Crystallography Open Database

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7119485 CIFC25 H26 O4P 1 21/n 114.1779; 7.8527; 19.28
90; 96.464; 90
2132.9Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974
7119486 CIFC27 H24 O3P -15.7885; 10.4613; 16.3808
92.216; 97.607; 92.531
981.26Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974
7119487 CIFC37.5 H32.5 Br Cl10.5 Mn N3 O3 P2P -112.8806; 15.305; 15.3667
113.734; 98.8175; 110.01
2452.06Gyandshwar; Kumar; Rao; Wendy; Pell; Ilia; Korobkov; Darrin; Richeson
Electrocatalytic reduction of CO2 using Mn complexes with unconventional coordination environments
Chem.Commun., 2016, 52, 8010
7119488 CIFC21 H17 Br Mn N2 O3 PP 1 21 18.312; 11.1704; 11.8045
90; 108.672; 90
1038.34Gyandshwar; Kumar; Rao; Wendy; Pell; Ilia; Korobkov; Darrin; Richeson
Electrocatalytic reduction of CO2 using Mn complexes with unconventional coordination environments
Chem.Commun., 2016, 52, 8010
7119615 CIFC219 H324 Gd18 N30 O147R -3 c :H33.1977; 33.1977; 59.4184
90; 90; 120
56711Kai; Wang; Zi-Lu; Chen; Hua-Hong; Zou; Kun; Hu; Hai-Ye; Li; Zhong; Zhang; Wei-Yin; Sun; Fu-Pei; Liang
A single-stranded {Gd18} nanowheel with a symmetric polydentate diacylhydrazone ligand
Chem.Commun., 2016, 52, 8297
7119616 CIFC15 H15 N O2P 21 21 217.965; 9.5073; 16.0506
90; 90; 90
1215.44Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119617 CIFC15 H15 N O2P 21 21 217.9647; 9.5076; 16.0492
90; 90; 90
1215.33Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119618 CIFC14 H12 Br N O2P 21 21 218.5431; 9.8089; 14.6636
90; 90; 90
1228.79Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119619 CIFC15 H15 N O3P 1 21/n 116.9222; 7.6509; 20.5384
90; 109.285; 90
2509.9Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119620 CIFC15 H12 F3 N O2P 1 21/c 19.6309; 7.8723; 17.274
90; 96.92; 90
1300.13Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119621 CIFC15 H12 F3 N O2P -18.7121; 11.7093; 14.2353
76.9998; 72.3793; 69.8941
1287.79Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119622 CIFC14 H12 Br N O2P 1 21/n 118.1984; 7.3629; 19.2858
90; 108.487; 90
2450.81Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119649 CIFC23 H20 Cl N O2P 21 21 219.4627; 11.1519; 18.1676
90; 90; 90
1917.17Yan Lu; Yuhang Zhou; Lili Lin; Haifeng Zheng; Kai Fu; Xiaohua Liu; Xiaoming Feng
N,N'-Dioxide/nickel(II)-catalyzed asymmetric Diels-Alder reaction of cyclopentadiene with 2,3-dioxopyrrolidines and 2=alkenoyl pyridines
Chem.Commun., 2016, 52, 8255
7119650 CIFC18 H21 N O4P 21 21 2116.2716; 21.2062; 10.0994
90; 90; 90
3484.9U. B. Rao Khandavilli; Matteo Lusi; Balakrishna R. Bhogala; Anita R. Maguire; Matthias Stein; Simon E. Lawrence
Diversity in a simple co-crystal: racemic and kryptoracemic behaviour
Chem.Commun., 2016, 52, 8309-8312
7119651 CIFC18 H21 N O4P 1 21 19.882; 20.953; 16.215
90; 93.913; 90
3350U. B. Rao Khandavilli; Matteo Lusi; Balakrishna R. Bhogala; Anita R. Maguire; Matthias Stein; Simon E. Lawrence
Diversity in a simple co-crystal: racemic and kryptoracemic behaviour
Chem.Commun., 2016, 52, 8309-8312
7119652 CIFC18 H21 N O4P 1 21/c 110.0661; 21.081; 16.584
90; 100.06; 90
3465.1U. B. Rao Khandavilli; Matteo Lusi; Balakrishna R. Bhogala; Anita R. Maguire; Matthias Stein; Simon E. Lawrence
Diversity in a simple co-crystal: racemic and kryptoracemic behaviour
Chem.Commun., 2016, 52, 8309-8312
7119653 CIFC11 H16 N2 O5 SP 1 21/n 19.03667; 6.90757; 21.7122
90; 99.8233; 90
1335.44Shuai Dong; Kiran Indukuri; Derrick L. J. Clive; Jin-Ming Gao
Synthesis of models of the BC ring systems of MPC1001 and MPC1001F
Chem.Commun., 2016, 52, 8271
7119654 CIFC16 H15 N3 O7 SP -16.7169; 7.9571; 16.1794
91.3062; 98.1391; 92.2828
855Shuai Dong; Kiran Indukuri; Derrick L. J. Clive; Jin-Ming Gao
Synthesis of models of the BC ring systems of MPC1001 and MPC1001F
Chem.Commun., 2016, 52, 8271
7119655 CIFC16 H14 F3 N3 O2P 1 21/c 110.013; 7.5562; 21.159
90; 93.102; 90
1598.5Xing-Long Yu; Jia-Rong Chen; Dong-Zhen Chen; Wen-Jing Xiao
Visible-light-induced photocatalytic azotrifluoromethylation of alkenes with aryldiazonium salts and sodium triflinate
Chem.Commun., 2016, 52, 8275
7119656 CIFC20 H17 B F4 OP 1 21/n 17.7761; 15.354; 14.48
90; 95.766; 90
1720.1Eliar Mosaferi; David Ripsman; Douglas W. Stephan
The air-stable carbocation salt [(MeOC6H4)CPh2][BF4] in Lewis acid catalyzed hydrothiolation of alkenes
Chem.Commun., 2016, 52, 8291
7119675 CIFC59 H59 B2 F24 N5 PtC 1 2/c 139.65; 13.44; 26.01
90; 111.476; 90
12898Marta Rosello-Merino; Raquel J. Rama; Josefina Diez; Salvador Conejero
Catalytic dehydrocoupling of amine-boranes and amines into diaminoboranes: isolation of a Pt(II), Shimoi-type, Eta1-BH complex
Chem.Commun., 2016, 52, 8389
7119676 CIFC68 H78 N8 O28 Zn3I -4 2 d28.2219; 28.2219; 9.7266
90; 90; 90
7747Jun-Cheng Jin; Ju Wu; Guo-Ping Yang; Yun-Long Wu; Yao-Yu Wang
A microporous anionic metal-organic framework for a highly selective and sensitive electrochemical sensor of Cu2+ ions
Chem.Commun., 2016, 52, 8475
7119677 CIFC19 H12 O4P -18.4472; 12.7834; 15.0002
100.217; 105.699; 108.939
1411Devenderan Ramanathan; Kayambu Namitharan; Kasi Pitchumani
Copper(I)-Y zeolite catalyzed N-sulfonylketenimine mediated annulation of hydroxynaphthoquinones: syntheses of naphtho[2,1-b]furan-2,5-diones and benzo[de]chromene-2,6-diones
Chem.Commun., 2016, 52, 8436
7119678 CIFC18.25 H10.5 O3P 1 21/n 19.081; 15.7891; 9.2543
90; 97.431; 90
1315.74Devenderan Ramanathan; Kayambu Namitharan; Kasi Pitchumani
Copper(I)-Y zeolite catalyzed N-sulfonylketenimine mediated annulation of hydroxynaphthoquinones: syntheses of naphtho[2,1-b]furan-2,5-diones and benzo[de]chromene-2,6-diones
Chem.Commun., 2016, 52, 8436
7119679 CIFC73 H82 Cl4 Co3 N10 O26P 1 21 114.3957; 18.2215; 16.1798
90; 102.476; 90
4143.9Roberto Berardozzi; Elena Badetti; Nadia Alessandra Carmo dos Santos; Klaus Wurst; Giulia Licini; Gennaro Pescitelli; Cristiano Zonta; Lorenzo Di Bari
Co(II)-induced giant vibrational CD provides a new design of methods for rapid and sensitive chirality recognition
Chem.Commun., 2016, 52, 8428
7119680 CIFC21 H17 N O3 S SeP -19.7234; 9.8305; 22.0952
102.367; 94.393; 107.218
1948.22Kai Sun; Xin Wang; Yunhe Lv; Gang Li; Hezhen Jiao; Changwei Dai; Yangyang Li; Chong Zhang; Lin Liu
Peroxodisulfate-mediated selenoamination of alkenes yielding amidoselenide-containing sulfamides and azoles
Chem.Commun., 2016, 52, 8471
7119681 CIFC24 H27 Co3 N12 O10P 63/m m c16.8676; 16.8676; 18.8186
90; 90; 120
4636.9Di-Ming Chen; Jia-Yue Tian; Chun-Sen Liu; Miao Du
A bracket approach to improve the stability and gas sorption performance of a metal-organic framework via in situ incorporating the size-matching molecular building blocks
Chem. Commun., 2016, 52, 8413
7119682 CIFC42 H24 Co5 N15 O15P 63/m m c18.8605; 18.8605; 16.6183
90; 90; 120
5119.5Di-Ming Chen; Jia-Yue Tian; Chun-Sen Liu; Miao Du
A bracket approach to improve the stability and gas sorption performance of a metal-organic framework via in situ incorporating the size-matching molecular building blocks
Chem. Commun., 2016, 52, 8413
7119826 CIFC193.68 H54 Cu18 N18 O117R -3 m18.2623; 18.2623; 39.6543
90; 90; 120
11453.3Xiaoping Zhang; Zhenjie Zhang; Jake Boissonnault; Seth M. Cohen
Design and synthesis of squaramide-based MOFs as efficient MOF-supported hydrogen-bonding organocatalysts
Chem.Commun., 2016, 52, 8585
7119827 CIFC180 H54 N18 O108 Zn18R -3 m18.816; 18.816; 38.416
90; 90; 120
11779Xiaoping Zhang; Zhenjie Zhang; Jake Boissonnault; Seth M. Cohen
