Crystallography Open Database

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1520452 CIFC24 H17 N4 OP 1 21/n 13.9114; 20.5945; 22.458
90; 91.758; 90		1808.2Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520453 CIFC28 H19 N4 OP 1 21 111.7763; 5.828; 16.1543
90; 104.773; 90		1072.06Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520454 CIFC32 H26 N4 OP 1 21/c 17.474; 9.2641; 35.865
90; 91.227; 90		2482.7Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520455 CIFC36 H28 N4 OP 1 21/c 111.2158; 10.0647; 24.8459
90; 97.414; 90		2781.25Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520456 CIFC21 H17 Br F3 N O2P 21 21 219.1964; 13.4028; 15.611
90; 90; 90		1924.2Zhang, Xiao; Liu, Wen-Bo; Tu, Hang-Fei; You, Shu-Li
Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles
Chem. Sci., 2015, 6, 4525
1520493 CIFC30 H26 Co F6 N6 O7 S2P -111.0341; 12.5779; 13.0044
82.865; 88.796; 66.687		1643.85Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520494 CIFC29 H35 F6 N7 O12 S2 ZnP 1 21/n 113.0156; 12.7488; 22.3963
90; 92.294; 90		3713.3Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520495 CIFC36 H42 Co F6 N6 O11 S2P 1 21/n 112.4657; 15.6171; 21.316
90; 91.047; 90		4149.1Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520496 CIFC30 H30 F6 N6 O11 S2 ZnP -114.707; 21.388; 25.657
67.683; 75.282; 89.683		7184Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520497 CIFC30 H32.5 F6 N6 O10 S2 ZnP -111.0677; 13.3087; 13.5558
71.591; 78.668; 67.235		1740.65Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520498 CIFC29 H27.5 Co F6 N7 O9.25 S2P -113.2461; 20.9848; 26.9609
111.361; 96.713; 94.455		6872.7Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520524 CIFC53 H69 N6 O25 P2 RuP n n a21.3561; 19.4016; 14.9635
90; 90; 90		6200.01Fielden, John; Sumliner, Jordan M.; Han, Nannan; Geletii, Yurii V.; Xiang, Xu; Musaev, Djamaladdin G.; Lian, Tianquan; Hill, Craig L.
Water splitting with polyoxometalate-treated photoanodes: enhancing performance through sensitizer design
Chem. Sci., 2015, 6, 5531
1520525 CIFC34 H20 Co2 N2 O8P -112.956; 13.122; 13.752
84.973; 67.595; 83.245		2144.1Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520526 CIFC17 H10 Co N O4P -17.7116; 10.2889; 11.0085
71.43; 86.282; 82.265		820.22Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520527 CIFC34 H20 Co2 N2 O8P -112.9698; 13.1304; 13.7579
85.041; 68.014; 83.544		2156.3Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520528 CIFC17 H10 Co N O4P -17.6397; 10.4311; 10.9968
71.121; 87.061; 83.361		823.5Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520529 CIFC51 H30 Co3 N3 O12C 1 2 117.173; 19.784; 13.887
90; 95.771; 90		4694Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520530 CIFC51 H30 Co3 N3 O12C 1 2 117.0391; 20.0278; 13.8334
90; 96.243; 90		4692.7Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520535 CIFC41 H46 N4 S2C 1 2/c 124.1082; 18.137; 16.7624
90; 106.002; 90		7045.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520536 CIFC65 H64 B2 N4 S2I 41/a :241.594; 41.594; 13.1413
90; 90; 90		22735.2Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520537 CIFC71 H56 B2 F20 N4 O2 S2P 1 21/c 114.5445; 22.7136; 19.7133
90; 98.039; 90		6448.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520538 CIFC42 H49 B N2 S3P -16.3487; 16.1168; 19.3671
74.649; 85.857; 83.373		1896.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520539 CIFC32 H45 B N2 S3P -16.524; 13.6675; 18.0034
98.64; 95.792; 101.67		1539.9Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520540 CIFC30 H39 B Br2 N2 S3P -110.2773; 12.1331; 14.8059
65.908; 79.793; 68.09		1563Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520543 CIFC25 H20 Au Br F3 PP 21 21 218.3781; 14.3827; 19.3153
90; 90; 90		2327.49Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520544 CIFC27 H22 Au2 Br Cl2 F6 PP 1 21/n 111.2208; 16.168; 17.031
90; 108.049; 90		2937.7Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520545 CIFC56 H40 Au6 Br2 F18 O2 P2C 1 2/m 111.61; 23.9064; 11.1568
90; 97.975; 90		3066.66Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520580 CIFC84 H118 Al3 N6 O6P 1 21/n 113.8521; 24.7127; 22.886
90; 93.263; 90		7821.7Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520581 CIFC27 H37 Al N2 O2P 1 21 19.9462; 10.3018; 12.8708
90; 108.547; 90		1250.3Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520582 CIFC29 H41 Al N2 O3P 21 21 218.0191; 13.4769; 25.379
90; 90; 90		2742.77Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520583 CIFC41 H65 Al N2 O3P 1 21/c 116.6845; 19.6643; 12.0401
90; 99.106; 90		3900.4Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520584 CIFC32 H48 Hf N2 O4P 1 21/c 114.0484; 13.4118; 16.8344
90; 101.404; 90		3109.22Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520585 CIFC32 H48 Hf N2 O4P 4310.3884; 10.3884; 28.732
90; 90; 90		3100.72Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520586 CIFC32 H48 Hf N2 O4P 4110.39461; 10.39461; 28.7569
90; 90; 90		3107.12Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520587 CIFC31 H45.67 Al N2 O3P a -326.2561; 26.2561; 26.2561
90; 90; 90		18100.5Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520588 CIFC32 H48 N2 O4 TiP 1 21/c 113.7916; 12.9946; 17.548
90; 102.79; 90		3066.86Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520589 CIFC45 H70 ThP 1 c 112.658; 10.48; 18.889
90; 127; 90		2001Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520590 CIFC48 H74 ThP 1 21/n 110.699; 26.148; 17.831
90; 98.273; 90		4936Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520591 CIFC49 H72 ThP -110.468; 11.297; 18.569
80.098; 82.085; 78.986		2110.8Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520592 CIFC53 H73 N ThP -111.109; 21.888; 21.958
97.052; 90.196; 90.925		5298Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520593 CIFC53 H73 N O ThP 1 21/c 115.278; 12.306; 25.718
90; 90.308; 90		4835.2Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520594 CIFC52 H77 N O ThP -110.9616; 11.0914; 20.157
77.206; 84.115; 75.93		2315.1Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520597 CIFC16 H12 Cl N OP 21 21 219.3918; 13.5329; 51.624
90; 90; 90		6561.3Pedroni, J.; Saget, T.; Donets, P. A.; Cramer, N.
