Crystallography Open Database

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1517271 CIFC371 H328 B16 Co8 F64 N72 O26C 1 2/c 127.3936; 39.1227; 41.964
90; 107.152; 90		42973Cullen, William; Turega, Simon; Hunter, Christopher A.; Ward, Michael D.
pH-dependent binding of guests in the cavity of a polyhedral coordination cage: reversible uptake and release of drug molecules
Chem. Sci., 2015, 6, 625
1517459 CIFC46 H44 Cl2 F6 N O7 P3 Ru S2P 1 21 112.731; 15.301; 13.247
90; 109.038; 90		2439.3Wesselbaum, Sebastian; Moha, Verena; Meuresch, Markus; Brosinski, Sandra; Thenert, Katharina M.; Kothe, Jens; Stein, Thorsten vom; Englert, Ulli; Hölscher, Markus; Klankermayer, Jürgen; Leitner, Walter
Hydrogenation of carbon dioxide to methanol using a homogeneous ruthenium‒Triphos catalyst: from mechanistic investigations to multiphase catalysis
Chem. Sci., 2015, 6, 693
1517514 CIFC12 H12 F6 P TcP 1 21/c 113.8831; 9.8745; 9.719
90; 94.232; 90		1328.73Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517515 CIFC14 H16 F6 P TcP 1 21/n 17.7559; 11.003; 8.9353
90; 98.474; 90		754.2Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517516 CIFC18 H24 F6 P TcP 21 21 219.2697; 13.0695; 15.815
90; 90; 90		1916Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517517 CIFC20 H24 F6 P TcP 1 21/n 18.7563; 12.1899; 9.5187
90; 108.089; 90		965.8Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517518 CIFC21 H49 Al Cl7 N7 O7 TcP 1 21 18.8724; 23.5963; 9.6318
90; 96.888; 90		2001.92Benz, Michael; Braband, Henrik; Schmutz, Paul; Halter, Jonathan; Alberto, Roger
From TcVIIto TcI; facile syntheses of bis-arene complexes [99(m)Tc(arene)2]+from pertechnetate
Chem. Sci., 2015, 6, 165
1517671 CIFC22 H19 F O2P 1 21/c 115.5436; 8.7069; 12.5382
90; 92.769; 90		1694.9Alza, Esther; Laraia, Luca; Ibbeson, Brett M.; Collins, Súil; Galloway, Warren R. J. D.; Stokes, Jamie E.; Venkitaraman, Ashok R.; Spring, David R.
Synthesis of a novel polycyclic ring scaffold with antimitotic properties via a selective domino Heck‒Suzuki reaction
Chem. Sci., 2015, 6, 390
1517680 CIFC39 H36 Ag3 F9 N12 O9.5 S3P 1 21/n 113.528; 20.05; 18.26
90; 107.1; 90		4733.8He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
A macrocycle-assisted nanoparticlization process for bulk Ag2S
Chem. Sci., 2015, 6, 654
1517681 CIFC40 H36 Ag5 F9 N12 O10 S4P 21 21 2110.57; 21.277; 23.103
90; 90; 90		5195.8He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
A macrocycle-assisted nanoparticlization process for bulk Ag2S
Chem. Sci., 2015, 6, 654
1517682 CIFC75 H72 Ag5 F9 N24 O9 S4C 1 2/c 123.725; 19.387; 18.732
90; 90.71; 90		8615He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
A macrocycle-assisted nanoparticlization process for bulk Ag2S
Chem. Sci., 2015, 6, 654
1517683 CIFC40 H36 Ag6 F10.5 N12 O16 S4.5P b c n12.772; 35.464; 25.664
90; 90; 90		11624He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
A macrocycle-assisted nanoparticlization process for bulk Ag2S
Chem. Sci., 2015, 6, 654
1517789 CIFC51 H54 O6P -113.7149; 15.9855; 20.8687
103.455; 105.879; 93.251		4244.3Chen, Huanqing; Fan, Jiazeng; Hu, Xiaoshi; Ma, Junwei; Wang, Shilu; Li, Jian; Yu, Yihua; Jia, Xueshun; Li, Chunju
Biphen[n]arenes
Chem. Sci., 2015, 6, 197
1517790 CIFC68 H72 O8P 1 21/c 111.5532; 30.664; 7.71
90; 90.771; 90		2731.2Chen, Huanqing; Fan, Jiazeng; Hu, Xiaoshi; Ma, Junwei; Wang, Shilu; Li, Jian; Yu, Yihua; Jia, Xueshun; Li, Chunju
Biphen[n]arenes
Chem. Sci., 2015, 6, 197
1517834 CIFC16 H15 N5 O2P 1 21/c 111.641; 8.7512; 14.7356
90; 92.598; 90		1499.61Foy, Justin T.; Ray, Debdas; Aprahamian, Ivan
Regulating signal enhancement with coordination-coupled deprotonation of a hydrazone switch
Chem. Sci., 2015, 6, 209
1517835 CIFC19 H20.5 Cl N6.5 O7 ZnC 1 2/c 122.782; 7.5608; 26.996
90; 102.942; 90		4531.9Foy, Justin T.; Ray, Debdas; Aprahamian, Ivan
Regulating signal enhancement with coordination-coupled deprotonation of a hydrazone switch
Chem. Sci., 2015, 6, 209
1517851 CIFC23 H17 N O6P b c a21.073; 7.448; 23.393
90; 90; 90		3671.6Velasco, V.; Aguilà, D.; Barrios, L. A.; Borilovic, I.; Roubeau, O.; Ribas-Ariño, J.; Fumanal, M.; Teat, S. J.; Aromí, G.
New coordination features; a bridging pyridine and the forced shortest non-covalent distance between two CO32−species
Chem. Sci., 2015, 6, 123
1517852 CIFC111 H92 Co4 N16 O16C 1 2/c 116.833; 19.112; 30.84
90; 101.398; 90		9726Velasco, V.; Aguilà, D.; Barrios, L. A.; Borilovic, I.; Roubeau, O.; Ribas-Ariño, J.; Fumanal, M.; Teat, S. J.; Aromí, G.
New coordination features; a bridging pyridine and the forced shortest non-covalent distance between two CO32−species
Chem. Sci., 2015, 6, 123
1517853 CIFC194 H158 B2 Co8 F8 N24 Na4 O34P 1 21/c 118.4101; 17.6277; 30.4003
90; 106.78; 90		9445.7Velasco, V.; Aguilà, D.; Barrios, L. A.; Borilovic, I.; Roubeau, O.; Ribas-Ariño, J.; Fumanal, M.; Teat, S. J.; Aromí, G.
New coordination features; a bridging pyridine and the forced shortest non-covalent distance between two CO32−species
Chem. Sci., 2015, 6, 123
1517854 CIFC62 H87 N O7 S UP -114.4228; 14.8678; 15.4212
112.831; 96.488; 108.933		2772.5Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517855 CIFC64 H83 N O5 Se UP -116.827; 17.007; 19.804
88.022; 80.746; 82.903		5550.2Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517856 CIFC58 H77 N O5 Te UP -111.2439; 12.9994; 18.636
102.273; 101.519; 100.806		2531.7Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517857 CIFC124.5 H154.5 N2 O6 S2 U2P -111.1756; 16.817; 28.662
85.233; 87.451; 88.366		5361.1Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517858 CIFC126 H156 N2 O6 Se2 U2P -111.217; 16.815; 28.68
85.324; 87.434; 88.412		5384.5Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517859 CIFC150 H179.5 N2 O6.35 Te2 U2P -116.773; 16.923; 25.039
105.196; 102.968; 101.507		6426.8Franke, Sebastian M.; Rosenzweig, Michael W.; Heinemann, Frank W.; Meyer, Karsten
Reactivity of uranium(iii) with H2E (E = S, Se, Te): synthesis of a series of mononuclear and dinuclear uranium(iv) hydrochalcogenido complexes
Chem. Sci., 2015, 6, 275
1517871 CIFC29 H17 Cl2 F12 Fe Hg3 P5P -111.733; 12.1852; 13.1641
85.129; 80.243; 74.103		1782.43Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517872 CIFC29 H17 As5 Cl2 F12 Fe Hg3P -111.9982; 13.3448; 14.1016
65.329; 78.072; 66.415		1878.24Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517873 CIFC9 H13 Fe P5P n m a11.4347; 23.4865; 15.1315
90; 90; 90		4063.73Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517874 CIFC13 H21 Fe P5P c a 2118.7588; 6.5778; 14.1509
90; 90; 90		1746.1Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517875 CIFC17 H29 Fe P5P 1 21/c 19.0507; 25.602; 10.1648
90; 115.783; 90		2120.87Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517876 CIFC31 H21 F12 Fe Hg3 P5P -112.0744; 12.2486; 14.5238
69.244; 82.395; 65.44		1826.58Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517877 CIFC36.5 H32 Cl3 F12 Fe Hg3 P5P 1 21 112.3145; 26.4751; 14.4338
90; 107.168; 90		4496.14Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517878 CIFC55 H53 As15 F12 Fe3 Hg3C 1 2/c 148.2155; 14.138; 22.3159
90; 109.887; 90		14304.9Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517879 CIFC19 H2 Cl2 F12 Hg3P -19.2776; 9.7199; 12.7689
103.463; 100.8; 97.447		1081.75Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517880 CIFC28 H15 Cl2 F12 Fe Hg3 P5P -111.6373; 11.8015; 15.7005
89.754; 68.252; 66.286		1806.94Fleischmann, Martin; Jones, James S.; Gabbaï, François P.; Scheer, Manfred
A comparative study of the coordination behavior of cyclo-P5and cyclo-As5ligand complexes towards the trinuclear Lewis acid complex (perfluoro-ortho-phenylene)mercury
Chem. Sci., 2015, 6, 132
1517881 CIFC26 H24 F18 Li2 O2P -19.0486; 12.7853; 14.6892
84.024; 74.906; 69.739		1539.05Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517882 CIFC28 H17 B F18P 1 21/n 19.1239; 24.4308; 12.5042
90; 97.114; 90		2765.78Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517883 CIFC36 H36 B NP 1 21/n 18.8391; 34.0268; 9.5807
90; 100.72; 90		2831.26Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517884 CIFC36 H18 B F18 NI 4123.5023; 23.5023; 25.182
90; 90; 90		13909.5Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517885 CIFC24 H9 B F18P b c a15.56; 8.7136; 35.624
90; 90; 90		4830Zhang, Zuolun; Edkins, Robert M.; Nitsch, Jörn; Fucke, Katharina; Steffen, Andreas; Longobardi, Lauren E.; Stephan, Douglas W.; Lambert, Christoph; Marder, Todd B.
Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups
Chem. Sci., 2015, 6, 308
1517951 CIFC252 H276 Co4 F36 N48 P6R -330.5162; 30.5162; 71.022
90; 90; 120		57278Symmers, P. R.; Burke, M. J.; August, D. P.; Thomson, P. I. T.; Nichol, G. S.; Warren, M. R.; Campbell, C. J.; Lusby, P. J.
Non-equilibrium cobalt(iii) “click” capsules
Chem. Sci., 2015, 6, 756
1517963 CIFF0.5 O32.5 Si16I m m m26.585; 24.926; 15.939
90; 90; 90		10562.1Jiang, Jiuxing; Yun, Yifeng; Zou, Xiaodong; Jorda, Jose Luis; Corma, Avelino
ITQ-54: a multi-dimensional extra-large pore zeolite with 20 ×14 ×12-ring channels
Chem. Sci., 2015, 6, 480
1517964 CIFC36 H30 Cl4 Ni P2P b c a17.435; 15.662; 24.139
90; 90; 90		6592Hwang, Seung Jun; Powers, David C.; Maher, Andrew G.; Nocera, Daniel G.
Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl
Chem. Sci., 2015, 6, 917
1517965 CIFC18 H15 Cl2 PP 1 21/c 113.338; 14.376; 8.7454
90; 102.53; 90		1637Hwang, Seung Jun; Powers, David C.; Maher, Andrew G.; Nocera, Daniel G.
Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl
Chem. Sci., 2015, 6, 917
1517966 CIFC19 H15 Cl F3 O3 P SP 1 21/n 111.255; 9.1501; 18.658
90; 93.04; 90		1918.8Hwang, Seung Jun; Powers, David C.; Maher, Andrew G.; Nocera, Daniel G.
Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl
Chem. Sci., 2015, 6, 917
1517967 CIFC40 H48 Cl4 Ni O4 P2P 1 21/n 110.1261; 23.4579; 17.8192
90; 106.355; 90		4061.4Hwang, Seung Jun; Powers, David C.; Maher, Andrew G.; Nocera, Daniel G.
Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl
Chem. Sci., 2015, 6, 917
1517970 CIFC12 H12 Au Br2 N OP -17.0801; 10.0993; 10.1771
97.689; 99.69; 92.96		708.82Wu, Qian; Du, Chenglong; Huang, Yumin; Liu, Xingyan; Long, Zhen; Song, Feijie; You, Jingsong
Stoichiometric to catalytic reactivity of the aryl cycloaurated species with arylboronic acids: insight into the mechanism of gold-catalyzed oxidative C(sp2)‒H arylation
Chem. Sci., 2015, 6, 288
1517971 CIFC18 H15 Au Br NP b c a15.9554; 11.7205; 16.839
90; 90; 90		3148.98Wu, Qian; Du, Chenglong; Huang, Yumin; Liu, Xingyan; Long, Zhen; Song, Feijie; You, Jingsong
Stoichiometric to catalytic reactivity of the aryl cycloaurated species with arylboronic acids: insight into the mechanism of gold-catalyzed oxidative C(sp2)‒H arylation
Chem. Sci., 2015, 6, 288
1517972 CIFC18 H16 Au Cl2 NP -17.8572; 8.2744; 15.3789
93.413; 103.381; 113.776		876.93Wu, Qian; Du, Chenglong; Huang, Yumin; Liu, Xingyan; Long, Zhen; Song, Feijie; You, Jingsong
Stoichiometric to catalytic reactivity of the aryl cycloaurated species with arylboronic acids: insight into the mechanism of gold-catalyzed oxidative C(sp2)‒H arylation
Chem. Sci., 2015, 6, 288
1517979 CIFC19 H16 N2 O3P 1 21 16.8436; 26.8023; 8.3932
90; 90.9; 90		1539.33Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517980 CIFC19 H16 N2 O3P 1 21 16.8507; 26.777; 8.4103
90; 90.84; 90		1542.63Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517981 CIFC26 H22 N2 O3P 1 21 15.4249; 16.5948; 11.417
90; 98.277; 90		1017.11Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517982 CIFC26 H22 N2 O3P 1 21 15.4288; 16.6067; 11.4114
90; 98.2867; 90		1018.05Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517983 CIFC57 H49.5 Eu N6 O11.5C 2 2 2126.0015; 26.4029; 30.8305
90; 90; 90		21165.6Kotova, Oxana; Blasco, Salvador; Twamley, Brendan; O'Brien, John; Peacock, Robert D.; Kitchen, Jonathan A.; Martínez-Calvo, Miguel; Gunnlaugsson, Thorfinnur
The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures
Chem. Sci., 2015, 6, 457
1517990 CIFC197.82 H137.82 Cl5.46C 1 2 153.108; 21.244; 26.197
90; 98.53; 90		29229Matsuno, Taisuke; Sato, Sota; Iizuka, Ryosuke; Isobe, Hiroyuki
Molecular recognition in curved π-systems: effects of π-lengthening of tubular molecules on thermodynamics and structures
Chem. Sci., 2015, 6, 909
1518019 CIFC36 H66 Al Cl5 P2 Pb PtP c a 2125.2527; 13.9068; 24.7327
90; 90; 90		8685.7Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518020 CIFC120 H156 B2 Cl18 P4 Pb2 Pt2P -110.5092; 15.3892; 20.0776
109.785; 90.439; 90.796		3054.9Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518021 CIFC36 H66 Al Cl4 I P2 Pb PtP -113.381; 13.612; 13.987
92.698; 111.864; 101.984		2291Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518022 CIFC36 H66 Al2 Cl8 P2 Pb PtC 1 2/c 120.719; 10.6901; 23.859
90; 111.311; 90		4923.1Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518023 CIFC72 H132 Br2 P4 Pt2 SnP -113.9687; 14.2448; 21.1628
96.439; 101.9; 114.878		3643.1Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518024 CIFC36 H66 Al Br5 P2 Pt SnP -111.5394; 12.469; 17.7
105.191; 100.053; 107.994		2245.2Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518025 CIFC60 H78 B Br Cl8 P2 Pt SnP -113.5049; 15.4437; 15.6528
82.203; 78.913; 85.651		3169.9Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518026 CIFC36 H66 Al2 Br8 P2 Pt SnP 1 21/n 113.2989; 22.907; 16.964
90; 99.008; 90		5104.1Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518027 CIFC56 H110 Br3 N O P2 Pt SnP -115.687; 20.715; 21.567
75.297; 82.231; 78.538		6617Braunschweig, Holger; Celik, Mehmet Ali; Dewhurst, Rian D.; Heid, Magdalena; Hupp, Florian; Sen, Sakya S.
Stepwise isolation of low-valent, low-coordinate Sn and Pb mono- and dications in the coordination sphere of platinum
Chem. Sci., 2015, 6, 425
1518028 CIFC36 H49.5 Cl F12 Fe Li2 N O6P -112.26; 12.5792; 15.8788
75.171; 71.664; 67.768		2125.4Pascualini, M. E.; Di Russo, N. V.; Thuijs, A. E.; Ozarowski, A.; Stoian, S. A.; Abboud, K. A.; Christou, G.; Veige, A. S.