Design and synthesis of squaramide-based MOFs as efficient MOF-supported hydrogen-bonding organocatalysts
Chem.Commun., 2016, 52, 8585
7119828 CIFC19 H21 B Cd N9 O4P -18.562; 8.839; 16.904
82.238; 89.592; 78.252
1240.7Min Liu; Shumei Chen; Tian Wen; Jian Zhang
Encapsulation of LnIII ions/Ag nanoparticles within Cd(II) boron imidazolate frameworks for tuning luminescence emission
Chem.Commun., 2016, 52, 8577
7119829 CIFC42 H31 B2 Cd3 N16 O12C 1 2/c 128.187; 14.002; 27.657
90; 116.228; 90
9792Min Liu; Shumei Chen; Tian Wen; Jian Zhang
Encapsulation of LnIII ions/Ag nanoparticles within Cd(II) boron imidazolate frameworks for tuning luminescence emission
Chem.Commun., 2016, 52, 8577
7119830 CIFC52 H68 N8 O8P 1 21/n 117.4535; 8.0246; 17.7712
90; 97.847; 90
2465.68Juhoon Lee; Nolan W. Waggoner; Luis Polanco; Ga Rim You; Vincent M. Lynch; Sung Kuk Kim; Simon M. Humphrey; Jonathan L. Sessler
Ship in a breakable bottle: fluoride-induced release of an organic molecule from a Pr(III)-linked molecular cage
Chem.Commun., 2016, 52, 8514
7119831 CIFC286 H338 N38 O40 Pr4P -120.6712; 21.0386; 21.6281
62.477; 79.558; 67.086
7683.2Juhoon Lee; Nolan W. Waggoner; Luis Polanco; Ga Rim You; Vincent M. Lynch; Sung Kuk Kim; Simon M. Humphrey; Jonathan L. Sessler
Ship in a breakable bottle: fluoride-induced release of an organic molecule from a Pr(III)-linked molecular cage
Chem.Commun., 2016, 52, 8514
7119832 CIFC60 H68 N16 O4 Pr2C 1 2 128.896; 8.6749; 14.2513
90; 116.056; 90
3209.29Juhoon Lee; Nolan W. Waggoner; Luis Polanco; Ga Rim You; Vincent M. Lynch; Sung Kuk Kim; Simon M. Humphrey; Jonathan L. Sessler
Ship in a breakable bottle: fluoride-induced release of an organic molecule from a Pr(III)-linked molecular cage
Chem.Commun., 2016, 52, 8514
7119833 CIFC21 H22 N2 O5P 1 21/n 114.2787; 9.4954; 14.5637
90; 98.003; 90
1955.34Yanan Li; Huihui Gao; Zhenlei Zhang; Peng Qian; Meixiang Bi; Zhenggen Zha; Zhiyong Wang
Electrochemical synthesis of alpha-enaminones from aryl ketones
Chem.Commun., 2016, 52, 8600
7120018 CIFC29 H46 N4 O2 S4P -18.58; 13.5581; 13.8786
85.002; 87.556; 85.019
1601.26Luyi Zong; Yujun Xie; Can Wang; Jian-Rong Li; Qianqian Li; Zhen Li
From ACQ to AIE: the suppression of the strong pi-pi interaction of naphthalene diimide derivatives through the adjustment of their flexible chains
Chem.Commun., 2016, 52, 11496
7121007 CIFC37 H43 N3 O3 S2P 1 21/c 114.0664; 27.41; 9.4754
90; 107.434; 90
3485.5Chris L. Vonnegut; Airlia M. Shonkwiler; Lev N. Zakharov; Michael M. Haley; Darren W. Johnson
Harnessing solid-state packing for selective detection of chloride in a macrocyclic anionophore
Chemical Communications, 2016, 52, 9506-9509
7121008 CIFC38.25 H44.5 Cl3.5 N3 O2 S2P 1 21/n 120.7737; 31.7155; 24.6016
90; 98.088; 90
16047.5Chris L. Vonnegut; Airlia M. Shonkwiler; Lev N. Zakharov; Michael M. Haley; Darren W. Johnson
Harnessing solid-state packing for selective detection of chloride in a macrocyclic anionophore
Chemical Communications, 2016, 52, 9506-9509
7121015 CIFC13 H54 N2 Na2 Ni O34 W6P -19.6825; 10.3943; 11.758
113.733; 102.543; 90.479
1051.34Nadiia I. Gumerova; Alexander Roller; Annette Rompel
[Ni(OH)3W6O18(OCH2)3CCH2OH]4-: the first tris-functionalized Anderson-type heteropolytungstate
Chemical Communications, 2016, 52, 9263-9266
7124582 CIFC31 H34 Cl2 N2 O3P 1 21/c 19.4917; 18.4515; 16.3576
90; 100.11; 90
2820.3Deardorff, Cassie L.; Eric Sikma, R.; Rhodes, Christopher P.; Hudnall, Todd W.
Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes.
Chemical communications (Cambridge, England), 2016, 52, 9024-9027
7124583 CIFC31 H35 Cl N2 O2P 1 21/c 110.4748; 17.8218; 15.4388
90; 105.179; 90
2781.6Deardorff, Cassie L.; Eric Sikma, R.; Rhodes, Christopher P.; Hudnall, Todd W.
Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes.
Chemical communications (Cambridge, England), 2016, 52, 9024-9027
7124584 CIFC35 H43 Cl3 N2 OP -111.4742; 11.8275; 12.891
81.869; 87.309; 88.774
1729.8Deardorff, Cassie L.; Eric Sikma, R.; Rhodes, Christopher P.; Hudnall, Todd W.
Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes.
Chemical communications (Cambridge, England), 2016, 52, 9024-9027
7124585 CIFC31 H33 N2 O3P 1 21/c 111.8892; 16.2557; 13.7767
90; 96.327; 90
2646.4Deardorff, Cassie L.; Eric Sikma, R.; Rhodes, Christopher P.; Hudnall, Todd W.
Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes.
Chemical communications (Cambridge, England), 2016, 52, 9024-9027
7124586 CIFC10 H10 N8 O S2P 1 21/n 19.3608; 11.0691; 13.0914
90; 110.3; 90
1272.2Kersten, Kortney M.; Matzger, Adam J.
Improved pharmacokinetics of mercaptopurine afforded by a thermally robust hemihydrate.
Chemical communications (Cambridge, England), 2016, 52, 5281-5284
7124587 CIFC54 H40 N2P b c a11.0573; 25.485; 28.816
90; 90; 90
8120.2Dai, Shengyu; Sui, Xuelin; Chen, Changle
Synthesis of high molecular weight polyethylene using iminopyridyl nickel catalysts.
Chemical communications (Cambridge, England), 2016, 52, 9113-9116
7124588 CIFC25 H22 N2 O4P 1 21/c 111.398; 11.272; 16.887
90; 98.34; 90
2146.7Wang, Nan-Nan; Hao, Wen-Juan; Zhang, Tian-Shu; Li, Guigen; Wu, Ya-Nan; Tu, Shu-Jiang; Jiang, Bo
Metal-free C(sp(3))-H functionalization: oxidative carbo-oxygenation of α-diazo carbonyls via radical dediazotization.
Chemical communications (Cambridge, England), 2016, 52, 5144-5147
7124589 CIFC14 H16 O3P 1 21/n 114.498; 5.9876; 14.857
90; 103.208; 90
1255.6Bankar, Siddheshwar K.; Mathew, Jopaul; Ramasastry, S. S. V.
Synthesis of benzofurans via an acid catalysed transacetalisation/Fries-type O →C rearrangement/Michael addition/ring-opening aromatisation cascade of β-pyrones.
Chemical communications (Cambridge, England), 2016, 52, 5569-5572
7124590 CIFC28 H30 Br2 O6P -17.84; 11.999; 15.345
102.86; 98.09; 90.08
1392.5Bankar, Siddheshwar K.; Mathew, Jopaul; Ramasastry, S. S. V.
Synthesis of benzofurans via an acid catalysed transacetalisation/Fries-type O →C rearrangement/Michael addition/ring-opening aromatisation cascade of β-pyrones.
Chemical communications (Cambridge, England), 2016, 52, 5569-5572
7124591 CIFC27 H30 N2 O6 SP 21 21 218.931; 10.538; 28.633
90; 90; 90
2695Zhang, Minmin; Yu, Shuowen; Hu, Fangzhi; Liao, Yijun; Liao, Lihua; Xu, Xiaoying; Yuan, Weicheng; Zhang, Xiaomei
Highly enantioselective [3+2] coupling of cyclic enamides with quinone monoimines promoted by a chiral phosphoric acid.
Chemical communications (Cambridge, England), 2016, 52, 8757-8760
7124592 CIFC15 H24 B N O2P 1 21/n 113.8539; 7.816; 15.243
90; 115.863; 90
1485.22Légaré, Marc-André; Rochette, Étienne; Légaré Lavergne, Julien; Bouchard, Nicolas; Fontaine, Frédéric-Georges
Bench-stable frustrated Lewis pair chemistry: fluoroborate salts as precatalysts for the C-H borylation of heteroarenes.
Chemical communications (Cambridge, England), 2016, 52, 5387-5390
7124593 CIFC16 H26 B F2 N OP 1 21/n 17.6884; 13.7157; 15.1094
90; 98.435; 90
1576.1Légaré, Marc-André; Rochette, Étienne; Légaré Lavergne, Julien; Bouchard, Nicolas; Fontaine, Frédéric-Georges
Bench-stable frustrated Lewis pair chemistry: fluoroborate salts as precatalysts for the C-H borylation of heteroarenes.
Chemical communications (Cambridge, England), 2016, 52, 5387-5390
7124594 CIFC15 H23 B F3 NP 1 21/c 114.8666; 7.633; 14.4543
90; 115.531; 90
1480.06Légaré, Marc-André; Rochette, Étienne; Légaré Lavergne, Julien; Bouchard, Nicolas; Fontaine, Frédéric-Georges
Bench-stable frustrated Lewis pair chemistry: fluoroborate salts as precatalysts for the C-H borylation of heteroarenes.