Enantioselective palladium(0)-catalyzed intramolecular cyclopropane functionalization: access to dihydroquinolones, dihydroisoquinolones and the BMS-791325 ring system
Chem. Sci., 2015, 6, 5164
1520598 CIFC40 H62 N2 Si2P -19.4109; 10.1841; 11.6538
91.036; 102.694; 116.006		970.92Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520599 CIFC20 H31 N OP 1 21/n 19.269; 17.342; 11.775
90; 96.71; 90		1880Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520600 CIFC46 H70 N2 Si2P -112.8; 13.86; 14.36
66.45; 79.9; 67.84		2162Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520601 CIFC46 H70 N2 Si2P -112.79; 13.783; 14.433
66.35; 79.58; 67.48		2152Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520602 CIFC24 H39 N O Se2 SiP 1 21/n 114.6952; 10.08; 17.7472
90; 109.567; 90		2477.04Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520618 CIFC56 H100 F N O4P -415.6111; 15.6111; 10.505
90; 90; 90		2560.14Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520619 CIFC22 H50 Cl2 F N O4P 1 21/c 19.9446; 18.0891; 15.7361
90; 103.523; 90		2752.27Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520620 CIFC26 H60 F N O6P b c n9.9133; 17.3454; 18.3631
90; 90; 90		3157.54Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520621 CIFC26 H60 F N O4C 1 2/c 122.5166; 14.2863; 19.8783
90; 103.626; 90		6214.47Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520622 CIFC38.39 H77.58 F N O12P 21 21 218.978; 24.2645; 10.3218
90; 90; 90		4753.1Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520623 CIFC22 H44 F0.5 N0.5 O7C 1 2 125.1923; 9.6565; 10.6715
90; 92.2457; 90		2594.06Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520624 CIFC28 H64 F N O4P b c a18.6017; 18.6158; 19.1084
90; 90; 90		6616.96Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520625 CIFC56 H64 F N O4P 21 21 2110.6859; 12.6528; 34.797
90; 90; 90		4704.78Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520626 CIFC49 H80 F N O7P 1 c 18.7551; 12.7463; 22.1115
90; 92.0698; 90		2465.93Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520627 CIFC73 H78 F N O3P -114.5683; 19.9837; 20.7534
91.2454; 94.4191; 103.901		5842.46Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520628 CIFC55 H72 F N O3P -19.4953; 12.1501; 21.4618
81.8444; 89.1604; 78.5486		2401.96Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520629 CIFC54 H68 F N O2P 1 21/n 111.2887; 17.6025; 24.966
90; 98.4318; 90		4907.35Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520630 CIFC60 H80 F N O2P -113.4717; 17.5643; 24.8506
78.8655; 80.5422; 69.645		5379Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520631 CIFC76 H96 F N3 O5C 1 2/c 127.7157; 9.7374; 25.2072
90; 105.664; 90		6550.2Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520638 CIFC29 H24 Au Fe O2 P SP -19.187; 9.964; 15.554
108.411; 96.805; 95.38		1328.34Fernández-Gallardo, Jacob; Elie, Benelita T.; Sadhukha, Tanmoy; Prabha, Swayam; Sanaú, Mercedes; Rotenberg, Susan A.; Ramos, Joe W.; Contel, María
Heterometallic titanium‒gold complexes inhibit renal cancer cells in vitro and in vivo
Chem. Sci., 2015, 6, 5269
1520639 CIFC33 H29 Cl N2 O2 SP 1 21 110.1227; 25.116; 11.547
90; 97.553; 90		2910.3Wang, Yidong; Zhang, Peichao; Liu, Yuan; Xia, Fei; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2+2] versus [4+2]-cycloadditions of 3-styrylindoles with N-allenamides: observation of interesting substituent effects
Chem. Sci., 2015, 6, 5564
1520640 CIFC35 H32 N2 O4 SP 21 21 216.0633; 11.5428; 42.4729
90; 90; 90		2972.57Wang, Yidong; Zhang, Peichao; Liu, Yuan; Xia, Fei; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2+2] versus [4+2]-cycloadditions of 3-styrylindoles with N-allenamides: observation of interesting substituent effects
Chem. Sci., 2015, 6, 5564
1520661 CIFC20 H16 Br2 OP -17.1574; 11.25; 22.434
84.231; 84.177; 89.834		1787.9Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520662 CIFC25 H36 OP 1 21/c 114.4666; 10.0707; 16.4037
90; 109.508; 90		2252.65Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520663 CIFC28 H34 OC 1 2/c 123.302; 11.4445; 18.904
90; 104.415; 90		4882.6Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520664 CIFC20 H16 Br2 OP -16.0698; 11.4589; 13.8421
67.027; 85.348; 76.337		861.26Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520665 CIFC62 H138 Ge2 Si14C 1 2/c 138.0616; 9.3192; 48.0059
90; 92.3498; 90		17013.6Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520666 CIFC80 H162 Ge2 Si14P 1 21/a 112.7486; 20.8969; 18.9393
90; 103.248; 90		4911.28Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520667 CIFC64 H142 Ge2 Si14P b c a21.4391; 21.7284; 36.5231
90; 90; 90		17013.8Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520675 CIFC16 H14 N2 OP 1 21/n 113.4616; 4.959; 19.7696
90; 93.71; 90		1316.98Li, Shangda; Ji, Huafang; Cai, Lei; Li, Gang
Pd(ii)-catalyzed remote regiodivergent ortho- and meta-C‒H functionalizations of phenylethylamines
Chem. Sci., 2015, 6, 5595
1520676 CIFC20 H18 N2 O3C 1 2/c 133.97; 6.299; 16.431
90; 92.257; 90		3513Li, Shangda; Ji, Huafang; Cai, Lei; Li, Gang
Pd(ii)-catalyzed remote regiodivergent ortho- and meta-C‒H functionalizations of phenylethylamines
Chem. Sci., 2015, 6, 5595
1520695 CIFC41 H29 N2 OP 21 21 219.7022; 14.1065; 22.5755
90; 90; 90		3089.78Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520696 CIFC41 H32 N2 OP b c a9.7137; 21.2283; 30.357
90; 90; 90		6259.8Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520697 CIFC28 H19 F3 N2 OP -19.7447; 10.0599; 12.2374
103.037; 100.267; 97.73		1130.75Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520698 CIFC27 H21 N O SP 1 21/n 111.5129; 21.7914; 17.1772
90; 98.718; 90		4259.66Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520699 CIFC42 H34 N2 OP 1 21/n 17.8222; 19.2845; 21.7791
90; 100.329; 90		3232.1Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520700 CIFC21 H23 N2 O RhP 1 21/n 17.9626; 12.2907; 18.1403
90; 102.579; 90		1732.7Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520709 CIFC324.95 H223.55 Cu4 N97.65 Na11.5 O115.55 S16 Zn12P 1 n 121.91216; 32.64068; 35.0386
90; 98.2694; 90		24800Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520710 CIFC326.45 H230.05 Cu10 N98.15 O119.55 S16 Zn6.4P -124.6339; 26.2771; 38.566
71.189; 77.8; 87.75		23086Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520711 CIFC325.25 H227.25 Cu16 N97.75 O116.25 S16P -124.6594; 26.1086; 38.5294
71.7131; 78.2731; 87.7169		23054.1Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520712 CIFC80 H52 N24 O20 S4 Zn4I 41/a16.4641; 16.4641; 53.397
90; 90; 90		14474.1Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520713 CIFC25 H24 N4 O4P 1 21/c 120.3743; 5.7348; 19.2424
90; 102.342; 90		2196.4Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520714 CIFC28 H28 N2 O4 S4P 1 21/c 16.5498; 20.4037; 11.0725
90; 100.469; 90		1455.1Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520715 CIFC28 H28 N2 O4 S4I 1 2/a 115.181; 15.559; 23.696
90; 105.016; 90		5406Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520741 CIFC39 H69 Ga N2 Si3P -110.5026; 11.3327; 19.4036
85.025; 85.154; 71.124		2173.1Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520742 CIFC43 H80 Ga Li N2 Si4P 1 21/m 111.519; 20.858; 11.942
90; 117.73; 90		2539.7Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520743 CIFC47 H84 Ga Li N2 O2 Si3P 1 21/n 111.5267; 18.7832; 24.68
90; 90.988; 90		5342.6Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520744 CIFC43 H77 Ga N2 O Si3P -111.3181; 13.8704; 17.8645
69.483; 71.891; 67.251		2371.9Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520745 CIFC40 H71 Ga N2 Si3P 1 21/c 121.8907; 11.0318; 20.6366
90; 117.951; 90		4402.3Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520746 CIFC35 H58 N2 Si2 ZnC 1 2/c 110.6838; 19.4876; 18.4437
90; 102.692; 90		3746.18Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520747 CIFC42 H69 Al N2 Rh SiP 1 21/n 110.8994; 20.7161; 18.9857
90; 92.16; 90		4283.79Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520748 CIFC45 H73 N2 Rh Si ZnP -110.3195; 11.6531; 19.8109
77.86; 75.973; 73.269		2188Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520749 CIFC45 H73 Mg N2 Rh SiP -110.3775; 11.6602; 19.854
77.684; 75.691; 73.192		2202.2Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520750 CIFC72 H98 Al2 N4 Rh2C 1 2/c 117.4233; 16.5193; 23.4839
90; 104.958; 90		6530.1Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520954 CIFC48 H64 Cl In N2 O2P -111.7715; 12.7462; 15.4167
105.421; 96.436; 103.43		2131.3Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520955 CIFC73 H103.5 In2 N8.5 O6P 21 21 2115.0752; 22.4148; 23.2893
90; 90; 90		7869.6Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520956 CIFC34 H46 Cl In N4 O2C 1 2 136.78; 8.3688; 24.188
90; 115.26; 90		6733.3Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520957 CIFC42 H58 In N3 O3P 21 21 219.192; 16.465; 25.858
90; 90; 90		3913.5Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520958 CIFC64 H58 In N3 O3 Si2P 21 21 2112.019; 20.066; 23.278
90; 90; 90		5614Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520959 CIFC25 H40 O2P 1 21 114.07; 10.406; 14.8885
90; 103.249; 90		2121.84Challinor, Victoria L.; Johnston, Ryne C.; Bernhardt, Paul V.; Lehmann, Reginald P.; Krenske, Elizabeth H.; De Voss, James J.
Biosynthetic insights provided by unusual sesterterpenes from the medicinal herb Aletris farinosa
Chem. Sci., 2015, 6, 5740
1520960 CIFC34 H30 Br N2 O5 P PdP 1 21 19.566; 10.649; 17.115
90; 95.18; 90		1736.4Xie, Lan-Gui; Bagutski, Viktor; Audisio, Davide; Wolf, Larry M.; Schmidts, Volker; Hofmann, Kathrin; Wirtz, Cornelia; Thiel, Walter; Thiele, Christina M.; Maulide, Nuno
Dynamic behaviour of monohaptoallylpalladium species: internal coordination as a driving force in allylic alkylation chemistry
Chem. Sci., 2015, 6, 5734
1521277 CIFC20 H27 Br N4 OP 1 21 18.9698; 18.4284; 12.3981
90; 98.31; 90		2027.88Zaretsky, Serge; Hickey, Jennifer L.; Tan, Joanne; Pichugin, Dmitry; St. Denis, Megan A.; Ler, Spencer; Chung, Benjamin K. W.; Scully, Conor C. G.; Yudin, Andrei K.
Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway
Chem. Sci., 2015, 6, 5446
1521278 CIFC33 H53 N7 O7P 1 21 110.0804; 9.9982; 19.7575
90; 103.299; 90		1937.88Zaretsky, Serge; Hickey, Jennifer L.; Tan, Joanne; Pichugin, Dmitry; St. Denis, Megan A.; Ler, Spencer; Chung, Benjamin K. W.; Scully, Conor C. G.; Yudin, Andrei K.
Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway
Chem. Sci., 2015, 6, 5446
1521279 CIFC43 H72 Cl7 N P2 Pt RuP -19.6223; 14.2389; 18.6464
85.8029; 78.4958; 76.9593		2437.81Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521280 CIFC73 H96 Cl5 N P4 Pd RuP -111.5671; 13.5147; 24.091
76.202; 88.744; 72.724		3487.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521281 CIFC81 H144 Cl11 Ir O2 P4 Ru2C 1 2/c 113.811; 40.893; 16.343
90; 97.877; 90		9143Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521282 CIFC51 H92 Cl3 Ir P2 RuP -110.9458; 15.8362; 16.7533
111.788; 96.293; 99.958		2607.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521283 CIFC63 H88 As Cl7 O2 P2 Pt RuP -111.307; 13.305; 24.398
75.582; 88.059; 71.085		3358.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521284 CIFC46 H80 Cl5 P2 Rh RuP -110.935; 12.995; 18.693
78.174; 75.183; 75.241		2455.3Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521285 CIFC40 H74 Cl6 O P2 Pt Ru SP -110.432; 12.713; 19.025
77.214; 80.085; 82.926		2414.3Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521286 CIFC61 H83 Ag Cl8 F3 N3 O3 P2 Ru SP -113.297; 14.55; 18.906
111.639; 93.007; 92.517		3387.4Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521287 CIFC81.47 H144.4 Cl8.53 O3.16 P4 Rh2 Ru2C 1 2/c 132.65; 13.4; 23.89
90; 109.79; 90		9835Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521288 CIFC55 H79 Ag Cl8 F3 N3 O3 P2 Ru SP -114.248; 15.814; 16.607
70.503; 74.933; 68.534		3241.9Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521289 CIFC76 H134 Au B Cl10 F4 P4 Ru2P 1 2/c 119.988; 16.619; 27.233
90; 100.779; 90		8887Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521290 CIFC37 H66 Au Cl3 P2 RuP 1 21/c 113.392; 17.683; 20.172
90; 121.735; 90		4062.7Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1523944 CIFC32 H30 N2 O4 S4P -111.2966; 12.1022; 12.7036
85.244; 70.619; 77.661		1600.36Yadagiri, Dongari; Anbarasan, Pazhamalai
Tandem 1,2-sulfur migration and (aza)-Diels‒Alder reaction of β-thio-α-diazoimines: rhodium catalyzed synthesis of (fused)-polyhydropyridines, and cyclohexenes
Chem. Sci., 2015, 6, 5847
1529061 CIFC37 H22 B F9P -110.1241; 10.1353; 17.3058
84.1092; 73.833; 63.9157		1531.42Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529062 CIFC28 H18 B F9P -19.7736; 16.1049; 16.4046
76.766; 74.775; 75.51		2375.1Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529063 CIFC28 H20 B F9 OP 1 21/n 18.6666; 35.693; 15.69
90; 91.689; 90		4851.4Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529064 CIFC37 H56 N8 O9P 1 21 19.2715; 36.7577; 11.3129
90; 90.098; 90		3855.4Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529065 CIFC40 H68 N8 O13P 1 21 113.3658; 9.4864; 17.7634
90; 104.204; 90		2183.42Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529066 CIFC36 H52 N8 O9I 1 2 116.9971; 9.2681; 25.8496
90; 99.408; 90		4017.3Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529067 CIFC39 H64 N8 O12P 1 21 117.7309; 9.6245; 26.236
90; 107.755; 90		4263.9Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529068 CIFC39 H64 N8 O12P 1 21 19.769; 13.318; 17.543
90; 103.191; 90		2222.2Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529075 CIFC28.52 H21.52 F6 N0.48 O2 S2P 1 21/c 118.2529; 6.5741; 21.2658
90; 100.998; 90		2504.95Ohshima, Satoko; Morimoto, Masakazu; Irie, Masahiro
Light-driven bending of diarylethene mixed crystals
Chem. Sci., 2015, 6, 5746
1529076 CIFC27 H20 F6 N2 O2 S2P -115.141; 18.267; 19.761
72.453; 86.674; 77.582		5089Ohshima, Satoko; Morimoto, Masakazu; Irie, Masahiro
Light-driven bending of diarylethene mixed crystals
Chem. Sci., 2015, 6, 5746
1529077 CIFC113.3 H88.95 Cl2 Cu2 F24 N15.65 O14 S2P 32 2 129.93; 29.93; 28.878
90; 90; 120		22403Mortezaei, Shahab; Catarineu, Noelle R.; Duan, Xueyou; Hu, Chunhua; Canary, James W.
Redox-configurable ambidextrous catalysis: structural and mechanistic insight
Chem. Sci., 2015, 6, 5904
1529078 CIFC65.36 H70.72 N4 O2.68C 1 2/c 134.794; 5.836; 28.131
90; 97.862; 90		5659Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529079 CIFC66 H67 N4 O2C 1 2/c 134.89; 5.8074; 28.103
90; 98.31; 90		5634.4Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529080 CIFC68 H71 N4 O4.5C 1 2/c 134.814; 5.8498; 27.956
90; 98.517; 90		5630.6Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529081 CIFC63 H69 N4 O3C 1 2/c 134.994; 5.7712; 28.005
90; 97.696; 90		5604.9Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529082 CIFC63 H69 N7 O6C 1 2/c 134.875; 5.794; 28.028
90; 98.453; 90		5602Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529083 CIFC68 H68 N4 O2C 1 2/c 135.119; 5.8515; 28.129
90; 96.944; 90		5738Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529084 CIFC68 H70 N4P -15.8032; 17.6171; 28.095
82.852; 89.95; 81.848		2820.8Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529085 CIFC70 H76 N4C 1 2 134.833; 5.8219; 28.205
90; 98.49; 90		5657.1Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529086 CIFC74 H72 N4P -15.8111; 17.553; 28.328
82.08; 89.417; 83.086		2841.1Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529087 CIFC70 H74 N6C 1 2 135.689; 5.9481; 28.84
90; 97.562; 90		6069Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529088 CIFC133 H99 Cu5.5 N17 O31R -3 :H29.5994; 29.5994; 52.255
90; 90; 120		39648Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529089 CIFC168 H156 Cu3 F0 N12 O27 S0C 1 2/c 157.029; 34.131; 24.4704
90; 95.496; 90		47412Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529090 CIFC128 H126 Br4 Cu2 N6 O17 S4P 1 21/n 111.0753; 32.119; 47.079
90; 92.659; 90		16729Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529091 CIFC108 H102 Cu2 F12 N10 O36 S4P -114.4856; 18.0721; 30.4166
96.787; 93.193; 102.088		7704.9Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529092 CIFC47 H44.5 B Cu F4 N5.5 O11P b c a9.459; 29.785; 34.465
90; 90; 90		9710Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529093 CIFC149 H187 B4 Cu2 F16 N19 O34.5P 1 21/c 128.9123; 20.7706; 29.7284
90; 101.224; 90		17511.2Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529094 CIFC93 H105 Br3 Cu2 N6 O16.5 S4.5P -115.4223; 19.5085; 28.1607
100.656; 105.671; 102.75		7682Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529194 CIFC94 H120 N6 O2 Y2P 1 21/n 113.16; 16.367; 19.701
90; 103.837; 90		4120Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529195 CIFC98 H128 N6 O2 Y2P 1 21/n 113.324; 16.849; 19.59
90; 104.35; 90		4261Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529196 CIFC98 H128 N6 O4 Y2P 1 21/n 113.2137; 17.8164; 18.8346
90; 102.372; 90		4331.1Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529197 CIFC70 H100 N6 O2 Y2C 1 2/c 116.313; 20.362; 20.231
90; 92.019; 90		6716Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529198 CIFC94 H120 N6 O2 Y2P 1 21/n 115.639; 17.514; 16.24
90; 104.711; 90		4302Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529199 CIFC72 H104 N6 O4 Y2P 1 21/n 113.492; 13.673; 19.028
90; 101.334; 90		3442Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529200 CIFC47 H62 N3 O2 YP 1 21/n 112.902; 21.925; 16.088
90; 106.222; 90		4370Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529203 CIFC43.5 H73 N6 O P Si6 UP -111.5703; 11.7055; 21.152
86.747; 83.81; 75.03		2750.1Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529204 CIFC40 H69 N6 O P Si6 ThP -111.4301; 21.3302; 24.614
99.881; 90.073; 95.606		5882.8Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529205 CIFC40 H69 N7 O Si6 UC 1 2/c 115.5201; 17.9868; 37.3806
