P.; Ungur, Liviu; Lenz, Samuel; Ringenberg, Mark R.; Frey, Wolfgang; Stoll, Hermann; Rauhut, Guntram; van Slageren, Joris Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes. Chemical science, 2018, 9, 1221-1230 |
| 1548427 | CIF | C38 H48 B2 N2 O2 | P 1 21/a 1 | 17.6; 19.466; 20.232 90; 96.305; 90 | 6889.6 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548428 | CIF | C48 H56 B2 F3 N3 O2 | P 1 21/c 1 | 11.335; 10.991; 35.202 90; 95.263; 90 | 4367 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548429 | CIF | C29 H39 B2 N O2 | P 1 21/n 1 | 8.723; 23.773; 13.264 90; 99.499; 90 | 2712.9 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548430 | CIF | C28 H38 B2 N2 O2 | P 1 21/n 1 | 10.134; 18.98; 13.58 90; 96.976; 90 | 2592.7 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548431 | CIF | C40 H50 B2 N2 O4 | P -1 | 8.4242; 15.698; 28.081 89.956; 87.717; 89.896 | 3710.6 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548432 | CIF | C49 H59 B2 N3 O4 | P -1 | 10.951; 14.21; 16.118 104.201; 92.6541; 111.94 | 2228.7 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548433 | CIF | C54 H69 B2 N3 O2 | P 1 21/c 1 | 10.6242; 20.635; 22.708 90; 100.578; 90 | 4893.7 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548434 | CIF | C37 H47 B2 N3 O2 | P 1 21/n 1 | 10.981; 10.43; 28.55 90; 94.578; 90 | 3259.5 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548435 | CIF | C37 H47 B2 N3 O2 | P 1 21/a 1 | 15.319; 13.7912; 17.481 90; 112.051; 90 | 3423 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548436 | CIF | C38 H48 B2 N2 O2 | P 1 21/n 1 | 8.565; 33.036; 11.991 90; 90.444; 90 | 3393 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548437 | CIF | C48 H56 B2 F3 N3 O2 | P 1 21/n 1 | 14.692; 11.21; 27.115 90; 105.567; 90 | 4302 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548438 | CIF | C45 H62 B2 N2 O4 | P -1 | 11.4491; 12.8149; 15.929 74.652; 86.76; 65.452 | 2046.2 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548439 | CIF | C49 H59 B2 N3 O4 | P -1 | 8.034; 10.856; 26.173 97.069; 97.132; 102.212 | 2187.4 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548440 | CIF | C53 H63 B2 N3 O2 | P -1 | 11.821; 12.93; 16.755 101.05; 95.8819; 111.862 | 2289.8 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548441 | CIF | C39 H37 B2 F3 N2 O2 | P 21 21 21 | 16.004; 21.403; 32.93 90; 90; 90 | 11280 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548442 | CIF | C39 H47 B2 F3 N2 O2 | P 1 21/c 1 | 14.252; 17.527; 14.877 90; 93.855; 90 | 3707.8 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548443 | CIF | C89 H112 B4 N4 O4 | P -1 | 9.894; 12.714; 16.323 101.384; 91.511; 100.757 | 1973.3 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548444 | CIF | C38 H47 B2 Cl N2 O2 | P 1 21/c 1 | 10.777; 8.468; 38.298 90; 95.088; 90 | 3481 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548445 | CIF | C45 H64 B2 N2 O3 | P n a 21 | 19.208; 13.253; 16.091 90; 90; 90 | 4096.2 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548455 | CIF | C22 H25 N O4 | P 21 21 21 | 10.3192; 11.0867; 17.4057 90; 90; 90 | 1991.31 | Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench. Chemical science, 2018, 9, 1352-1357 |
| 1548456 | CIF | C20 H23 N O2 | P 21 21 21 | 6.1094; 14.2823; 19.8409 90; 90; 90 | 1731.24 | Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench. Chemical science, 2018, 9, 1352-1357 |
| 1548457 | CIF | C27 H21 N O2 | P -1 | 7.9717; 9.2791; 14.2492 95.3798; 105.336; 98.2795 | 996.24 | Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench. Chemical science, 2018, 9, 1352-1357 |
| 1548458 | CIF | C23 H27 N O4 | P 1 21 1 | 9.495; 8.8357; 12.0617 90; 90.258; 90 | 1011.91 | Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench. Chemical science, 2018, 9, 1352-1357 |
| 1548459 | CIF | C106 H66 B4 F40 O2 P2 | P n a 21 | 23.2043; 30.9754; 14.803 90; 90; 90 | 10639.8 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
| 1548460 | CIF | C88 H62 B4 F40 O2 P2 | P -1 | 11.163; 16.2067; 24.8378 76.432; 87.505; 76.034 | 4238.6 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
| 1548461 | CIF | C31 H32 B F10 P | P 1 21/n 1 | 17.6792; 8.532; 19.5972 90; 99.052; 90 | 2919.2 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
| 1548462 | CIF | C40 H34 B F10 P | P 1 21/n 1 | 13.2212; 16.1944; 19.5088 90; 94.223; 90 | 4165.7 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
| 1548463 | CIF | C34 H38 B F10 P | P -1 | 13.2091; 14.4202; 17.4143 102.465; 96.491; 91.561 | 3213.5 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
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