Crystallography Open Database

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1559979 CIFC30 H36 N2 O S2P -16.7333; 7.2344; 14.884
85.396; 80.658; 74.043		687.4Sinclair, Geoffrey S.; Claridge, Robert C. M.; Kukor, Andrew J.; Hopkins, W. Scott; Schipper, Derek J.
N-Oxide S‒O chalcogen bonding in conjugated materials
Chemical Science, 2021, 12, 2304-2312
1559980 CIFC18 H15 N O3P 1 21/c 15.974; 16.697; 14.741
90; 91.617; 90		1469.8Cheng, Yaohang; Yu, Shijie; He, Yuhang; An, Guanghui; Li, Guangming; Yang, Zhenyu
C4-arylation and domino C4-arylation/3,2-carbonyl migration of indoles by tuning Pd catalytic modes: Pd(i)‒Pd(ii) catalysis vs. Pd(ii) catalysis
Chemical Science, 2021, 12, 3216-3225
1559981 CIFC18 H15 N O3P -18.1516; 8.1871; 11.8093
96.901; 107.557; 92.751		743.01Cheng, Yaohang; Yu, Shijie; He, Yuhang; An, Guanghui; Li, Guangming; Yang, Zhenyu
C4-arylation and domino C4-arylation/3,2-carbonyl migration of indoles by tuning Pd catalytic modes: Pd(i)–Pd(ii) catalysis vs. Pd(ii) catalysis
Chemical Science, 2021, 12, 3216-3225
1559982 CIFC285 H325 Ag21 Au B2 Cl2 Fe3 O2 P6 S12P -121.3948; 27.211; 29.938
80.347; 70.094; 67.283		15103Zou, Xuejuan; He, Shuping; Kang, Xi; Chen, Shuang; Yu, Haizhu; Jin, Shan; Astruc, Didier; Zhu, Manzhou
New atomically precise M1Ag21 (M = Au/Ag) nanoclusters as excellent oxygen reduction reaction catalysts
Chemical Science, 2021, 12, 3660-3667
1559983 CIFC298 H333 Ag22 B2 Fe3 P6 S12P -121.412; 27.2727; 29.7612
79.123; 70.493; 66.956		15040.9Zou, Xuejuan; He, Shuping; Kang, Xi; Chen, Shuang; Yu, Haizhu; Jin, Shan; Astruc, Didier; Zhu, Manzhou
New atomically precise M1Ag21 (M = Au/Ag) nanoclusters as excellent oxygen reduction reaction catalysts
Chemical Science, 2021, 12, 3660-3667
1559984 CIFC84 H116 Fe2 K2 N4 Si4 Sm2C 1 2/c 114.315; 21.977; 26.509
90; 95.58; 90		8300Xiao, Yuyuan; Zhao, Xiao-Kun; Wu, Tianpin; Miller, Jeffrey T.; Hu, Han-Shi; Li, Jun; Huang, Wenliang; Diaconescu, Paula L.
Distinct electronic structures and bonding interactions in inverse-sandwich samarium and ytterbium biphenyl complexes.
Chemical science, 2020, 12, 227-238
1559985 CIFC34 H62 Fe N2 O3 Si2 YbP 21 21 2113.9723; 15.8539; 16.9858
90; 90; 90		3762.62Xiao, Yuyuan; Zhao, Xiao-Kun; Wu, Tianpin; Miller, Jeffrey T.; Hu, Han-Shi; Li, Jun; Huang, Wenliang; Diaconescu, Paula L.
Distinct electronic structures and bonding interactions in inverse-sandwich samarium and ytterbium biphenyl complexes.
Chemical science, 2020, 12, 227-238
1559986 CIFC52 H92 Fe2 N4 O2 Si4 Yb2P -111.5553; 12.3812; 12.4512
112.215; 96.684; 113.262		1439.25Xiao, Yuyuan; Zhao, Xiao-Kun; Wu, Tianpin; Miller, Jeffrey T.; Hu, Han-Shi; Li, Jun; Huang, Wenliang; Diaconescu, Paula L.
Distinct electronic structures and bonding interactions in inverse-sandwich samarium and ytterbium biphenyl complexes.
Chemical science, 2020, 12, 227-238
1559987 CIFC104 H182 Fe2 K2 N4 O18 Si4 Sm2P -115.0158; 15.8062; 28.2213
83.357; 79.591; 66.665		6041.8Xiao, Yuyuan; Zhao, Xiao-Kun; Wu, Tianpin; Miller, Jeffrey T.; Hu, Han-Shi; Li, Jun; Huang, Wenliang; Diaconescu, Paula L.
Distinct electronic structures and bonding interactions in inverse-sandwich samarium and ytterbium biphenyl complexes.
Chemical science, 2020, 12, 227-238
1559988 CIFC34 H62 Fe N2 O6 Si2 YbP -111.3145; 13.0374; 14.2432
87.291; 81.628; 71.282		1968.71Xiao, Yuyuan; Zhao, Xiao-Kun; Wu, Tianpin; Miller, Jeffrey T.; Hu, Han-Shi; Li, Jun; Huang, Wenliang; Diaconescu, Paula L.
Distinct electronic structures and bonding interactions in inverse-sandwich samarium and ytterbium biphenyl complexes.
Chemical science, 2020, 12, 227-238
1559989 CIFC64 H106 Fe2 K2 N4 O2 Si4 Yb2P 1 21/n 113.2467; 18.78; 14.5436
90; 100.579; 90		3556.6Xiao, Yuyuan; Zhao, Xiao-Kun; Wu, Tianpin; Miller, Jeffrey T.; Hu, Han-Shi; Li, Jun; Huang, Wenliang; Diaconescu, Paula L.
Distinct electronic structures and bonding interactions in inverse-sandwich samarium and ytterbium biphenyl complexes.
Chemical science, 2020, 12, 227-238
1559990 CIFC34 H62 Fe N2 O6 Si2 YbP 1 21 110.201; 33.0414; 12.1739
90; 105.418; 90		3955.6Xiao, Yuyuan; Zhao, Xiao-Kun; Wu, Tianpin; Miller, Jeffrey T.; Hu, Han-Shi; Li, Jun; Huang, Wenliang; Diaconescu, Paula L.
Distinct electronic structures and bonding interactions in inverse-sandwich samarium and ytterbium biphenyl complexes.
Chemical science, 2020, 12, 227-238
1559991 CIFC23 H35 Fe N O3 SP 1 21/c 126.9077; 7.4341; 11.4663
90; 100.496; 90		2255.3Bitter, Stefan; Schlötter, Moritz; Schilling, Markus; Krumova, Marina; Polarz, Sebastian; Winter, Rainer F.
Ferro-self-assembly: magnetic and electrochemical adaptation of a multiresponsive zwitterionic metalloamphiphile showing a shape-hysteresis effect.
