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
1518870 CIFC67 H57.75 N7 O7P -110.4583; 13.5669; 19.947
76.564; 75.557; 80.757		2649.9Martinez-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
1518871 CIFC31 H22 O SP 1 21 15.594; 47.1662; 9.2545
90; 103.425; 90		2375.06Xu, Bingjia; He, Jiajun; Mu, Yingxiao; Zhu, Qiangzhong; Wu, Sikai; Wang, Yifan; Zhang, Yi; Jin, Chongjun; Lo, Changcheng; Chi, Zhenguo; Lien, Alan; Liu, Siwei; Xu, Jiarui
Very bright mechanoluminescence and remarkable mechanochromism using a tetraphenylethene derivative with aggregation-induced emission
Chem. Sci., 2015, 6, 3236
1518875 CIFC42 H84 N0 O26 Zn8C 1 2/c 122.502; 12.882; 21.773
90; 98.995; 90		6233.7Kubisiak, Marcin; Zelga, Karolina; Bury, Wojciech; Justyniak, Iwona; Budny-Godlewski, Krzysztof; Ochal, Zbigniew; Lewiński, Janusz
Development of zinc alkyl/air systems as radical initiators for organic reactions
Chem. Sci., 2015, 6, 3102
1518876 CIFC38 H64 O26 Zn8P -19.5731; 10.8542; 13.0771
77.371; 83.044; 80.914		1304.01Kubisiak, Marcin; Zelga, Karolina; Bury, Wojciech; Justyniak, Iwona; Budny-Godlewski, Krzysztof; Ochal, Zbigniew; Lewiński, Janusz
Development of zinc alkyl/air systems as radical initiators for organic reactions
Chem. Sci., 2015, 6, 3102
1518882 CIFC82.5 H86 B Cr F24 N2P -113.468; 14.272; 20.836
85.98; 89.96; 87.39		3991Samuel, Prinson P.; Neufeld, Roman; Chandra Mondal, Kartik; Roesky, Herbert W.; Herbst-Irmer, Regine; Stalke, Dietmar; Demeshko, Serhiy; Meyer, Franc; Rojisha, Vallyanga Chalil; De, Susmita; Parameswaran, Pattiyil; Stückl, A. Claudia; Kaim, Wolfgang; Christian, Jonathan H.; Bindra, Jasleen K.; Dalal, Naresh S.
Cr(i)Cl as well as Cr+are stabilised between two cyclic alkyl amino carbenes
Chem. Sci., 2015, 6, 3148
1518883 CIFC40 H62 Cl2 Cr N2C 1 2/c 116.958; 10.973; 22.073
90; 108.91; 90		3885.7Samuel, Prinson P.; Neufeld, Roman; Chandra Mondal, Kartik; Roesky, Herbert W.; Herbst-Irmer, Regine; Stalke, Dietmar; Demeshko, Serhiy; Meyer, Franc; Rojisha, Vallyanga Chalil; De, Susmita; Parameswaran, Pattiyil; Stückl, A. Claudia; Kaim, Wolfgang; Christian, Jonathan H.; Bindra, Jasleen K.; Dalal, Naresh S.
Cr(i)Cl as well as Cr+are stabilised between two cyclic alkyl amino carbenes
Chem. Sci., 2015, 6, 3148
1518884 CIFC47 H70 Cl Cr N2P -19.636; 12.053; 19.94
102.29; 95.37; 106.71		2137.4Samuel, Prinson P.; Neufeld, Roman; Chandra Mondal, Kartik; Roesky, Herbert W.; Herbst-Irmer, Regine; Stalke, Dietmar; Demeshko, Serhiy; Meyer, Franc; Rojisha, Vallyanga Chalil; De, Susmita; Parameswaran, Pattiyil; Stückl, A. Claudia; Kaim, Wolfgang; Christian, Jonathan H.; Bindra, Jasleen K.; Dalal, Naresh S.
Cr(i)Cl as well as Cr+are stabilised between two cyclic alkyl amino carbenes
Chem. Sci., 2015, 6, 3148
1518906 CIFC34 H18 O2C 1 2 113.707; 6.3468; 13.269
90; 103.472; 90		1122.6Sbargoud, Kamal; Mamada, Masashi; Marrot, Jérôme; Tokito, Shizuo; Yassar, Abderrahim; Frigoli, Michel
Diindeno[1,2-b:2′,1′-n]perylene: a closed shell related Chichibabin's hydrocarbon, the synthesis, molecular packing, electronic and charge transport properties
Chem. Sci., 2015, 6, 3402
1518907 CIFC34 H16 O2P b c n18.9562; 15.493; 14.8168
90; 90; 90		4351.5Sbargoud, Kamal; Mamada, Masashi; Marrot, Jérôme; Tokito, Shizuo; Yassar, Abderrahim; Frigoli, Michel
Diindeno[1,2-b:2′,1′-n]perylene: a closed shell related Chichibabin's hydrocarbon, the synthesis, molecular packing, electronic and charge transport properties
Chem. Sci., 2015, 6, 3402
1518908 CIFC59 H61 Si2P b c a34.006; 7.6167; 36.832
90; 90; 90		9540Sbargoud, Kamal; Mamada, Masashi; Marrot, Jérôme; Tokito, Shizuo; Yassar, Abderrahim; Frigoli, Michel
Diindeno[1,2-b:2′,1′-n]perylene: a closed shell related Chichibabin's hydrocarbon, the synthesis, molecular packing, electronic and charge transport properties
Chem. Sci., 2015, 6, 3402
1518942 CIFC26 H40 O5 SiP 1 21 16.7367; 22.9731; 16.5877
90; 90.862; 90		2566.9Mukai, Ken; Kasuya, Satoshi; Nakagawa, Yuki; Urabe, Daisuke; Inoue, Masayuki
A convergent total synthesis of ouabagenin
Chem. Sci., 2015, 6, 3383
1518943 CIFC18 H30 O5 SiP 1 21 111.0079; 6.36439; 13.7975
90; 110.712; 90		904.16Mukai, Ken; Kasuya, Satoshi; Nakagawa, Yuki; Urabe, Daisuke; Inoue, Masayuki
A convergent total synthesis of ouabagenin
Chem. Sci., 2015, 6, 3383
1518946 CIFC11 H9 F3 N2 OP -111.5587; 11.8263; 17.672
92.233; 102.972; 108.187		2220.9Chen, Zhang-Pei; Chen, Mu-Wang; Shi, Lei; Yu, Chang-Bin; Zhou, Yong-Gui
Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers
Chem. Sci., 2015, 6, 3415
1518947 CIFC10 H9 F3 N2 OP 1 21 19.0634; 5.8062; 9.8369
90; 90.567; 90		517.63Chen, Zhang-Pei; Chen, Mu-Wang; Shi, Lei; Yu, Chang-Bin; Zhou, Yong-Gui
Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers
Chem. Sci., 2015, 6, 3415
1518948 CIFC17 H15 F3 N2 OP 21 21 215.7467; 9.4574; 27.5934
90; 90; 90		1499.67Chen, Zhang-Pei; Chen, Mu-Wang; Shi, Lei; Yu, Chang-Bin; Zhou, Yong-Gui
Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers
Chem. Sci., 2015, 6, 3415
1518949 CIFC46 H46 N2 S2P 1 21/c 123.6399; 5.207; 15.042
90; 107.545; 90		1765.4He, Bo; Dai, Jing; Zherebetskyy, Danylo; Chen, Teresa L.; Zhang, Benjamin A.; Teat, Simon J.; Zhang, Qichun; Wang, Linwang; Liu, Yi
A divergent route to core- and peripherally functionalized diazacoronenes that act as colorimetric and fluorescence proton sensors
Chem. Sci., 2015, 6, 3180
1518950 CIFC42 H42 N2 S4R -3 :H43.2109; 43.2109; 5.0578
90; 90; 120		8178.6He, Bo; Dai, Jing; Zherebetskyy, Danylo; Chen, Teresa L.; Zhang, Benjamin A.; Teat, Simon J.; Zhang, Qichun; Wang, Linwang; Liu, Yi
A divergent route to core- and peripherally functionalized diazacoronenes that act as colorimetric and fluorescence proton sensors
Chem. Sci., 2015, 6, 3180
1518951 CIFC46 H46 N2 O2P 1 21/c 115.3148; 5.2027; 21.5181
90; 93.605; 90		1711.13He, Bo; Dai, Jing; Zherebetskyy, Danylo; Chen, Teresa L.; Zhang, Benjamin A.; Teat, Simon J.; Zhang, Qichun; Wang, Linwang; Liu, Yi