Chemical communications (Cambridge, England), 2016, 52, 5387-5390
7124595 CIFC21 H32 Cl N OP 21 21 2111.6015; 12.822; 13.428
90; 90; 90
1997.5McCarty, Zachary R.; Lastovickova, Dominika N.; Bielawski, Christopher W.
A cyclic (alkyl)(amido)carbene: synthesis, study and utility as a desulfurization reagent.
Chemical communications (Cambridge, England), 2016, 52, 5447-5450
7124596 CIFC21 H31 N OP 1 21/c 18.9044; 11.5431; 17.771
90; 92.232; 90
1825.2McCarty, Zachary R.; Lastovickova, Dominika N.; Bielawski, Christopher W.
A cyclic (alkyl)(amido)carbene: synthesis, study and utility as a desulfurization reagent.
Chemical communications (Cambridge, England), 2016, 52, 5447-5450
7124597 CIFC31 H41 N OP 1 21/n 18.6897; 29.0766; 10.8005
90; 106.809; 90
2612.3McCarty, Zachary R.; Lastovickova, Dominika N.; Bielawski, Christopher W.
A cyclic (alkyl)(amido)carbene: synthesis, study and utility as a desulfurization reagent.
Chemical communications (Cambridge, England), 2016, 52, 5447-5450
7124598 CIFC29 H43 Cl Ir N OP 1 21/c 115.8695; 11.8315; 14.6016
90; 96.061; 90
2726.3McCarty, Zachary R.; Lastovickova, Dominika N.; Bielawski, Christopher W.
A cyclic (alkyl)(amido)carbene: synthesis, study and utility as a desulfurization reagent.
Chemical communications (Cambridge, England), 2016, 52, 5447-5450
7124599 CIFC23 H7 F18 N3 O7 S2 SmP b c a19.8011; 14.62079; 21.27781
90; 90; 90
6160.09Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124600 CIFC23 H7 F18 N3 O7 S2 SmP b c a19.9769; 14.811; 21.41308
90; 90; 90
6335.66Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124601 CIFC23 H7 F18 N3 O7 S2 SmP b c a20.0503; 14.9396; 21.463
90; 90; 90
6429.1Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124602 CIFC23 H7 F18 N3 O7 S2 SmP b c a20.1162; 15.14532; 21.5437
90; 90; 90
6563.64Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124603 CIFC23 H7 F18 N3 O7 S2 SmP b c a19.85308; 14.68673; 21.32145
90; 90; 90
6216.84Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124604 CIFC62.5 H70 N4 Ni2 P4P -112.4093; 13.1987; 18.3557
79.4323; 76.229; 84.6926
2866.71Pelties, Stefan; Ehlers, Andreas W.; Wolf, Robert
Insertion of phenyl isothiocyanate into a P-P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane.
Chemical communications (Cambridge, England), 2016, 52, 6601-6604
7124605 CIFC76.5 H83 N5 Ni2 P4 SP -113.6251; 14.0607; 19.7007
99.8667; 99.819; 98.0922
3607.33Pelties, Stefan; Ehlers, Andreas W.; Wolf, Robert
Insertion of phenyl isothiocyanate into a P-P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane.
Chemical communications (Cambridge, England), 2016, 52, 6601-6604
7124606 CIFC73 H79 N5 Ni2 P4 SP -112.4533; 15.594; 19.3068
104.227; 103.128; 106.371
3305.15Pelties, Stefan; Ehlers, Andreas W.; Wolf, Robert
Insertion of phenyl isothiocyanate into a P-P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane.
Chemical communications (Cambridge, England), 2016, 52, 6601-6604
7124607 CIFC51 H38 Al B F20 N2P 1 21/n 114.3392; 22.0014; 16.1601
90; 107.299; 90
4867.6Cao, Levy L.; Daley, Erika; Johnstone, Timothy C.; Stephan, Douglas W.
Cationic aluminum hydride complexes: reactions of carbene-alane adducts with trityl-borate.
Chemical communications (Cambridge, England), 2016, 52, 5305-5307
7124608 CIFC17 H19 Al N2P 1 21/n 111.8284; 11.5141; 12.6491
90; 113.135; 90
1584.2Cao, Levy L.; Daley, Erika; Johnstone, Timothy C.; Stephan, Douglas W.
Cationic aluminum hydride complexes: reactions of carbene-alane adducts with trityl-borate.
Chemical communications (Cambridge, England), 2016, 52, 5305-5307
7124609 CIFC88 H38 Al B2 Br F40 N4P -112.4696; 13.5438; 23.9484
89.208; 88.213; 79.504
3974.8Cao, Levy L.; Daley, Erika; Johnstone, Timothy C.; Stephan, Douglas W.
Cationic aluminum hydride complexes: reactions of carbene-alane adducts with trityl-borate.
Chemical communications (Cambridge, England), 2016, 52, 5305-5307
7124610 CIFC17 H15 Br O2P 1 21 15.9605; 32.909; 7.1915
90; 91.991; 90
1409.8Kondoh, Azusa; Tran, Hoa Thi Quynh; Kimura, Kyoko; Terada, Masahiro
Enantioselective intramolecular cyclization of alkynyl esters catalyzed by a chiral Brønsted base.
Chemical communications (Cambridge, England), 2016, 52, 5726-5729
7124611 CIFC29 H27 N3 O3P 1 21/n 117.181; 26.757; 21.323
90; 96.526; 90
9739Selvaraju, Manikandan; Ye, Tzuen-Yang; Li, Chia-Hsin; Ho, Pei-Heng; Sun, Chung-Ming
Copper catalyzed aerobic oxidative cyclization and ketonization: one pot synthesis of benzoimidazo[1,2-a]imidazolones.
Chemical communications (Cambridge, England), 2016, 52, 6621-6624
7124612 CIFC36 H44 Cl6 Cu N4 O4P -111.6428; 13.6677; 14.1795
84.481; 68.11; 72.003
1990.8Gautam, R.; Chang, T. M.; Astashkin, A. V.; Lincoln, K. M.; Tomat, E.
Propentdyopent: the scaffold of a heme metabolite as an electron reservoir in transition metal complexes.
Chemical communications (Cambridge, England), 2016, 52, 6585-6588
7124613 CIFC37 H44 N4 O4 ZnP -111.175; 11.683; 14.705
92.05; 105.445; 110.322
1717.8Gautam, R.; Chang, T. M.; Astashkin, A. V.; Lincoln, K. M.; Tomat, E.
Propentdyopent: the scaffold of a heme metabolite as an electron reservoir in transition metal complexes.
Chemical communications (Cambridge, England), 2016, 52, 6585-6588
7124614 CIFC35 H44 Cl2 Co N4 O4C 1 2/c 117.3525; 13.834; 14.8976
90; 102.894; 90
3486.1Gautam, R.; Chang, T. M.; Astashkin, A. V.; Lincoln, K. M.; Tomat, E.
Propentdyopent: the scaffold of a heme metabolite as an electron reservoir in transition metal complexes.
Chemical communications (Cambridge, England), 2016, 52, 6585-6588
7124615 CIFC36 H42 Cl6 D2 N4 Ni O4P -112.2982; 14.0284; 14.0382
76.426; 67.944; 64.685
2021.2Gautam, R.; Chang, T. M.; Astashkin, A. V.; Lincoln, K. M.; Tomat, E.
Propentdyopent: the scaffold of a heme metabolite as an electron reservoir in transition metal complexes.
Chemical communications (Cambridge, England), 2016, 52, 6585-6588
7124616 CIFC342 H280 B16 Co8 F64 N72 O3.5 PC 1 2/c 132.8826; 30.1786; 40.0732
90; 96.498; 90
39511.2Taylor, Christopher G. P.; Piper, Jerico R.; Ward, Michael D.
Binding of chemical warfare agent simulants as guests in a coordination cage: contributions to binding and a fluorescence-based response.
Chemical communications (Cambridge, England), 2016, 52, 6225-6228
7124617 CIFC343 H281 B16 Co8 F64 N72 O3 PC 1 2/c 132.7148; 29.7919; 39.8554
90; 96.733; 90
38576.6Taylor, Christopher G. P.; Piper, Jerico R.; Ward, Michael D.
Binding of chemical warfare agent simulants as guests in a coordination cage: contributions to binding and a fluorescence-based response.
Chemical communications (Cambridge, England), 2016, 52, 6225-6228
7124618 CIFC366 H330 B16 Co8 F64 N72 O30 P2C 1 2/c 127.477; 39.201; 41.992
90; 107.133; 90
43223Taylor, Christopher G. P.; Piper, Jerico R.; Ward, Michael D.
Binding of chemical warfare agent simulants as guests in a coordination cage: contributions to binding and a fluorescence-based response.
Chemical communications (Cambridge, England), 2016, 52, 6225-6228
7124619 CIFC60 H56 Cl2 O8C 1 2/c 112.0691; 21.178; 20.726
90; 105.081; 90
5115.1Ma, Yingjie; Chen, Long; Li, Chen; Müllen, Klaus
A fishing rod-like conjugated polymer bearing pillar[5]arenes.