Chemical science, 2020, 12, 270-281
1559992 CIFC29 H21 N3 O PtP 1 21/n 110.309; 13.9097; 15.4326
90; 101.658; 90		2167.31Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559993 CIFC29 H17 F4 N3 O PdP -111.8675; 12.4514; 17.2457
94.655; 96.279; 113.088		2308.6Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559994 CIFC29 H19 F2 N3 O PtP -19.3869; 11.7589; 11.9012
117.792; 105.826; 94.593		1084.42Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559995 CIFC29 H17 F4 N3 O PtP 1 2/c 122.8339; 9.8626; 22.7576
90; 117.704; 90		4537.52Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559996 CIFC29 H17 F4 N3 O PtP -19.6007; 11.7181; 12.0959
118.283; 95.325; 104.556		1123.48Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559997 CIFC23 H40 Cl O2 P PdP 1 21/n 19.7932; 13.0955; 19.8473
90; 93.9044; 90		2539.4Kim, Daeun; Choi, Geunho; Kim, Weonjeong; Kim, Dongwook; Kang, Youn K.; Hong, Soon Hyeok
The site-selectivity and mechanism of Pd-catalyzed C(sp<sup>2</sup>)-H arylation of simple arenes.
Chemical science, 2020, 12, 363-373
1559998 CIFC126 H53 N5 Ni S2 U2P 1 21/c 117.6663; 16.9578; 26.7308
90; 106.76; 90		7667.88Li, Xiaomeng; Roselló, Yannick; Yao, Yang-Rong; Zhuang, Jiaxin; Zhang, Xingxing; Rodríguez-Fortea, Antonio; de Graaf, Coen; Echegoyen, Luis; Poblet, Josep M.; Chen, Ning
U<sub>2</sub>N@<i>I</i> <sub>h</sub>(7)-C<sub>80</sub>: fullerene cage encapsulating an unsymmetrical U(iv)[double bond, length as m-dash]N[double bond, length as m-dash]U(v) cluster.
Chemical science, 2020, 12, 282-292
1559999 CIFC64.5 H59.5 Cl1.5 F6 P2 Pd2 Ru S3 SbP -111.9921; 12.28439; 21.733
94.518; 91.0356; 101.524		3125.45Kulichenko, Maksim; Fedik, Nikita; Monfredini, Anna; Muñoz-Castro, Alvaro; Balestri, Davide; Boldyrev, Alexander I.; Maestri, Giovanni
"Bottled" spiro-doubly aromatic trinuclear [Pd<sub>2</sub>Ru]<sup>+</sup> complexes.
Chemical science, 2020, 12, 477-486
1560000 CIFC28 H46 Li N2 O P3P 1 21/n 110.215; 30.038; 10.723
90; 116.107; 90		2954.5Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560001 CIFC58.28 H98.56 Br2 Cl6.56 Cu2 N6 P6 Ti2P 1 21/c 111.6149; 16.6838; 20.0416
90; 90.81; 90		3883.3Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560002 CIFC40 H38 Cl2 N2 O P3 TiP 1 21/n 110.1219; 16.662; 22.432
90; 99.27; 90		3733.8Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560003 CIFC45 H44 Cl N4 P3 TiP -112.209; 12.264; 15.876
97.041; 99.249; 98.343		2295.3Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560004 CIFC24 H38 Cl3 N2 P3 ZrP b c a16.455; 16.291; 22.0025
90; 90; 90		5898.2Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560005 CIFC29 H49 Au Cl4 N3 P3 TiP n m a14.2921; 13.7871; 18.9179
90; 90; 90		3727.7Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560006 CIFC147 H126 Cl18 N8 P12 Zr4P -111.8938; 12.0699; 27.548
82.319; 80.357; 70.217		3656.1Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560007 CIFC77 H70 B Cl2 N2 O2 P3 TiP -111.7665; 13.781; 20.643
82.299; 86.711; 80.965		3273.7Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560008 CIFC48 H76 Cu2 N4 P6C 1 2/c 131.2123; 11.3573; 16.6578
90; 111.69; 90		5486.9Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560009 CIFC28 H47 Cl N3 P3 TiP 1 21/n 119.7139; 17.7743; 20.2496
90; 112.411; 90		6559.6Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560010 CIFC24 H38 Cl2 N2 P3 TiP 1 21/n 111.1686; 15.39; 16.608
90; 99.796; 90		2813Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560011 CIFC45 H44 Cl N4 P3 TiP -112.209; 12.264; 15.876
97.041; 99.249; 98.343		2295.3Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560012 CIFC47 H47 Cl N3 P3 TiP 1 21/c 112.4622; 22.1019; 15.1862
90; 94.567; 90		4169.6Normand, Adrien T.; Sosa Carrizo, E. Daiann; Magnoux, Corentin; Lobato, Esteban; Cattey, Hélène; Richard, Philippe; Brandès, Stéphane; Devillers, Charles H.; Romieu, Anthony; Le Gendre, Pierre; Fleurat-Lessard, Paul
Reappraising Schmidpeter's bis(iminophosphoranyl)phosphides: coordination to transition metals and bonding analysis.
Chemical science, 2020, 12, 253-269
1560015 CIFC18 H24 O2P -18.3649; 10.0504; 10.2831
73.682; 70.348; 86.635		780.74Kleinmans, Roman; Will, Leon E.; Schwarz, J. Luca; Glorius, Frank
Photoredox-enabled 1,2-dialkylation of α-substituted acrylates via Ireland‒Claisen rearrangement
Chemical Science, 2021, 12, 2816-2822
1560016 CIFC12 H21 N O2 SP -16.3005; 10.5228; 10.9791
65.837; 82.374; 88.124		658.07Kleinmans, Roman; Will, Leon E.; Schwarz, J. Luca; Glorius, Frank
Photoredox-enabled 1,2-dialkylation of α-substituted acrylates via Ireland‒Claisen rearrangement
Chemical Science, 2021, 12, 2816-2822
1560017 CIFC22 H26 O2P 1 21/n 110.5885; 8.3629; 20.6387
90; 99.927; 90		1800.21Kleinmans, Roman; Will, Leon E.; Schwarz, J. Luca; Glorius, Frank
Photoredox-enabled 1,2-dialkylation of α-substituted acrylates via Ireland‒Claisen rearrangement
Chemical Science, 2021, 12, 2816-2822
1560018 CIFC35 H35 N2 O PP -18.9009; 10.4501; 17.0815
104.343; 91.133; 112.507		1410.37Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560019 CIFC33 H30 N O PP -18.2229; 12.4346; 13.1943
108.632; 96.25; 93.485		1264.24Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560020 CIFC32 H22 F3 O4 P SP 1 21/c 17.4114; 15.707; 22.5898
90; 92.536; 90		2627.1Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560021 CIFC33 H25 F3 N O3 P SP n a 218.0035; 27.389; 12.6664
90; 90; 90		2776.6Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560022 CIFC34 H29 F3 N O3 P SP 1 21/c 18.9602; 11.4072; 28.9126
90; 93.074; 90		2950.9Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560023 CIFC33 H25 F3 N O3 P SP 1 21/c 116.162; 12.9217; 14.4246
90; 107.362; 90		2875.2Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560024 CIFC36 H34 F3 N2 O3 P SP 1 21/c 111.0775; 19.2817; 15.3042
90; 104; 90		3171.8Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560025 CIFC33 H29 Au B Cl F4 N PP 1 21 18.2171; 20.0635; 9.9302
90; 111.472; 90		1523.51Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560026 CIFC36 H33 Au B2 F8 N P SP 1 21/c 116.5012; 15.8634; 13.7254
90; 92.673; 90		3588.9Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560027 CIFC37 H37 Au B2 F8 N P SP 1 21 18.2911; 15.0763; 14.2431