90; 97.783; 90		10338.9Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529206 CIFC43.5 H73 N7 O Si6 ThP -111.2966; 23.057; 23.27
66.405; 87.39; 77.614		5419.5Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529207 CIFC43.5 H73 N7 S Si6 UP -111.581; 11.6278; 21.115
86.775; 83.982; 75.259		2733.3Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529208 CIFC43.5 H73 N7 S Si6 ThP -111.6047; 11.6602; 21.204
86.479; 83.836; 75.464		2759.5Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529209 CIFC52.5 H91.5 N6 Ni O P Si6 ThP -114.8598; 19.6824; 24.2681
105.87; 101.321; 96.5472		6587.8Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529210 CIFC114 H143 Cl N14 O5P 1 21/n 110.9481; 39.559; 24.446
90; 92.404; 90		10578Galán, Albano; Valderrey, Virginia; Ballester, Pablo
Ordered co-encapsulation of chloride with polar neutral guests in a tetraurea calix[4]pyrrole dimeric capsule
Chem. Sci., 2015, 6, 6325
1529211 CIFC16 H11 N O2P 1 21/c 115.281; 3.8302; 24.754
90; 125.705; 90		1176.5Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles
Chem. Sci., 2015, 6, 5964
1529212 CIFC16 H12 O3P 1 21/n 16.0914; 8.5177; 23.947
90; 90.598; 90		1242.4Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles
Chem. Sci., 2015, 6, 5964
1529213 CIFC18 H16 O3P 1 21 17.946; 9.4371; 9.6309
90; 100.506; 90		710.09Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles
Chem. Sci., 2015, 6, 5964
1529214 CIFC92 H76 Dy N11 OP 1 21/c 117.5705; 22.6256; 24.6091
90; 100.073; 90		9632.4Cao, Wei; Gao, Chen; Zhang, Yi-Quan; Qi, Dongdong; Liu, Tao; Wang, Kang; Duan, Chunying; Gao, Song; Jiang, Jianzhuang
Rational enhancement of the energy barrier of bis(tetrapyrrole) dysprosium SMMs via replacing atom of porphyrin core
Chem. Sci., 2015, 6, 5947
1529215 CIFC189 H157 Cl15 Dy2 N22 S2C 1 2/c 131.8037; 17.264; 32.0054
90; 102.045; 90		17186Cao, Wei; Gao, Chen; Zhang, Yi-Quan; Qi, Dongdong; Liu, Tao; Wang, Kang; Duan, Chunying; Gao, Song; Jiang, Jianzhuang
Rational enhancement of the energy barrier of bis(tetrapyrrole) dysprosium SMMs via replacing atom of porphyrin core
Chem. Sci., 2015, 6, 5947
1529216 CIFC26 H21 Cl N2 O2P 21 21 219.5286; 10.2653; 21.7873
90; 90; 90		2131.1Li, Bao-Sheng; Wang, Yuhuang; Jin, Zhichao; Chi, Yonggui Robin
Cycloaddition of cyclobutenone and azomethine imine enabled by chiral isothiourea organic catalysts
Chem. Sci., 2015, 6, 6008
1529251 CIFC42 H3 B F32 N3 PP -110.7013; 11.2094; 17.8097
90.007; 104.509; 98.16		2045.87Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529252 CIFC60 H30 B F20 N3 P2P 1 21/n 112.8405; 18.5144; 22.501
90; 90.649; 90		5348.9Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529253 CIFC48 H54 B F20 N3 P2P -112.7734; 14.9217; 15.1042
107.504; 95.932; 111.054		2489Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529254 CIFC42 H50 B Cl0 F2 N7P -111.7044; 16.5009; 18.3335
86.77; 76.082; 83.169		3411Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529255 CIFC42 H15 B F20 N3 PP 1 21/n 112.226; 23.2442; 14.116
90; 107.089; 90		3834.42Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529258 CIFC19.5 H15 N4 O0.5P 1 21/c 111.4678; 19.447; 15.154
90; 112.202; 90		3129He, Liang; Li, Yi; Tan, Cai-Ping; Ye, Rui-Rong; Chen, Mu-He; Cao, Jian-Jun; Ji, Liang-Nian; Mao, Zong-Wan
Cyclometalated iridium(iii) complexes as lysosome-targeted photodynamic anticancer and real-time tracking agents
Chem. Sci., 2015, 6, 5409
1529259 CIFC44 H36 F10 Ir N6 O2 PP -18.5758; 14.436; 17.199
79.43; 89.672; 84.686		2084He, Liang; Li, Yi; Tan, Cai-Ping; Ye, Rui-Rong; Chen, Mu-He; Cao, Jian-Jun; Ji, Liang-Nian; Mao, Zong-Wan
Cyclometalated iridium(iii) complexes as lysosome-targeted photodynamic anticancer and real-time tracking agents
Chem. Sci., 2015, 6, 5409
1529260 CIFC17 H18 O3P -16.2616; 9.355; 11.752
87.526; 88.241; 86.453		686.17Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529261 CIFC20 H19 N OR -3 :H25.0795; 25.0795; 13.9752
90; 90; 120		7612.5Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529262 CIFC22 H23 N O2P 1 21/c 114.0542; 15.9871; 7.7187
90; 91.974; 90		1733.25Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529263 CIFC23 H25 N O2P b c a7.5352; 16.1007; 30.3669
90; 90; 90		3684.2Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529264 CIFC23 H23 N O3P 21 21 217.2261; 13.4245; 18.999
90; 90; 90		1843.03Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529265 CIFC21 H23 N OP -112.0196; 12.4522; 14.0202
94.894; 114.29; 113.544		1673.4Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529286 CIFC60 H64 O6 P2P -111.135; 11.644; 12.132
97.161; 111.866; 112.432		1282.5Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529287 CIFC50 H52 Cl12 O6 P2P 1 21/c 112.0579; 17.329; 27.445
90; 91.263; 90		5733.3Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529288 CIFC152 H96 O12 P4P 1 21/c 124.148; 23.858; 22.983
90; 117.759; 90		11717Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529289 CIFC152 H96 O12 P4C 1 2/m 134.54; 42.038; 17.4446
90; 100.248; 90		24925Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529290 CIFC156 H100 Cl12 O12 P4C 1 2/c 125.827; 22.684; 22.259
90; 99.466; 90		12863Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529291 CIFC164 H98 Cl6 O12 P4P 21 21 221.98; 17.101; 17.472
90; 90; 90		6567Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529292 CIFC166 H100 Cl12 O12 P4C 1 2/c 134.079; 13.764; 27.024
90; 103.463; 90		12328Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529299 CIFC43 H68 N6 O9P 1 21 18.3147; 19.2037; 14.1567
90; 102.128; 90		2210Cayuela, Angelina; Kennedy, Stuart R.; Soriano, M. Laura; Jones, Christopher D.; Valcárcel, Miguel; Steed, Jonathan W.
Fluorescent carbon dot‒molecular salt hydrogels
Chem. Sci., 2015, 6, 6139
1529300 CIFC13 H14 N3 O2P 1 21/c 18.5132; 21.0477; 7.2003
90; 113.595; 90		1182.31Weiss, Ryan J.; Gordts, Philip L. S. M.; Le, Dzung; Xu, Ding; Esko, Jeffrey D.; Tor, Yitzhak
Small molecule antagonists of cell-surface heparan sulfate and heparin‒protein interactions
Chem. Sci., 2015, 6, 5984
1529301 CIFC13 H18 N3 O3P -16.2877; 8.8655; 12.0399
102.993; 91.548; 92.63		652.79Weiss, Ryan J.; Gordts, Philip L. S. M.; Le, Dzung; Xu, Ding; Esko, Jeffrey D.; Tor, Yitzhak
Small molecule antagonists of cell-surface heparan sulfate and heparin‒protein interactions
Chem. Sci., 2015, 6, 5984
1529302 CIFC24 H29 Cl2 N6 O5P 1 21/m 15.0339; 37.994; 7.136
90; 110.533; 90		1278.1Weiss, Ryan J.; Gordts, Philip L. S. M.; Le, Dzung; Xu, Ding; Esko, Jeffrey D.; Tor, Yitzhak
Small molecule antagonists of cell-surface heparan sulfate and heparin‒protein interactions
Chem. Sci., 2015, 6, 5984
1529303 CIFC26 H26 F7.5 N6 Na0.5 O9C 1 2/m 114.0292; 22.3313; 9.5059
90; 92.95; 90		2974.2Weiss, Ryan J.; Gordts, Philip L. S. M.; Le, Dzung; Xu, Ding; Esko, Jeffrey D.; Tor, Yitzhak
Small molecule antagonists of cell-surface heparan sulfate and heparin‒protein interactions
Chem. Sci., 2015, 6, 5984
1529308 CIFC106 H120 Cl6 N8 PtP 1 21/c 120.8774; 15.8099; 30.488
90; 99.1261; 90		9935.8Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529309 CIFC111 H123 Cl9 N8 O4 Pt Zn2P -114.8426; 20.11; 21.2677
63.3696; 78.2695; 71.6398		5371.33Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529310 CIFC147.31 H169.64 Cl21.9 N8 Ni2 Pt2P -119.4832; 20.2466; 21.267
86.76; 81.4; 67.434		7659.8Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529311 CIFC164.8 H174 Cl12 N8 Ni2 O P2 PtC 1 2/c 164.086; 12.967; 40.547
90; 102.6; 90		32883Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529312 CIFC107 H113 Cl3 N10 Zn2C 1 2/c 131.53; 8.731; 36.552
90; 113.582; 90		9222Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529314 CIFC52 H66 Co2 F12 N8 O5P 1 21/n 110.072; 38.683; 14.706
90; 98.28; 90		5670Villanueva, Omar; Weldy, Nina Mace; Blakey, Simon B.; MacBeth, Cora E.