Chemical communications (Cambridge, England), 2016, 52, 6662-6664
7124620 CIFC39 H54 N3 NbP 19.6363; 10.354; 10.4978
107.019; 113.605; 91.585
905.11Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124621 CIFC39 H55 N6 NbP 1 21/n 111.649; 18.9555; 17.0768
90; 97.526; 90
3738.3Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124622 CIFC38 H49 N3 NbP n n m12.4801; 13.772; 19.2824
90; 90; 90
3314.2Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124623 CIFC67 H72 B F15 N5 NbP -112.5396; 17.4757; 29.99
84.127; 82.987; 73.602
6241.6Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124624 CIFC57 H55 B F15 N6 NbP -112.2684; 12.7008; 19.2268
79.4526; 83.1067; 68.923
2743.4Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124625 CIFC121 H118 B2 F30 N8 Nb2P b c a19.3473; 22.4336; 25.5172
90; 90; 90
11075.2Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124626 CIFC15 H32 Cu3 N12 O16P -112.6421; 14.2612; 17.0125
90.192; 96.38; 113.941
2782Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124627 CIFC15 H44 Cl3 N9 Ni3 O13P 1 21/c 117.1605; 13.4761; 14.8097
90; 111.774; 90
3180.5Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124628 CIFC18 H32 N8 O14 U2P 1 21/n 18.3529; 21.2854; 8.9198
90; 111.884; 90
1471.61Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124629 CIFC31 H32 F2 I N O4 SP 1 21/c 114.4081; 22.6704; 19.5045
90; 109.072; 90
6021.2Yu, Liu-Zhu; Zhu, Zi-Zhong; Hu, Xu-Bo; Tang, Xiang-Ying; Shi, Min
Palladium-catalyzed cascade cyclization of allylamine-tethered alkylidenecyclopropanes: facile access to iodine/difluoromethylene- and perfluoroalkyl-containing 1-benzazepine scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 6581-6584
7124630 CIFC30 H36 B F2 PP -19.9138; 10.3236; 13.6951
76.806; 71.844; 82.615
1294.2Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124631 CIFC54 H32 B2 F25 PP 1 21 110.7299; 19.7985; 12.1281
90; 95.89; 90
2562.84Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124632 CIFC30 H32 B F6 PP 1 21/n 111.4351; 9.5654; 24.6131
90; 92.863; 90
2688.9Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124633 CIFC54 H36 B2 F21 PP -19.9916; 15.7747; 16.8287
86.925; 79.345; 75.871
2527.8Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124634 CIFC11 H13 N O2P 1 21/n 18.9638; 10.52; 11.467
90; 109.75; 90
1017.7Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124635 CIFC11 H12 F N O2P 1 21/c 17.7034; 22.119; 12.573
90; 105.27; 90
2066.7Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124636 CIFC12 H15 N O3P 1 21/n 17.4266; 11.889; 13.141
90; 102.2; 90
1134.1Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124637 CIFC11 H12 F N O2P 1 21/n 19.0682; 10.39; 11.58
90; 109.17; 90
1030.6Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124638 CIFC158 H178 Au24 Pd S18P -116.1244; 17.6398; 17.7651
65.152; 64.342; 81.391
4129.8Tian, Shubo; Liao, Lingwen; Yuan, Jinyun; Yao, Chuanhao; Chen, Jishi; Yang, Jinlong; Wu, Zhikun
Structures and magnetism of mono-palladium and mono-platinum doped Au25(PET)18 nanoclusters.
Chemical communications (Cambridge, England), 2016, 52, 9873-9876
7124639 CIFC158 H178 Au24 Pt S18P -116.19; 17.714; 17.8666
65.106; 64.289; 81.343
4184.5Tian, Shubo; Liao, Lingwen; Yuan, Jinyun; Yao, Chuanhao; Chen, Jishi; Yang, Jinlong; Wu, Zhikun
Structures and magnetism of mono-palladium and mono-platinum doped Au25(PET)18 nanoclusters.
Chemical communications (Cambridge, England), 2016, 52, 9873-9876
7124640 CIFC44 H42 Co4 N4 O14P 42/m b c25.569; 25.569; 16.707
90; 90; 90
10923Su, Lei; Song, Wei-Chao; Zhao, Jiong-Peng; Liu, Fu-Chen
Crystal engineering to control the magnetic interaction between weak ferromagnetic single-chain magnets assembled in a 3D framework.
Chemical communications (Cambridge, England), 2016, 52, 8722-8725
7124641 CIFC43 H51 Cl3 Co N2 O2 S2P 1 21/c 119.3263; 9.6193; 25.4228
90; 108.384; 90
4485Sarkar, Prasenjit; Tiwari, Archana; Sarmah, Amrit; Bhandary, Subhrajyoti; Roy, Ram Kinkar; Mukherjee, Chandan
An elusive vinyl radical isolated as an appended unit in a five-coordinate Co(iii)-bis(iminobenzosemiquinone) complex formed via ligand-centered C-S bond cleavage.
Chemical communications (Cambridge, England), 2016, 52, 10613-10616
7124642 CIFC21 H15 O7 PP 1 21/n 17.7879; 20.327; 11.9549
90; 93.558; 90
1888.9Feng, Genfeng; Liu, Wei; Peng, Yuxin; Zhao, Bo; Huang, Wei; Dai, Yafei
Cavity partition and functionalization of a [2+3] organic molecular cage by inserting polar P[double bond, length as m-dash]O bonds.
Chemical communications (Cambridge, England), 2016, 52, 9267-9270
7124643 CIFC60 H60 N6 O8 P2P 21 319.1327; 19.1327; 19.1327
90; 90; 90
7003.7Feng, Genfeng; Liu, Wei; Peng, Yuxin; Zhao, Bo; Huang, Wei; Dai, Yafei
Cavity partition and functionalization of a [2+3] organic molecular cage by inserting polar P[double bond, length as m-dash]O bonds.
Chemical communications (Cambridge, England), 2016, 52, 9267-9270
7124644 CIFC38 H32 F12 N4 P2P -18.8259; 9.7216; 12.7688
104.695; 100.791; 108.868
958.4Wang, Zhaoyang; Bai, Wei; Tong, Jiaqi; Wang, Yi Jia; Qin, Anjun; Sun, Jing Zhi; Tang, Ben Zhong
A macrocyclic 1,4-bis(4-pyridylethynyl)benzene showing unique aggregation-induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10365-10368
7124645 CIFC21 H27 N3 O4I 1 2 116.8244; 6.0896; 41.9414
90; 101.245; 90
4214.6Li, Dan; Wang, Yijie; Wang, Linqing; Wang, Jie; Wang, Pengxin; Wang, Kezhou; Lin, Li; Liu, Dongsheng; Jiang, Xianxing; Yang, Dongxu
Simple magnesium catalyst mediated γ-butyrolactams in desymmetrization of meso-aziridines.
Chemical communications (Cambridge, England), 2016, 52, 9640-9643
7124646 CIFC18 H13 N OP 1 21/c 110.016; 9.223; 13.978
90; 94.662; 90
1287Wu, Shanchao; Liu, Na; Dong, Guoqiang; Ma, Lin; Wang, Shengzheng; Shi, Wencai; Fang, Kun; Chen, Shuqiang; Li, Jian; Zhang, Wannian; Sheng, Chunquan; Wang, Wei
Facile construction of pyrrolo[1,2-b]isoquinolin-10(5H)-ones via a redox-amination-aromatization-Friedel-Crafts acylation cascade reaction and discovery of novel topoisomerase inhibitors.
Chemical communications (Cambridge, England), 2016, 52, 9593-9596
7124647 CIFC36 H45 F12 N7 O4 P2 RuP -18.4109; 11.4169; 11.725
74.801; 76.758; 87.087
1057.59He, Lei; Chen, Xiang; Meng, Zhenyu; Wang, Jintao; Tian, Keyin; Li, Tianhu; Shao, Fangwei
Octahedral ruthenium complexes selectively stabilize G-quadruplexes.
Chemical communications (Cambridge, England), 2016, 52, 8095-8098
7124648 CIFC29 H32 F12 N6 O3 P2 Ru SP 1 21/c 111.5273; 12.9572; 24.0256
90; 97.6261; 90
3556.8He, Lei; Chen, Xiang; Meng, Zhenyu; Wang, Jintao; Tian, Keyin; Li, Tianhu; Shao, Fangwei
Octahedral ruthenium complexes selectively stabilize G-quadruplexes.
Chemical communications (Cambridge, England), 2016, 52, 8095-8098
7124649 CIFC64 H59 Cl2 N6 O14P 21 21 2115.8312; 18.6954; 21.7724
90; 90; 90
6444Liu, Kang; Xiong, Yong; Wang, Zuo-Fei; Tao, Hai-Yan; Wang, Chun-Jiang
Ligand-controlled stereodivergent 1,3-dipolar cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles.
Chemical communications (Cambridge, England), 2016, 52, 9458-9461
7124650 CIFC29 H24 Cl N3 O8P 15.8187; 11.7632; 11.9555
79.413; 87.509; 78.478
788.2Liu, Kang; Xiong, Yong; Wang, Zuo-Fei; Tao, Hai-Yan; Wang, Chun-Jiang
Ligand-controlled stereodivergent 1,3-dipolar cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles.
Chemical communications (Cambridge, England), 2016, 52, 9458-9461
7124651 CIFC25 H31 B Br4 Ga PP 1 21/n 112.2483; 15.51; 15.3013
90; 90.094; 90
2906.8Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124652 CIFC18 H21 B F6 N O4 P S2P b c n30.337; 7.7017; 19.3533
90; 90; 90
4521.8Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124653 CIFC34 H26 B Br4 Ga N PP 1 21/n 112.5932; 14.1435; 19.2716
90; 107.068; 90
3281.3Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124654 CIFC31 H29 B N PP 1 21/n 16.9184; 22.8078; 16.1979
90; 101.927; 90
2500.7Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124655 CIFC33 H30 B F6 N2 O4 P S2P -18.9898; 12.2194; 15.5624
91.453; 91.387; 106.552
1637.28Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124656 CIFC12 H10 N4 O4 ZnP 43 21 27.8691; 7.8691; 22.353
90; 90; 90
1384.2Cepeda, Javier; Sebastian, Eider San; Padro, Daniel; Rodríguez-Diéguez, Antonio; García, Jose A; Ugalde, Jesus M.; Seco, Jose M.
A Zn based coordination polymer exhibiting long-lasting phosphorescence.
Chemical communications (Cambridge, England), 2016, 52, 8671-8674
7124657 CIFC21 H19 B O2P 1 21/a 114.9097; 6.6345; 16.6553
90; 92.822; 90
1645.52Wang, Taisheng; Zhang, Na; Zhang, Ke; Dai, Jingwen; Bai, Wei; Bai, Ruke
Pyrene boronic acid cyclic ester: a new fast self-recovering mechanoluminescent material at room temperature.
Chemical communications (Cambridge, England), 2016, 52, 9679-9682
7124658 CIFC22 H21 B O2P 1 21/c 111.7096; 10.8168; 14.2151
90; 91.551; 90
1799.8Wang, Taisheng; Zhang, Na; Zhang, Ke; Dai, Jingwen; Bai, Wei; Bai, Ruke
Pyrene boronic acid cyclic ester: a new fast self-recovering mechanoluminescent material at room temperature.