90; 97.96; 90		1763.2Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560028 CIFC39 H42 Au B2 F8 N2 P SP 1 21/n 110.2268; 8.5127; 45.347
90; 94.336; 90		3936.5Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560029 CIFC35 H34 Au B Cl F4 N2 PP 1 21/c 120.6017; 8.5026; 20.569
90; 118.012; 90		3180.9Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560030 CIFC36 H32 Au B2 Cl2 F8 O P SP -18.0106; 12.2124; 19.0728
99.359; 93.578; 101.894		1792.6Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560031 CIFC52 H96 O Si8 U2P 21 21 2110.5444; 18.4631; 31.5083
90; 90; 90		6134.1Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560032 CIFC26 H50 O Si4 UP 1 21/n 117.5935; 9.977; 18.6747
90; 110.001; 90		3080.27Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560033 CIFC58.34 H113.47 O Si9 U2P -420.3708; 20.3708; 16.6734
90; 90; 90		6918.95Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560034 CIFC84 H168 Si12 U2P 1 21/c 126.7057; 15.99077; 26.5612
90; 117.35; 90		10074.9Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560035 CIFC24 H44 Si4 UI 41/a :231.8409; 31.8409; 11.0234
90; 90; 90		11176Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560036 CIFC28 H52 O Si4 UP 21 21 2111.40224; 16.98119; 17.03377
90; 90; 90		3298.14Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560037 CIFC34 H48 N4 P2P -17.5552; 9.5169; 11.8279
76.651; 84.11; 72.543		788.85Lücke, Marcel-Philip; Yao, Shenglai; Driess, Matthias
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst
Chemical Science, 2021, 12, 2909-2915
1560038 CIFC48 H58 N4 Si2C 1 2/c 125.072; 9.1667; 19.7603
90; 99.889; 90		4474Lücke, Marcel-Philip; Yao, Shenglai; Driess, Matthias
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst
Chemical Science, 2021, 12, 2909-2915
1560039 CIFC34 H48 N4 Ni P2P -110.1955; 10.3773; 16.0898
76.412; 80.446; 88.451		1631.6Lücke, Marcel-Philip; Yao, Shenglai; Driess, Matthias
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst
Chemical Science, 2021, 12, 2909-2915
1560040 CIFC55 H66 N4 Ni Si2P 1 21/m 19.1662; 26.4418; 9.8935
90; 90.567; 90		2397.8Lücke, Marcel-Philip; Yao, Shenglai; Driess, Matthias
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst
Chemical Science, 2021, 12, 2909-2915
1560078 CIFC19 H13 N OP 21 21 2117.214; 14.4042; 5.5668
90; 90; 90		1380.3Li, Hui; Li, Huanhuan; Gu, Jie; He, Fei; Peng, Hao; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Ping; Zheng, Chao; Huang, Wei; Chen, Runfeng
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime
Chemical Science, 2021, 12, 3580-3586
1560079 CIFC19 H12 F N OP b c a11.8585; 10.3783; 22.8559
90; 90; 90		2812.9Li, Hui; Li, Huanhuan; Gu, Jie; He, Fei; Peng, Hao; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Ping; Zheng, Chao; Huang, Wei; Chen, Runfeng
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime
Chemical Science, 2021, 12, 3580-3586
1560080 CIFC19 H12 F N OP 1 21/n 114.608; 5.4287; 18.371
90; 107.996; 90		1385.6Li, Hui; Li, Huanhuan; Gu, Jie; He, Fei; Peng, Hao; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Ping; Zheng, Chao; Huang, Wei; Chen, Runfeng
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime
Chemical Science, 2021, 12, 3580-3586
1560081 CIFC19 H12 F N OP 1 21/c 18.9406; 22.597; 7.0302
90; 91.313; 90		1419.9Li, Hui; Li, Huanhuan; Gu, Jie; He, Fei; Peng, Hao; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Ping; Zheng, Chao; Huang, Wei; Chen, Runfeng
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime
Chemical Science, 2021, 12, 3580-3586
1560082 CIFC56 H63 N5 O4P 1 21/c 114.7734; 17.4936; 18.6427
90; 90.2338; 90		4817.98Villarón, David; Siegler, Maxime A.; Wezenberg, Sander J.
A photoswitchable strapped calix[4]pyrrole receptor: highly effective chloride binding and release
Chemical Science, 2021, 12, 3188-3193
1560083 CIFC108 H98 Mn4 Mo9 N3 O43 P5P -116.1432; 18.3888; 24.571
94.772; 109.004; 106.661		6480.2Li, Chifeng; Jimbo, Atsuhiro; Yamaguchi, Kazuya; Suzuki, Kosuke
A protecting group strategy to access stable lacunary polyoxomolybdates for introducing multinuclear metal clusters
Chemical Science, 2021, 12, 1240-1244
1560084 CIFC174 H174 Cl20 Mn6 Mo18 O74 P8P -117.3006; 19.39; 20.7716
95.31; 112.975; 99.33		6236.6Li, Chifeng; Jimbo, Atsuhiro; Yamaguchi, Kazuya; Suzuki, Kosuke
A protecting group strategy to access stable lacunary polyoxomolybdates for introducing multinuclear metal clusters
Chemical Science, 2021, 12, 1240-1244
1560085 CIFC22 H33 IrP 1 21/n 18.01647; 16.3246; 15.049
90; 92.985; 90		1966.73Tian, Yancong; Jakoobi, Martin; Boulatov, Roman; Sergeev, Alexey G.
Selective cleavage of unactivated arene ring C‒C bonds by iridium: key roles of benzylic C‒H activation and metal‒metal cooperativity
Chemical Science, 2021, 12, 3568-3579
1560086 CIFC20 H23 IrC 1 c 122.2884; 22.2818; 26.1267
90; 97.5244; 90		12863.5Tian, Yancong; Jakoobi, Martin; Boulatov, Roman; Sergeev, Alexey G.
Selective cleavage of unactivated arene ring C–C bonds by iridium: key roles of benzylic C–H activation and metal–metal cooperativity
Chemical Science, 2021, 12, 3568-3579
1560094 CIFC51 H48 O6 SP 21 21 218.0941; 17.5936; 32.602
90; 90; 90		4642.7Bartelmann, Thomas; Gnannt, Frederik; Zitzmann, Max; Mayer, Peter; Dube, Henry
Sulfoxide hemithioindigo tweezers ‒ visible light addressable capture and release
Chemical Science, 2021, 12, 3651-3659
1560095 CIFC36 H53 B N6 O3 P2 Pd WP 1 21/c 116.8853; 15.2569; 15.7122
90; 91.701; 90		4046Osipova, Elena S.; Gulyaeva, Ekaterina S.; Gutsul, Evgenii I.; Kirkina, Vladislava A.; Pavlov, Alexander A.; Nelyubina, Yulia V.; Rossin, Andrea; Peruzzini, Maurizio; Epstein, Lina M.; Belkova, Natalia V.; Filippov, Oleg A.; Shubina, Elena S.
Bifunctional activation of amine-boranes by the W/Pd bimetallic analogs of “frustrated Lewis pairs”
Chemical Science, 2021, 12, 3682-3692
1560096 CIFC32 H48 O3 P2 Pd WP 1 21/c 18.2012; 37.372; 10.9355
90; 103.388; 90		3260.59Osipova, Elena S.; Gulyaeva, Ekaterina S.; Gutsul, Evgenii I.; Kirkina, Vladislava A.; Pavlov, Alexander A.; Nelyubina, Yulia V.; Rossin, Andrea; Peruzzini, Maurizio; Epstein, Lina M.; Belkova, Natalia V.; Filippov, Oleg A.; Shubina, Elena S.