Cobalt catalyzed sp3C‒H amination utilizing aryl azides
Chem. Sci., 2015, 6, 6672
1529315 CIFC44 H52 Co2 K2 N6 O4F d d d10.8136; 27.533; 29.5266
90; 90; 90		8791Villanueva, Omar; Weldy, Nina Mace; Blakey, Simon B.; MacBeth, Cora E.
Cobalt catalyzed sp3C‒H amination utilizing aryl azides
Chem. Sci., 2015, 6, 6672
1529316 CIFC70 H79 Co2 N9 O4P 32 2 114.064; 14.064; 27.143
90; 90; 120		4649.5Villanueva, Omar; Weldy, Nina Mace; Blakey, Simon B.; MacBeth, Cora E.
Cobalt catalyzed sp3C‒H amination utilizing aryl azides
Chem. Sci., 2015, 6, 6672
1529321 CIFC56 H68 N4 O13F 4 3 236.2659; 36.2659; 36.2659
90; 90; 90		47697.5Barker, Emily C.; Goh, Ching Yong; Jones, Franca; Mocerino, Mauro; Skelton, Brian W.; Becker, Thomas; Ogden, Mark I.
Investigating hydrogel formation using in situ variable-temperature scanning probe microscopy
Chem. Sci., 2015, 6, 6133
1529322 CIFC24 H27 N O3P -111.3191; 11.464; 18.1291
93.847; 101.554; 114.578		2065.9Tan, Wei Wen; Yoshikai, Naohiko
Copper-catalyzed condensation of imines and α-diazo-β-dicarbonyl compounds: modular and regiocontrolled synthesis of multisubstituted pyrroles
Chem. Sci., 2015, 6, 6448
1529323 CIFC27 H23 N O3P 1 21/c 19.9721; 14.3477; 15.3171
90; 106.912; 90		2096.7Tan, Wei Wen; Yoshikai, Naohiko
Copper-catalyzed condensation of imines and α-diazo-β-dicarbonyl compounds: modular and regiocontrolled synthesis of multisubstituted pyrroles
Chem. Sci., 2015, 6, 6448
1529324 CIFC25 H19 Bi F9 N5 O9 S3P -19.3667; 13.6119; 13.6823
77.1774; 87.8299; 79.1523		1670.6Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529325 CIFC41 H51 F9 N5 O9 P S3P -111.6535; 14.5562; 14.588
88.2712; 80.7875; 88.0482		2440.47Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529326 CIFC44.67 H56.5 As F9 N6.83 O9 S3P -115.0217; 18.4434; 31.1243
93.909; 101.339; 99.3536		8297.5Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529327 CIFC41 H51 F9 N5 O9 S3 SbP 1 21/n 114.0078; 17.6534; 22.0396
90; 108.34; 90		5173.3Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529328 CIFC27 H34.5 F9 N7.5 O9 P S3P -113.2699; 15.788; 20.4958
76.0415; 87.922; 73.566		3994.6Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529329 CIFC28 H36 As F9 N8 O9 S3P -112.3457; 13.3802; 14.5721
81.4461; 66.6056; 72.0828		2101.1Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529330 CIFC27 H22 F9 N6 O9 P S3C 1 2/c 128.5371; 13.8414; 21.8775
90; 124.553; 90		7117.1Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529345 CIFC41 H59 B Ir N O2 P2P -114.2754; 16.7152; 18.3801
66.601; 89.641; 87.421		4020.7Lee, Chun-I; DeMott, Jessica C.; Pell, Christopher J.; Christopher, Alyson; Zhou, Jia; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Ligand survey results in identification of PNP pincer complexes of iridium as long-lived and chemoselective catalysts for dehydrogenative borylation of terminal alkynes
Chem. Sci., 2015, 6, 6572
1529346 CIFC38 H64 B2 Ir N O4 P2P 1 21/c 115.139; 11.8769; 23.409
90; 95.654; 90		4188.6Lee, Chun-I; DeMott, Jessica C.; Pell, Christopher J.; Christopher, Alyson; Zhou, Jia; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Ligand survey results in identification of PNP pincer complexes of iridium as long-lived and chemoselective catalysts for dehydrogenative borylation of terminal alkynes
Chem. Sci., 2015, 6, 6572
1529347 CIFC47 H61 B F4 Ir N O2 P2P 1 21/c 114.781; 26.065; 12.544
90; 107.16; 90		4618Lee, Chun-I; DeMott, Jessica C.; Pell, Christopher J.; Christopher, Alyson; Zhou, Jia; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Ligand survey results in identification of PNP pincer complexes of iridium as long-lived and chemoselective catalysts for dehydrogenative borylation of terminal alkynes
Chem. Sci., 2015, 6, 6572
1529348 CIFC32 H53 B Ir N O2 P2P 1 21/c 114.792; 17.546; 14.1242
90; 110.435; 90		3435.1Lee, Chun-I; DeMott, Jessica C.; Pell, Christopher J.; Christopher, Alyson; Zhou, Jia; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Ligand survey results in identification of PNP pincer complexes of iridium as long-lived and chemoselective catalysts for dehydrogenative borylation of terminal alkynes
Chem. Sci., 2015, 6, 6572
1529364 CIFC24 H41 F8 N2 Ni O3 PP 1 21/c 115.5474; 9.9548; 19.6379
90; 92.862; 90		3035.6Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529365 CIFC31 H38 F8 N2 NiP 21 21 2110.8851; 15.544; 18.9208
90; 90; 90		3201.4Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529366 CIFC35 H45 F10 N2 Ni O3 SP 1 21/c 110.2361; 16.5042; 22.6115
90; 90.96; 90		3819.4Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529367 CIFC33 H41 F7 N2 Ni O2P 1 21/c 19.7181; 18.216; 19.2228
90; 92.18; 90		3400.5Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529368 CIFC37 H46 F8 N2 Ni OP 1 21/c 116.5255; 10.6186; 20.8839
90; 101.931; 90		3585.5Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529378 CIFC87 H75 N4 O4P -111.962; 15.81; 19.746
97.277; 99.848; 100.275		3572Katoono, Ryo; Kawai, Shunsuke; Fujiwara, Kenshu; Suzuki, Takanori
Controllability of dynamic double helices: quantitative analysis of the inversion of a screw-sense preference upon complexation
Chem. Sci., 2015, 6, 6592
1529389 CIFC68 H60 Ce Li4 N12F d d d :211.4483; 43.06; 24.522
90; 90; 90		12088.5Levin, Jessica R.; Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Control of cerium oxidation state through metal complex secondary structures
Chem. Sci., 2015, 6, 6925
1529390 CIFC88 H80 Ce N16 Na4P -113.9504; 16.2467; 19.0053
83.136; 83.696; 84.993		4238.8Levin, Jessica R.; Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Control of cerium oxidation state through metal complex secondary structures
Chem. Sci., 2015, 6, 6925
1529391 CIFC83 H75 Ce K5 N15P -115.2003; 15.4668; 18.0353
93.849; 101.333; 107.292		3933.7Levin, Jessica R.; Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Control of cerium oxidation state through metal complex secondary structures
Chem. Sci., 2015, 6, 6925
1529403 CIFC57 H79 Br2 N4 Si2C 1 2/c 138.86; 15.6626; 22.7308
90; 125.774; 90		11224.8Arz, Marius I.; Geiß, Daniel; Straßmann, Martin; Schnakenburg, Gregor; Filippou, Alexander C.
Silicon(i) chemistry: the NHC-stabilised silicon(i) halides Si2X2(Idipp)2(X = Br, I) and the disilicon(i)-iodido cation [Si2(I)(Idipp)2]+
Chem. Sci., 2015, 6, 6515
1529404 CIFC57 H79 I2 N4 Si2C 1 2/c 138.872; 15.6801; 22.7851
90; 125.507; 90		11305.4Arz, Marius I.; Geiß, Daniel; Straßmann, Martin; Schnakenburg, Gregor; Filippou, Alexander C.