Chemical communications (Cambridge, England), 2016, 52, 9679-9682
7124659 CIFC42 F28P 21 21 218.45; 11.0004; 42.68
90; 90; 90
3967.3Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124660 CIFC42 F28P 1 21/n 116.6651; 11.1489; 19.1918
90; 90.213; 90
3565.8Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124661 CIFC42 F28P -112.5285; 17.8163; 24.7339
90.202; 101.264; 90.695
5414Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124662 CIFC44 H61 N O10P -112.0803; 12.3966; 14.483
106.375; 96.145; 108.074
1932.7Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Kalenius, Elina; Ras, Robin H. A.; Rissanen, Kari
2-Methylresorcinarene: a very high packing coefficient in a mono-anion based dimeric capsule and the X-ray crystal structure of the tetra-anion.
Chemical communications (Cambridge, England), 2016, 52, 8115-8118
7124663 CIFC125 H227 N10 O31.5P -113.3506; 15.7389; 17.8889
69.234; 75.125; 87.036
3393.7Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Kalenius, Elina; Ras, Robin H. A.; Rissanen, Kari
2-Methylresorcinarene: a very high packing coefficient in a mono-anion based dimeric capsule and the X-ray crystal structure of the tetra-anion.
Chemical communications (Cambridge, England), 2016, 52, 8115-8118
7124664 CIFC98 H120 N16 O18P 43 21 215.4204; 15.4204; 43.9852
90; 90; 90
10459.2Chung, Mee-Kyung; Lee, Stephen J.; Waters, Marcey L.; Gagné, Michel R
Tetrameric psuedo-peptide receptors with allosteric properties.
Chemical communications (Cambridge, England), 2016, 52, 8103-8106
7124665 CIFC68 H80 N16 O12P 21 21 2122.2194; 26.8073; 30.7909
90; 90; 90
18340.4Chung, Mee-Kyung; Lee, Stephen J.; Waters, Marcey L.; Gagné, Michel R
Tetrameric psuedo-peptide receptors with allosteric properties.
Chemical communications (Cambridge, England), 2016, 52, 8103-8106
7124666 CIFC31 H35 N O2 SiP 1 21/n 110.5604; 12.5871; 20.6289
90; 103.411; 90
2667.3Shinde, Popat S.; Shaikh, Aslam C.; Patil, Nitin T.
Efficient access to alkynylated quinalizinones via the gold(i)-catalyzed aminoalkynylation of alkynes.
Chemical communications (Cambridge, England), 2016, 52, 8152-8155
7124667 CIFC31 H33 N O2 SiP 1 21/c 117.0259; 19.7058; 8.2013
90; 101.746; 90
2694Shinde, Popat S.; Shaikh, Aslam C.; Patil, Nitin T.
Efficient access to alkynylated quinalizinones via the gold(i)-catalyzed aminoalkynylation of alkynes.
Chemical communications (Cambridge, England), 2016, 52, 8152-8155
7124668 CIFC78 H68 Cl2 F6 N4 Pt2 S2P 1 21/c 112.1203; 21.6638; 27.3069
90; 91.372; 90
7168Boixel, Julien; Zhu, Yifan; Le Bozec, Hubert; Benmensour, Mohamed Ali; Boucekkine, Abdou; Wong, Keith Man-Chung; Colombo, Alessia; Roberto, Dominique; Guerchais, Véronique; Jacquemin, Denis
Contrasted photochromic and luminescent properties in dinuclear Pt(ii) complexes linked through a central dithienylethene unit.
Chemical communications (Cambridge, England), 2016, 52, 9833-9836
7124669 CIFC34 H58 F4 Mo N6 P4P 1 n 110.2417; 18.3288; 21.5881
90; 95.3341; 90
4034.93Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124670 CIFC34 H58 Cr F4 N6 P4P 1 21/c 110.8985; 13.441; 13.4741
90; 101.392; 90
1934.89Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124671 CIFC34 H58 Cr F4 N6 P4P 1 21/n 110.301; 18.8047; 20.7192
90; 93.77; 90
4004.77Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124672 CIFC34 H58 F4 N6 P4 WP 1 n 110.2469; 18.3292; 21.5498
90; 95.426; 90
4029.29Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124673 CIFC105 H105 N5P b c a32.7165; 16.1948; 39.103
90; 90; 90
20718.2Qiao, Bo; Anderson, Joseph R.; Pink, Maren; Flood, Amar H.
Size-matched recognition of large anions by cyanostar macrocycles is saved when solvent-bias is avoided.
Chemical communications (Cambridge, England), 2016, 52, 8683-8686
7124674 CIFC17 H13 N O2P 1 21/c 18.9419; 20.446; 7.9832
90; 111.874; 90
1354.5Li, Jiu-Ling; Li, Wei-Ze; Wang, Ying-Chun; Ren, Qiu; Wang, Heng-Shan; Pan, Ying-Ming
Palladium(ii)-catalyzed C-C and C-O bond formation for the synthesis of C1-benzoyl isoquinolines from isoquinoline N-oxides and nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10028-10031
7124675 CIFC9 H9 N O3P 21 21 215.43; 7.8748; 20.6997
90; 90; 90
885.12Vidal-Albalat, A; Swiderek, K.; Izquierdo, J.; Rodríguez, S; Moliner, V.; González, F V
Catalytic enantioselective epoxidation of nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10060-10063
7124676 CIFC14 H11 N O3P 1 21 18.6028; 6.2292; 11.4861
90; 94.415; 90
613.7Vidal-Albalat, A; Swiderek, K.; Izquierdo, J.; Rodríguez, S; Moliner, V.; González, F V
Catalytic enantioselective epoxidation of nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10060-10063
7124677 CIFC42 H76 Cl3 Dy O35P -112.741; 13.235; 17.923
89.94; 85.741; 86.594
3008.6Al Hareri, M.; Gavey, E. L.; Regier, J.; Ras Ali, Z.; Carlos, L. D.; Ferreira, R. A. S.; Pilkington, M.
Encapsulation of a [Dy(OH2)8](3+) cation: magneto-optical and theoretical studies of a caged, emissive SMM.
Chemical communications (Cambridge, England), 2016, 52, 11335-11338
7124678 CIFC19 H20 N2 O4P 1 21/n 17.791; 13.1164; 16.9526
90; 96.895; 90
1719.86Briones, John F.; Basarab, Gregory S.
Expedient synthesis of tetrahydroquinoline-3-spirohydantoin derivatives via the Lewis acid-catalyzed tert-amino effect reaction.
Chemical communications (Cambridge, England), 2016, 52, 8541-8544
7124679 CIFC52 H62 F12 N2 O14 P2P -113.595; 20.8235; 23.687
74.639; 84.656; 76.364
6280.5Cheng, Ming; Yao, Chenhao; Cao, Yihan; Wang, Qi; Pan, Yi; Jiang, Juli; Wang, Leyong
4-Methylcoumarin-bridged fluorescent responsive cryptand: from [2+2] photodimerization to supramolecular polymer.
Chemical communications (Cambridge, England), 2016, 52, 8715-8718
7124680 CIFC26 H24 N2 O3P 1 21/n 19.1828; 9.0675; 26.107
90; 91.376; 90
2173.2An, Yuanyuan; Xia, Hongguang; Wu, Jie
Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10415-10418
7124681 CIFC26 H24 N2 O3C 1 2/c 138.327; 12.158; 9.715
90; 95.51; 90
4506An, Yuanyuan; Xia, Hongguang; Wu, Jie
Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10415-10418
7124682 CIFC66 H57 Ce F15 N3 O2 P2 S6 Si3P -113.5981; 14.8764; 21.2531
75.799; 87.413; 75.372
4032.2Yin, Haolin; Carroll, Patrick J.; Schelter, Eric J.
Reactions of a cerium(iii) amide with heteroallenes: insertion, silyl-migration and de-insertion.
Chemical communications (Cambridge, England), 2016, 52, 9813-9816
7124683 CIFC48 H69 Ce F15 N9 Si3C 1 2/c 123.8; 12.7595; 40.727
90; 97.599; 90
12259.2Yin, Haolin; Carroll, Patrick J.; Schelter, Eric J.
Reactions of a cerium(iii) amide with heteroallenes: insertion, silyl-migration and de-insertion.
Chemical communications (Cambridge, England), 2016, 52, 9813-9816
7124684 CIFC21 H16 OP 1 21/c 113.33; 15.13; 7.59
90; 100.77; 90
1504Jin, Ruiwen; Chen, Yiyong; Liu, Wangsheng; Xu, Dawen; Li, Yawei; Ding, Aishun; Guo, Hao
Merging photoredox catalysis with Lewis acid catalysis: activation of carbon-carbon triple bonds.
Chemical communications (Cambridge, England), 2016, 52, 9909-9912
7124685 CIFC16 H14 O5P 1 21/c 18.4933; 10.7736; 14.1815
90; 92.817; 90
1296.1Chen, Dong; Xu, Wen-Dan; Liu, Hao-Miao; Li, Ming-Ming; Yan, Yong-Min; Li, Xiao-Nian; Li, Yan; Cheng, Yong-Xian; Qin, Hong-Bo
Enantioselective total synthesis of (+)-Lingzhiol via tandem semipinacol rearrangement/Friedel-Crafts type cyclization.
Chemical communications (Cambridge, England), 2016, 52, 8561-8564
7124686 CIFC16 H13 Br O5P 21 21 218.1765; 10.7366; 16.4944
90; 90; 90
1448Chen, Dong; Xu, Wen-Dan; Liu, Hao-Miao; Li, Ming-Ming; Yan, Yong-Min; Li, Xiao-Nian; Li, Yan; Cheng, Yong-Xian; Qin, Hong-Bo
Enantioselective total synthesis of (+)-Lingzhiol via tandem semipinacol rearrangement/Friedel-Crafts type cyclization.