Bifunctional activation of amine-boranes by the W/Pd bimetallic analogs of “frustrated Lewis pairs”
Chemical Science, 2021, 12, 3682-3692
1560097 CIFC21 H30 B F2 N O5P 1 21/c 114.1856; 17.0247; 9.5406
90; 94.364; 90		2297.4Wang, Yandong; Bai, Jingyi; Yang, Youqing; Zhao, Wenxuan; Liang, Yong; Wang, Di; Zhao, Yue; Shi, Zhuangzhi
Rhodium-catalysed selective C‒C bond activation and borylation of cyclopropanes
Chemical Science, 2021, 12, 3599-3607
1560098 CIFC22 H34 Cl2 N2 O6 Rh2P 1 21/n 19.2163; 11.7129; 13.3216
90; 108.006; 90		1367.63Wang, Yandong; Bai, Jingyi; Yang, Youqing; Zhao, Wenxuan; Liang, Yong; Wang, Di; Zhao, Yue; Shi, Zhuangzhi
Rhodium-catalysed selective C‒C bond activation and borylation of cyclopropanes
Chemical Science, 2021, 12, 3599-3607
1560099 CIFC14 H19 N OP 21 21 219.9241; 11.0168; 24.6334
90; 90; 90		2693.21Wang, Yandong; Bai, Jingyi; Yang, Youqing; Zhao, Wenxuan; Liang, Yong; Wang, Di; Zhao, Yue; Shi, Zhuangzhi
Rhodium-catalysed selective C‒C bond activation and borylation of cyclopropanes
Chemical Science, 2021, 12, 3599-3607
1560100 CIFC23 H16 OP 1 21/n 19.3347; 10.0778; 16.957
90; 101.582; 90		1562.7Uraguchi, Daisuke; Kato, Kohsuke; Ooi, Takashi
o-Quinone methide with overcrowded olefin component as a dehydridation catalyst under aerobic photoirradiation conditions
Chemical Science, 2021, 12, 2778-2783
1560101 CIFC26 H20 OP 1 21/c 110.294; 16.632; 11.319
90; 112.274; 90		1793.3Uraguchi, Daisuke; Kato, Kohsuke; Ooi, Takashi
o-Quinone methide with overcrowded olefin component as a dehydridation catalyst under aerobic photoirradiation conditions
Chemical Science, 2021, 12, 2778-2783
1560102 CIFC26 H21 B F4 OP 1 21/n 17.4982; 19.0172; 14.6488
90; 99.675; 90		2059.13Uraguchi, Daisuke; Kato, Kohsuke; Ooi, Takashi
o-Quinone methide with overcrowded olefin component as a dehydridation catalyst under aerobic photoirradiation conditions
Chemical Science, 2021, 12, 2778-2783
1560103 CIFC4 H2.67 Bi0.67 N4.67 Ni0.67 S4P -18.441; 8.6899; 11.8177
97.574; 92.137; 91.817		858.1Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560104 CIFC4 H2.67 Bi0.67 N4.67 Ni0.67 S4P -18.4472; 8.7119; 11.9671
97.041; 90.364; 91.558		873.67Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560105 CIFC2 H6 N4 SP -16.9352; 7.0096; 12.3675
90.894; 104.311; 101.787		568.89Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560106 CIFC7 Bi N7 Ni S6P 1 2/n 112.216; 36.8375; 24.5263
90; 90.224; 90		11036.9Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560107 CIFC6 H4 Bi N7 Ni S6P -18.4699; 8.6913; 11.9058
97.187; 91.149; 91.61		868.96Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560108 CIFC6 Bi K N6 Ni S6P -18.5073; 8.5686; 11.9651
97.573; 89.781; 90.997		864.46Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560109 CIFC0.92 Bi0.15 N1.25 Ni0.17 S0.86P n -3 :212.12528; 12.12528; 12.12528
90; 90; 90		1782.69Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560111 CIFC74 H86 Li4 O2 P2 Si4P -111.4716; 12.6646; 12.7092
85.944; 86.346; 68.446		1711.6Brand, Alexander; Schulz, Stephen; Hepp, Alexander; Weigand, Jan J.; Uhl, Werner
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P‒C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
Chemical Science, 2021, 12, 3460-3474
1560112 CIFC37 H32 O5 P2 Si2 WP 1 21/c 110.6448; 12.9069; 26.22
90; 92.664; 90		3598.5Brand, Alexander; Schulz, Stephen; Hepp, Alexander; Weigand, Jan J.; Uhl, Werner
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P‒C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
Chemical Science, 2021, 12, 3460-3474
1560113 CIFC32 H32 P2 Si2P 1 21/c 112.2157; 10.4934; 22.6538
90; 99.262; 90		2866Brand, Alexander; Schulz, Stephen; Hepp, Alexander; Weigand, Jan J.; Uhl, Werner
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P‒C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
Chemical Science, 2021, 12, 3460-3474
1560114 CIFC53 H60 Cl2 O4 P2 Si4P 1 21/n 110.1186; 18.8541; 27.477
90; 91.367; 90		5240.5Brand, Alexander; Schulz, Stephen; Hepp, Alexander; Weigand, Jan J.; Uhl, Werner
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P‒C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
Chemical Science, 2021, 12, 3460-3474
1560116 CIFC12 H32 Cl5 N4 Ti2P n a 2119.796; 8.413; 13.102
90; 90; 90		2182.1Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560117 CIFC14 H36 Cl10 N4 Ti2P 1 21/c 113.348; 13.855; 17.166
90; 112.468; 90		2933.6Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560118 CIFC10 H24 Cl3 N2 O TiP 1 21/n 110.972; 12.308; 12.075
90; 101.587; 90		1597.4Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560119 CIFC13 H34 Cl4 N4 Ti2C 1 2/c 123.348; 8.843; 12.648
90; 121.198; 90		2233.7Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560120 CIFC6 H16 Cl I N2 ZnC 1 2/c 123.149; 7.256; 15.032
90; 111.169; 90		2354.5Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560121 CIFC13 H34 I2 N4 Zn2P 21 21 2111.494; 13.09; 14.921
90; 90; 90		2245Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560122 CIFC24 H28 N2 O6P 1 21 118.5604; 7.5949; 8.0212
90; 96.383; 90		1123.69Arhangelskis, Mihails; Bučar, Dejan-Krešimir; Bordignon, Simone; Chierotti, Michele R.; Stratford, Samuel A.; Voinovich, Dario; Jones, William; Hasa, Dritan
Mechanochemical reactivity inhibited, prohibited and reversed by liquid additives: examples from crystal-form screens
Chemical Science, 2021, 12, 3264-3269
1560123 CIFC24 H28 N2 O6C 1 2 117.9007; 6.3022; 20.9554
90; 105.356; 90		2279.66Arhangelskis, Mihails; Bučar, Dejan-Krešimir; Bordignon, Simone; Chierotti, Michele R.; Stratford, Samuel A.; Voinovich, Dario; Jones, William; Hasa, Dritan
Mechanochemical reactivity inhibited, prohibited and reversed by liquid additives: examples from crystal-form screens
Chemical Science, 2021, 12, 3264-3269
1560124 CIFC24.63 H29.26 N2 O6.32C 1 2 117.8855; 6.3218; 21.0313
90; 105.346; 90		2293.19Arhangelskis, Mihails; Bučar, Dejan-Krešimir; Bordignon, Simone; Chierotti, Michele R.; Stratford, Samuel A.; Voinovich, Dario; Jones, William; Hasa, Dritan
Mechanochemical reactivity inhibited, prohibited and reversed by liquid additives: examples from crystal-form screens
Chemical Science, 2021, 12, 3264-3269
1560125 CIFC24 H20 O4P 21 21 218.9924; 19.5139; 23.2425
90; 90; 90		4078.52Yang, Chi; Wu, Tian-Rui; Li, Yan; Wu, Bing-Bing; Jin, Ruo-Xing; Hu, Duo-Duo; Li, Yuan-Bo; Bian, Kang-Jie; Wang, Xi-Sheng
Facile synthesis of axially chiral styrene-type carboxylic acids via palladium-catalyzed asymmetric C‒H activation
Chemical Science, 2021, 12, 3726-3732
1560126 CIFC25 H18 O2P 18.6935; 11.1218; 12.2142
87.376; 70.785; 81.619		1103.26Yang, Chi; Wu, Tian-Rui; Li, Yan; Wu, Bing-Bing; Jin, Ruo-Xing; Hu, Duo-Duo; Li, Yuan-Bo; Bian, Kang-Jie; Wang, Xi-Sheng
Facile synthesis of axially chiral styrene-type carboxylic acids via palladium-catalyzed asymmetric C‒H activation
Chemical Science, 2021, 12, 3726-3732
1560133 CIFC19 H16 Br NP 1 21 110.077; 5.678; 13.478
90; 96.922; 90		765.6Jiang, Feng; Fu, Chunling; Ma, Shengming
Asymmetric construction of pyrido[1,2-<i>a</i>]-1<i>H</i>-indole derivatives <i>via</i> a gold-catalyzed cycloisomerization.