Silicon(i) chemistry: the NHC-stabilised silicon(i) halides Si2X2(Idipp)2(X = Br, I) and the disilicon(i)-iodido cation [Si2(I)(Idipp)2]+
Chem. Sci., 2015, 6, 6515
1529405 CIFC84 H77 B F21 I N4 Si2P 1 21/n 119.9019; 20.2022; 20.2072
90; 99.189; 90		8020.3Arz, Marius I.; Geiß, Daniel; Straßmann, Martin; Schnakenburg, Gregor; Filippou, Alexander C.
Silicon(i) chemistry: the NHC-stabilised silicon(i) halides Si2X2(Idipp)2(X = Br, I) and the disilicon(i)-iodido cation [Si2(I)(Idipp)2]+
Chem. Sci., 2015, 6, 6515
1529407 CIFC166 H146 B4 Cr2 N12P -115.3682; 15.9908; 17.5923
72.813; 69.832; 68.859		3712.1DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529408 CIFC134 H90 B2 F48 Mn2 N12P -115.0589; 15.8311; 18.4096
75.382; 67.031; 68.819		3736DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529409 CIFC140 H102 B2 F48 Fe2 N12 O1.5P -115.1719; 15.9218; 18.3985
75.334; 66.781; 68.243		3763.5DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529410 CIFC134 H76 B2 Co2 F48 N12P -114.8476; 15.9017; 18.21
75.56; 67.648; 68.82		3676.39DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529411 CIFC292 H264 B6 Cr4 N28P -115.17; 15.9112; 30.3415
90.924; 97.35; 115.288		6546.9DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529425 CIFC131 H158 N8 O15 P6 Pt3P 63/m23.8013; 23.8013; 13.6022
90; 90; 120		6673.3Loughrey, Jonathan J.; Patmore, Nathan J.; Baldansuren, Amgalanbaatar; Fielding, Alistair J.; McInnes, Eric J. L.; Hardie, Michaele J.; Sproules, Stephen; Halcrow, Malcolm A.
Platinum(ii) complexes of mixed-valent radicals derived from cyclotricatechylene, a macrocyclic tris-dioxolene
Chem. Sci., 2015, 6, 6935
1529426 CIFC104.7 H101.78 N1.3 O9.84 P6 Pt3P 1 21 114.86; 23.898; 15.103
90; 98.87; 90		5299.3Loughrey, Jonathan J.; Patmore, Nathan J.; Baldansuren, Amgalanbaatar; Fielding, Alistair J.; McInnes, Eric J. L.; Hardie, Michaele J.; Sproules, Stephen; Halcrow, Malcolm A.
Platinum(ii) complexes of mixed-valent radicals derived from cyclotricatechylene, a macrocyclic tris-dioxolene
Chem. Sci., 2015, 6, 6935
1529427 CIFC52.59 H37.19 Cl1.19 N6 O4F d d d23.5964; 37.347; 40.0789
90; 90; 90		35319.7Windle, Christopher D.; George, Michael W.; Perutz, Robin N.; Summers, Peter A.; Sun, Xue Zhong; Whitwood, Adrian C.
Comparison of rhenium‒porphyrin dyads for CO2photoreduction: photocatalytic studies and charge separation dynamics studied by time-resolved IR spectroscopy
Chem. Sci., 2015, 6, 6847
1529428 CIFC67.5 H49 Cl5 F6 N8 O4 P Re ZnP -112.9474; 15.8804; 17.3277
98.752; 92.264; 106.821		3357.4Windle, Christopher D.; George, Michael W.; Perutz, Robin N.; Summers, Peter A.; Sun, Xue Zhong; Whitwood, Adrian C.
Comparison of rhenium‒porphyrin dyads for CO2photoreduction: photocatalytic studies and charge separation dynamics studied by time-resolved IR spectroscopy
Chem. Sci., 2015, 6, 6847
1529471 CIFC56.5 H50 B2 F15 Mg N3 O3P -111.7916; 13.46; 18.239
86.434; 88.133; 69.802		2711.3Lampland, Nicole L.; Pindwal, Aradhana; Neal, Steven R.; Schlauderaff, Shealyn; Ellern, Arkady; Sadow, Aaron D.
Magnesium-catalyzed hydrosilylation of α,β-unsaturated esters
Chem. Sci., 2015, 6, 6901
1529474 CIFC15 H21 I OC 1 2 122.448; 6.0248; 11.443
90; 97.517; 90		1534.3Shen, Zhigao; Pan, Xixian; Lai, Yisheng; Hu, Jiadong; Wan, Xiaolong; Li, Xiaoge; Zhang, Hui; Xie, Weiqing
Chiral ion-pair organocatalyst promotes highly enantioselective 3-exo iodo-cycloetherification of allyl alcohols
Chem. Sci., 2015, 6, 6986
1529475 CIFC19 H19 I N4 O4P 1 21 110.31; 7.955; 11.875
90; 90.15; 90		973.9Shen, Zhigao; Pan, Xixian; Lai, Yisheng; Hu, Jiadong; Wan, Xiaolong; Li, Xiaoge; Zhang, Hui; Xie, Weiqing
Chiral ion-pair organocatalyst promotes highly enantioselective 3-exo iodo-cycloetherification of allyl alcohols
Chem. Sci., 2015, 6, 6986
1529476 CIFC22 H18 Br2 O4P 3 c 140.346; 40.346; 17.984
90; 90; 120		25352White, Nicholas G.; MacLachlan, Mark J.
Anion-templated hexagonal nanotubes
Chem. Sci., 2015, 6, 6245
1529477 CIFC54 H90 Br2 N2 O4P 3 c 140.346; 40.346; 17.984
90; 90; 120		25352White, Nicholas G.; MacLachlan, Mark J.
Anion-templated hexagonal nanotubes
Chem. Sci., 2015, 6, 6245
1529478 CIFC54 H88 Br2 N2 O6R 3 c :H39.973; 39.973; 18.0631
90; 90; 120		24995White, Nicholas G.; MacLachlan, Mark J.
Anion-templated hexagonal nanotubes
Chem. Sci., 2015, 6, 6245
1529479 CIFC54 H88 Br2 N2 O6R 3 c :H39.896; 39.896; 18.0796
90; 90; 120		24922White, Nicholas G.; MacLachlan, Mark J.
Anion-templated hexagonal nanotubes
Chem. Sci., 2015, 6, 6245
1529506 CIFC19 H16 O2C 1 2 114.321; 8.9769; 11.71
90; 91.66; 90		1504.78Lin, Che-Hung; Pursley, Dominik; Klein, Johannes E. M. N.; Teske, Johannes; Allen, Jennifer A.; Rami, Fabian; Köhn, Andreas; Plietker, Bernd
Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] ‒ the Fe-catalyzed Cloke‒Wilson rearrangement of vinyl and arylcyclopropanes
Chem. Sci., 2015, 6, 7034
1529507 CIFC19 H16 O2P 1 21 16.3155; 7.7433; 15.0935
90; 100.579; 90		725.57Lin, Che-Hung; Pursley, Dominik; Klein, Johannes E. M. N.; Teske, Johannes; Allen, Jennifer A.; Rami, Fabian; Köhn, Andreas; Plietker, Bernd
Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] ‒ the Fe-catalyzed Cloke‒Wilson rearrangement of vinyl and arylcyclopropanes
Chem. Sci., 2015, 6, 7034
1529508 CIFC19 H16 O2C 1 2 114.3185; 8.9738; 11.7148
90; 91.675; 90		1504.61Lin, Che-Hung; Pursley, Dominik; Klein, Johannes E. M. N.; Teske, Johannes; Allen, Jennifer A.; Rami, Fabian; Köhn, Andreas; Plietker, Bernd
Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] ‒ the Fe-catalyzed Cloke‒Wilson rearrangement of vinyl and arylcyclopropanes
Chem. Sci., 2015, 6, 7034
1529509 CIFC19 H16 O2P 1 21 16.309; 7.753; 15.117
90; 100.736; 90		726.5Lin, Che-Hung; Pursley, Dominik; Klein, Johannes E. M. N.; Teske, Johannes; Allen, Jennifer A.; Rami, Fabian; Köhn, Andreas; Plietker, Bernd
Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] ‒ the Fe-catalyzed Cloke‒Wilson rearrangement of vinyl and arylcyclopropanes
Chem. Sci., 2015, 6, 7034
1530394 CIFC273 H261 Cl14 N O4P 1 21/n 116.1937; 43.708; 33.799
90; 92.7924; 90		23894Golling, Florian E.; Osella, Silvio; Quernheim, Martin; Wagner, Manfred; Beljonne, David; Müllen, Klaus
π-extended [12]cycloparaphenylenes: from a hexaphenylbenzene cyclohexamer to its unexpected C2-symmetric congener
Chem. Sci., 2015, 6, 7072
1530395 CIFC46 H52 Br2P 1 21/c 112.9767; 10.3514; 15.6662
90; 105.739; 90		2025.5Golling, Florian E.; Osella, Silvio; Quernheim, Martin; Wagner, Manfred; Beljonne, David; Müllen, Klaus
π-extended [12]cycloparaphenylenes: from a hexaphenylbenzene cyclohexamer to its unexpected C2-symmetric congener
Chem. Sci., 2015, 6, 7072
1530396 CIFC14 H30 Cl4 N4 Ni O4P c a 2112.3629; 12.8888; 13.1011
90; 90; 90		2087.6Marriott, Katie E. R.; Bhaskaran, Lakshmi; Wilson, Claire; Medarde, Marisa; Ochsenbein, Stefan T.; Hill, Stephen; Murrie, Mark
Pushing the limits of magnetic anisotropy in trigonal bipyramidal Ni(ii)
Chem. Sci., 2015, 6, 6823
1530691 CIFC42 H52 Cl Co N4P 1 21/c 123.591; 10.436; 15.7392
90; 101.118; 90		3802.2Meng, Yin-Shan; Mo, Zhenbo; Wang, Bing-Wu; Zhang, Yi-Quan; Deng, Liang; Gao, Song