A divergent route to core- and peripherally functionalized diazacoronenes that act as colorimetric and fluorescence proton sensors
Chem. Sci., 2015, 6, 3180
1518952 CIFC34 H36 Cl2 Mo2 N6 O4P 1 21/c 112.536; 12.3769; 13.069
90; 115.499; 90		1830.2Tsurugi, Hayato; Hayakawa, Akio; Kando, Shun; Sugino, Yoshitaka; Mashima, Kazushi
Mixed-ligand complexes of paddlewheel dinuclear molybdenum as hydrodehalogenation catalysts for polyhaloalkanes
Chem. Sci., 2015, 6, 3434
1518953 CIFC62 H102 Cl4 Mo2 N6 O4P 1 21/n 112.6064; 14.1061; 19.183
90; 101.372; 90		3344.3Tsurugi, Hayato; Hayakawa, Akio; Kando, Shun; Sugino, Yoshitaka; Mashima, Kazushi
Mixed-ligand complexes of paddlewheel dinuclear molybdenum as hydrodehalogenation catalysts for polyhaloalkanes
Chem. Sci., 2015, 6, 3434
1518954 CIFC48 H69 Cl4 Mo2 N6 O4P -112.142; 13.615; 17.274
78.896; 84.467; 69.112		2616.8Tsurugi, Hayato; Hayakawa, Akio; Kando, Shun; Sugino, Yoshitaka; Mashima, Kazushi
Mixed-ligand complexes of paddlewheel dinuclear molybdenum as hydrodehalogenation catalysts for polyhaloalkanes
Chem. Sci., 2015, 6, 3434
1518955 CIFC34 H36 Cl4 Mo2 N6 O4P 1 21/c 111.752; 15.014; 11.14
90; 109.276; 90		1855.4Tsurugi, Hayato; Hayakawa, Akio; Kando, Shun; Sugino, Yoshitaka; Mashima, Kazushi
Mixed-ligand complexes of paddlewheel dinuclear molybdenum as hydrodehalogenation catalysts for polyhaloalkanes
Chem. Sci., 2015, 6, 3434
1518956 CIFC216 H130 N12 O32 Zr6P m -3 m25.4376; 25.4376; 25.4376
90; 90; 90		16459.9Zheng, Jun; Wu, Mingyan; Jiang, Feilong; Su, Weiping; Hong, Maochun
Stable porphyrin Zr and Hf metal‒organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses
Chem. Sci., 2015, 6, 3466
1518957 CIFC216 H124 Cu3 N12 O32 Zr6P m -3 m25.4213; 25.4213; 25.4213
90; 90; 90		16428.3Zheng, Jun; Wu, Mingyan; Jiang, Feilong; Su, Weiping; Hong, Maochun
Stable porphyrin Zr and Hf metal‒organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses
Chem. Sci., 2015, 6, 3466
1518958 CIFC216 H130 Hf6 N12 O32P m -3 m25.3976; 25.3976; 25.3976
90; 90; 90		16382.4Zheng, Jun; Wu, Mingyan; Jiang, Feilong; Su, Weiping; Hong, Maochun
Stable porphyrin Zr and Hf metal‒organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses
Chem. Sci., 2015, 6, 3466
1518959 CIFC216 H124 Cu3 Hf6 N12 O32P m -3 m25.357; 25.357; 25.357
90; 90; 90		16304Zheng, Jun; Wu, Mingyan; Jiang, Feilong; Su, Weiping; Hong, Maochun
Stable porphyrin Zr and Hf metal‒organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses
Chem. Sci., 2015, 6, 3466
1518983 CIFC40 H28P 1 21/c 19.0462; 22.0677; 14.1102
90; 91.134; 90		2816.25He, Zikai; Shan, Liang; Mei, Ju; Wang, Hong; Lam, Jacky W. Y.; Sung, Herman H. Y.; Williams, Ian D.; Gu, Xiao; Miao, Qian; Tang, Ben Zhong
Aggregation-induced emission and aggregation-promoted photochromism of bis(diphenylmethylene)dihydroacenes
Chem. Sci., 2015, 6, 3538
1518984 CIFC45 H31 Cl3P 1 21/n 19.6681; 17.2389; 20.8625
90; 90.222; 90		3477.07He, Zikai; Shan, Liang; Mei, Ju; Wang, Hong; Lam, Jacky W. Y.; Sung, Herman H. Y.; Williams, Ian D.; Gu, Xiao; Miao, Qian; Tang, Ben Zhong
Aggregation-induced emission and aggregation-promoted photochromism of bis(diphenylmethylene)dihydroacenes
Chem. Sci., 2015, 6, 3538
1518985 CIFC48 H32C 1 2/c 128.4; 12.0889; 20.7374
90; 110.271; 90		6678.7He, Zikai; Shan, Liang; Mei, Ju; Wang, Hong; Lam, Jacky W. Y.; Sung, Herman H. Y.; Williams, Ian D.; Gu, Xiao; Miao, Qian; Tang, Ben Zhong
Aggregation-induced emission and aggregation-promoted photochromism of bis(diphenylmethylene)dihydroacenes
Chem. Sci., 2015, 6, 3538
1518986 CIFC44 H30P 1 21 19.2686; 7.5344; 22.0069
90; 91.349; 90		1536.39He, Zikai; Shan, Liang; Mei, Ju; Wang, Hong; Lam, Jacky W. Y.; Sung, Herman H. Y.; Williams, Ian D.; Gu, Xiao; Miao, Qian; Tang, Ben Zhong
Aggregation-induced emission and aggregation-promoted photochromism of bis(diphenylmethylene)dihydroacenes
Chem. Sci., 2015, 6, 3538
1518987 CIFC93 H95 N2 P PdP 1 21/n 114.1659; 25.5435; 20.2558
90; 95.695; 90		7293.3Henwood, Adam F.; Lesieur, Mathieu; Bansal, Ashu K.; Lemaur, Vincent; Beljonne, David; Thompson, David G.; Graham, Duncan; Slawin, Alexandra M. Z.; Samuel, Ifor D. W.; Cazin, Catherine S. J.; Zysman-Colman, Eli
Palladium(0) NHC complexes: a new avenue to highly efficient phosphorescence
Chem. Sci., 2015, 6, 3248
1518988 CIFC54 H76 N4 PdP 1 21/n 112.889; 27.082; 14.073
90; 92.483; 90		4908Henwood, Adam F.; Lesieur, Mathieu; Bansal, Ashu K.; Lemaur, Vincent; Beljonne, David; Thompson, David G.; Graham, Duncan; Slawin, Alexandra M. Z.; Samuel, Ifor D. W.; Cazin, Catherine S. J.; Zysman-Colman, Eli
Palladium(0) NHC complexes: a new avenue to highly efficient phosphorescence
Chem. Sci., 2015, 6, 3248
1519000 CIFC136 H142 N4 Ni O2P -112.8361; 15.5717; 15.9281
100.921; 109.976; 108.18		2682Zeng, Wangdong; Lee, Sangsu; Son, Minjung; Ishida, Masatoshi; Furukawa, Ko; Hu, Pan; Sun, Zhe; Kim, Dongho; Wu, Jishan
Phenalenyl-fused porphyrins with different ground states
Chem. Sci., 2015, 6, 2427
1519001 CIFC136 H142 N4 Ni O2P -112.85; 15.5881; 15.9283
100.951; 110.033; 108.118		2687.2Zeng, Wangdong; Lee, Sangsu; Son, Minjung; Ishida, Masatoshi; Furukawa, Ko; Hu, Pan; Sun, Zhe; Kim, Dongho; Wu, Jishan
Phenalenyl-fused porphyrins with different ground states
Chem. Sci., 2015, 6, 2427
1519002 CIFC85.5 H87 N5 NiP -115.0498; 15.6708; 17.4668
111.901; 107.076; 102.416		3400.2Zeng, Wangdong; Lee, Sangsu; Son, Minjung; Ishida, Masatoshi; Furukawa, Ko; Hu, Pan; Sun, Zhe; Kim, Dongho; Wu, Jishan
Phenalenyl-fused porphyrins with different ground states
Chem. Sci., 2015, 6, 2427
1519367 CIFC10 H10 Cl I N2 O4P 1 21/n 112.2849; 16.0628; 14.7939
90; 113.273; 90		2681.74Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519368 CIFC10 H10 F6 I N2 PC 1 2/m 113.6827; 6.7491; 8.4045
90; 106.045; 90		745.89Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519369 CIFC10 H10 F6 I N2 SbP -16.9674; 7.1797; 7.7358