Chemical science, 2020, 12, 696-701
1560134 CIFC17 H20 Cl N OP 1 21 110.4093; 6.0139; 12.2223
90; 100.849; 90		751.45Jiang, Feng; Fu, Chunling; Ma, Shengming
Asymmetric construction of pyrido[1,2-<i>a</i>]-1<i>H</i>-indole derivatives <i>via</i> a gold-catalyzed cycloisomerization.
Chemical science, 2020, 12, 696-701
1560135 CIFC167 H154 Cl3 F4 N34 O30P 1 21/n 122.99; 45.82; 40.8
90; 90.92; 90		42973Mateus, Pedro; Jacquet, Antoine; Méndez-Ardoy, Alejandro; Boulloy, Alice; Kauffmann, Brice; Pecastaings, Gilles; Buffeteau, Thierry; Ferrand, Yann; Bassani, Dario M.; Huc, Ivan
Sensing a binding event through charge transport variations using an aromatic oligoamide capsule
Chemical Science, 2021, 12, 3743-3750
1560136 CIFC25 H23 N3 O5P 1 21/c 111.2876; 21.068; 9.751
90; 106.139; 90		2227.5Park, Hyunchang; Lee, Dongwhan
Biomimetic hydrogen-bonding cascade for chemical activation: telling a nucleophile from a base.
Chemical science, 2020, 12, 590-598
1560137 CIFC17 H14 Br Cl3 N2 O4P 1 21/c 125.8801; 6.9453; 23.8077
90; 116.121; 90		3842.25Park, Hyunchang; Lee, Dongwhan
Biomimetic hydrogen-bonding cascade for chemical activation: telling a nucleophile from a base.
Chemical science, 2020, 12, 590-598
1560138 CIFC16 H14 N2 O4I 1 2/a 117.4514; 4.6477; 35.608
90; 102.334; 90		2821.46Park, Hyunchang; Lee, Dongwhan
Biomimetic hydrogen-bonding cascade for chemical activation: telling a nucleophile from a base.
Chemical science, 2020, 12, 590-598
1560139 CIFC27 H43 N O3P 1 21/c 18.2116; 14.8475; 20.2921
90; 96.28; 90		2459.2Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560140 CIFC116 H190.67 K4 N4 O12I -4 3 d32.4579; 32.4579; 32.4579
90; 90; 90		34194.9Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560141 CIFC58 H94 Li2 N2 O7C 1 2/c 116.8366; 13.6239; 24.398
90; 91.454; 90		5594.6Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560142 CIFC144 H224 N6 Na12 O12P 1 21/n 116.206; 29.7416; 30.0188
90; 102.473; 90		14127.3Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560143 CIFC108 H172 N4 Na4 O12I -4 3 d32.0084; 32.0084; 32.0084
90; 90; 90		32793.8Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560144 CIFC115 H175 K10 N5 O10P 1 21/c 125.5103; 27.8549; 16.3237
90; 90.336; 90		11599.2Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560145 CIFC77 H121 Li6 N3 O8P 1 21 114.2409; 14.1749; 20.804
90; 104.449; 90		4066.7Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560146 CIFC138 H210 Li12 N6 O12P -115.9758; 16.9105; 29.646
84.635; 79.342; 87.435		7833.4Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560147 CIFC22 H24 O8P 1 21/n 18.5666; 14.3257; 9.2306
90; 112.196; 90		1048.86Zhou, Jiawang; Stojanović, Ljiljana; Berezin, Andrey A.; Battisti, Tommaso; Gill, Abigail; Kariuki, Benson M.; Bonifazi, Davide; Crespo-Otero, Rachel; Wasielewski, Michael R.; Wu, Yi-Lin
Organic room-temperature phosphorescence from halogen-bonded organic frameworks: hidden electronic effects in rigidified chromophores.
Chemical science, 2020, 12, 767-773
1560148 CIFC22 H20 Br4 O8P -19.5351; 12.0414; 12.8133
72.585; 69.31; 89.363		1305.8Zhou, Jiawang; Stojanović, Ljiljana; Berezin, Andrey A.; Battisti, Tommaso; Gill, Abigail; Kariuki, Benson M.; Bonifazi, Davide; Crespo-Otero, Rachel; Wasielewski, Michael R.; Wu, Yi-Lin
Organic room-temperature phosphorescence from halogen-bonded organic frameworks: hidden electronic effects in rigidified chromophores.
Chemical science, 2020, 12, 767-773
1560149 CIFC22 H23 Br O8P 1 21 19.6364; 9.8092; 11.8602
90; 90.442; 90		1121.06Zhou, Jiawang; Stojanović, Ljiljana; Berezin, Andrey A.; Battisti, Tommaso; Gill, Abigail; Kariuki, Benson M.; Bonifazi, Davide; Crespo-Otero, Rachel; Wasielewski, Michael R.; Wu, Yi-Lin
Organic room-temperature phosphorescence from halogen-bonded organic frameworks: hidden electronic effects in rigidified chromophores.
Chemical science, 2020, 12, 767-773
1560150 CIFC65 H80 Cl N6 O6P -112.0771; 13.4199; 18.1881
75.562; 80.992; 87.013		2819.2Martinez-Cuezva, Alberto; Pastor, Aurelia; Marin-Luna, Marta; Diaz-Marin, Carmen; Bautista, Delia; Alajarin, Mateo; Berna, Jose
Cyclization of interlocked fumaramides into β-lactams: experimental and computational mechanistic assessment of the key intercomponent proton transfer and the stereocontrolling active pocket.