Observation of the single-ion magnet behavior of d8ions on two-coordinate Co(i)‒NHC complexes
Chem. Sci., 2015, 6, 7156
1530692 CIFC66 H72 B Co N4C 1 2/c 129.581; 11.9267; 32.317
90; 101.11; 90		11187.9Meng, Yin-Shan; Mo, Zhenbo; Wang, Bing-Wu; Zhang, Yi-Quan; Deng, Liang; Gao, Song
Observation of the single-ion magnet behavior of d8ions on two-coordinate Co(i)‒NHC complexes
Chem. Sci., 2015, 6, 7156
1530693 CIFC78 H76 B Co F24 N4P 42/n :214.0529; 14.0529; 18.2643
90; 90; 90		3606.9Meng, Yin-Shan; Mo, Zhenbo; Wang, Bing-Wu; Zhang, Yi-Quan; Deng, Liang; Gao, Song
Observation of the single-ion magnet behavior of d8ions on two-coordinate Co(i)‒NHC complexes
Chem. Sci., 2015, 6, 7156
1531037 CIFC180 H48 O32 Zr6F m -3 m45.887; 45.887; 45.887
90; 90; 90		96620Sawano, Takahiro; Ji, Pengfei; McIsaac, Alexandra R.; Lin, Zekai; Abney, Carter W.; Lin, Wenbin
The first chiral diene-based metal‒organic frameworks for highly enantioselective carbon‒carbon bond formation reactions
Chem. Sci., 2015, 6, 7163
1531038 CIFC107 H168 Fe2 N14 P2 Si6P -111.5288; 12.5203; 21.155
73.555; 75.604; 74.65		2774Metsänen, Toni T.; Gallego, Daniel; Szilvási, Tibor; Driess, Matthias; Oestreich, Martin
Peripheral mechanism of a carbonyl hydrosilylation catalysed by an SiNSi iron pincer complex
Chem. Sci., 2015, 6, 7143
1531040 CIFC16 H16 F N2 O5 VP 1 21/c 17.9908; 17.1771; 11.9692
90; 100.208; 90		1616.87Gazi, Sarifuddin; Hung Ng, Wilson Kwok; Ganguly, Rakesh; Putra Moeljadi, Adhitya Mangala; Hirao, Hajime; Soo, Han Sen
Selective photocatalytic C‒C bond cleavage under ambient conditions with earth abundant vanadium complexes
Chem. Sci., 2015, 6, 7130
1531041 CIFC30 H44 N2 O8 V2C 1 2/c 112.1706; 11.0345; 23.8844
90; 100.883; 90		3149.9Gazi, Sarifuddin; Hung Ng, Wilson Kwok; Ganguly, Rakesh; Putra Moeljadi, Adhitya Mangala; Hirao, Hajime; Soo, Han Sen
Selective photocatalytic C‒C bond cleavage under ambient conditions with earth abundant vanadium complexes
Chem. Sci., 2015, 6, 7130
1531042 CIFC15 H22 N O4 VP n a 2114.7897; 13.1867; 7.8841
90; 90; 90		1537.62Gazi, Sarifuddin; Hung Ng, Wilson Kwok; Ganguly, Rakesh; Putra Moeljadi, Adhitya Mangala; Hirao, Hajime; Soo, Han Sen
Selective photocatalytic C‒C bond cleavage under ambient conditions with earth abundant vanadium complexes
Chem. Sci., 2015, 6, 7130
1531044 CIFC30 H22 O4P 1 21 17.0717; 8.8439; 19.5443
90; 96.556; 90		1214.33Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531045 CIFC38.5 H29 Cl O4C 1 2 116.8074; 10.9989; 16.649
90; 92.018; 90		3075.9Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531046 CIFC27 H23 N O4P 1 21 18.1626; 12.2302; 11.0742
90; 101.402; 90		1083.72Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531316 CIFC24 H17 N OP 1 21/n 112.9997; 21.3361; 13.502
90; 106.398; 90		3592.6Poudel, Tej Narayan; Lee, Yong Rok
Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group
Chem. Sci., 2015, 6, 7028
1531937 CIFC98 H96 B F24 N2 O Pd TlP -112.7422; 26.6786; 28.5026
99.098; 90.144; 90.509		9566.9Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531938 CIFC108 H102 B F24 N2 Pd TlP -112.5519; 20.2591; 21.647
105.597; 102.325; 97.308		5079.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531939 CIFC152 H172 Ag4 F12 N4 O12 Pt2 S4P 1 21/n 111.7798; 29.62; 20.9358
90; 90.39; 90		7304.7Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531940 CIFC81 H92 Ag F3 N2 O3 Pt SP 1 21/n 118.6061; 19.7722; 20.9507
90; 106.515; 90		7389.5Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531941 CIFC71 H94 F3 N2 O5 Pt S TlP -113.95; 16.2777; 17.6213
66.887; 70.018; 71.465		3379.6Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531942 CIFC93 H134 Ag F3 N2 O10.5 Pd SP 21 21 2115.5936; 21.315; 24.141
90; 90; 90		8023.9Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531943 CIFC79 H106 Ag F3 N5 O4 Pt SP 21 21 2115.6478; 21.2503; 24.077
90; 90; 90		8006.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531944 CIFC84 H98 Ag F3 N2 O3 Pd SP -114.5289; 15.663; 17.673
96.662; 109.412; 94.019		3742.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531945 CIFC98 H96 B F24 N2 O Pt TlP -112.7326; 26.642; 28.428
99.2; 90.224; 90.514		9518.8Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531946 CIFC94 H86 B F24 N2 Pt TlP -114.6265; 20.6542; 31.1986
76.597; 79.378; 89.566		9005.2Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531947 CIFC3 H7 Cl3 I0 N O0 PbP 43 21 210.4482; 10.4482; 14.7573
90; 90; 90		1611Wang, Guan-E; Xu, Gang; Wang, Ming-Sheng; Cai, Li-Zhen; Li, Wen-Hua; Guo, Guo-Cong
Semiconductive 3-D haloplumbate framework hybrids with high color rendering index white-light emission
Chem. Sci., 2015, 6, 7222
1531948 CIFC80 H180 Cl59 N16 O2 Pb21P 1 21/c 121.2016; 15.9211; 26.4092
90; 91.811; 90		8910Wang, Guan-E; Xu, Gang; Wang, Ming-Sheng; Cai, Li-Zhen; Li, Wen-Hua; Guo, Guo-Cong
Semiconductive 3-D haloplumbate framework hybrids with high color rendering index white-light emission
Chem. Sci., 2015, 6, 7222
1532452 CIFC15 H34 I2 N4 Ni O4 S2P -110.141; 11.619; 11.643
86.263; 69.71; 76.551		1251.3Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532453 CIFC15 H29 Co N2 O6 S2P -17.5419; 8.0477; 16.687
78.174; 82.069; 86.421		981.2Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532454 CIFC15 H28 Fe N2 O6 S2P -17.486; 8.04; 16.74
78.165; 82.235; 86.603		976.6Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532455 CIFC30 H56 Cu2 N4 O12 S4C 1 2/c 119.683; 12.1661; 19.517
90; 106.346; 90		4484.7Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532456 CIFC11 H24 N2 O2 S2P 1 21/c 19.6252; 12.3461; 12.2335
90; 103.606; 90		1413Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532465 CIFC47.5 H62.5 F6 N1.5 O6.5 PP 1 2/c 115.9874; 18.0758; 18.1871
90; 107.85; 90		5002.8Jia, Fei; He, Zhenfeng; Yang, Liu-Pan; Pan, Zhi-Sheng; Yi, Min; Jiang, Ren-Wang; Jiang, Wei
Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities
Chem. Sci., 2015, 6, 6731
1532466 CIFC138 H129 F18 N3 O18 P3R -3 :H43.2165; 43.2165; 12.4664
90; 90; 120		20163.7Jia, Fei; He, Zhenfeng; Yang, Liu-Pan; Pan, Zhi-Sheng; Yi, Min; Jiang, Ren-Wang; Jiang, Wei
Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities
Chem. Sci., 2015, 6, 6731
1532468 CIFC82 H116 Cd2 N24 O25C 1 2/c 130.664; 17.225; 27.371
90; 105.9; 90		13904Sun, Chun-Yi; To, Wai-Pong; Wang, Xin-Long; Chan, Kaai-Tung; Su, Zhong-Min; Che, Chi-Ming
Metal‒organic framework composites with luminescent gold(iii) complexes. Strongly emissive and long-lived excited states in open air and photo-catalysis
Chem. Sci., 2015, 6, 7105
1532469 CIFC91.5 H111.5 Ge2 N2 Si2P -110.806; 18.897; 21.557
108.61; 90.43; 103.93		4032.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532470 CIFC104 H122 Ge2 N2 O2 Si2P 1 21/n 113.373; 21.643; 15.884
90; 102.62; 90		4486.3Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532471 CIFC46 H57 Ge N SiP -110.783; 11.465; 16.298
97.01; 91.76; 92.77		1996.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532472 CIFC52 H61 Ge N SiP 1 21/n 111.543; 23.7164; 16.3022