A high-spin square-planar Fe(ii) complex stabilized by a trianionic pincer-type ligand and conclusive evidence for retention of geometry and spin state in solution
Chem. Sci., 2015, 6, 608
1518079 CIFC12 As2 F21 Se2P -18.5406; 8.5891; 14.093
84.9; 84.781; 88.091		1025.1Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518080 CIFC48 H50 S2P 1 21/n 115.695; 15.264; 16.274
90; 93.45; 90		3891.7Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518081 CIFC48 H50 F6 S2 SbP 1 21/n 116.17; 15.837; 17.339
90; 92.97; 90		4434.3Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518082 CIFC49 H52 Cl2 F6 Sb Se2P 1 21/c 119.147; 15.238; 16.653
90; 90.08; 90		4859Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518083 CIFC51 H55 F6 N Sb Te2C 1 2/c 119.854; 14.726; 17.178
90; 92.07; 90		5019Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518084 CIFC12 F21 S2 Sb2P 1 21/n 112.029; 12.276; 14.44
90; 97.662; 90		2113.3Mallow, Ole; Khanfar, Monther A.; Malischewski, Moritz; Finke, Pamela; Hesse, Malte; Lork, Enno; Augenstein, Timo; Breher, Frank; Harmer, Jeffrey R.; Vasilieva, Nadezhda V.; Zibarev, Andrey; Bogomyakov, Artem S.; Seppelt, Konrad; Beckmann, Jens
Diaryldichalcogenide radical cations
Chem. Sci., 2015, 6, 497
1518097 CIFC60 H78 Cl2 Ir N2 O6.5 P2 S2P -111.6106; 17.2668; 18.6161
113.198; 95.475; 105.211		3226Oldenhof, Sander; Lutz, Martin; de Bruin, Bas; Ivar van der Vlugt, Jarl; Reek, Joost N. H.
Dehydrogenation of formic acid by Ir‒bisMETAMORPhos complexes: experimental and computational insight into the role of a cooperative ligand
Chem. Sci., 2015, 6, 1027
1518098 CIFC30 H25 N O4P -112.1231; 12.9429; 17.2915
95.734; 108.021; 113.144		2295Berger, Reinhard; Wagner, Manfred; Feng, Xinliang; Müllen, Klaus
Polycyclic aromatic azomethine ylides: a unique entry to extended polycyclic heteroaromatics
Chem. Sci., 2015, 6, 436
1518099 CIFC38.5 H20 Cl F10 NP -112.6166; 16.35; 16.738
87.227; 75.478; 67.501		3083.7Berger, Reinhard; Wagner, Manfred; Feng, Xinliang; Müllen, Klaus
Polycyclic aromatic azomethine ylides: a unique entry to extended polycyclic heteroaromatics
Chem. Sci., 2015, 6, 436
1518139 CIFC40 H60 Cu3 K N8 O54 Ru Si W11P -4 21 m24.415; 24.415; 15.337
90; 90; 90		9142Shi, Dongying; He, Cheng; Qi, Bo; Chen, Cong; Niu, Jingyang; Duan, Chunying
Merging of the photocatalysis and copper catalysis in metal‒organic frameworks for oxidative C‒C bond formation
Chem. Sci., 2015, 6, 1035
1518140 CIFC40 H58 Cu2 K N8 O52 Ru Si W11P c c n17.8663; 22.1923; 22.2835
90; 90; 90		8835.3Shi, Dongying; He, Cheng; Qi, Bo; Chen, Cong; Niu, Jingyang; Duan, Chunying
Merging of the photocatalysis and copper catalysis in metal‒organic frameworks for oxidative C‒C bond formation
Chem. Sci., 2015, 6, 1035
1518141 CIFC13 H14 N2 O2P 1 21/c 111.6434; 10.03245; 20.857
90; 103.161; 90		2372.35Brachet, E.; Ghosh, T.; Ghosh, I.; König, B.
Visible light C‒H amidation of heteroarenes with benzoyl azides
Chem. Sci., 2015, 6, 987
1518142 CIFC13 H10 N2 O4P 1 21/n 18.3156; 9.9732; 14.574
90; 102.762; 90		1178.81Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518143 CIFC13 H9 N2 O4P 1 21 18.3745; 10.0838; 14.5833
90; 103.496; 90		1197.51Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518144 CIFC13 H9 F N2 O4P 1 21/c 17.24677; 14.8112; 11.0943
90; 99.3083; 90		1175.11Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518145 CIFC13 H9 F N2 O4P 1 21 17.1667; 5.2718; 15.7374
90; 101.26; 90		583.14Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518146 CIFC13 H9 F N2 O4P 1 21 17.1322; 5.2282; 15.7662
90; 101.237; 90		576.63Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518147 CIFC13 H9 F N2 O4P 21 21 216.56098; 13.5445; 13.6122
90; 90; 90		1209.65Maeno, Mayaka; Tokunaga, Etsuko; Yamamoto, Takeshi; Suzuki, Toshiya; Ogino, Yoshiyuki; Ito, Emi; Shiro, Motoo; Asahi, Toru; Shibata, Norio
Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
Chem. Sci., 2015, 6, 1043
1518148 CIFC12 H40 B4 N4 O6P 1 21/n 116.026; 8.7017; 17.485
90; 115.469; 90		2201.4Kalviri, Hassan A.; Gärtner, Felix; Ye, Gang; Korobkov, Ilia; Baker, R. Tom
Probing the second dehydrogenation step in ammonia-borane dehydrocoupling: characterization and reactivity of the key intermediate, B-(cyclotriborazanyl)amine-borane
Chem. Sci., 2015, 6, 618
1518149 CIFC4 H26 B4 N4 O2P -16.9419; 8.8077; 12.4471
91.79; 103.761; 111.731		680.64Kalviri, Hassan A.; Gärtner, Felix; Ye, Gang; Korobkov, Ilia; Baker, R. Tom
Probing the second dehydrogenation step in ammonia-borane dehydrocoupling: characterization and reactivity of the key intermediate, B-(cyclotriborazanyl)amine-borane
Chem. Sci., 2015, 6, 618
1518154 CIFC22 H22.5 B Cl Cr F4 N4.5 O3P b c n14.5572; 13.9044; 24.0822
90; 90; 90		4874.5Kotani, Hiroaki; Kaida, Suzue; Ishizuka, Tomoya; Sakaguchi, Miyuki; Ogura, Takashi; Shiota, Yoshihito; Yoshizawa, Kazunari; Kojima, Takahiko
Formation and characterization of a reactive chromium(v)‒oxo complex: mechanistic insight into hydrogen-atom transfer reactions
Chem. Sci., 2015, 6, 945
1518155 CIFC21 H20 B2 Cr F8 N5 O2P 1 21/c 19.683; 22.83; 11.317
90; 104.712; 90		2419.7Kotani, Hiroaki; Kaida, Suzue; Ishizuka, Tomoya; Sakaguchi, Miyuki; Ogura, Takashi; Shiota, Yoshihito; Yoshizawa, Kazunari; Kojima, Takahiko
Formation and characterization of a reactive chromium(v)‒oxo complex: mechanistic insight into hydrogen-atom transfer reactions
Chem. Sci., 2015, 6, 945
1518167 CIFC51 H99 K N2 O6 Si6 ThP -112.1595; 12.7622; 22.2587
100.93; 104.448; 95.5814		3246.1Langeslay, Ryan R.; Fieser, Megan E.; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1−anion containing thorium in the formal +2 oxidation state
Chem. Sci., 2015, 6, 517
1518168 CIFC53 H103 K O8 Si6 ThP 1 21/n 117.1884; 18.0161; 22.654
90; 99.6558; 90		6915.8Langeslay, Ryan R.; Fieser, Megan E.; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1−anion containing thorium in the formal +2 oxidation state
Chem. Sci., 2015, 6, 517
1518169 CIFC33 H63 Si6 ThP 1 21/c 117.547; 13.6955; 19.1293
90; 112.595; 90		4244.2Langeslay, Ryan R.; Fieser, Megan E.; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1−anion containing thorium in the formal +2 oxidation state
Chem. Sci., 2015, 6, 517
1518170 CIFC30 H50 Si4 ThC 1 2/c 120.2007; 8.1694; 19.9544
90; 91.3531; 90		3292.1Langeslay, Ryan R.; Fieser, Megan E.; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1−anion containing thorium in the formal +2 oxidation state
Chem. Sci., 2015, 6, 517
1518200 CIFC28 H20 N4P -17.8497; 10.7861; 14.7876
109.56; 91.8983; 111.312		1081.87Rijeesh, K.; Hashim, P. K.; Noro, Shin-ichiro; Tamaoki, Nobuyuki
Dynamic induction of enantiomeric excess from a prochiral azobenzene dimer under circularly polarized light
Chem. Sci., 2015, 6, 973
1518209 CIFC11 H7 Au Cl2 F NP 1 21/c 19.1445; 7.8648; 15.71
90; 106.294; 90		1084.5Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518210 CIFC24 H18 Au F2 NP -114.8527; 16.3867; 17.62
90.156; 91.414; 114.256		3908.3Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518211 CIFC27 H20 Au Cl2 F6 NP -19.334; 11.4331; 12.8416
73.407; 81.938; 73.869		1258.9Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518212 CIFC24 H18 Au N3 O4P b c n11.1263; 14.1527; 26.2319
90; 90; 90		4130.7Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518213 CIFC28 H20 Au N S2I 41/a35.5669; 35.5669; 7.2973
90; 90; 90		9231.1Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518214 CIFC26 H24 Au NP 1 21/n 17.5722; 16.2301; 16.7076
90; 93.349; 90		2049.8Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518215 CIFC30 H32 Au N O2C 1 2/c 119.4071; 15.6565; 19.6251
90; 112.078; 90		5525.8Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518216 CIFC18 H14 Au Cl F NP 1 21/c 19.4066; 13.227; 13.1786
90; 110.251; 90		1538.3Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518217 CIFC22 H17 Au Cl NP 1 21/c 110.34; 18.881; 9.579
90; 110.408; 90		1752.7Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518218 CIFC20.62 H17.23 Au Cl1.23 N OP c a 2122.3204; 11.4097; 7.0554
90; 90; 90		1796.79Maity, Ayan; Sulicz, Amanda N.; Deligonul, Nihal; Zeller, Matthias; Hunter, Allen D.; Gray, Thomas G.