Chemical science, 2020, 12, 747-756
1560151 CIFC20 H20 N O2 S2P 1 21/n 112.3021; 7.9076; 18.7346
90; 97.095; 90		1808.5Hu, Jiefeng; Yang, Xianyu; Shi, Shasha; Cheng, Bo; Luo, Xiaoling; Lan, Yu; Loh, Teck-Peng
Metal-free C(sp3)‒H functionalization of sulfonamides via strain-release rearrangement
Chemical Science, 2021, 12, 4034-4040
1560152 CIFC47 H62 F6 Fe N O10 PP -111.2754; 11.2786; 19.1955
81.762; 83.501; 76.134		2337.6Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560153 CIFC47 H62 F6 Fe N O10 PP -111.3327; 11.4193; 19.3877
82.951; 80.729; 77.436		2406.89Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560154 CIFC47 H62 F6 Fe N O10 PP -111.2781; 11.2893; 19.213
83.432; 81.586; 76.335		2343.29Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560155 CIFC47 H62 F6 Fe N O10 PP -111.2958; 11.3414; 19.2872
83.238; 81.374; 76.703		2368.53Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560156 CIFC47 H62 F6 Fe N O10 PP -111.3259; 11.3917; 19.3628
83.024; 80.932; 77.121		2395.24Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560157 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.2236; 25.2061; 13.5364
90; 110.914; 90		3258.5Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560158 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.2753; 25.224; 13.5486
90; 111.171; 90		3274.6Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560159 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.3328; 25.4063; 13.6255
90; 111.122; 90		3336.6Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560160 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.361; 25.435; 13.645
90; 111.064; 90		3356Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560161 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.28; 25.269; 13.5675
90; 111.092; 90		3288.2Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560162 CIFC47 H62 F6 Fe N O10 PP -111.2892; 11.3208; 19.2519
83.33; 81.46; 76.478		2357.22Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560163 CIFC47 H62 F6 Fe N O10 PP -111.3088; 11.3689; 19.3307
83.1; 81.166; 76.913		2382.63Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560164 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.844; 11.6767; 16.7383
94.74; 95.623; 104.722		1840.28Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560165 CIFC47 H62 F6 Fe N O10 PP -111.3611; 11.5447; 19.4228
82.91; 80.543; 77.861		2446.24Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560166 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.8233; 11.6256; 16.7174
94.917; 95.464; 104.784		1825.52Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560167 CIFC47 H62 F6 Fe N O10 PP -111.3456; 11.4668; 19.414
82.907; 80.58; 77.69		2424.07Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560168 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.7522; 11.4459; 16.6761
95.5; 95.052; 104.805		1779.06Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560169 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.3108; 25.3315; 13.5949
90; 111.123; 90		3312.2Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560170 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.7269; 11.4193; 16.6601
95.565; 95.014; 104.744		1769.03Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560171 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.3821; 25.543; 13.668
90; 111.172; 90		3380Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560172 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.8091; 11.5747; 16.7136
95.109; 95.249; 104.806		1814.42Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560173 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.354; 25.443; 13.638
90; 111.061; 90		3352.7Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560174 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.8649; 11.7188; 16.7606
94.613; 95.802; 104.684		1853.36Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560175 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.691; 11.3787; 16.6251
95.673; 94.963; 104.636		1753.22Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560176 CIFC47 H62 F6 Fe N O10 PP -111.3733; 11.6068; 19.427
83.003; 80.579; 77.986		2464.26Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560177 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.7922; 11.5185; 16.7041
95.266; 95.19; 104.874		1800.49Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560178 CIFC26 H42 Si2P 1 21/c 112.1094; 11.0077; 9.4271
90; 103.617; 90		1221.28He, Tao; Wang, Guoqiang; Long, Peng-Wei; Kemper, Sebastian; Irran, Elisabeth; Klare, Hendrik F. T.; Oestreich, Martin
Intramolecular Friedel-Crafts alkylation with a silylium-ion-activated cyclopropyl group: formation of tricyclic ring systems from benzyl-substituted vinylcyclopropanes and hydrosilanes.
Chemical science, 2020, 12, 569-575
1560179 CIFC62 H26 Al F20 N6P 1 21/n 110.6538; 21.0744; 27.7419
90; 90.186; 90		6228.6Arnold, Amela; Sherbow, Tobias J.; Bohanon, Amanda M.; Sayler, Richard I.; Britt, R. David; Smith, Allison M.; Fettinger, James C.; Berben, Louise A.
Delocalization tunable by ligand substitution in [L<sub>2</sub>Al] <sup><i>n</i>-</sup> complexes highlights a mechanism for strong electronic coupling.
Chemical science, 2020, 12, 675-682
1560180 CIFC35 H21 Al Cl2 F10 N3 OP 1 21/n 113.3802; 15.1258; 17.4402
90; 110.95; 90		3296.3Arnold, Amela; Sherbow, Tobias J.; Bohanon, Amanda M.; Sayler, Richard I.; Britt, R. David; Smith, Allison M.; Fettinger, James C.; Berben, Louise A.
Delocalization tunable by ligand substitution in [L<sub>2</sub>Al] <sup><i>n</i>-</sup> complexes highlights a mechanism for strong electronic coupling.
Chemical science, 2020, 12, 675-682
1560181 CIFC44 H39 Al Cl F10 N3 O2.5P 1 21 19.8433; 10.2481; 20.401
90; 103.193; 90		2003.63Arnold, Amela; Sherbow, Tobias J.; Bohanon, Amanda M.; Sayler, Richard I.; Britt, R. David; Smith, Allison M.; Fettinger, James C.; Berben, Louise A.
Delocalization tunable by ligand substitution in [L<sub>2</sub>Al] <sup><i>n</i>-</sup> complexes highlights a mechanism for strong electronic coupling.
Chemical science, 2020, 12, 675-682
1560182 CIFC88 H84 Al N10C 1 2/c 124.1574; 16.2905; 19.344
90; 110.105; 90		7148.7Arnold, Amela; Sherbow, Tobias J.; Bohanon, Amanda M.; Sayler, Richard I.; Britt, R. David; Smith, Allison M.; Fettinger, James C.; Berben, Louise A.
Delocalization tunable by ligand substitution in [L<sub>2</sub>Al] <sup><i>n</i>-</sup> complexes highlights a mechanism for strong electronic coupling.
Chemical science, 2020, 12, 675-682
1560183 CIFC26 H28 Co Ho N10 O8C m c m14.7754; 14.9336; 14.0276
90; 90; 90		3095.2Wang, Junhao; Zakrzewski, Jakub J.; Zychowicz, Mikolaj; Vieru, Veacheslav; Chibotaru, Liviu F.; Nakabayashi, Koji; Chorazy, Szymon; Ohkoshi, Shin-Ichi
Holmium(iii) molecular nanomagnets for optical thermometry exploring the luminescence re-absorption effect.
Chemical science, 2020, 12, 730-741
1560184 CIFC26 H28 Ho Ir N10 O8C m c m14.872; 15.2339; 14.1487
90; 90; 90		3205.51Wang, Junhao; Zakrzewski, Jakub J.; Zychowicz, Mikolaj; Vieru, Veacheslav; Chibotaru, Liviu F.; Nakabayashi, Koji; Chorazy, Szymon; Ohkoshi, Shin-Ichi
Holmium(iii) molecular nanomagnets for optical thermometry exploring the luminescence re-absorption effect.