90; 97.979; 90		4419.7Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532473 CIFC49 H61 Ge N SiP 1 21/c 110.319; 18.286; 22.437
90; 91.27; 90		4232.7Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532474 CIFC50 H63 Ge N SiP 1 21 110.2741; 14.6818; 14.6417
90; 102.077; 90		2159.71Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532475 CIFC52 H67 Ge N SiP 1 21/n 19.942; 15.413; 28.793
90; 97.18; 90		4377.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532476 CIFC46 H57 N Si SnP -110.673; 12.534; 15.493
82.27; 85.09; 73.63		1968Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532477 CIFC52 H68 N Si SnP -110.2591; 13.6505; 17.3164
99.111; 105.293; 95.189		2287.3Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532478 CIFC53 H61 Ge N SiP 1 21/n 110.0813; 15.796; 28.096
90; 96.916; 90		4441.6Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532479 CIFC53 H61 N Si SnP 1 21/n 110.1088; 15.7379; 28.106
90; 96.853; 90		4439.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532480 CIFC52 H65 Ge N SiP 1 21/n 110.003; 15.4017; 28.92
90; 97.698; 90		4415.4Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532481 CIFC49 H63 Ge N SiP 1 21/n 111.374; 23.3065; 16.3439
90; 97.891; 90		4291.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532482 CIFC49 H62 Cl Ge N SiP -110.731; 14.446; 15.647
77.83; 78.54; 69.06		2194.2Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532483 CIFC48 H63 Ge N O SiP -110.399; 14.2109; 15.4524
90.483; 101.026; 105.118		2159.72Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532484 CIFC53 H70 N2 O Si SnP -114.604; 15.84; 20.773
88.61; 82.84; 84.99		4749.2Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532485 CIFC112 H154 Ge2 N2 O2 Si2P 1 21/n 115.0392; 12.4994; 26.2128
90; 93.127; 90		4920.17Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532486 CIFC112 H158 N2 O2 Si2 Sn2P -115.4827; 16.4448; 23.7823
72.311; 88.259; 62.908		5094.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532490 CIFC27 H30 B2 D3 N2 O2P -16.2435; 13.8921; 14.2338
100.533; 92.139; 100.164		1191.63Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532491 CIFC30 H34 B2 N2 O2P -112.0335; 13.357; 17.045
73.663; 81.968; 79.686		2575Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532492 CIFC31 H36 B2 N2 O2P 1 21/n 19.498; 9.09; 30.647
90; 94.119; 90		2639.1Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532493 CIFC30 H33 B2 Br N2 O2P 1 21/n 19.5066; 9.248; 30.632
90; 94.399; 90		2685.1Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532494 CIFC32 H39 B2 N2 O2P 1 21/n 18.8862; 21.985; 14.0495
90; 96.2349; 90		2728.5Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532495 CIFC33 H52 I P2 PdP b c a14.978; 16.438; 29.361
90; 90; 90		7229Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532496 CIFC65 H64 B F24 I P2 PdP 1 21/n 114.0602; 28.6171; 16.9031
90; 92.0331; 90		6796.9Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532497 CIFC33 H53 I P2 PdP 1 21/c 112.8203; 14.834; 19.174
90; 106.641; 90		3493.7Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532498 CIFC40 H60 I N P2 PdP 1 21/n 117.0891; 14.014; 18.4206
90; 100.081; 90		4343.4Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532499 CIFC39 H57 I O P2 PdP -111.8764; 14.433; 25.1741
101.297; 93.5784; 111.2		3903Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532500 CIFC68 H72 B F24 I P3 PdP 1 21 110.0901; 23.7955; 31.205
90; 90.532; 90		7492Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532501 CIFC44 H67 F3 O4 P2 Pd S2P 21 21 2114.0266; 15.2323; 21.3735
90; 90; 90		4566.6Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532502 CIFC50 H74 P2 Pd S2P 1 21/n 111.297; 11.59; 36.768
90; 92.926; 90		4808Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1533007 CIFC75 H88 Mo4 O8 P2 Sm2P -19.5023; 12.6103; 15.1418
97.784; 90.79; 100.069		1768.68Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533008 CIFC68 H80 Mo4 O8 P2 Yb2P -19.4563; 12.5189; 14.9787
84.903; 71.669; 76.285		1635Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533009 CIFC68 H86 Mo2 O4 P4 Sm2P -19.6185; 10.2667; 17.5096
83.519; 77.307; 78.461		1648.4Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533010 CIFC81 H105 Mo3 O6 P5 Sm3P 1 21/m 110.13; 25.686; 15.724
90; 96.36; 90		4066.2Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533011 CIFC78 H106 Mo2 O4 P6 Sm2P -111.1671; 12.7931; 14.7276
98.952; 110.227; 95.319		1925.7Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533012 CIFC78 H106 Mo2 O4 P6 Yb2P -111.1924; 12.6285; 14.6371
99.581; 110.455; 94.847		1888.44Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533373 CIFC28 H42 Au Cl3 N4 OI 41/a37.1846; 37.1846; 9.743
90; 90; 90		13471.6Ramsay, William J.; Foster, Jonathan A.; Moore, Katharine L.; Ronson, Tanya K.; Mirgalet, Raphaël J.; Jefferson, David A.; Nitschke, Jonathan R.
AuICl-bound N-heterocyclic carbene ligands form MII4(LAuCl)6integrally gilded cages
Chem. Sci., 2015, 6, 7326
1534135 CIFC40 H59 Cl2 N2 P RuP 1 21/n 112.2117; 18.0562; 18.2926
90; 103.741; 90		3918Lummiss, Justin A. M.; Higman, Carolyn S.; Fyson, Devon L.; McDonald, Robert; Fogg, Deryn E.
The divergent effects of strong NHC donation in catalysis
Chem. Sci., 2015, 6, 6739
1540648 CIFC81 H141 K2 La2 N4 O13 Si4P c c n20.3261; 54.668; 16.5827
90; 90; 90		18426.5Kotyk, Christopher M.; Fieser, Megan E.; Palumbo, Chad T.; Ziller, Joseph W.; Darago, Lucy E.; Long, Jeffrey R.; Furche, Filipp; Evans, William J.
Isolation of +2 rare earth metal ions with three anionic carbocyclic rings: bimetallic bis(cyclopentadienyl) reduced arene complexes of La2+and Ce2+are four electron reductants
Chem. Sci., 2015, 6, 7267
1553083 CIFC23 H21 B F10 N2P 1 21/c 119.6299; 19.4566; 12.265
90; 101.938; 90		4583.1Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553084 CIFC23 H18.711 B F10 N2P 1 21/n 111.5423; 12.863; 15.801
90; 93.409; 90		2341.8Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553085 CIFC29 H39 B N2P c c n16.756; 19.073; 15.93
90; 90; 90		5091Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553086 CIFC18 H25 B N2P 1 21 18.4021; 10.0498; 9.2882
90; 93.645; 90		782.7Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553087 CIFC13 H23 B N2P 1 21 19.2454; 7.0797; 9.5352
90; 100.812; 90		613.04Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553088 CIFC15 H27 B N2P 1 21/c 17.4085; 9.5348; 20.4481
90; 97.479; 90		1432.14Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553089 CIFC13 H21 B Cl2 N2P 1 21/n 18.8877; 14.4614; 10.8854
90; 91.815; 90		1398.38Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553090 CIFC37 H20 B2 Cl2 F20 N2P 1 c 110.6012; 10.7318; 16.8601
90; 105.327; 90		1849.9Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015
1553091 CIFC11 H24 B PP 1 21/c 111.0408; 6.6868; 16.9825
90; 97.038; 90		1244.3Farrell, Jeffrey M.; Posaratnanathan, Roy T.; Stephan, Douglas W.
A family of N-heterocyclic carbene-stabilized borenium ions for metal-free imine hydrogenation catalysis.
Chemical science, 2015, 6, 2010-2015

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