Chemical communications (Cambridge, England), 2016, 52, 8561-8564
7124687 CIFC15 H14 N2 O3P 1 21/c 19.7836; 19.184; 7.2536
90; 110.113; 90
1278.4Alcaide, Benito; Almendros, Pedro; Cembellín, Sara; Fernández, Israel; Martínez Del Campo, Teresa
Stereoselective synthesis of strained cage compounds via gold-catalyzed allene functionalization.
Chemical communications (Cambridge, England), 2016, 52, 10265-10268
7124688 CIFC2 H4 N6 O2C 1 2/c 112.8179; 4.8463; 18.2472
90; 100.494; 90
1114.55He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124689 CIFC3 H4 N6 O4P n a 2112.7338; 9.977; 5.136
90; 90; 90
652.5He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124690 CIFC2 H4 N6 O2P 1 21 13.5852; 16.3937; 9.4278
90; 98.448; 90
548.1He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124691 CIFC2 H4 N6 O2P 1 21/n 18.0055; 6.4742; 10.7844
90; 96.224; 90
555.65He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124692 CIFC H N O SP 1 21/c 115.924; 8.289; 15.498
90; 99.13; 90
2019.7Wang, Sasa; Chen, Xinzheng; Ao, Qiaoqiao; Wang, Huifei; Zhai, Hongbin
Decarboxylative Csp(3)-Csp(3) coupling for benzylation of unstable ketone enolates: synthesis of p-(acylethyl)phenols.
Chemical communications (Cambridge, England), 2016, 52, 9454-9457
7124693 CIFC22 H26 F6 N2 Rh SbP 1 21/n 112.6576; 14.5099; 13.416
90; 106.523; 90
2362.24Hou, Wei; Yang, Yaxi; Wu, Yunxiang; Feng, Huijin; Li, Yuanchao; Zhou, Bing
Rhodium(iii)-catalyzed alkylation of primary C(sp(3))-H bonds with α-diazocarbonyl compounds.
Chemical communications (Cambridge, England), 2016, 52, 9672-9675
7124694 CIFC64 H256 Co16 N64 Nb32 O205 S4 V39P n m a23.9036; 21.2261; 18.0968
90; 90; 90
9182Hu, Ju-Fang; Han, Tian; Chi, Ying-Nan; Lin, Zheng-Guo; Xu, Yan-Qing; Yang, Song; Wei, Ding; Zheng, Yan-Zhen; Hu, Chang-Wen
Sulfur-centred polyoxoniobate-based 3D organic-inorganic hybrid compound and its magnetic behavior.
Chemical communications (Cambridge, England), 2016, 52, 10846-10849
7124695 CIFC21 H30 Li N3P 1 21 110.1048; 12.9834; 15.341
90; 102.567; 90
1964.4Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124696 CIFC38 H48 Li2 O2 P2C 1 c 110.592; 18.626; 9.119
90; 95.24; 90
1791.5Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124697 CIFC24 H37 Li N4P 1 21/c 110.1275; 8.6095; 27.5008
90; 91.558; 90
2396.98Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124698 CIFC51 H57 N9 O6P 1 21/c 126.8526; 13.8261; 26.9848
90; 111.812; 90
9301.3Pfletscher, Michael; Wölper, Christoph; Gutmann, Jochen S.; Mezger, Markus; Giese, Michael
A modular approach towards functional supramolecular aggregates - subtle structural differences inducing liquid crystallinity.
Chemical communications (Cambridge, England), 2016, 52, 8549-8552
7124699 CIFC25 H39 Br Co P2 SiP 1 21/n 112.1709; 14.4443; 15.9292
90; 97.855; 90
2774.1Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124700 CIFC30 H41 Br Co P2 SiP 1 21/c 111.0181; 18.0167; 15.4914
90; 98.734; 90
3039.5Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124701 CIFC25 H42 Br4 Co P2 SiP b c a17.6793; 16.195; 23.2286
90; 90; 90
6650.7Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124702 CIFC30 H42 P2 SiP 1 21/c 113.1415; 14.3471; 16.6192
90; 112.798; 90
2888.6Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124703 CIFC25 H40 Br2 Co P2 SiP 1 21/c 117.1233; 9.7303; 17.9002
90; 110.977; 90
2784.8Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124704 CIFC12 H32 Br4 Co N2P b c a12.3228; 13.1299; 26.5742
90; 90; 90
4299.6Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124705 CIFC30 H42 Br2 Co P2 SiP 1 21/c 117.387; 11.5644; 15.641
90; 92.891; 90
3140.9Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124706 CIFC62 H59 F12 N11 O11 P2 Ru3P -115.8008; 16.2412; 19.6284
107.027; 102.696; 109.127
4263.5Zhang, Biaobiao; Li, Fei; Zhang, Rong; Ma, Chengbing; Chen, Lin; Sun, Licheng
Characterization of a trinuclear ruthenium species in catalytic water oxidation by Ru(bda)(pic)2 in neutral media.
Chemical communications (Cambridge, England), 2016, 52, 8619-8622
7124707 CIFC47 H34 N6 O3P c a 2126.853; 10.1988; 27.005
90; 90; 90
7395.8Luciano, M.; Tardie, W.; Zeller, M.; Brückner, C
Supersizing pyrrole-modified porphyrins by reversal of the 'breaking and mending' strategy.
Chemical communications (Cambridge, England), 2016, 52, 10133-10136
7124708 CIFC24 H20 O3P 1 21/c 111.887; 10.4572; 14.8193
90; 100.36; 90
1812.08Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124709 CIFC24 H20 O4P 1 21/n 112.6203; 10.0898; 15.4768
90; 106.857; 90
1886.08Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124710 CIFC23 H16 Br2 O4P -18.0971; 11.2035; 12.1077
87.795; 71.122; 74.233
998.7Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124711 CIFC18 H22 Cl2 O6P c a 2112.3202; 4.6501; 32.022
90; 90; 90
1834.5Kaufmann, Lena; Kennedy, Stuart R.; Jones, Christopher D.; Steed, Jonathan W.
Cavity-containing supramolecular gels as a crystallization tool for hydrophobic pharmaceuticals.
Chemical communications (Cambridge, England), 2016, 52, 10113-10116
7124712 CIFC19 H24 N O6 P SP 319.7393; 9.7393; 18.532
90; 90; 120
1522.3Yan, Zhong; Wu, Bo; Gao, Xiang; Zhou, Yong-Gui
Enantioselective synthesis of quaternary α-aminophosphonates by Pd-catalyzed arylation of cyclic α-ketiminophosphonates with arylboronic acids.
Chemical communications (Cambridge, England), 2016, 52, 10882-10885
7124713 CIFC36 H41 N3 O10 S3P 6314.5223; 14.5223; 10.2703
90; 90; 120
1875.8Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124714 CIFC288 H264 Ag12 N24 O96 Re12 S24F 4 3 235.7237; 35.7237; 35.7237
90; 90; 90
45590Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124715 CIFC288 H264 Ag12 B12 F48 N24 O48 S24F 4 3 235.4548; 35.4548; 35.4548
90; 90; 90
44568.2Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124716 CIFC39 H42 N6 O12 S3R 3 :H28.138; 28.138; 4.4445
90; 90; 120
3047.5Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124717 CIFC42.98 H46.96 Ag Cl3.96 N3 O4 PP 21 21 2114.018; 17.0222; 19.3743
90; 90; 90
4623.04de la Campa, Raquel; Gammack Yamagata, Adam D.; Ortín, Irene; Franchino, Allegra; Thompson, Amber L.; Odell, Barbara; Dixon, Darren J.
Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketimines.
Chemical communications (Cambridge, England), 2016, 52, 10632-10635
7124718 CIFC28 H20 O2P 1 21 19.4569; 19.807; 21.941
90; 96.83; 90
4080.7Zhang, Xin; Chen, Lin; Chen, Xiang-Yu; Zhang, Hanzhi; Yang, Liuqing; Yang, Fengchun
Effective separation of single-walled carbon nanotubes and their very different electrochemical behaviours.
Chemical communications (Cambridge, England), 2016, 52, 9287-9290
7124719 CIFC20 H14 O2P 3110.784; 10.784; 10.863
90; 90; 120
1094.1Zhang, Xin; Chen, Lin; Chen, Xiang-Yu; Zhang, Hanzhi; Yang, Liuqing; Yang, Fengchun
Effective separation of single-walled carbon nanotubes and their very different electrochemical behaviours.
Chemical communications (Cambridge, England), 2016, 52, 9287-9290
7124720 CIFC39 H84 Ge10 N7 O12 Rb2P -110.8759; 13.4395; 21.2985
85.907; 88.885; 88.995
3104.2Bentlohner, Manuel M.; Fischer, Christina; Fässler, Thomas F
Synthesis and characterization of pristine closo-[Ge10](2.).
Chemical communications (Cambridge, England), 2016, 52, 9841-9843
7124721 CIFC38 H32 N4 O2P 1 21/n 111.4777; 15.9325; 17.0968
90; 103.233; 90
3043.4Krick, Marcel; Holstein, Julian; Würtele, Christian; Clever, Guido H.
Endohedral dynamics of push-pull rotor-functionalized cages.
Chemical communications (Cambridge, England), 2016, 52, 10411-10414
7124722 CIFC46 H32 D8 N4 O3P -19.7141; 13.7175; 13.8642
92.206; 97.198; 98.744
1808.46Krick, Marcel; Holstein, Julian; Würtele, Christian; Clever, Guido H.
Endohedral dynamics of push-pull rotor-functionalized cages.
Chemical communications (Cambridge, England), 2016, 52, 10411-10414
7124723 CIFC40 H43 Br6 N9 P2P 1 21/c 115.79; 17.796; 16.457
90; 104.672; 90
4473.6Đorđević, Nemanja; Ganguly, Rakesh; Petković, Milena; Vidović, Dragoslav
Bis(carbodicarbene)phosphenium trication: the case against hypervalency.
Chemical communications (Cambridge, England), 2016, 52, 9789-9792
7124724 CIFC84 H93.9 Br2 F24 N19.05 O0.47 P2 Sb4P -112.1048; 13.7318; 16.1379
108.884; 98.2298; 102.753
2407.61Đorđević, Nemanja; Ganguly, Rakesh; Petković, Milena; Vidović, Dragoslav
Bis(carbodicarbene)phosphenium trication: the case against hypervalency.