Chemical science, 2020, 12, 730-741
1560185 CIFC26 H28 Ho N10 O8 RhC m c m14.8236; 15.1198; 14.066
90; 90; 90		3152.6Wang, Junhao; Zakrzewski, Jakub J.; Zychowicz, Mikolaj; Vieru, Veacheslav; Chibotaru, Liviu F.; Nakabayashi, Koji; Chorazy, Szymon; Ohkoshi, Shin-Ichi
Holmium(iii) molecular nanomagnets for optical thermometry exploring the luminescence re-absorption effect.
Chemical science, 2020, 12, 730-741
1560186 CIFC8 H8 N2 O2P -16.931; 7.59; 7.735
60.94; 82.44; 75.12		343.75Nicks, Joshua; Boer, Stephanie A.; White, Nicholas G.; Foster, Jonathan A.
Monolayer nanosheets formed by liquid exfoliation of charge-assisted hydrogen-bonded frameworks
Chemical Science, 2021, 12, 3322-3327
1560187 CIFC8 H8 N2 O2P -17.0348; 7.8512; 7.8827
61.268; 74.309; 82.32		367.54Nicks, Joshua; Boer, Stephanie A.; White, Nicholas G.; Foster, Jonathan A.
Monolayer nanosheets formed by liquid exfoliation of charge-assisted hydrogen-bonded frameworks
Chemical Science, 2021, 12, 3322-3327
1560188 CIFC8 H8 N2 O2P -15.5557; 7.8957; 9.0549
71.386; 83.555; 74.217		362.09Nicks, Joshua; Boer, Stephanie A.; White, Nicholas G.; Foster, Jonathan A.
Monolayer nanosheets formed by liquid exfoliation of charge-assisted hydrogen-bonded frameworks
Chemical Science, 2021, 12, 3322-3327
1560189 CIFC9 H11 N O3P 1 21/c 16.0794; 23.851; 6.5545
90; 114.294; 90		866.24Ma, Liang; Kou, Luyao; Jin, Feng; Cheng, Xionglve; Tao, Suyan; Jiang, Gangzhong; Bao, Xiaoguang; Wan, Xiaobing
Acyclic nitronate olefin cycloaddition (ANOC): regio- and stereospecific synthesis of isoxazolines.
Chemical science, 2020, 12, 774-779
1560190 CIFC9 H11 N O3P c a 2110.2859; 10.6455; 7.6374
90; 90; 90		836.28Ma, Liang; Kou, Luyao; Jin, Feng; Cheng, Xionglve; Tao, Suyan; Jiang, Gangzhong; Bao, Xiaoguang; Wan, Xiaobing
Acyclic nitronate olefin cycloaddition (ANOC): regio- and stereospecific synthesis of isoxazolines.
Chemical science, 2020, 12, 774-779
1560191 CIFC12 H11 N O3P 1 21/c 112.4596; 7.5335; 10.8814
90; 92.749; 90		1020.2Ma, Liang; Kou, Luyao; Jin, Feng; Cheng, Xionglve; Tao, Suyan; Jiang, Gangzhong; Bao, Xiaoguang; Wan, Xiaobing
Acyclic nitronate olefin cycloaddition (ANOC): regio- and stereospecific synthesis of isoxazolines.
Chemical science, 2020, 12, 774-779
1560192 CIFC12 H11 N O3P 1 21/c 19.4978; 19.9607; 11.2962
90; 91.786; 90		2140.5Ma, Liang; Kou, Luyao; Jin, Feng; Cheng, Xionglve; Tao, Suyan; Jiang, Gangzhong; Bao, Xiaoguang; Wan, Xiaobing
Acyclic nitronate olefin cycloaddition (ANOC): regio- and stereospecific synthesis of isoxazolines.
Chemical science, 2020, 12, 774-779
1560197 CIFC33 H17 NP 1 21/c 19.5983; 7.4141; 28.155
90; 97.017; 90		1988.6Ghosh, Animesh; Csókás, Dániel; Budanović, Maja; Webster, Richard D.; Pápai, Imre; Stuparu, Mihaiela C.
Synthesis of azahelicenes through Mallory reaction of imine precursors: corannulene substrates provide an exception to the rule in oxidative photocyclizations of diarylethenes
Chemical Science, 2021, 12, 3977-3983
1560198 CIFAs B F H4 N O4C 1 c 14.4453; 8.1098; 12.7463
90; 90; 90		459.51Bai, Zhiyong; Liu, Lehui; Wang, Dongmei; Hu, Chun-Li; Lin, Zhoubin
To improve the key properties of nonlinear optical crystals assembled with tetrahedral functional building units
Chemical Science, 2021, 12, 4014-4020
1560199 CIFC65 H65 Cu F3 N4 O4 P3 SP -110.6937; 10.7364; 25.1952
88.365; 83.658; 83.887		2858.25Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560200 CIFC43 H49 B Cl Cu F20 N4 O P3P 1 21/c 116.4423; 20.739; 15.7833
90; 104.388; 90		5213.2Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560201 CIFC15 H39 Cl2 Cu N4 P3P b c a16.2129; 16.8046; 17.8201
90; 90; 90		4855.1Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560202 CIFC54 H45 B Cu F20 N4 P3P 1 21/n 112.8794; 28.2479; 15.6613
90; 110.76; 90		5327.9Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560203 CIFC39 H39 B Cu F20 N4 P3P -113.443; 14.253; 14.599
93.503; 105.397; 107.916		2534.8Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560204 CIFC19 H18 N2 O2 S2P 1 21 19.6009; 10.3983; 9.9867
90; 115.222; 90		901.95Zhong, Xia; Zhong, Ziwei; Wu, Zhikun; Ye, Zhen; Feng, Yuxiang; Dong, Shunxi; Liu, Xiaohua; Peng, Qian; Feng, Xiaoming
Chiral Lewis acid-bonded picolinaldehyde enables enantiodivergent carbonyl catalysis in the Mannich/condensation reaction of glycine ester
Chemical Science, 2021, 12, 4353-4360
1560205 CIFC38 H56 F9 N4 O16 S3 YbP 21 21 223.069; 24.5839; 9.5501
90; 90; 90		5416.1Zhong, Xia; Zhong, Ziwei; Wu, Zhikun; Ye, Zhen; Feng, Yuxiang; Dong, Shunxi; Liu, Xiaohua; Peng, Qian; Feng, Xiaoming
Chiral Lewis acid-bonded picolinaldehyde enables enantiodivergent carbonyl catalysis in the Mannich/condensation reaction of glycine ester
Chemical Science, 2021, 12, 4353-4360
1560206 CIFC49 H78 F9 N4 O17 S3 YbP 1 21 111.9789; 20.7474; 12.9099
90; 106.293; 90		3079.7Zhong, Xia; Zhong, Ziwei; Wu, Zhikun; Ye, Zhen; Feng, Yuxiang; Dong, Shunxi; Liu, Xiaohua; Peng, Qian; Feng, Xiaoming
Chiral Lewis acid-bonded picolinaldehyde enables enantiodivergent carbonyl catalysis in the Mannich/condensation reaction of glycine ester
Chemical Science, 2021, 12, 4353-4360
1560207 CIFC122 H112 O4 S2P -18.9363; 15.5536; 17.3731
106.709; 97.475; 95.961		2267.6Lu, Xuefeng; An, Dongyue; Han, Yi; Zou, Ya; Qiao, Yanjun; Zhang, Ning; Chang, Dongdong; Wu, Jishan; Liu, Yunqi
A cyclopenta-fused dibenzo[b,d]thiophene-co-phenanthrene macrocyclic tetraradicaloid
Chemical Science, 2021, 12, 3952-3957
1560208 CIFC63 H66 Cu3 N9P -19.7333; 27.941; 42.675