91.775; 101.402; 96.682		376.18Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519370 CIFC11 H10 F3 I N2 O3 SP -17.0091; 10.6722; 10.7542
93.455; 105.677; 104.138		744.16Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519371 CIFC17 H17 I N2 O3 SP 1 21/n 19.0892; 21.1577; 10.0924
90; 115.781; 90		1747.65Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519372 CIFC10 H10 I N3 O3P -17.0864; 7.4613; 13.5366
99.491; 94.725; 117.637		614.97Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519373 CIFC12 H14 Ag B Cl2 F4 N2P 1 21/n 17.2894; 13.3581; 16.9874
90; 101.989; 90		1618.03Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519374 CIFC12 H14 Ag Cl3 N2 O4P 1 21/n 17.2442; 13.3604; 16.9657
90; 101.394; 90		1609.67Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519375 CIFC12 H14 Ag Cl2 F6 N2 PP -19.968; 10.512; 10.679
111.37; 116.82; 97.43		869.9Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519376 CIFC12 H14 Ag Cl2 F6 N2 SbP 1 21/c 112.6882; 13.8467; 11.1581
90; 112.12; 90		1816.08Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519377 CIFC11 H10 Ag F3 N2 O3 SP 1 21/c 17.952; 17.294; 10.7947
90; 95.624; 90		1477.36Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519378 CIFC17 H17 Ag N2 O3 SP 1 21/c 19.8088; 15.4242; 11.5973
90; 100.033; 90		1727.76Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519379 CIFC15 H15 Ag2 N5 O6P -17.4958; 10.0405; 12.7988
82.991; 83.259; 76.743		926.59Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519380 CIFC10 H12 Ag N3 O4I 1 2/a 15.7265; 14.7681; 14.6482
90; 96.59; 90		1230.61Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519381 CIFC22.5 H17 Ag Cl5 N3 O3P -17.2198; 13.3083; 14.6862
116.693; 90.96; 90.319		1260.4Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté
Counterion influence on the N‒I‒N halogen bond
Chem. Sci., 2015, 6, 3746
1519382 CIFC59 H79 B Cl N6 O13 S6P -117.809; 18.594; 22.412
73.894; 83.175; 71.769		6768.1Rudolf, Marc; Trukhina, Olga; Perles, Josefina; Feng, Lai; Akasaka, Takeshi; Torres, Tomas; Guldi, Dirk M.
Taming C60fullerene: tuning intramolecular photoinduced electron transfer process with subphthalocyanines
Chem. Sci., 2015, 6, 4141
1519383 CIFC72 H116 Fe2 Mo2 N12 P4P -114.749; 15.266; 18.081
72.467; 83.794; 81.014		3826.2Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki
Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site
Chem. Sci., 2015, 6, 3940
1519384 CIFC72 H116 Mo2 N12 P4 Ru2P -114.7212; 15.3604; 18.0121
72.7582; 84.4816; 81.1096		3837.72Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki
Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site
Chem. Sci., 2015, 6, 3940
1519385 CIFC39 H65 Cl3 Fe Mo N P2C 1 c 121.9221; 15.852; 14.007
90; 121.631; 90		4144.4Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki
Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site
Chem. Sci., 2015, 6, 3940
1519386 CIFC39 H64 Cl5 Fe Mo N P2P -113.2456; 15.6143; 24.2272
90.538; 102.695; 112.964		4475.5Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki
Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site
Chem. Sci., 2015, 6, 3940
1519387 CIFC40 H57 Cl5 Fe Mo N P2C 1 c 118.9384; 19.521; 13.7984
90; 120.86; 90		4379Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki
Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site
Chem. Sci., 2015, 6, 3940
1519388 CIFC27 H25 N5 O2P 21 21 2111.295; 12.39; 16.088
90; 90; 90		2251.4Li, Qi; Xia, Tingting; Yao, Licheng; Deng, Haiteng; Liao, Xuebin
Enantioselective and diastereoselective azo-coupling/iminium-cyclizations: a unified strategy for the total syntheses of (−)-psychotriasine and (+)-pestalazine B
Chem. Sci., 2015, 6, 3599
1519389 CIFC60 H70 N2 O4P -110.8676; 12.3446; 19.476
75.286; 86.422; 86.274		2518.9Yatham, Veera Reddy; Neudörfl, Jörg-M.; Schlörer, Nils E.; Berkessel, Albrecht
Carbene catalyzed umpolung of α,β-enals: a reactivity study of diamino dienols vs. azolium enolates, and the characterization of advanced reaction intermediates
Chem. Sci., 2015, 6, 3706
1519390 CIFC55 H72 N2 O6P 1 21/c 112.309; 37.444; 10.6821
90; 91.78; 90		4921Yatham, Veera Reddy; Neudörfl, Jörg-M.; Schlörer, Nils E.; Berkessel, Albrecht
Carbene catalyzed umpolung of α,β-enals: a reactivity study of diamino dienols vs. azolium enolates, and the characterization of advanced reaction intermediates
Chem. Sci., 2015, 6, 3706
1519391 CIFC18 H54 Cl N3 Si6 ThR 3 c :H18.4298; 18.4298; 16.84
90; 90; 120		4953.5Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W.
Thorium‒ligand multiple bonds via reductive deprotection of a trityl group
Chem. Sci., 2015, 6, 3891
1519392 CIFC36 H82 Cl2 N3 Na O4.5 Si6 ThR -3 :H18.404; 18.404; 29.626
90; 90; 120		8690Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W.
Thorium‒ligand multiple bonds via reductive deprotection of a trityl group
Chem. Sci., 2015, 6, 3891
1519393 CIFC18 H54 I N3 Si6 ThR 3 c :H18.328; 18.328; 17.356
90; 90; 120		5049Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W.
Thorium‒ligand multiple bonds via reductive deprotection of a trityl group
Chem. Sci., 2015, 6, 3891
1519394 CIFC53 H73 N2 O2 Si4 ThP -112.955; 13.0253; 16.867
85.654; 77.178; 79.336		2725.5Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W.
Thorium‒ligand multiple bonds via reductive deprotection of a trityl group
Chem. Sci., 2015, 6, 3891
1519395 CIFC37 H69 N3 S Si6 ThP -110.5938; 11.5867; 19.595
96.883; 91.006; 96.27		2372.5Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W.
Thorium‒ligand multiple bonds via reductive deprotection of a trityl group
Chem. Sci., 2015, 6, 3891
1519396 CIFC32 H83 K N3 O7.5 Si6 ThP b c a20.457; 20.307; 25.358
90; 90; 90		10534Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W.
Thorium‒ligand multiple bonds via reductive deprotection of a trityl group
Chem. Sci., 2015, 6, 3891
1519397 CIFC30 H78 K N3 O6 S Si6 ThP -112.7484; 18.891; 21.817
91.554; 105.863; 92.564		5044.8Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W.