Chemical communications (Cambridge, England), 2016, 52, 9789-9792
7124725 CIFC38 H26 F2P -19.3318; 16.3035; 18.6019
94.673; 90.768; 100.362
2773.6Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124726 CIFC37 H28 Cl2 N2P 1 21/n 110.2875; 9.5469; 30.516
90; 90.739; 90
2996.8Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124727 CIFC40 H32 S2P 1 21/c 19.6317; 9.5173; 33.0419
90; 96.269; 90
3010.8Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124728 CIFC40 H32 S2P 1 21/c 116.2653; 11.5962; 18.2995
90; 115.9; 90
3104.9Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124729 CIFC35 H36 Br Cl4 Ir N2P 1 21/n 111.5187; 12.8279; 23.1283
90; 96.529; 90
3395.29Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124730 CIFC41 H36 Br Ir N2P 21 21 2113.7643; 14.1122; 16.9238
90; 90; 90
3287.4Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124731 CIFC33 H32 Br Ir N2P 21 21 219.2873; 16.9087; 17.495
90; 90; 90
2747.3Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124732 CIFC20 H20 N2 O2P 1 21/n 19.797; 9.3477; 19.3037
90; 103.385; 90
1719.8Kim, Won Young; Shi, Hu; Jung, Hyo Sung; Cho, Daeheum; Verwilst, Peter; Lee, Jin Yong; Kim, Jong Seung
Coumarin-decorated Schiff base hydrolysis as an efficient driving force for the fluorescence detection of water in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 8675-8678
7124733 CIFC19 H19 N3 O2P 1 21/c 17.9685; 10.0372; 20.628
90; 91.778; 90
1649.1Kim, Won Young; Shi, Hu; Jung, Hyo Sung; Cho, Daeheum; Verwilst, Peter; Lee, Jin Yong; Kim, Jong Seung
Coumarin-decorated Schiff base hydrolysis as an efficient driving force for the fluorescence detection of water in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 8675-8678
7124734 CIFC14 H14 F N O3P 21 21 218.2754; 12.082; 13.332
90; 90; 90
1333Liu, Jianchao; Xu, Xiaobing; Li, Jiuyi; Liu, Bo; Jiang, Huanfeng; Yin, Biaolin
Palladium-catalyzed dearomatizing 2,5-alkoxyarylation of furan rings: diastereospecific access to spirooxindoles.
Chemical communications (Cambridge, England), 2016, 52, 9550-9553
7124735 CIFC17 H19 N O4P 1 21/n 114.349; 7.2477; 14.692
90; 105.12; 90
1475Liu, Jianchao; Xu, Xiaobing; Li, Jiuyi; Liu, Bo; Jiang, Huanfeng; Yin, Biaolin
Palladium-catalyzed dearomatizing 2,5-alkoxyarylation of furan rings: diastereospecific access to spirooxindoles.
Chemical communications (Cambridge, England), 2016, 52, 9550-9553
7124736 CIFC14 H12 N2 O2P -16.0661; 7.8841; 12.8564
91.07; 94.098; 97.33
608.04Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124737 CIFC16 H16 N2 O2P -19.2837; 9.9699; 9.9836
92.401; 112.162; 116.147
743.75Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124738 CIFC18 H16 N2 O2 SP 1 21/c 18.4209; 28.5775; 6.9049
90; 101.544; 90
1628.04Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124739 CIFC18 H17 N O4 SP -16.5556; 11.4813; 12.6356
113.781; 98.198; 93.092
854.85Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124740 CIFC162 H66 Cl8 N2 O14P -116.2768; 16.3003; 23.6077
94.242; 95.588; 115.579
5575.6Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784
7124741 CIFC156 H51 Cl8 O12P -113.8208; 17.4812; 24.2884
76.082; 87.204; 70.991
5382.5Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784
7124742 CIFC93 H55 Cl6 N O13P -112.0893; 17.1939; 24.6711
104.88; 90.051; 98.347
4899.8Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784
7124743 CIFC18 H23 Cl2 N O2 RuP 1 21/n 113.7506; 7.06591; 19.8176
90; 109.476; 90
1815.31Ma, Lili; Ma, Rong; Wang, Zhigang; Yiu, Shek-Man; Zhu, Guangyu
Heterodinuclear Pt(iv)-Ru(ii) anticancer prodrugs to combat both drug resistance and tumor metastasis.
Chemical communications (Cambridge, England), 2016, 52, 10735-10738
7124744 CIFC9.5 H20 Cl3 N3 O4 Pt S0.5P -18.8701; 12.497; 17.2431
92.445; 103.722; 104.921
1783.24Ma, Lili; Ma, Rong; Wang, Zhigang; Yiu, Shek-Man; Zhu, Guangyu
Heterodinuclear Pt(iv)-Ru(ii) anticancer prodrugs to combat both drug resistance and tumor metastasis.
Chemical communications (Cambridge, England), 2016, 52, 10735-10738
7124745 CIFC28 H46 Ir O2 P3P 1 21/c 112.8054; 12.7662; 20.774
90; 104.821; 90
3283.1Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124746 CIFC29 H48 Ir O2 P3P -110.2215; 11.864; 16.0253
103.712; 100.633; 93.622
1843.9Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124747 CIFC31 H52 Ir O2 P3C 1 2/c 110.5197; 20.993; 30.334
90; 99.463; 90
6607.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124748 CIFC28 H48 Ir O2 P3P 1 21/c 112.8121; 12.7747; 20.771
90; 104.573; 90
3290.2Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124749 CIFC29 H50 Ir O2 P3P -110.23; 11.9105; 15.9818
103.735; 100.957; 93.714
1844.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124750 CIFC36 H66 Ir O2 P3P -110.901; 12.686; 15.2272
78.184; 72.973; 73.418
1912.8Paul, Ursula S. D.; Braunschweig, Holger; Radius, Udo
Iridium-catalysed dehydrocoupling of aryl phosphine-borane adducts: synthesis and characterisation of high molecular weight poly(phosphinoboranes).
Chemical communications (Cambridge, England), 2016, 52, 8573-8576
7124751 CIFC40 H30 N2 O2P -17.2874; 14.4206; 15.0229
64.011; 79.684; 83.373
1394.93Das, Amrita; Ghosh, Indrajit; König, Burkhard
Synthesis of pyrrolo[1,2-a]quinolines and ullazines by visible light mediated one- and twofold annulation of N-arylpyrroles with arylalkynes.
Chemical communications (Cambridge, England), 2016, 52, 8695-8698
7124752 CIFC20 H14 Cl N OP 1 21/c 116.4245; 7.25848; 13.1153
90; 108.39; 90
1483.72Das, Amrita; Ghosh, Indrajit; König, Burkhard
Synthesis of pyrrolo[1,2-a]quinolines and ullazines by visible light mediated one- and twofold annulation of N-arylpyrroles with arylalkynes.
Chemical communications (Cambridge, England), 2016, 52, 8695-8698
7124753 CIFC25 H24 Cl N3 OP 21 21 2110.3206; 11.6585; 18.3971
90; 90; 90
2213.59Ma, Jiajia; Harms, Klaus; Meggers, Eric
Enantioselective rhodium/ruthenium photoredox catalysis en route to chiral 1,2-aminoalcohols.
Chemical communications (Cambridge, England), 2016, 52, 10183-10186
7124754 CIFC48.4 H49.6 Cl2 F6 N4 O P Rh S2P -117.1583; 17.7095; 18.8292
66.918; 69.054; 76.796
4889.7Ma, Jiajia; Harms, Klaus; Meggers, Eric
Enantioselective rhodium/ruthenium photoredox catalysis en route to chiral 1,2-aminoalcohols.
Chemical communications (Cambridge, England), 2016, 52, 10183-10186
7124755 CIFC16 H46 Mo2 N2 Ni2 O16P 1 21/n 112.0683; 10.1464; 12.6315
90; 91.893; 90
1545.88Kuznetsov, Denis A.; Konev, Dmitry V.; Komarova, Natal'ya S.; Ionov, Andrey M.; Mozhchil, Rais N.; Fedyanin, Ivan V.
Ni-based heterogeneous catalyst from a designed molecular precursor for the efficient electrochemical water oxidation.
Chemical communications (Cambridge, England), 2016, 52, 9255-9258
7124756 CIFC106 H74.5 B3.5 F13.88 I0.5 N21 O4 Pd2C 1 2/c 142.9184; 20.7337; 28.9827
90; 125.086; 90
21104.1Li, Yu-Hao; Jiang, Ji-Jun; Fan, Yan-Zhong; Wei, Zhang-Wen; Chen, Cheng-Xia; Yu, Hui-Juan; Zheng, Shao-Ping; Fenske, Dieter; Su, Cheng-Yong; Barboiu, Mihail
Solvent- and anion-induced interconversions of metal-organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8745-8748
7124757 CIFC98 H75 B4 F16 N17 O4 Pd2C 1 2/c 143.0462; 20.744; 28.9748
90; 125.766; 90
20993.7Li, Yu-Hao; Jiang, Ji-Jun; Fan, Yan-Zhong; Wei, Zhang-Wen; Chen, Cheng-Xia; Yu, Hui-Juan; Zheng, Shao-Ping; Fenske, Dieter; Su, Cheng-Yong; Barboiu, Mihail
Solvent- and anion-induced interconversions of metal-organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8745-8748
7124758 CIFC106 H56 N6 O2P -116.792; 19.978; 23.171
102.93; 101.11; 112.55
6654Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124759 CIFC110 H60 N2 O2P b c n31.58; 18.296; 20.075
90; 90; 90
11599Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124760 CIFC116 H66 N2 O2I 41/a c d :239.28; 39.28; 39.78
90; 90; 90
61377Burgun, Alexandre; Valente, Peter; Evans, Jack D.; Huang, David M.; Sumby, Christopher J.; Doonan, Christian J.
Endohedrally functionalised porous organic cages.