Suzuki‒Miyaura coupling of arylboronic acids to gold(iii)
Chem. Sci., 2015, 6, 981
1518232 CIFC48 H30 F6 O4C 1 2/c 113.07527; 16.18867; 19.01027
90; 100.1; 90		3961.57Rives, Arnaud; Baglai, Iaroslav; Barthes, Cécile; Maraval, Valérie; Saffon-Merceron, Nathalie; Saquet, Alix; Voitenko, Zoia; Volovenko, Yulian; Chauvin, Remi
Carbo-cyclohexadienes vs. carbo-benzenes: structure and conjugative properties
Chem. Sci., 2015, 6, 1139
1518233 CIFC47 H28 Cl2 F6 O2P -112.5119; 12.6648; 14.9565
70.805; 66.621; 67.665		1967.5Rives, Arnaud; Baglai, Iaroslav; Barthes, Cécile; Maraval, Valérie; Saffon-Merceron, Nathalie; Saquet, Alix; Voitenko, Zoia; Volovenko, Yulian; Chauvin, Remi
Carbo-cyclohexadienes vs. carbo-benzenes: structure and conjugative properties
Chem. Sci., 2015, 6, 1139
1518234 CIFC49 H25 Cl3 F12 O2P 1 21/c 112.8182; 35.815; 9.7626
90; 92.841; 90		4476.3Rives, Arnaud; Baglai, Iaroslav; Barthes, Cécile; Maraval, Valérie; Saffon-Merceron, Nathalie; Saquet, Alix; Voitenko, Zoia; Volovenko, Yulian; Chauvin, Remi
Carbo-cyclohexadienes vs. carbo-benzenes: structure and conjugative properties
Chem. Sci., 2015, 6, 1139
1518242 CIFC81 H86 Cl6 N6 O8 Rh2P 21 21 2113.919; 19.144; 28.616
90; 90; 90		7625Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518243 CIFC39 H40 Cl2 F6 N4 O2 P RhP 21 21 2113.1445; 13.6427; 22.5166
90; 90; 90		4037.8Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518244 CIFC14 H18 N2 O5P 21 21 215.4571; 15.3289; 17.4084
90; 90; 90		1456.24Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518245 CIFC22 H26 N2 O4P 1 21/c 110.1905; 11.5731; 17.4203
90; 97.5045; 90		2036.88Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518246 CIFC51 H52 Cl4 F6 N4 O3 P RhP n a 2117.7761; 22.9437; 13.1111
90; 90; 90		5347.4Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518247 CIFC47 H45 Cl2 Ir N4 O3C 1 2/c 138.9286; 13.3583; 17.0015
90; 111.479; 90		8227.1Wang, Chuanyong; Chen, Liang-An; Huo, Haohua; Shen, Xiaodong; Harms, Klaus; Gong, Lei; Meggers, Eric
Asymmetric Lewis acid catalysis directed by octahedral rhodium centrochirality
Chem. Sci., 2015, 6, 1094
1518248 CIFC98 H110 B Cl2 F20 N6 Nb2P 1 21/c 114.224; 21.737; 31.247
90; 90.83; 90		9660Gianetti, Thomas L.; Nocton, Grégory; Minasian, Stefan G.; Kaltsoyannis, Nikolas; Kilcoyne, A. L. David; Kozimor, Stosh A.; Shuh, David K.; Tyliszczak, Tolek; Bergman, Robert G.; Arnold, John
Electron localization in a mixed-valence diniobium benzene complex
Chem. Sci., 2015, 6, 993
1518249 CIFC65 H66 B F20 N3 Nb O2P 1 21/c 118.1669; 17.1279; 19.7092
90; 90.559; 90		6132.4Gianetti, Thomas L.; Nocton, Grégory; Minasian, Stefan G.; Kaltsoyannis, Nikolas; Kilcoyne, A. L. David; Kozimor, Stosh A.; Shuh, David K.; Tyliszczak, Tolek; Bergman, Robert G.; Arnold, John
Electron localization in a mixed-valence diniobium benzene complex
Chem. Sci., 2015, 6, 993
1518250 CIFC95 H110 B Cl9 F20 N6 Nb2P 1 21/c 120.744; 20.888; 22.683
90; 90.709; 90		9827.8Gianetti, Thomas L.; Nocton, Grégory; Minasian, Stefan G.; Kaltsoyannis, Nikolas; Kilcoyne, A. L. David; Kozimor, Stosh A.; Shuh, David K.; Tyliszczak, Tolek; Bergman, Robert G.; Arnold, John
Electron localization in a mixed-valence diniobium benzene complex
Chem. Sci., 2015, 6, 993
1518251 CIFC61 H60 B Cl0 F20 N4 NbP 1 n 115.2666; 16.9177; 25.577
90; 97.658; 90		6547Gianetti, Thomas L.; Nocton, Grégory; Minasian, Stefan G.; Kaltsoyannis, Nikolas; Kilcoyne, A. L. David; Kozimor, Stosh A.; Shuh, David K.; Tyliszczak, Tolek; Bergman, Robert G.; Arnold, John
Electron localization in a mixed-valence diniobium benzene complex
Chem. Sci., 2015, 6, 993
1518252 CIFC24 H28 B2 Cl6 Fe N8 O6C 1 2/c 124.287; 8.1945; 20.396
90; 120.269; 90		3505.8Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518253 CIFC31 H44 B2 Fe N8 O9P -110.435; 12.522; 14.568
110.05; 98.25; 92.93		1759.4Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518254 CIFC270 H327 B29.5 F22 Fe12 N96 O73.5 Pd6F 4 3 277.1812; 77.1812; 77.1812
90; 90; 90		459764Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518255 CIFC193 H230 B12 Fe6 N59 O53 Pd3P -124.07; 25.09; 26.26
111.25; 101.84; 110.6		12790Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518256 CIFC453.5 H476.75 B33.75 F9 Fe12 N100.75 O83.5 Pd6P -137.76; 37.914; 49.64
109.87; 111.57; 90.72		61382Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518257 CIFC350 H400 B24 Fe12 N105 O99 Pd6P -126.3697; 37.7311; 41.401
113.826; 96.68; 90.021		37375Wise, Matthew D.; Holstein, Julian J.; Pattison, Philip; Besnard, Celine; Solari, Euro; Scopelliti, Rosario; Bricogne, Gerard; Severin, Kay
Large, heterometallic coordination cages based on ditopic metallo-ligands with 3-pyridyl donor groups
Chem. Sci., 2015, 6, 1004
1518278 CIFC20 H20 N2 O3 SC 1 2/c 111.5572; 15.5085; 20.8957
90; 94.733; 90		3732.5Zhou, Ai-Hua; He, Qiao; Shu, Chao; Yu, Yong-Fei; Liu, Shuang; Zhao, Tian; Zhang, Wei; Lu, Xin; Ye, Long-Wu
Atom-economic generation of gold carbenes: gold-catalyzed formal [3+2] cycloaddition between ynamides and isoxazoles
Chem. Sci., 2015, 6, 1265
1518279 CIFC24 H20 N2 O2P 21 21 217.58; 13.2149; 18.5282
90; 90; 90		1855.95Hesping, Lena; Biswas, Anup; Daniliuc, Constantin G.; Mück-Lichtenfeld, Christian; Studer, Armido
Stereoselective Lewis base catalyzed formal 1,3-dipolar cycloaddition of azomethine imines with mixed anhydrides
Chem. Sci., 2015, 6, 1252
1518308 CIFC90 H64 F24 N14 P4 Ru2P -113.811; 18.252; 20.803
84.81; 82.76; 72.33		4949Cui, Bin-Bin; Mao, Zupan; Chen, Yuxia; Zhong, Yu-Wu; Yu, Gui; Zhan, Chuanlang; Yao, Jiannian
Tuning of resistive memory switching in electropolymerized metallopolymeric films
Chem. Sci., 2015, 6, 1308
1518338 CIFC36 H54 F18 N15 P3 Ru3 S9C 1 2 127.5079; 16.0629; 14.4082
90; 108.033; 90		6053.6Zubi, Ahmed; Wragg, Ashley; Turega, Simon; Adams, Harry; Costa, Paulo J.; Félix, Vítor; Thomas, Jim A.
Modulating the electron-transfer properties of a mixed-valence system through host‒guest chemistry
Chem. Sci., 2015, 6, 1334
1518339 CIFC15 H12 Au N O2P -17.3807; 11.755; 15.94
102.912; 92.025; 100.595		1320.8Seki, Tomohiro; Sakurada, Kenta; Muromoto, Mai; Ito, Hajime
Photoinduced single-crystal-to-single-crystal phase transition and photosalient effect of a gold(i) isocyanide complex with shortening of intermolecular aurophilic bonds
Chem. Sci., 2015, 6, 1491
1518340 CIFC15 H12 Au N O2P -16.0552; 7.0297; 15.9689
96.315; 93.979; 90.279		673.93Seki, Tomohiro; Sakurada, Kenta; Muromoto, Mai; Ito, Hajime
Photoinduced single-crystal-to-single-crystal phase transition and photosalient effect of a gold(i) isocyanide complex with shortening of intermolecular aurophilic bonds
Chem. Sci., 2015, 6, 1491
1518342 CIFC33 H27 Br N2 O4P 1 21 19.7143; 22.5934; 12.6641
90; 106.703; 90		2662.23Cabanillas, Alejandro; Davies, Christopher D.; Male, Louise; Simpkins, Nigel S.
Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions
Chem. Sci., 2015, 6, 1350
1518343 CIFC33 H28 N2 O4P 21 21 2112.1648; 12.4912; 17.107
90; 90; 90		2599.46Cabanillas, Alejandro; Davies, Christopher D.; Male, Louise; Simpkins, Nigel S.
Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions
Chem. Sci., 2015, 6, 1350
1518344 CIFC24 H26 N2 O5P 16.25441; 12.592; 13.61853
100.755; 92.7028; 95.0674		1047.35Cabanillas, Alejandro; Davies, Christopher D.; Male, Louise; Simpkins, Nigel S.
Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions
Chem. Sci., 2015, 6, 1350
1518345 CIFC22 H22 N2 O5P 1 21 112.14306; 6.28576; 13.0165
90; 108.566; 90		941.82Cabanillas, Alejandro; Davies, Christopher D.; Male, Louise; Simpkins, Nigel S.
Highly enantioselective access to diketopiperazines via cinchona alkaloid catalyzed Michael additions
Chem. Sci., 2015, 6, 1350
1518346 CIFC8 H4 Cr2 O8 P2C m c a12.2545; 11.5949; 9.7196
90; 90; 90		1381.06Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518347 CIFC8 H4 O8 P2 W2C m c a12.4977; 12.0462; 10.1185
90; 90; 90		1523.3Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518348 CIFC7 H7 Cr2 O7 P3P -16.9134; 7.3239; 8.761
111.796; 92.15; 115.204		362.43Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518352 CIFC3 H3 Cl Cu N3 S3P a -311.70071; 11.70071; 11.70071
90; 90; 90		1601.9Tominaka, S.; Hamoudi, H.; Suga, T.; Bennett, T. D.; Cairns, A. B.; Cheetham, A. K.
Topochemical conversion of a dense metal‒organic framework from a crystalline insulator to an amorphous semiconductor
Chem. Sci., 2015, 6, 1465
1518353 CIFC3 H3 Cl Cu N3 S3P a -311.74713; 11.74713; 11.74713
90; 90; 90		1621.05Tominaka, S.; Hamoudi, H.; Suga, T.; Bennett, T. D.; Cairns, A. B.; Cheetham, A. K.
Topochemical conversion of a dense metal‒organic framework from a crystalline insulator to an amorphous semiconductor
Chem. Sci., 2015, 6, 1465
1518354 CIFC3 H3 Cl Cu N3 S3P a -311.78842; 11.78842; 11.78842
90; 90; 90		1638.2Tominaka, S.; Hamoudi, H.; Suga, T.; Bennett, T. D.; Cairns, A. B.; Cheetham, A. K.
Topochemical conversion of a dense metal‒organic framework from a crystalline insulator to an amorphous semiconductor
Chem. Sci., 2015, 6, 1465
1518355 CIFC32 H44 K N2 O13 RhC 1 c 113.6052; 19.6523; 14.3113
90; 105.559; 90		3686.2Murphy, Stephen K.; Bruch, Achim; Dong, Vy M.
Mechanistic insights into hydroacylation with non-chelating aldehydes
Chemical Science, 2015, 6, 174-180
1518358 CIFC18 H32 N4 PdP 1 21/c 19.5147; 8.7236; 12.2763
90; 96.21; 90		1012.98Hering, Florian; Nitsch, Jörn; Paul, Ursula; Steffen, Andreas; Bickelhaupt, F. Matthias; Radius, Udo
Bite-angle bending as a key for understanding group-10 metal reactivity of d10-[M(NHC)2] complexes with sterically modest NHC ligands
Chem. Sci., 2015, 6, 1426
1518359 CIFC28 H50 Cl4 N6 PdP -19.5437; 12.6519; 14.7569
81.229; 83.044; 81.137		1731.26Hering, Florian; Nitsch, Jörn; Paul, Ursula; Steffen, Andreas; Bickelhaupt, F. Matthias; Radius, Udo
Bite-angle bending as a key for understanding group-10 metal reactivity of d10-[M(NHC)2] complexes with sterically modest NHC ligands
Chem. Sci., 2015, 6, 1426
1518360 CIFC145 H149 Cl6 Cs3 N8 O14P -111.649; 18.299; 18.362
60.833; 80.132; 86.221		3366.6Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518361 CIFC74 H78 Cl6 Cs F N4 O8P -112.5824; 16.3849; 18.0859
89.08; 89.123; 70.854		3521.7Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518362 CIFC82 H92 N4 O12P -116.284; 21.681; 24.254
65.823; 87.933; 77.172		7602Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518363 CIFC75 H71 Cl3 N4 O12P 1 21/c 118.865; 17.828; 20.315
90; 107.064; 90		6532Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518364 CIFC81 H94 Cl6 F N5 O6P 1 21/n 118.1082; 20.262; 21.408
90; 105.284; 90		7577Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518365 CIFC78 H81 N7 O6P 1 21/n 119.8344; 17.7442; 20.5845
90; 109.128; 90		6844.6Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518366 CIFC74 H77 Cl4 Cs N4 O7P 1 2/n 128.4416; 17.3237; 28.5922
90; 90.135; 90		14087.7Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518367 CIFC74 H77 Cl3 Cs F N4 O7P 1 21/n 117.1643; 20.272; 20.1109
90; 99.129; 90		6909Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518368 CIFC163 H193 Cl6 F2 N10 O15P -117.7069; 19.2391; 27.8205
71.903; 75.381; 69.249		8315.5Kim, Sung Kuk; Lynch, Vincent M.; Hay, Benjamin P.; Kim, Jong Seung; Sessler, Jonathan L.
Ion pair-induced conformational motion in calix[4]arene-strapped calix[4]pyrroles
Chem. Sci., 2015, 6, 1404
1518371 CIFC279.28 H164 N37 O100C 1 2/c 133.067; 14.8252; 17.1809
90; 121.19; 90		7205.1Mallick, Arijit; Garai, Bikash; Addicoat, Matthew A.; Petkov, Petko St.; Heine, Thomas; Banerjee, Rahul
Solid state organic amine detection in a photochromic porous metal organic framework
Chem. Sci., 2015, 6, 1420
1518372 CIFC69 H35 Mg4 N7 O30P 1 2/c 134.3413; 10.0447; 17.7382
90; 96.234; 90		6082.6Mallick, Arijit; Garai, Bikash; Addicoat, Matthew A.; Petkov, Petko St.; Heine, Thomas; Banerjee, Rahul
Solid state organic amine detection in a photochromic porous metal organic framework
Chem. Sci., 2015, 6, 1420
1518407 CIFC74 H86 N6 O3P -19.827; 16.9659; 21.6298
69.273; 81.505; 87.976		3335.2Slater, Anna G.; Hu, Ya; Yang, Lixu; Argent, Stephen P.; Lewis, William; Blunt, Matthew O.; Champness, Neil R.
Thymine functionalised porphyrins, synthesis and heteromolecular surface-based self-assembly
Chem. Sci., 2015, 6, 1562
1518408 CIFC86 H92 Cl18 N6 O3P -115.4721; 16.3717; 19.0278
92.068; 110.731; 99.28		4426Slater, Anna G.; Hu, Ya; Yang, Lixu; Argent, Stephen P.; Lewis, William; Blunt, Matthew O.; Champness, Neil R.
Thymine functionalised porphyrins, synthesis and heteromolecular surface-based self-assembly
Chem. Sci., 2015, 6, 1562
1518409 CIFC28 H20 N2P 21 21 215.9763; 11.5786; 29.273
90; 90; 90		2025.6Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission
Chem. Sci., 2015, 6, 1932
1518410 CIFC40 H28 N2P -110.6571; 11.1264; 13.1685
88; 76.566; 74.575		1463.4Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission
Chem. Sci., 2015, 6, 1932
1518411 CIFC42 H32 N2 O2P -111.1806; 11.4458; 12.861
101.527; 91.283; 99.274		1589.02Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission
Chem. Sci., 2015, 6, 1932
1518412 CIFC32 H28 N2 O4P -19.768; 12.3063; 12.4687
68.542; 70.492; 88.089		1308.1Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong
Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission
Chem. Sci., 2015, 6, 1932
1518432 CIFC6 H12 O6P 21 21 2110.336; 14.852; 4.924
90; 90; 90		755.9Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518433 CIFC6 H12 O6P 21 21 2110.26; 14.837; 4.8169
90; 90; 90		733.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518434 CIFC6 H12 O6P 21 21 2110.22; 14.832; 4.7689
90; 90; 90		722.9Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518435 CIFC6 H12 O6P 21 21 2110.218; 14.823; 4.7439
90; 90; 90		718.5Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518436 CIFC6 H12 O6P 21 21 2110.181; 14.808; 4.693
90; 90; 90		707.5Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518437 CIFC6 H12 O6P 21 21 2110.11; 14.808; 4.5801
90; 90; 90		685.7Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518438 CIFC6 H12 O6P 21 21 2110.06; 14.798; 4.537
90; 90; 90		675.4Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518439 CIFC6 H12 O6P 21 21 2110.05; 14.807; 4.4206
90; 90; 90		657.8Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518440 CIFC6 H12 O6P 21 21 2110.04; 14.796; 4.3879
90; 90; 90		651.8Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518441 CIFC6 H12 O6P 21 21 2110.056; 14.779; 4.275
90; 90; 90		635.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518442 CIFC6 H12 O6P 21 21 2110.059; 14.776; 4.261
90; 90; 90		633.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518443 CIFC6 H12 O6P 21 21 2110.063; 14.787; 4.256
90; 90; 90		633.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518444 CIFC6 H12 O6P 21 21 219.714; 14.99; 4.262
90; 90; 90		621Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518445 CIFC6 H12 O6P 21 21 219.73; 14.987; 4.234
90; 90; 90		617.4Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518446 CIFC6 H12 O6P 21 21 219.694; 14.931; 4.2234
90; 90; 90		611.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518447 CIFC67 F6P b c a9.9998; 20.6538; 31.3512
90; 90; 90		6475.1San, Long K.; Bukovsky, Eric V.; Larson, Bryon W.; Whitaker, James B.; Deng, S. H. M.; Kopidakis, Nikos; Rumbles, Garry; Popov, Alexey A.; Chen, Yu-Sheng; Wang, Xue-Bin; Boltalina, Olga V.; Strauss, Steven H.