Thorium‒ligand multiple bonds via reductive deprotection of a trityl group
Chem. Sci., 2015, 6, 3891
1519398 CIFC8 H6 F4 O6P 1 21/c 18.5417; 8.0442; 7.4465
90; 99.017; 90		505.33Gong, Yongyang; Zhao, Lifang; Peng, Qian; Fan, Di; Yuan, Wang Zhang; Zhang, Yongming; Tang, Ben Zhong
Crystallization-induced dual emission from metal- and heavy atom-free aromatic acids and esters
Chem. Sci., 2015, 6, 4438
1519399 CIFC10 H6 F4 O4P 1 21/n 16.332; 4.701; 17.423
90; 95.605; 90		516.1Gong, Yongyang; Zhao, Lifang; Peng, Qian; Fan, Di; Yuan, Wang Zhang; Zhang, Yongming; Tang, Ben Zhong
Crystallization-induced dual emission from metal- and heavy atom-free aromatic acids and esters
Chem. Sci., 2015, 6, 4438
1519400 CIFC94 H93.62 Ga4 Gd2 N15 O31.31C 1 2/c 125.233; 22.054; 17.997
90; 99.09; 90		9889Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal
Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative
Chem. Sci., 2015, 6, 4148
1519401 CIFC94 H93 Ga4 N15 O31 Tb2C 1 2/c 125.1697; 22.1217; 17.9895
90; 99.302; 90		9884.8Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal
Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative
Chem. Sci., 2015, 6, 4148
1519402 CIFC94 H93 Dy2 Ga4 N15 O31C 1 2/c 125.1638; 22.1781; 18.0649
90; 99.353; 90		9947.7Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal
Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative
Chem. Sci., 2015, 6, 4148
1519403 CIFC93 H91 Er2 Ga4 N15 O31C 1 2/c 125.1476; 22.138; 18.0285
90; 99.177; 90		9908.3Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal
Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative
Chem. Sci., 2015, 6, 4148
1519404 CIFC94 H93 Ga4 N15 O31 Y2C 1 2/c 125.1053; 22.1794; 18.0733
90; 99.377; 90		9929.1Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal
Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative
Chem. Sci., 2015, 6, 4148
1519405 CIFC26 H20 O3P 21 21 215.8732; 11.684; 28.383
90; 90; 90		1947.7Li, Guo-Tai; Gu, Qing; You, Shu-Li
Enantioselective annulation of enals with 2-naphthols by triazolium salts derived froml-phenylalanine
Chem. Sci., 2015, 6, 4273
1519406 CIFC35 H38 B F4 N3 O SiP 31 2 111.541; 11.541; 52.812
90; 90; 120		6091.9Li, Guo-Tai; Gu, Qing; You, Shu-Li
Enantioselective annulation of enals with 2-naphthols by triazolium salts derived froml-phenylalanine
Chem. Sci., 2015, 6, 4273
1519407 CIFC154 H96 N14 O32 Ti7P 1 2/m 117.6073; 17.0188; 25.0871
90; 101.722; 90		7360.7Yuan, Shuai; Liu, Tian-Fu; Feng, Dawei; Tian, Jian; Wang, Kecheng; Qin, Junsheng; Zhang, Qiang; Chen, Ying-Pin; Bosch, Mathieu; Zou, Lanfang; Teat, Simon J.; Dalgarno, Scott J.; Zhou, Hong-Cai
A single crystalline porphyrinic titanium metal‒organic framework
Chem. Sci., 2015, 6, 3926
1519408 CIFC25 H21 Cl N5 O4 PtP -17.2307; 12.06; 14.471
74.425; 82.9797; 79.6363		1192.09Tsai, Johnson Lui-Lui; Zou, Taotao; Liu, Jia; Chen, Tianfeng; Chan, Anna On-Yee; Yang, Chen; Lok, Chun-Nam; Che, Chi-Ming
Luminescent platinum(ii) complexes with self-assembly and anti-cancer properties: hydrogel, pH dependent emission color and sustained-release properties under physiological conditions
Chem. Sci., 2015, 6, 3823
1519409 CIFC17 H17 Cl O3P 21 21 216.2836; 12.6214; 37.0026
90; 90; 90		2934.6Burns, Alan R.; Madec, Amaël G. E.; Low, Darryl W.; Roy, Iain D.; Lam, Hon Wai
Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations
Chem. Sci., 2015, 6, 3550
1519410 CIFC17 H18 O3P 1 21 112.1037; 6.87725; 16.6432
90; 92.6683; 90		1383.88Burns, Alan R.; Madec, Amaël G. E.; Low, Darryl W.; Roy, Iain D.; Lam, Hon Wai
Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations
Chem. Sci., 2015, 6, 3550
1519411 CIFC18 H19 Cl O3P 1 21 17.0438; 11.6921; 9.8846
90; 108.47; 90		772.13Burns, Alan R.; Madec, Amaël G. E.; Low, Darryl W.; Roy, Iain D.; Lam, Hon Wai
Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations
Chem. Sci., 2015, 6, 3550
1519412 CIFC18 H19 N O5P 21 21 216.71816; 13.19234; 17.888
90; 90; 90		1585.38Burns, Alan R.; Madec, Amaël G. E.; Low, Darryl W.; Roy, Iain D.; Lam, Hon Wai
Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations
Chem. Sci., 2015, 6, 3550
1519413 CIFC12 H9 Cl O3P 21 21 219.632; 9.726; 11.729
90; 90; 90		1098.8Yin, Qin; Wang, Shou-Guo; Liang, Xiao-Wei; Gao, De-Wei; Zheng, Jun; You, Shu-Li
Organocatalytic asymmetric chlorinative dearomatization of naphthols
Chem. Sci., 2015, 6, 4179
1519414 CIFC12 H8 Br Cl O3P 21 21 217.45; 7.796; 21.193
90; 90; 90		1230.9Yin, Qin; Wang, Shou-Guo; Liang, Xiao-Wei; Gao, De-Wei; Zheng, Jun; You, Shu-Li
Organocatalytic asymmetric chlorinative dearomatization of naphthols
Chem. Sci., 2015, 6, 4179
1519415 CIFC114 H86 O52 Y6P m -3 m19.3042; 19.3042; 19.3042
90; 90; 90		7193.8Luebke, Ryan; Belmabkhout, Youssef; Weseliński, Łukasz J.; Cairns, Amy J.; Alkordi, Mohamed; Norton, George; Wojtas, Łukasz; Adil, Karim; Eddaoudi, Mohamed
Versatile rare earth hexanuclear clusters for the design and synthesis of highly-connectedftw-MOFs
Chem. Sci., 2015, 6, 4095
1519416 CIFC138 H78 O35 Y6I m -340.048; 40.048; 40.048
90; 90; 90		64231Luebke, Ryan; Belmabkhout, Youssef; Weseliński, Łukasz J.; Cairns, Amy J.; Alkordi, Mohamed; Norton, George; Wojtas, Łukasz; Adil, Karim; Eddaoudi, Mohamed
Versatile rare earth hexanuclear clusters for the design and synthesis of highly-connectedftw-MOFs
Chem. Sci., 2015, 6, 4095
1519417 CIFC162 H78 O32 Y6I m -348.111; 48.111; 48.111
90; 90; 90		111361Luebke, Ryan; Belmabkhout, Youssef; Weseliński, Łukasz J.; Cairns, Amy J.; Alkordi, Mohamed; Norton, George; Wojtas, Łukasz; Adil, Karim; Eddaoudi, Mohamed
Versatile rare earth hexanuclear clusters for the design and synthesis of highly-connectedftw-MOFs
Chem. Sci., 2015, 6, 4095
1519418 CIFC17 H17 F SP 21 21 217.9685; 11.0136; 16.1416
90; 90; 90		1416.6Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R.
Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect?
Chem. Sci., 2015, 6, 3565
1519419 CIFC17 H17 F O SP 21 21 219.4841; 9.9993; 14.7157
90; 90; 90		1395.55Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R.
Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect?
Chem. Sci., 2015, 6, 3565
1519420 CIFC17 H17 F O2 SP 1 21/c 114.663; 9.5972; 10.7876
90; 109.646; 90		1429.7Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R.
Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect?
Chem. Sci., 2015, 6, 3565
1519421 CIFC8 H8 F N O3 SP n a 2120.3421; 4.6595; 9.8133
90; 90; 90		930.14Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R.
Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect?
Chem. Sci., 2015, 6, 3565
1519422 CIFC8 H8 F N O4 SP -17.2161; 7.3574; 9.1736
86.045; 76.993; 78.266		464.49Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R.
Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect?
Chem. Sci., 2015, 6, 3565
1519423 CIFC15 H20 N2 O2P 1 21 19.4882; 10.3774; 15.575
90; 107.509; 90		1462.5Kim, Jinhee; Sim, Mikyung; Kim, Namhoon; Hong, Sungwoo
Asymmetric C‒H functionalization of cyclopropanes using an isoleucine-NH2bidentate directing group
Chem. Sci., 2015, 6, 3611
1519424 CIFC19 H21 Cu N4 O4.5P 1 21/c 112.1843; 13.6819; 22.5624
90; 99.683; 90		3707.7Moore, Cameron M.; Szymczak, Nathaniel K.
Nitrite reduction by copper through ligand-mediated proton and electron transfer
Chem. Sci., 2015, 6, 3373
1519425 CIFC36 H34 Cu2 N8 O6P b c n14.1161; 15.8051; 14.538
90; 90; 90		3243.5Moore, Cameron M.; Szymczak, Nathaniel K.