75.096; 83.457; 84.935		11121.3Xie, Mo; Chen, Xiao-Ru; Wu, Kun; Lu, Zhou; Wang, Kai; Li, Nan; Wei, Rong-Jia; Zhan, Shun-Ze; Ning, Guo-Hong; Zou, Bo; Li, Dan
Pressure-induced phosphorescence enhancement and piezochromism of a carbazole-based cyclic trinuclear Cu(i) complex
Chemical Science, 2021, 12, 4425-4431
1560209 CIFC63 H66 Cu3 N9P 1 c 111.4093; 28.8937; 17.7109
90; 104.338; 90		5656.66Xie, Mo; Chen, Xiao-Ru; Wu, Kun; Lu, Zhou; Wang, Kai; Li, Nan; Wei, Rong-Jia; Zhan, Shun-Ze; Ning, Guo-Hong; Zou, Bo; Li, Dan
Pressure-induced phosphorescence enhancement and piezochromism of a carbazole-based cyclic trinuclear Cu(i) complex
Chemical Science, 2021, 12, 4425-4431
1560210 CIFC63 H66 Cu3 N9P 1 21/c 111.52641; 29.1085; 17.85854
90; 103.99; 90		5814.11Xie, Mo; Chen, Xiao-Ru; Wu, Kun; Lu, Zhou; Wang, Kai; Li, Nan; Wei, Rong-Jia; Zhan, Shun-Ze; Ning, Guo-Hong; Zou, Bo; Li, Dan
Pressure-induced phosphorescence enhancement and piezochromism of a carbazole-based cyclic trinuclear Cu(i) complex
Chemical Science, 2021, 12, 4425-4431
1560211 CIFC22 H45 Fe N4 O7P 1 21/c 113.571; 11.046; 19.406
90; 102.992; 90		2834.6Keshari, Kritika; Bera, Moumita; Velasco, Lucía; Munshi, Sandip; Gupta, Geetika; Moonshiram, Dooshaye; Paria, Sayantan
Characterization and reactivity study of non-heme high-valent iron‒hydroxo complexes
Chemical Science, 2021, 12, 4418-4424
1560212 CIFC30 H16 O2P 1 21/c 18.1656; 15.1358; 15.7979
90; 102.468; 90		1906.5Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560213 CIFC30 H18 N2P 1 21/c 115.9958; 15.9492; 7.8148
90; 91.516; 90		1993.02Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560214 CIFC15 H8 O2 SC 1 2/c 117.7976; 10.4721; 11.7388
90; 99.158; 90		2159.97Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560215 CIFC57 H34 Cl2P 21 21 218.57192; 20.53361; 22.43166
90; 90; 90		3948.25Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560216 CIFC30 H16 S2P 1 21/n 19.338; 13.622; 16.299
90; 102.204; 90		2026.4Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560217 CIFC28.5 H16.5 Cl1.5 OP 41 2 29.0201; 9.0201; 49.382
90; 90; 90		4017.8Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560218 CIFC70 H86 B P2 YP 1 21/c 119.84621; 15.33735; 19.6362
90; 91.1824; 90		5975.76Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560219 CIFC39 H57 Cl2 F6 P2 Ru SbP 1 21/n 114.68263; 10.27641; 28.8561
90; 94.9221; 90		4337.89Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560220 CIFC26 H36 Cl4 Hf P2P 1 21/c 113.847; 11.756; 17.937
90; 95.395; 90		2907Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560221 CIFC33 H43 Cl5 N P2 TaP b c a20.20265; 16.84883; 20.7566
90; 90; 90		7065.36Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560222 CIFC30.5 H39 Br Cl3 Mn O3 P2P 1 21/c 112.12; 18.798; 15.683
90; 111.303; 90		3329Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560223 CIFC30 H36 Cr O4 P2P 1 21/n 111.87864; 15.68278; 15.58857
90; 102.773; 90		2832.13Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560224 CIFC45 H60 Cl N O2 P2 PtP 1 21/c 118.1766; 11.59885; 21.4296
90; 114.947; 90		4096.41Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560225 CIFC38 H55 Cl5 F6 P2 Rh SbP 1 21/c 18.68119; 24.5831; 20.7842
90; 96.7728; 90		4404.61Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560226 CIFC33 H42 N2 O3 P2 WP 1 21/n 110.771; 18.02; 16.983
90; 97.989; 90		3264Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560227 CIFC29 H36 O3 P2 WP b c a15.652; 16.072; 22.3038
90; 90; 90		5610.7Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560228 CIFC33 H42 Mo N2 O3 P2P 1 21/n 110.771; 18.08; 16.992
90; 97.838; 90		3278Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560229 CIFC38 H52 Mo O6 P2P 1 21/c 110.8424; 15.9246; 22.3877
90; 101.63; 90		3786.12Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560230 CIFC35 H48 Mo O4.5 P2C 1 2/c 132.514; 11.57882; 39.5477
90; 113.917; 90		13610.2Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560231 CIFC86 H100 Au B F2 O P2P 1 21/c 111.28458; 13.79053; 47.7699
90; 90.5291; 90		7433.65Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560232 CIFC29 H36 Mo O3 P2P b c a15.65317; 16.11165; 22.26048
90; 90; 90		5614.06Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560233 CIFC56 H82 O3 P2 S2 ZnP 1 21/c 120.688; 26.218; 40.07
90; 95.99; 90		21615Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560236 CIFC32 H43 Ba N6 O11 S2P c a 2117.6827; 10.4422; 22.5408
90; 90; 90		4162.08Abou, Diane S.; Thiele, Nikki A.; Gutsche, Nicholas T.; Villmer, Alexandria; Zhang, Hanwen; Woods, Joshua J.; Baidoo, Kwamena E.; Escorcia, Freddy E.; Wilson, Justin J.; Thorek, Daniel L. J.
Towards the stable chelation of radium for biomedical applications with an 18-membered macrocyclic ligand
Chemical Science, 2021, 12, 3733-3742
1560237 CIFC59 H76 Cl Ir N2P 21 21 2116.297; 17.0451; 17.8125
90; 90; 90		4948.03Foster, Daven; Gao, Pengchao; Zhang, Ziyun; Sipos, Gellért; Sobolev, Alexandre N.; Nealon, Gareth; Falivene, Laura; Cavallo, Luigi; Dorta, Reto
Design, scope and mechanism of highly active and selective chiral NHC‒iridium catalysts for the intramolecular hydroamination of a variety of unactivated aminoalkenes
Chemical Science, 2021, 12, 3751-3767
1560238 CIFC55 H64 Br2 N4 O13P -19.3936; 16.783; 17.8687
75.171; 83.247; 84.427		2697.7Wilson, Benjamin H.; Abdulla, Louae M.; Schurko, Robert W.; Loeb, Stephen J.
Translational dynamics of a non-degenerate molecular shuttle imbedded in a zirconium metal‒organic framework
Chemical Science, 2021, 12, 3944-3951

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