A faux hawk fullerene with PCBM-like properties
Chem. Sci., 2015, 6, 1801
1518448 CIFC60 H60 Li4 O5 Rb4C m c m14.166; 13.519; 25.901
90; 90; 90		4960Filatov, Alexander S.; Spisak, Sarah N.; Zabula, Alexander V.; McNeely, James; Rogachev, Andrey Yu.; Petrukhina, Marina A.
Self-assembly of tetrareduced corannulene with mixed Li‒Rb clusters: dynamic transformations, unique structures and record7Li NMR shifts
Chem. Sci., 2015, 6, 1959
1518449 CIFC66 H80 Li3 O12.5 Rb5P -110.064; 15.27; 22.129
90.416; 93.102; 94.532		3384.9Filatov, Alexander S.; Spisak, Sarah N.; Zabula, Alexander V.; McNeely, James; Rogachev, Andrey Yu.; Petrukhina, Marina A.
Self-assembly of tetrareduced corannulene with mixed Li‒Rb clusters: dynamic transformations, unique structures and record7Li NMR shifts
Chem. Sci., 2015, 6, 1959
1518450 CIFC28 H46 N4 O19 TmC 1 c 123.1686; 9.677; 16.8001
90; 118.272; 90		3317.3Funk, Alexander M.; Finney, Katie-Louise N. A.; Harvey, Peter; Kenwright, Alan M.; Neil, Emily R.; Rogers, Nicola J.; Kanthi Senanayake, P.; Parker, David
Critical analysis of the limitations of Bleaney's theory of magnetic anisotropy in paramagnetic lanthanide coordination complexes
Chem. Sci., 2015, 6, 1655
1518469 CIFC21 H10 Au B Cl10 N6 PbP -18.5794; 13.7444; 13.7913
110.805; 93.371; 101.13		1477.17Echeverría, Raquel; López-de-Luzuriaga, José M.; Monge, Miguel; Olmos, M. Elena
The gold(i)⋯lead(ii) interaction: a relativistic connection
Chem. Sci., 2015, 6, 2022
1518476 CIFC14 H23 F6 O6 Pd SbP -19.539; 10.408; 11.253
115.767; 97.422; 91.945		992.6Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518477 CIFC15 H22 F6 N O6 Pd SbP n m a18.89; 16.805; 13.196
90; 90; 90		4189Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518478 CIFC22 H35 F6 O6 Pd SbP n a 2116.758; 16.947; 9.5046
90; 90; 90		2699.3Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518479 CIFC17 H28 F6 N3 O10 Pd SbP 1 21/c 110.0271; 19.0026; 14.5138
90; 92.747; 90		2762.3Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518480 CIFC66 H86 Cl20 F24 O16 Pd4 Sb4P -116.4284; 19.3745; 21.4447
66.181; 88.434; 72.775		5930.9Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518496 CIFC34 H58 As4 Co2P 1 21/n 18.4386; 13.7676; 16.0276
90; 100.27; 90		1832.24Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518497 CIFC35 H60 As4 Cl2 Co2C 1 2/c 117.893; 19.9249; 11.6299
90; 107.903; 90		3945.5Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518498 CIFC68 H116 As10 Co4P -110.3921; 14.3707; 14.8262
62.53; 76.535; 79.819		1904.35Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518499 CIFC72 H124 As10 Cl8 Co4P -113.7956; 14.0892; 15.0382
62.971; 69.895; 61.292		2254Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518500 CIFC51 H87 As12 Co3C 1 2/c 128.9202; 15.7899; 29.9375
90; 112.752; 90		12607.1Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518501 CIFC23 H32 N2 SeP n a 2123.3; 7.0807; 11.6415
90; 90; 90		1920.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518502 CIFC15 H24 N2 SeP 1 21/c 111.8147; 11.1443; 12.2088
90; 108.21; 90		1527Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518503 CIFC27 H48 N2 SeP 1 21/n 114.4058; 7.4133; 25.023
90; 97.856; 90		2647.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518504 CIFC19 H20 N2 SeP 1 2/n 18.3318; 7.4265; 13.6459
90; 98.798; 90		834.42Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518505 CIFC21 H24 N2 SeP b c n16.043; 7.3937; 16.055
90; 90; 90		1904.4Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518506 CIFC35 H52 N2 SeP 1 21/c 120.433; 7.6327; 21.563
90; 106.66; 90		3221.8Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518507 CIFC27 H34 Cl2 N2 SeI 1 2/a 117.366; 9.4565; 21.295
90; 109.08; 90		3305Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518508 CIFC21 H26 N2 SeP b c n15.9194; 7.4418; 16.1915
90; 90; 90		1918.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518509 CIFC11 H6 F5 N3 SeP 1 21/c 19.3746; 15.527; 8.3524
90; 90.357; 90		1215.7Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518510 CIFC11 H11 N3 O SeP -17.8283; 7.9731; 18.447
97.93; 94.637; 90.042		1136.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518511 CIFC21 H21 N3 O SeP -18.5326; 10.637; 11.589
107.558; 101.546; 107.498		906.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518512 CIFC30 H35 N3 O Se SiP b c a13.2692; 19.8926; 20.979
90; 90; 90		5537.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518526 CIFC12 H11 N O2P -14.00444; 11.1381; 12.202
71.955; 89.514; 80.992		510.62Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518527 CIFC38 H48 N2 O4P 1 21/c 114.93217; 14.22602; 15.93712
90; 100.89; 90		3324.49Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518528 CIFC30 H40 N2 O4 Si4P -18.5558; 11.887; 17.0071
99.115; 92.129; 94.397		1700.67Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518529 CIFC34 H52 N2 O4 Si6P -18.6514; 11.8373; 20.4256
82.751; 87.339; 86.175		2068.9Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518530 CIFC152.05 H75.74 Cl2.21 F40 N12 S8P -118.9073; 20.7452; 21.091
67.38; 77.21; 65.257		6917.2Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518531 CIFC87.05 H40.13 Cl3.96 F20 N6 S6C 1 2/c 149.998; 12.402; 35.242
90; 131.613; 90		16338Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518532 CIFC95.3 H48 Cl2.3 F20 N6 O0.5 S8P -117.2734; 18.9028; 30.1289
105; 92.92; 107.23		8989Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518536 CIFC18 H11 F6 N O3C 1 2/c 132.403; 6.8959; 15.25
90; 97.03; 90		3382Lu, Yi; Wang, Huai-Wei; Spangler, Jillian E.; Chen, Kai; Cui, Pei-Pei; Zhao, Yue; Sun, Wei-Yin; Yu, Jin-Quan
Rh(iii)-catalyzed C‒H olefination of N-pentafluoroaryl benzamides using air as the sole oxidant
Chem. Sci., 2015, 6, 1923
1518540 CIFC18 H33 N2 O8 S2P -17.8956; 9.6557; 14.916
77.311; 81.835; 86.214		1097.43Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518541 CIFC36 H66 N4 O16 S4I 1 2/c 119.4827; 7.7013; 30.1416
90; 101.758; 90		4427.61Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518542 CIFC28.7552 H49.5104 N8 O14 S4P -19.7673; 9.8143; 10.2046
94.88; 96.822; 95.184		962.76Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518545 CIFC14 H34 Cl Mo P3P 21 21 2111.8282; 12.449; 13.6005
90; 90; 90		2002.7Neary, Michelle C.; Parkin, Gerard
Dehydrogenation, disproportionation and transfer hydrogenation reactions of formic acid catalyzed by molybdenum hydride compounds
Chem. Sci., 2015, 6, 1859
1518548 CIFC44.71 H22.16 Cl4 F14 N6 Na2 O7.22P -114.6741; 15.8676; 24.1918
91.946; 106.327; 115.228		4812.8Seifert, Sabine; Schmidt, David; Würthner, Frank
An ambient stable core-substituted perylene bisimide dianion: isolation and single crystal structure analysis
Chem. Sci., 2015, 6, 1663
1518587 CIFC56 H92 Cl2 Co2 I2 N4 P4 Ti2P b c a18.6991; 16.4217; 21.8753
90; 90; 90		6717.3Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518588 CIFC31 H55 Cl Co N2 P3 TiP 1 21/n 19.0138; 18.8395; 21.5085
90; 90.54; 90		3652.3Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518589 CIFC68 H104 Co2 I2 N4 O2 P4 Ti2P -112.5912; 13.4571; 13.5956
110.682; 94.623; 117.15		1835.07Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518590 CIFC24 H16 Au2 F8 N4 O2P -13.5452; 14.0087; 14.249
109.292; 91.673; 91.322		667.23Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518591 CIFC18 H4 Au2 F8 N4P -13.5707; 10.3087; 14.2742
107.689; 92.505; 100.205		489.99Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518592 CIFC18 H4 Au2 F8 N4P 1 21/c 17.79058; 18.7202; 6.74157
90; 103.167; 90		957.35Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518593 CIFC30 H51 Ir P2P -110.264; 16.311; 19.425
103.753; 105.008; 93.129		3027.6Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518594 CIFC31 H55 Ir O P2P 1 21/c 117.003; 20.0591; 9.4403
90; 102.986; 90		3137.41Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518595 CIFC24 H46 Cl Ir P2P 1 21/c 111.4108; 13.6574; 17.7933
90; 104.097; 90		2689.4Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518596 CIFC34 H26 F4 P2P 1 21/n 19.2062; 16.7452; 17.6319
90; 101.286; 90		2665.6Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518597 CIFC25 H22 F4 P2C 1 2 121.0973; 8.3882; 6.3567
90; 102.383; 90		1098.76Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518598 CIFC58 H26 B F21 P2P 1 21 18.4256; 21.123; 13.804
90; 95.055; 90		2447.2Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518599 CIFC59.25 H28.5 B Cl2.5 F23 P2P 1 21/c 118.8002; 17.1372; 17.8001
90; 102.564; 90		5597.6Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518609 CIFC35 H28 F6 N3 P S2 Se4P 1 21/n 119.6176; 7.5992; 25.2231
90; 93.7263; 90		3752.3Bedics, Matthew A.; Kearns, Hayleigh; Cox, Jordan M.; Mabbott, Sam; Ali, Fatima; Shand, Neil C.; Faulds, Karen; Benedict, Jason B.; Graham, Duncan; Detty, Michael R.