Nitrite reduction by copper through ligand-mediated proton and electron transfer
Chem. Sci., 2015, 6, 3373
1519426 CIFC26 H44 B Cl2 N2P 1 21/n 18.7727; 16.781; 18.22
90; 91.317; 90		2681.5Braunschweig, H.; Gackstatter, A.; Kupfer, T.; Scheller, T.; Hupp, F.; Damme, A.; Arnold, N.; Ewing, W. C.
Generation of 1,2-azaboretidines via reduction of ADC borane adducts
Chem. Sci., 2015, 6, 3461
1519427 CIFC22 H39 B Cl2 N2P 1 21/n 18.4091; 23.915; 13.429
90; 91.008; 90		2700.2Braunschweig, H.; Gackstatter, A.; Kupfer, T.; Scheller, T.; Hupp, F.; Damme, A.; Arnold, N.; Ewing, W. C.
Generation of 1,2-azaboretidines via reduction of ADC borane adducts
Chem. Sci., 2015, 6, 3461
1519428 CIFC13 H28 B Br2 N2P 1 21/n 17.1189; 15.9168; 15.0043
90; 91.677; 90		1699.4Braunschweig, H.; Gackstatter, A.; Kupfer, T.; Scheller, T.; Hupp, F.; Damme, A.; Arnold, N.; Ewing, W. C.
Generation of 1,2-azaboretidines via reduction of ADC borane adducts
Chem. Sci., 2015, 6, 3461
1519429 CIFC23 H41 B N2P -18.8938; 9.258; 15.064
73.468; 79.717; 77.485		1151.7Braunschweig, H.; Gackstatter, A.; Kupfer, T.; Scheller, T.; Hupp, F.; Damme, A.; Arnold, N.; Ewing, W. C.
Generation of 1,2-azaboretidines via reduction of ADC borane adducts
Chem. Sci., 2015, 6, 3461
1519430 CIFC20 H16 N2 O2C 1 2/c 117.37; 29.0684; 8.8805
90; 94.498; 90		4470.1He, Xiaoyan; Benniston, Andrew C.; Saarenpää, Hanna; Lemmetyinen, Helge; Tkachenko, Nikolia V.; Baisch, Ulrich
Polymorph crystal packing effects on charge transfer emission in the solid state
Chem. Sci., 2015, 6, 3525
1519431 CIFC20 H16 N2 O2P -19.4336; 9.5749; 9.9183
115.803; 97.324; 104.839		749.69He, Xiaoyan; Benniston, Andrew C.; Saarenpää, Hanna; Lemmetyinen, Helge; Tkachenko, Nikolia V.; Baisch, Ulrich
Polymorph crystal packing effects on charge transfer emission in the solid state
Chem. Sci., 2015, 6, 3525
1519432 CIFC394 H336 Cl20 N62 O76 Zn10P 1 2/n 121.4479; 30.381; 34.189
90; 97.46; 90		22089Riddell, Imogen A.; Ronson, Tanya K.; Nitschke, Jonathan R.
Mutual stabilisation between MII4L6tetrahedra and MIIX42−metallate guests
Chem. Sci., 2015, 6, 3533
1519433 CIFC156 H132 B6 Br4 Co5 F24 N24F 41 3 234.5284; 34.5284; 34.5284
90; 90; 90		41165.1Riddell, Imogen A.; Ronson, Tanya K.; Nitschke, Jonathan R.
Mutual stabilisation between MII4L6tetrahedra and MIIX42−metallate guests
Chem. Sci., 2015, 6, 3533
1519434 CIFC156 H132 Co4 F48 N24 P4.96 Sb3.04C 1 2/c 143.7451; 25.115; 39.7763
90; 100.245; 90		43003.8Riddell, Imogen A.; Ronson, Tanya K.; Nitschke, Jonathan R.
Mutual stabilisation between MII4L6tetrahedra and MIIX42−metallate guests
Chem. Sci., 2015, 6, 3533
1519435 CIFC390 H330 Br Cl19 N60 O76 Zn10P 1 2/n 121.4814; 30.514; 34.022
90; 97.399; 90		22115Riddell, Imogen A.; Ronson, Tanya K.; Nitschke, Jonathan R.
Mutual stabilisation between MII4L6tetrahedra and MIIX42−metallate guests
Chem. Sci., 2015, 6, 3533
1519436 CIFC8 H20 Br4 Cl4 N2 PbP -17.792; 8.315; 16.462
97.337; 96.252; 90.184		1051.4Solis-Ibarra, D.; Smith, I. C.; Karunadasa, H. I.
Post-synthetic halide conversion and selective halogen capture in hybrid perovskites
Chem. Sci., 2015, 6, 4054
1519437 CIFC8 H20 Br4 Cl4 N2 PbP 1 21/c 15.4158; 5.4438; 35.809
90; 93.3655; 90		1053.9Solis-Ibarra, D.; Smith, I. C.; Karunadasa, H. I.
Post-synthetic halide conversion and selective halogen capture in hybrid perovskites
Chem. Sci., 2015, 6, 4054
1519438 CIFC8 H20 Br8 N2 PbP -17.9735; 8.3877; 16.775
95.611; 95.889; 90.377		1110.5Solis-Ibarra, D.; Smith, I. C.; Karunadasa, H. I.
Post-synthetic halide conversion and selective halogen capture in hybrid perovskites
Chem. Sci., 2015, 6, 4054
1519439 CIFC17 H18 F3 N SP 1 21 19.1167; 7.9295; 11.3854
90; 105.727; 90		792.25Chen, Jiean; Meng, Sixuan; Wang, Leming; Tang, Hongmei; Huang, Yong
Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a non-covalent organocatalyst
Chem. Sci., 2015, 6, 4184
1519440 CIFC28 H27 Br O4P 21 21 218.7857; 16.2342; 17.0357
90; 90; 90		2429.8Verrier, Charlie; Melchiorre, Paolo
Diastereodivergent organocatalysis for the asymmetric synthesis of chiral annulated furans
Chem. Sci., 2015, 6, 4242
1519441 CIFC28 H28 O4C 1 2 122.183; 7.95; 15.744
90; 122.929; 90		2330.5Verrier, Charlie; Melchiorre, Paolo
Diastereodivergent organocatalysis for the asymmetric synthesis of chiral annulated furans
Chem. Sci., 2015, 6, 4242
1519442 CIFC68 H87 Cl5 Cu5 N16 O48 P2P 21 21 2116.4315; 18.87; 30.286
90; 90; 90		9390.5Marino, Nadia; Armentano, Donatella; Pardo, Emilio; Vallejo, Julia; Neve, Francesco; Di Donna, Leonardo; De Munno, Giovanni
Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion
Chem. Sci., 2015, 6, 4300
1519443 CIFC219 H238.34 Cu15 F45 N48 O117.67 P6 S15P 1 21 117.821; 49.945; 18.529
90; 108.269; 90		15661Marino, Nadia; Armentano, Donatella; Pardo, Emilio; Vallejo, Julia; Neve, Francesco; Di Donna, Leonardo; De Munno, Giovanni
Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion
Chem. Sci., 2015, 6, 4300
1519634 CIFC63.2 H72.55 I6 N13.06 Zn3C 1 2 135.1081; 14.6516; 31.3279
90; 101.649; 90		15782.8Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519635 CIFC60.26 H61.53 I6 N14 Zn3C 1 2 135.2721; 14.6427; 31.6037
90; 102.029; 90		15964.2Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519636 CIFC84.5 H64 I12.04 N24 S0.5 Zn6C 1 2 134.8299; 14.9133; 31.5387
90; 102.403; 90		15999.8Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519637 CIFC87.64 H68.04 I12 N24 S0.62 Zn6C 1 2 134.4391; 15.0959; 29.9556
90; 101.454; 90		15263.4Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519638 CIFC85.6 H63.3 I12 N24 O1.7 Zn6C 1 2 134.2; 15.1265; 31.003
90; 102.385; 90		15665Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519639 CIFC86.95 H64.82 I12 N24 O1.87 Zn6C 1 2 134.627; 15.0818; 31.194
90; 102.792; 90		15886Yoshioka, Shota; Inokuma, Yasuhide; Hoshino, Manabu; Sato, Takashi; Fujita, Makoto
Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method
Chem. Sci., 2015, 6, 3765
1519640 CIFC34 H50 N2 Na O4 PP 1 21/n 110.6728; 15.0865; 21.8147
90; 93.643; 90		3505.4Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519641 CIFC24 H44 N4 Na O5 PP 1 21/n 119.3693; 14.6742; 21.9183
90; 111.339; 90		5802.7Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519642 CIFC32 H54 N4 Na O6 PP 21 21 2110.4709; 17.4983; 18.6976
90; 90; 90		3425.83Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519643 CIFC38 H58 K N2 O8 PP 1 21/n 110.7457; 17.6496; 21.5074
90; 99.87; 90		4018.66Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519644 CIFC64 H92 K N4 O10 PP 1 21 113.233; 19.9093; 13.5733
90; 115.271; 90		3233.79Heift, Dominikus; Benkő, Zoltán; Grützmacher, Hansjörg; Jupp, Andrew R.; Goicoechea, Jose M.
Cyclo-oligomerization of isocyanates with Na(PH2) or Na(OCP) as “P−” anion sources
Chem. Sci., 2015, 6, 4017
1519645 CIFC43 H65 Dy N2 O6P -111.0343; 12.2286; 17.5339
77.103; 85.701; 69.694		2162.9Qian, Kang; Baldoví, José J.; Jiang, Shang-Da; Gaita-Ariño, Alejandro; Zhang, Yi-Quan; Overgaard, Jacob; Wang, Bing-Wu; Coronado, Eugenio; Gao, Song
Does the thermal evolution of molecular structures critically affect the magnetic anisotropy?
Chem. Sci., 2015, 6, 4587
1519646 CIFC43 H65 Dy N2 O6P -111.0141; 12.2286; 17.5325
77.161; 85.753; 69.723		2159.67Qian, Kang; Baldoví, José J.; Jiang, Shang-Da; Gaita-Ariño, Alejandro; Zhang, Yi-Quan; Overgaard, Jacob; Wang, Bing-Wu; Coronado, Eugenio; Gao, Song
Does the thermal evolution of molecular structures critically affect the magnetic anisotropy?
Chem. Sci., 2015, 6, 4587
1519647 CIFC43 H65 Dy N2 O6P -111.087; 12.2243; 18.3363
79.664; 85.44; 68.727		2277.9Qian, Kang; Baldoví, José J.; Jiang, Shang-Da; Gaita-Ariño, Alejandro; Zhang, Yi-Quan; Overgaard, Jacob; Wang, Bing-Wu; Coronado, Eugenio; Gao, Song
Does the thermal evolution of molecular structures critically affect the magnetic anisotropy?
Chem. Sci., 2015, 6, 4587
1519705 CIFC104 H154 I4 O P8 Pd4P 1 21/c 116.2343; 15.9423; 20.8753
90; 94.704; 90		5384.6Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519706 CIFC25 H36 Br P2 PdP 1 21/n 112.5686; 13.9781; 14.9939
90; 97.33; 90		2612.7Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519707 CIFC25 H37 Br P2 PdP 1 21/n 111.2438; 13.7677; 17.4246
90; 106.978; 90		2579.8Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519708 CIFC25 H36 Cl P2 PdP 1 21/n 111.6639; 13.5934; 16.568
90; 105.116; 90		2536Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519709 CIFC29 H47 P3 PdP 1 21/n 110.3086; 24.0617; 12.5709
90; 107.577; 90		2972.5Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519710 CIFC26 H40 Cl2 P2 PdC 1 2/c 113.0569; 16.808; 31.261
90; 93.209; 90		6849.8Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519711 CIFC26 H39 Cl P2 PdP 1 21/c 111.2685; 20.7303; 23.1605
90; 99.234; 90		5340.2Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519712 CIFC25 H37 I P2 PdC 1 2/c 129.176; 12.515; 22.247
90; 105.315; 90		7835Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519713 CIFC51 H78 Br4 Cl2 P4 Pd2P 1 21/n 110.3876; 16.2993; 17.0895
90; 103.477; 90		2813.8Comanescu, C. C.; Vyushkova, M.; Iluc, V. M.
Palladium carbene complexes as persistent radicals
Chem. Sci., 2015, 6, 4570
1519714 CIFC56 H33 D6 N O5P -112.741; 16.6787; 20.596
102.918; 90.565; 106.517		4077.3Hwang, Jungwun; Dial, Brent E.; Li, Ping; Kozik, Michael E.; Smith, Mark D.; Shimizu, Ken D.
How important are dispersion interactions to the strength of aromatic stacking interactions in solution?
Chem. Sci., 2015, 6, 4358
1519715 CIFC42 H29 N O4P 21 21 218.0214; 18.267; 21.084
90; 90; 90		3089.4Hwang, Jungwun; Dial, Brent E.; Li, Ping; Kozik, Michael E.; Smith, Mark D.; Shimizu, Ken D.
How important are dispersion interactions to the strength of aromatic stacking interactions in solution?
Chem. Sci., 2015, 6, 4358
1519716 CIFC54 H36 N O4P -19.7344; 12.477; 16.268
91.644; 99.097; 94.093		1944.4Hwang, Jungwun; Dial, Brent E.; Li, Ping; Kozik, Michael E.; Smith, Mark D.; Shimizu, Ken D.
How important are dispersion interactions to the strength of aromatic stacking interactions in solution?
Chem. Sci., 2015, 6, 4358
1519717 CIFC78 H76 B F24 P Ru S Si2P -113.1832; 16.891; 20.072
67.256; 76.552; 73.916		3920.8Stahl, Timo; Hrobárik, Peter; Königs, C. David F.; Ohki, Yasuhiro; Tatsumi, Kazuyuki; Kemper, Sebastian; Kaupp, Martin; Klare, Hendrik F. T.; Oestreich, Martin
Mechanism of the cooperative Si‒H bond activation at Ru‒S bonds
Chem. Sci., 2015, 6, 4324
1519718 CIFC66 H64 B F24 P Ru S SiP 1 21/n 113.56; 27.705; 18.609
90; 102.006; 90		6838Stahl, Timo; Hrobárik, Peter; Königs, C. David F.; Ohki, Yasuhiro; Tatsumi, Kazuyuki; Kemper, Sebastian; Kaupp, Martin; Klare, Hendrik F. T.; Oestreich, Martin
Mechanism of the cooperative Si‒H bond activation at Ru‒S bonds
Chem. Sci., 2015, 6, 4324
1519719 CIFC46 H38 B F24 O P SiP 1 21/c 116.929; 18.161; 16.113
90; 97.045; 90		4916.5Stahl, Timo; Hrobárik, Peter; Königs, C. David F.; Ohki, Yasuhiro; Tatsumi, Kazuyuki; Kemper, Sebastian; Kaupp, Martin; Klare, Hendrik F. T.; Oestreich, Martin
Mechanism of the cooperative Si‒H bond activation at Ru‒S bonds
Chem. Sci., 2015, 6, 4324
1519720 CIFC104 H154 I4 O P8 Pd4P 1 21/c 116.2343; 15.9423; 20.8753
90; 94.704; 90		5384.6Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519721 CIFC25 H36 Br P2 PdP 1 21/n 112.5686; 13.9781; 14.9939
90; 97.33; 90		2612.7Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519722 CIFC25 H37 Br P2 PdP 1 21/n 111.2438; 13.7677; 17.4246
90; 106.978; 90		2579.8Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519723 CIFC25 H36 Cl P2 PdP 1 21/n 111.6639; 13.5934; 16.568
90; 105.116; 90		2536Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519724 CIFC29 H47 P3 PdP 1 21/n 110.3086; 24.0617; 12.5709
90; 107.577; 90		2972.5Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519725 CIFC26 H40 Cl2 P2 PdC 1 2/c 113.0569; 16.808; 31.261
90; 93.209; 90		6849.8Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519726 CIFC26 H39 Cl P2 PdP 1 21/c 111.2685; 20.7303; 23.1605
90; 99.234; 90		5340.2Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519727 CIFC25 H37 I P2 PdC 1 2/c 129.176; 12.515; 22.247
90; 105.315; 90		7835Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519728 CIFC51 H78 Br4 Cl2 P4 Pd2P 1 21/n 110.3876; 16.2993; 17.0895
90; 103.477; 90		2813.8Yang, Sung Ho; Choi, Jinsu; Palanikumar, L.; Choi, Eun Seong; Lee, Juno; Kim, Juan; Choi, Insung S.; Ryu, Ja-Hyoung
Cytocompatible in situ cross-linking of degradable LbL films based on thiol‒exchange reaction
Chem. Sci., 2015, 6, 4698
1519764 CIFC15 H22 N2 O5P 21 21 2110.7542; 11.2346; 13.4066
90; 90; 90		1619.77Wang, Chao; Zhang, Li; Chen, Changpeng; Han, Jian; Yao, Yingming; Zhao, Yingsheng
Oxalyl amide assisted palladium-catalyzed synthesis of pyrrolidones via carbonylation of γ-C(sp3)‒H bonds of aliphatic amine substrates
Chem. Sci., 2015, 6, 4610