Extreme red shifted SERS nanotags
Chem. Sci., 2015, 6, 2302
1518610 CIFC20 H14P -19.6321; 11.0943; 14.7022
67.862; 79.883; 69.219		1359Collins, Karl D.; Honeker, Roman; Vásquez-Céspedes, Suhelen; Tang, Dan-Tam D.; Glorius, Frank
C‒H arylation of triphenylene, naphthalene and related arenes using Pd/C
Chem. Sci., 2015, 6, 1816
1518611 CIFC24 H16P 1 21/c 119.1157; 5.7556; 29.6669
90; 108.002; 90		3104.2Collins, Karl D.; Honeker, Roman; Vásquez-Céspedes, Suhelen; Tang, Dan-Tam D.; Glorius, Frank
C‒H arylation of triphenylene, naphthalene and related arenes using Pd/C
Chem. Sci., 2015, 6, 1816
1518661 CIFC64 H48 S4P 1 21/n 120.159; 5.0166; 25.728
90; 109.164; 90		2457.7Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518662 CIFC65 H50 S4P 1 21/n 120.1; 5.1652; 25.159
90; 109.501; 90		2462.2Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518663 CIFC68 H56 Cl2 S4P 1 21/c 17.6706; 17.4871; 20.506
90; 100.272; 90		2706.5Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518664 CIFC66 H52 S4P 1 21/n 121.43; 5.2798; 24.95
90; 111.599; 90		2624.8Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518665 CIFC66 H52 S4P 1 21/n 120.0834; 5.2324; 24.6005
90; 109.019; 90		2444.01Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518666 CIFC8 H16 F7 O6 P2 S2 SbP 1 21/n 114.5029; 8.9034; 14.9927
90; 97.26; 90		1920.41Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518667 CIFC43 H71 F9 N3 O9 P3 S3 Sb4P -111.4789; 11.9874; 26.0864
91.82; 97.564; 112.074		3284.57Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518668 CIFC29 H61.5 F12 N0.5 O12 P4 S4 Sb4P 1 21/c 123.986; 21.83; 22.193
90; 106.57; 90		11138Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518669 CIFC31 H41 F6 N2 O6 S2 SbP 1 21/c 112.3127; 17.4575; 17.0214
90; 91.03; 90		3658.1Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518670 CIFC4 H9 F4 O3 P SP 1 21/m 110.2147; 8.6511; 11.0323
90; 94.5503; 90		971.83Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518671 CIFC14 H30 F6 O6 P2 S2P 1 21/n 113.4271; 11.8532; 15.7504
90; 110.993; 90		2340.4Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518672 CIFC27 H24 Cl5 F6 N5 O P2 RuP -111.1445; 12.0548; 14.8726
67.197; 84.942; 67.025		1691.09Walden, Andrew G.; Miller, Alexander J. M.
Rapid water oxidation electrocatalysis by a ruthenium complex of the tripodal ligand tris(2-pyridyl)phosphine oxide
Chem. Sci., 2015, 6, 2405
1518676 CIFC17 H25 N O2 SiP 1 21/n 17.8451; 10.8055; 41.681
90; 92.188; 90		3530.7Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming
Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams
Chem. Sci., 2015, 6, 2275
1518677 CIFC19 H19 Cl2 N O SP 1 21/c 19.4678; 22.465; 8.4857
90; 94.892; 90		1798.3Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming
Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams
Chem. Sci., 2015, 6, 2275
1518714 CIFC14 H26 Cl3 N4 O P RuP 1 21/n 16.9163; 23.66; 11.8396
90; 97.078; 90		1922.7Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G.
Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action
Chem. Sci., 2015, 6, 2449
1518715 CIFC15 H23 Cl2 N4 O P RuP -110.5379; 12.8283; 13.7451
100.766; 97.279; 91.491		1808.34Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G.
Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action
Chem. Sci., 2015, 6, 2449
1518716 CIFC42 H55 Cl2 N5 O10C 1 2 125.187; 8.1556; 21.154
90; 99.308; 90		4288.1Rose, Tristan E.; Lawson, Kenneth V.; Harran, Patrick. G.
Large ring-forming alkylations provide facile access to composite macrocycles
Chem. Sci., 2015, 6, 2219
1518727 CIFC53 H53 F3 N4 O3 P2 SC 1 c 124.05898; 12.60445; 17.26646
90; 109.899; 90		4923.42Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518728 CIFC67 H72 Cl Ir N4 P2P -111.53121; 15.09347; 16.48026
91.4726; 100.955; 90.9436		2814.45Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518729 CIFC54 H52 Cl Ir N4 O2 P2R -330.1754; 30.1754; 27.5094
90; 90; 120		21692.9Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518730 CIFC71.5 H80 Cl2 Ir2 N4 P2P -113.28816; 15.4534; 18.6095
66.4438; 87.7181; 64.8361		3131.28Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518731 CIFC55.5 H62 Au2 Cl3 Ir N4 P2P 1 21/c 112.88426; 13.46559; 30.9781
90; 99.5872; 90		5299.46Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H.
Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system
Chem. Sci., 2015, 6, 2506
1518738 CIFC19.5 H18.5 As3 Cl6.5 S6P n m a20.703; 9.885; 14.702
90; 90; 90		3008.8Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518739 CIFC24 H24 Cl3 S6 Sb3R -3 c :H14.2066; 14.2066; 33.41
90; 90; 120		5839.7Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518740 CIFC36 H42 As3 Cl3 S6P -110.0055; 12.424; 16.522
81.285; 88.456; 84.579		2020.9Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518741 CIFC30 H42 As3 Cl3 S6R -3 :H16.413; 16.413; 23.8
90; 90; 120		5552.4Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518742 CIFC24 H30 Cl3 S6 Sb3P 1 21/n 116.0971; 11.4604; 16.3368
90; 91.867; 90		3012.2Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518743 CIFC30 H42 Cl3 S6 Sb3R -3 :H16.458; 16.458; 23.9449
90; 90; 120		5616.9Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518744 CIFC32 H30 N8 O5 Zn4P 42/m c m11.5382; 11.5382; 25.813
90; 90; 90		3436.5Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming
Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications
Chem. Sci., 2015, 6, 2516
1518745 CIFC34 H32 N8 O5 Zn4P 42/m c m11.517; 11.517; 34.474
90; 90; 90		4573Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming
Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications
Chem. Sci., 2015, 6, 2516
1518753 CIFC37 H31 Cu F12 N4P -112.1667; 12.1867; 13.5954
81.549; 77.873; 65.444		1788.5Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl
Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal‒ligand interactions
Chem. Sci., 2015, 6, 2474
1518754 CIFC16 H6 F12 N2I 41/a :236.71; 36.71; 4.9148
90; 90; 90		6623.3Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl
Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal‒ligand interactions
Chem. Sci., 2015, 6, 2474
1518755 CIFC18 H27 Au B Cl N2 O2P 1 21/n 111.295; 10.512; 16.9583
90; 102.328; 90		1967.1Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518756 CIFC53 H79 Au B Cl N4 O4P 1 21/c 115.396; 14.4925; 24.966
90; 100.935; 90		5469.4Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518757 CIFC19 H27 B F3 Li N2 O5 SP -15.9513; 10.9562; 17.3953
96.176; 93.242; 97.646		1114.73Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518758 CIFC26 H39 B Cl N2 O2 RhP 1 21/c 116.46; 13.8072; 11.9483
90; 104.628; 90		2627.4Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518759 CIFC33 H47 B Cl Ir N2 O2C 1 2/c 135.4699; 10.667; 18.1337
90; 115.404; 90		6197.6Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518761 CIFC25 H23 F12 Fe2 O10P -19.507; 11.729; 16.605
102.703; 96.771; 112.595		1625Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518762 CIFC35 H25 F24 Fe3 O14P 1 21 19.7834; 20.8414; 12.0955
90; 102.57; 90		2407.2Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518763 CIFC35 H25 F24 Fe3 O14P 1 21 19.7979; 20.819; 12.0998
90; 102.659; 90		2408.2Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518764 CIFC35 H19 F30 Fe3 O14C 1 2/c 120.934; 13.481; 17.739
90; 92.848; 90		5000Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518765 CIFC25 H23 F12 Fe Mn O10P -19.464; 11.8255; 16.508
102.022; 97.859; 112.682		1618.3Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518766 CIFC35 H25 F24 Fe Ni2 O14P 1 21 19.7682; 20.7583; 12.0575
90; 103.126; 90		2381Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518779 CIFC38 H34 Cl2 Ir N P2I b a m30.868; 17.517; 24.155
90; 90; 90		13061Liu, Chong; Xie, Jian-Hua; Tian, Gui-Long; Li, Wei; Zhou, Qi-Lin
Highly efficient hydrogenation of carbon dioxide to formate catalyzed by iridium(iii) complexes of imine‒diphosphine ligands
Chem. Sci., 2015, 6, 2928
1518780 CIFGa1.67 O10 P2.5 Zn0.83C 1 2/m 116.767; 19.047; 10.248
90; 127.038; 90		2612.5Wu, Junbiao; Tao, Chunyao; Li, Yi; Li, Jiyang; Yu, Jihong
Methyl viologen-templated zinc gallophosphate zeolitic material with dual photo-/thermochromism and tuneable photovoltaic activity
Chem. Sci., 2015, 6, 2922
1518781 CIFC63 H59 B F29 Fe N3 P2P -112.7767; 13.894; 38.0545
90.4567; 92.9881; 96.475		6702.5Darmon, Jonathan M.; Kumar, Neeraj; Hulley, Elliott B.; Weiss, Charles J.; Raugei, Simone; Bullock, R. Morris; Helm, Monte L.
Increasing the rate of hydrogen oxidation without increasing the overpotential: a bio-inspired iron molecular electrocatalyst with an outer coordination sphere proton relay
Chem. Sci., 2015, 6, 2737
1518782 CIFC38 H55 Co N2 O4P 1 21/n 117.569; 10.302; 19.781
90; 100.629; 90		3518.8Zhao, Yaguang; Yu, Mengmeng; Zhang, Shuailin; Wu, Zhenqiang; Liu, Yuchu; Peng, Chi-How; Fu, Xuefeng
A well-defined, versatile photoinitiator (salen)Co‒CO2CH3for visible light-initiated living/controlled radical polymerization
Chem. Sci., 2015, 6, 2979
1518784 CIFC16 H29 B I N3C 1 2/c 117.3182; 19.7092; 12.0924
90; 120.773; 90		3546.3Chauvier, Clément; Tlili, Anis; Das Neves Gomes, Christophe; Thuéry, Pierre; Cantat, Thibault
Metal-free dehydrogenation of formic acid to H2and CO2using boron-based catalysts
Chem. Sci., 2015, 6, 2938
1518785 CIFC17 H30 B N3 O4P 21 21 217.1546; 12.8526; 20.4294
90; 90; 90		1878.59Chauvier, Clément; Tlili, Anis; Das Neves Gomes, Christophe; Thuéry, Pierre; Cantat, Thibault
Metal-free dehydrogenation of formic acid to H2and CO2using boron-based catalysts
Chem. Sci., 2015, 6, 2938
1518786 CIFC23 H17 NP n a 217.4701; 19.7919; 11.1894
90; 90; 90		1654.32Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J.
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
Chem. Sci., 2015, 6, 2843
1518787 CIFC58 H46 F6 Ir N4 O PP n a 2113.128; 37.8916; 10.29
90; 90; 90		5118.7Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J.
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
Chem. Sci., 2015, 6, 2843
1518788 CIFC44 H32 F6 Ir N4 PP 1 21/n 115.0877; 13.1747; 18.093
90; 96.094; 90		3576.1Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J.
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
Chem. Sci., 2015, 6, 2843
1518789 CIFC76 H60 F6 Ir N4 PP -110.8073; 13.5065; 20.8777
80.953; 86.577; 78.797		2950.9Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J.
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
Chem. Sci., 2015, 6, 2843
1518821 CIFC65 H80 Au N OP -111.6132; 14.7425; 16.9669
87.393; 71.112; 80.062		2707Ming Tong, Glenna So; Chan, Kaai Tung; Chang, Xiaoyong; Che, Chi-Ming
Theoretical studies on the photophysical properties of luminescent pincer gold(iii) arylacetylide complexes: the role of π-conjugation at the C-deprotonated [C^N^C] ligand
Chem. Sci., 2015, 6, 3026
1518822 CIFC35 H34 Au B Mn O2 PP -110.071; 11.844; 13.4
86.394; 79.387; 74.371		1512.8Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518823 CIFC43 H40 Au B Mn O2 PC 1 2/c 141.848; 10.898; 15.941
90; 91.024; 90		7269Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518824 CIFC30 H29 Au B Mn N O2 P SP 1 21/n 113.491; 13.559; 16.412
90; 101.959; 90		2937Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518825 CIFC46 H40 Au B3 Cl8 Mn2 O4P 1 21/c 118.435; 33.798; 17.288
90; 113.832; 90		9853Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518826 CIFC98 H85 Ag2 B6 Cl16 F Mn4 O8P -112.2946; 13.8214; 16.0619
88.083; 67.993; 83.916		2516.2Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518827 CIFC53 H48 Ag B3 Cl8 Mn2 O4P 1 21/n 111.184; 36.556; 13.609
90; 93.434; 90		5554Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518828 CIFC46 H40 Ag B3 Cl8 Mn2 O4P 1 21/c 118.444; 33.901; 17.285
90; 113.909; 90		9880Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518829 CIFC53 H48 B3 Cl8 Cu Mn2 O4P 1 21/n 111.0743; 36.198; 13.711
90; 93.21; 90		5488Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518830 CIFC55 H50 B3 Cl12 Cu2 Mn3 O6P -111.952; 14.576; 20.573
70.672; 73.21; 68.233		3084Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518831 CIFC67 H62 B3 Cl8 Cu2 Mn3 O6P -111.301; 14.461; 21.311
97.172; 96.19; 102.139		3345.8Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518832 CIFC75 H50 Au B F24 P2P -112.38; 15.772; 18.327
83.065; 74.699; 81.63		3402.1Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518843 CIFC22 H23 N O3P 1 21/n 16.0325; 20.594; 14.3515
90; 97.425; 90		1768Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando
Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans
Chem. Sci., 2015, 6, 2903
1518844 CIFC25 H27 N O3P 1 21/n 110.6026; 12.0053; 16.5199
90; 105.806; 90		2023.27Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando
Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans
Chem. Sci., 2015, 6, 2903
1518845 CIFC24 H25 N O3P 1 21/c 119.6584; 6.7792; 14.62
90; 104.609; 90		1885.39Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando
Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans
Chem. Sci., 2015, 6, 2903
1518846 CIFC10 H9 Br Cl N O2P 1 21 15.928; 7.6682; 11.3533
90; 95.944; 90		513.31Zhu, Cheng-Liang; Tian, Jun-Shan; Gu, Zhen-Yuan; Xing, Guo-Wen; Xu, Hao
Iron(ii)-catalyzed asymmetric intramolecular olefin aminochlorination using chloride ion
Chem. Sci., 2015, 6, 3044
1518866 CIFC11 H9 Dy N3 O6P 1 21/c 113.672; 7.313; 12.481
90; 94.296; 90		1244.4Yin, Dan-Dan; Chen, Qi; Meng, Yin-Shan; Sun, Hao-Ling; Zhang, Yi-Quan; Gao, Song
Slow magnetic relaxation in a novel carboxylate/oxalate/hydroxyl bridged dysprosium layer
Chem. Sci., 2015, 6, 3095
1518867 CIFC11 H9 N3 O6 YP 1 21/c 113.655; 7.278; 12.428
90; 94.424; 90		1231.4Yin, Dan-Dan; Chen, Qi; Meng, Yin-Shan; Sun, Hao-Ling; Zhang, Yi-Quan; Gao, Song
Slow magnetic relaxation in a novel carboxylate/oxalate/hydroxyl bridged dysprosium layer
Chem. Sci., 2015, 6, 3095
1518869 CIFC42 H34 N6 O10P -18.8838; 20.6864; 22.5136
68.276; 78.717; 89.509		3760Martinez-Cuezva, Alberto; Pastor, Aurelia; Cioncoloni, Giacomo; Orenes, Raul-Angel; Alajarin, Mateo; Symes, Mark D.; Berna, Jose
Versatile control of the submolecular motion of di(acylamino)pyridine-based [2]rotaxanes
Chem. Sci., 2015, 6, 3087

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