1519852 CIFC40 H46 N2P 1 21/c 110.701; 27.6694; 11.1215
90; 98.764; 90		3254.52Pandit, Palash; Yamamoto, Koji; Nakamura, Toshikazu; Nishimura, Katsuyuki; Kurashige, Yuki; Yanai, Takeshi; Nakamura, Go; Masaoka, Shigeyuki; Furukawa, Ko; Yakiyama, Yumi; Kawano, Masaki; Higashibayashi, Shuhei
Acid/base-regulated reversible electron transfer disproportionation of N‒N linked bicarbazole and biacridine derivatives
Chem. Sci., 2015, 6, 4160
1519853 CIFC46 H51 I6 N2P 1 21/c 115.047; 24.399; 13.754
90; 108.9; 90		4777.3Pandit, Palash; Yamamoto, Koji; Nakamura, Toshikazu; Nishimura, Katsuyuki; Kurashige, Yuki; Yanai, Takeshi; Nakamura, Go; Masaoka, Shigeyuki; Furukawa, Ko; Yakiyama, Yumi; Kawano, Masaki; Higashibayashi, Shuhei
Acid/base-regulated reversible electron transfer disproportionation of N‒N linked bicarbazole and biacridine derivatives
Chem. Sci., 2015, 6, 4160
1519854 CIFC46 H58 N2P 1 21/n 113.312; 18.813; 15.401
90; 97.762; 90		3821.7Pandit, Palash; Yamamoto, Koji; Nakamura, Toshikazu; Nishimura, Katsuyuki; Kurashige, Yuki; Yanai, Takeshi; Nakamura, Go; Masaoka, Shigeyuki; Furukawa, Ko; Yakiyama, Yumi; Kawano, Masaki; Higashibayashi, Shuhei
Acid/base-regulated reversible electron transfer disproportionation of N‒N linked bicarbazole and biacridine derivatives
Chem. Sci., 2015, 6, 4160
1519855 CIFC86 H108 N4C 1 2/c 130.6695; 12.1512; 23.0584
90; 119.572; 90		7473.9Pandit, Palash; Yamamoto, Koji; Nakamura, Toshikazu; Nishimura, Katsuyuki; Kurashige, Yuki; Yanai, Takeshi; Nakamura, Go; Masaoka, Shigeyuki; Furukawa, Ko; Yakiyama, Yumi; Kawano, Masaki; Higashibayashi, Shuhei
Acid/base-regulated reversible electron transfer disproportionation of N‒N linked bicarbazole and biacridine derivatives
Chem. Sci., 2015, 6, 4160
1519925 CIFC80 H56 Co7 F18 N16 O18 SiP a -324.5063; 24.5063; 24.5063
90; 90; 90		14717.5Chen, Kai-Jie; Perry IV, John J.; Scott, Hayley S.; Yang, Qing-Yuan; Zaworotko, Michael J.
Double-walled pyr topology networks from a novel fluoride-bridged heptanuclear metal cluster
Chem. Sci., 2015, 6, 4784
1519926 CIFC54 H62 Co N2 O4P -110.6748; 11.9906; 19.6875
101.316; 101.953; 103.763		2313.24Witt, Alexander; Heinemann, Frank W.; Khusniyarov, Marat M.
Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism
Chem. Sci., 2015, 6, 4599
1519927 CIFC54 H62 Co N2 O4P -110.7956; 12.0991; 19.834
102.162; 101.446; 104.036		2370.3Witt, Alexander; Heinemann, Frank W.; Khusniyarov, Marat M.
Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism
Chem. Sci., 2015, 6, 4599
1519928 CIFC54 H62 Co N2 O4P -19.8997; 10.812; 12.1278
104.002; 102.27; 101.408		1187.5Witt, Alexander; Heinemann, Frank W.; Khusniyarov, Marat M.
Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism
Chem. Sci., 2015, 6, 4599
1519929 CIFC82 H94 Co N2 O4P 1 21/n 116.5308; 11.7257; 18.9821
90; 107.445; 90		3510.2Witt, Alexander; Heinemann, Frank W.; Khusniyarov, Marat M.
Bidirectional photoswitching of magnetic properties at room temperature: ligand-driven light-induced valence tautomerism
Chem. Sci., 2015, 6, 4599
1519930 CIFC18 H26 Sn0.5P b c m10.9013; 12.0601; 25.222
90; 90; 90		3315.96Sindlinger, Christian P.; Stasch, Andreas; Bettinger, Holger F.; Wesemann, Lars
A nitrogen-base catalyzed generation of organotin(ii) hydride from an organotin trihydride under reductive dihydrogen elimination
Chem. Sci., 2015, 6, 4737
1519931 CIFC89 H134 N2 Sn2P -112.7122; 15.3521; 22.5773
84.881; 89.932; 82.556		4351.4Sindlinger, Christian P.; Stasch, Andreas; Bettinger, Holger F.; Wesemann, Lars
A nitrogen-base catalyzed generation of organotin(ii) hydride from an organotin trihydride under reductive dihydrogen elimination
Chem. Sci., 2015, 6, 4737
1519932 CIFC48.5 H70 SnP 1 21/c 115.9849; 15.9056; 17.7408
90; 100.754; 90		4431.37Sindlinger, Christian P.; Stasch, Andreas; Bettinger, Holger F.; Wesemann, Lars
A nitrogen-base catalyzed generation of organotin(ii) hydride from an organotin trihydride under reductive dihydrogen elimination
Chem. Sci., 2015, 6, 4737
1519944 CIFC35 H36 Cl2 F12 N2 O6C 1 2/c 129.3901; 13.5696; 21.1866
90; 105.652; 90		8136.1Vishe, Mahesh; Hrdina, Radim; Poblador-Bahamonde, Amalia I.; Besnard, Céline; Guénée, Laure; Bürgi, Thomas; Lacour, Jérôme
Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions
Chem. Sci., 2015, 6, 4923
1519945 CIFC33 H42 N4 O9P 1 21/n 110.4318; 18.5656; 17.6555
90; 90.817; 90		3419.04Vishe, Mahesh; Hrdina, Radim; Poblador-Bahamonde, Amalia I.; Besnard, Céline; Guénée, Laure; Bürgi, Thomas; Lacour, Jérôme
Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions
Chem. Sci., 2015, 6, 4923
1519946 CIFC32 H32 F12 N2 O9P 1 21/c 111.9175; 19.021; 17.226
90; 108.787; 90		3696.8Vishe, Mahesh; Hrdina, Radim; Poblador-Bahamonde, Amalia I.; Besnard, Céline; Guénée, Laure; Bürgi, Thomas; Lacour, Jérôme
Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions
Chem. Sci., 2015, 6, 4923
1519947 CIFC45 H38 Cl2 N4 O4P -19.5715; 18.5858; 23.8686
67.485; 81.597; 88.411		3878.5Vishe, Mahesh; Hrdina, Radim; Poblador-Bahamonde, Amalia I.; Besnard, Céline; Guénée, Laure; Bürgi, Thomas; Lacour, Jérôme
Remote stereoselective deconjugation of α,β-unsaturated esters by simple amidation reactions
Chem. Sci., 2015, 6, 4923
1520035 CIFC38 H34 Cl6 Cr Fe Mn N6 O14C 1 2/c 114.2177; 22.9278; 14.5428
90; 105.118; 90		4576.6Abhervé, Alexandre; Mañas-Valero, Samuel; Clemente-León, Miguel; Coronado, Eugenio
Graphene related magnetic materials: micromechanical exfoliation of 2D layered magnets based on bimetallic anilate complexes with inserted [FeIII(acac2-trien)]+and [FeIII(sal2-trien)]+molecules
Chem. Sci., 2015, 6, 4665
1520036 CIFC38 H34 Br6 Cr Fe Mn N6 O14C 1 2/c 114.1914; 23.0061; 14.788
90; 104.703; 90		4670Abhervé, Alexandre; Mañas-Valero, Samuel; Clemente-León, Miguel; Coronado, Eugenio
Graphene related magnetic materials: micromechanical exfoliation of 2D layered magnets based on bimetallic anilate complexes with inserted [FeIII(acac2-trien)]+and [FeIII(sal2-trien)]+molecules
Chem. Sci., 2015, 6, 4665
1520037 CIFC38 H34 Br6 Cr Ga Mn N6 O14C 1 2/c 114.1613; 23.0839; 14.8676
90; 104.296; 90		4709.7Abhervé, Alexandre; Mañas-Valero, Samuel; Clemente-León, Miguel; Coronado, Eugenio
Graphene related magnetic materials: micromechanical exfoliation of 2D layered magnets based on bimetallic anilate complexes with inserted [FeIII(acac2-trien)]+and [FeIII(sal2-trien)]+molecules
Chem. Sci., 2015, 6, 4665
1520038 CIFC26 H24 N2 O4P 1 21/c 19.7172; 11.762; 19.84
90; 99.84; 90		2234.2Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520039 CIFC26 H24 N2 O4P 1 21/n 19.591; 14.916; 15.744
90; 91.79; 90		2251.2Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520040 CIFC26 H22 Br2 N2 O4P -110.6774; 10.7451; 12.3472
107.453; 103.856; 103.585		1238.02Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520041 CIFC26 H22 Br2 N2 O4P -112.571; 13.241; 15.845
87.14; 76.74; 74.96		2479.1Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520042 CIFC26 H22 Br2 N2 O4P b c a11.755; 20.78; 21.031
90; 90; 90		5137Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520043 CIFC28 H22 Br2 N6 O2P 1 21/c 113.5422; 19.675; 10.2805
90; 100.796; 90		2690.7Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520044 CIFC28 H22 Br2 N6 O2P 1 21/c 114.5095; 20.268; 9.5541
90; 97.192; 90		2787.6Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520045 CIFC28 H22 Cl2 N6 O2P 1 21/c 115.6181; 15.7722; 10.6301
90; 95.137; 90		2608Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520046 CIFC28 H22 Cl2 N6 O2P 1 21/c 115.6347; 15.989; 10.646
90; 95.252; 90		2650.1Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520047 CIFC28 H22 Cl2 N6 O2P 1 21/c 114.4187; 19.4064; 9.7692
90; 95.552; 90		2720.7Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520048 CIFC28 H22 Cl2 N6 O2P 1 21/c 114.4; 19.51; 9.757
90; 95.784; 90		2727.2Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520049 CIFC28 H22 I2 N6 O2P -18.982; 12.5271; 26.146
84.5; 89.331; 74.563		2822.4Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520050 CIFC28 H22 I2 N6 O2P -19.048; 12.5933; 26.305
83.815; 89.271; 75.005		2878Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520051 CIFC11 H9 N3P 21 21 215.9077; 7.4479; 21.752
90; 90; 90		957.1Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520052 CIFC11 H9 N3P 21 21 215.911; 7.496; 21.82
90; 90; 90		967Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520069 CIFC17 H39 Cl2 Fe N P2P 21 21 2110.9222; 11.7618; 17.7375
90; 90; 90		2278.64Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520070 CIFC17 H44 B Fe N P2C 1 2/c 131.925; 7.968; 21.06
90; 121.335; 90		4575.8Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520071 CIFC18 H44 B Fe N O P2P 1 21/n 18.4128; 31.269; 9.8709
90; 114.779; 90		2357.6Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520072 CIFC18 H41 Fe N O P2P 1 21/n 18.0283; 12.8902; 21.842
90; 98.351; 90		2236.4Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520073 CIFC18 H41 Fe N O P2P 1 21/n 111.5836; 15.4917; 13.1032
90; 110.887; 90		2196.85Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520074 CIFC19 H41 Fe N O3 P2P 4111.736; 11.736; 16.678
90; 90; 90		2297.1Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520075 CIFC23 H49 Fe N O3 P2P 1 21/n 115.4197; 12.0975; 16.0962
90; 114.498; 90		2732.3Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520213 CIFC46 H40 N12 O2 Zn4P -110.283; 10.474; 20.857
95.09; 94.25; 96.25		2216.3Cheng, Gang; So, Gary Kwok-Ming; To, Wai-Pong; Chen, Yong; Kwok, Chi-Chung; Ma, Chensheng; Guan, Xiangguo; Chang, Xiaoyong; Kwok, Wai-Ming; Che, Chi-Ming
Luminescent zinc(ii) and copper(i) complexes for high-performance solution-processed monochromic and white organic light-emitting devices
Chem. Sci., 2015, 6, 4623
1520214 CIFC42 H48 B9 Cu N2 O P2P -110.828; 13.677; 14.95
90.64; 106.555; 95.534		2110.6Cheng, Gang; So, Gary Kwok-Ming; To, Wai-Pong; Chen, Yong; Kwok, Chi-Chung; Ma, Chensheng; Guan, Xiangguo; Chang, Xiaoyong; Kwok, Wai-Ming; Che, Chi-Ming
Luminescent zinc(ii) and copper(i) complexes for high-performance solution-processed monochromic and white organic light-emitting devices
Chem. Sci., 2015, 6, 4623
1520215 CIFC53 H52 B9 Cl2 Cu N2 P2P 1 21/c 115.5324; 15.5957; 20.6244
90; 98.789; 90		4937.4Cheng, Gang; So, Gary Kwok-Ming; To, Wai-Pong; Chen, Yong; Kwok, Chi-Chung; Ma, Chensheng; Guan, Xiangguo; Chang, Xiaoyong; Kwok, Wai-Ming; Che, Chi-Ming
Luminescent zinc(ii) and copper(i) complexes for high-performance solution-processed monochromic and white organic light-emitting devices
Chem. Sci., 2015, 6, 4623
1520226 CIFC5 H11 Cl N6P m n a6.4782; 9.5193; 14.311
90; 90; 90		882.5Xu, Jun; Yu, Hongde; Yang, Liulin; Wu, Guanglu; Wang, Zhiqiang; Wang, Dong; Zhang, Xi
Self-assembling 1D core/shell microrods by the introduction of additives: a one-pot and shell-tunable method
Chem. Sci., 2015, 6, 4907
1520227 CIFC58 H55 B F24 Fe N P3P 1 21/c 118.4232; 13.0618; 25.9802
90; 99.53; 90		6165.6Lindley, Brian M.; Swidan, Ala'aeddeen; Lobkovsky, Emil B.; Wolczanski, Peter T.; Adelhardt, Mario; Sutter, Jörg; Meyer, Karsten
Fe(iv) alkylidenes via protonation of Fe(ii) vinyl chelates and a comparative Mössbauer spectroscopic study
Chem. Sci., 2015, 6, 4730
1520228 CIFC61 H60 B F24 Fe N O P3C 1 2/m 119.963; 17.492; 19.586
90; 93.869; 90		6824Lindley, Brian M.; Swidan, Ala'aeddeen; Lobkovsky, Emil B.; Wolczanski, Peter T.; Adelhardt, Mario; Sutter, Jörg; Meyer, Karsten
Fe(iv) alkylidenes via protonation of Fe(ii) vinyl chelates and a comparative Mössbauer spectroscopic study
Chem. Sci., 2015, 6, 4730
1520229 CIFC58 H45 B F24 Fe N2 P2P 1 21/c 119.6517; 12.5655; 25.3645
90; 109.745; 90		5895.1Lindley, Brian M.; Swidan, Ala'aeddeen; Lobkovsky, Emil B.; Wolczanski, Peter T.; Adelhardt, Mario; Sutter, Jörg; Meyer, Karsten
Fe(iv) alkylidenes via protonation of Fe(ii) vinyl chelates and a comparative Mössbauer spectroscopic study
Chem. Sci., 2015, 6, 4730
1520230 CIFC26 H32 Fe N2 P2P -110.2138; 10.6014; 12.4208
88.674; 67.062; 89.687		1238.24Lindley, Brian M.; Swidan, Ala'aeddeen; Lobkovsky, Emil B.; Wolczanski, Peter T.; Adelhardt, Mario; Sutter, Jörg; Meyer, Karsten
Fe(iv) alkylidenes via protonation of Fe(ii) vinyl chelates and a comparative Mössbauer spectroscopic study
Chem. Sci., 2015, 6, 4730

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All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.