Chemical communications (Cambridge, England), 2016, 52, 8850-8853
7124761 CIFC17 H21 N O3P -18.0877; 8.9461; 10.5339
93.626; 92.834; 94.652
756.99Kaishap, Partha Pratim; Sarma, Bipul; Gogoi, Sanjib
The amide C-N bond of isatins as the directing group and the internal oxidant in Ru-catalyzed C-H activation and annulation reactions: access to 8-amido isocoumarins.
Chemical communications (Cambridge, England), 2016, 52, 9809-9812
7124762 CIFC798 H638 Ca17 N72 O322P 1 21/c 144.593; 51.642; 38.959
90; 107.1; 90
85751Mandal, Pradeep K.; Kauffmann, Brice; Destecroix, Harry; Ferrand, Yann; Davis, Anthony P.; Huc, Ivan
Crystal structure of a complex between β-glucopyranose and a macrocyclic receptor with dendritic multicharged water solubilizing chains.
Chemical communications (Cambridge, England), 2016, 52, 9355-9358
7124763 CIFC54 H72 Br N9 O8P 1 21/n 112.865; 18.623; 22.483
90; 90.143; 90
5387Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124764 CIFC54 H72 Cl N9 O8P 1 21/n 113.0109; 18.833; 22.702
90; 90.423; 90
5562.6Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124765 CIFC54 H72 I N9 O8P c a 2121.335; 15.168; 37.948
90; 90; 90
12280Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124766 CIFC54 H72 Cl0.63 F0.37 N9 O8P 1 21/n 112.9168; 18.9009; 22.5896
90; 90.65; 90
5514.7Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124767 CIFC72 H116 Cl3 N10 O18 P2P -118.5581; 19.3272; 23.1017
86.218; 87.845; 81.721
8178.5Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124768 CIFC58 H60 Cl6 N10 O14P -111.224; 13.636; 22.374
101.011; 98.751; 91.381
3317Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124769 CIFC70 H110 N10 O16 S2P 1 21/n 114.239; 21.245; 24.51
90; 92.19; 90
7409Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124770 CIFC54 H72 N10 O11P 1 21/n 112.8705; 18.6776; 23.141
90; 90.418; 90
5562.7Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124771 CIFC56 H75 N9 O10P 1 21/n 112.773; 19.067; 23.221
90; 91.69; 90
5653Kim, Ajeong; Ali, Rashid; Park, Seok Ho; Kim, Yong-Hoon; Park, Jung Su
Probing and evaluating anion-π interaction in meso-dinitrophenyl functionalized calix[4]pyrrole isomers.
Chemical communications (Cambridge, England), 2016, 52, 11139-11142
7124772 CIFC87 H129 N4 O16 Zn2P -114.3039; 17.603; 20.104
64.648; 74.715; 86.046
4407.1Gonawala, Sunalee; Leopoldino, Verônica R; Kpogo, Kenneth; Verani, Cláudio N
Langmuir-Blodgett films of salophen-based metallosurfactants as surface pretreatment coatings for corrosion mitigation.
Chemical communications (Cambridge, England), 2016, 52, 11155-11158
7124773 CIFC44 H28 Br4 N8 O12 Pb4 PdP -17.634; 13.084; 14.166
105.216; 105.376; 94.884
1298.1Dong, Ying; Li, Yue; Wei, Yong-Liang; Wang, Jian-Cheng; Ma, Jian-Ping; Ji, Jun; Yao, Bing-Jian; Dong, Yu-Bin
A N-heterocyclic tetracarbene Pd(ii) moiety containing a Pd(ii)-Pb(ii) bimetallic MOF for three-component cyclotrimerization via benzyne.
Chemical communications (Cambridge, England), 2016, 52, 10505-10508
7124774 CIFC126 H250 N10 O102 S4 V24I -4 3 m21.927; 21.927; 21.927
90; 90; 90
10542Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124775 CIFC123.5 H250.5 N15.5 O101.5 S4 V24I -4 3 m21.841; 21.841; 21.841
90; 90; 90
10419Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124776 CIFC121 H152 Br6 O101 S4 V24I -4 3 m22.108; 22.108; 22.108
90; 90; 90
10806Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124777 CIFC106.5 H221.5 N8.5 O100.5 S4 V24I -421.848; 21.848; 19.081
90; 90; 90
9108Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124778 CIFC183.5 H280.5 N9.5 O101.5 S4 V24I -428.983; 28.983; 25.744
90; 90; 90
21625Zhang, Yu-Teng; Wang, Xin-Long; Li, Shuang-Bao; Gong, Ya-Ru; Song, Bai-Qiao; Shao, Kui-Zhan; Su, Zhong-Min
Anderson-like alkoxo-polyoxovanadate clusters serving as unprecedented second building units to construct metal-organic polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 9632-9635
7124779 CIFC48 H69 N O6 Si2P 21 21 2110.50766; 14.738; 35.4339
90; 90; 90
5487.36Gan, Zubao; Chu, Zhiwen; Hu, Jia; Su, Zhishan; Hu, Changwei; Gao, Lu; Song, Zhenlei
Tunable reactivity of geminal bis(silyl) enol derivatives leading to selective exo-IEDDA or Sakurai allylation with a β,γ-unsaturated ketoester.
Chemical communications (Cambridge, England), 2016, 52, 10137-10140
7124780 CIFC226 H226 Cl16 F24 N26 O68 Pd4 S8P -117.8945; 19.5103; 20.507
90.134; 99.808; 110.635
6587.2Szalóki, György; Croué, Vincent; Allain, Magali; Goeb, Sébastien; Sallé, Marc
Neutral versus polycationic coordination cages: a comparison regarding neutral guest inclusion.
Chemical communications (Cambridge, England), 2016, 52, 10012-10015
7124781 CIFC210 H199 Cl16 F24 N21 O32 Pd4 S8P 1 21/c 116.3201; 29.0112; 27.2545
90; 105.883; 90
12411.4Szalóki, György; Croué, Vincent; Allain, Magali; Goeb, Sébastien; Sallé, Marc
Neutral versus polycationic coordination cages: a comparison regarding neutral guest inclusion.
Chemical communications (Cambridge, England), 2016, 52, 10012-10015
7124782 CIFC21 H28 B2 F8 N2 O2P -16.8103; 12.0335; 15.7289
70.566; 78.711; 88.033
1191.39Catalán, Aldo C; Tiburcio, Jorge
Self-assembly of pseudo-rotaxane and rotaxane complexes using an electrostatic slippage approach.
Chemical communications (Cambridge, England), 2016, 52, 9526-9529
7124783 CIFC24 H25 N3 O4I 1 2/a 122.3944; 10.7588; 19.4913
90; 105.44; 90
4526.69Ren, Shichao; Song, Shengjin; Ye, Lu; Feng, Chao; Loh, Teck-Peng
Copper-catalyzed oxyamination of electron-deficient alkenes with N-acyloxyamines.
Chemical communications (Cambridge, England), 2016, 52, 10373-10376
7124784 CIFC118 H108 Cl6 Co3 Ir2 N24 O29C 1 2/c 131.23; 17.481; 26.747
90; 102.845; 90
14237Li, Xuezhao; Wu, Jinguo; Chen, Liyong; Zhong, Xiaoming; He, Cheng; Zhang, Rong; Duan, Chunying
Engineering an iridium-containing metal-organic molecular capsule for induced-fit geometrical conversion and dual catalysis.
Chemical communications (Cambridge, England), 2016, 52, 9628-9631
7124785 CIFC121 H107 Cl4 Co3 Ir2 N25 O22P 43 21 220.973; 20.973; 30.067
90; 90; 90
13225Li, Xuezhao; Wu, Jinguo; Chen, Liyong; Zhong, Xiaoming; He, Cheng; Zhang, Rong; Duan, Chunying
Engineering an iridium-containing metal-organic molecular capsule for induced-fit geometrical conversion and dual catalysis.
Chemical communications (Cambridge, England), 2016, 52, 9628-9631
7124786 CIFC29 H20 OP -19.5812; 10.2719; 12.371
114.389; 96.569; 105.237
1034.9Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124787 CIFC33 H31 N OP -19.688; 9.724; 14.142
92.269; 93.742; 99.428
1309.8Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124788 CIFC29 H22 O2P -18.5465; 11.111; 12.403
109.873; 101.743; 90.448
1080.7Chen, Ling; Cao, Jian; Xu, Zheng; Zheng, Zhan-Jiang; Cui, Yu-Ming; Xu, Li-Wen
Lewis acid catalyzed [2+2] cycloaddition of ynamides and propargyl silyl ethers: synthesis of alkylidenecyclobutenones and their reactivity in ring-opening and ring expansion.
Chemical communications (Cambridge, England), 2016, 52, 9574-9577
7124789 CIFC21 H23 N O4C 1 c 18.12275; 19.6409; 11.31395
90; 92.5884; 90
1803.16Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124790 CIFC22 H25 N O4P 1 21/c 111.06181; 9.47232; 18.5215
90; 97.9172; 90
1922.2Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124791 CIFC21 H22 F3 N O4P -111.7112; 15.2229; 22.2156
78.173; 76.486; 89.949
3764.55Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124792 CIFC21 H23 N O4P b c n22.8332; 9.84289; 16.7747
90; 90; 90
3770.02Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124793 CIFC22 H28 N2 O4P 1 21/c 120.1612; 9.24516; 10.76938
90; 96.7643; 90
1993.37Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124794 CIFC22 H25 N O4P 1 21/n 19.8686; 23.9445; 33.107
90; 90.065; 90
7823.1Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124795 CIFC22 H28 N2 O4P 1 21 19.67334; 11.20885; 18.6086
90; 94.3265; 90
2011.93Firth, James D.; Craven, Philip G. E.; Lilburn, Matthew; Pahl, Axel; Marsden, Stephen P.; Nelson, Adam
A biosynthesis-inspired approach to over twenty diverse natural product-like scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 9837-9840
7124796 CIFC14 H23 O6 P Si2 WP 21 21 219.7786; 9.9521; 21.9977
90; 90; 90
2140.76Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124797 CIFC14 H24 I O6 P Si2 WP -19.179; 10.433; 14.066
86.293; 81.81; 65.584
1214Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124798 CIFC15 H25 O6 P Si2 WP 21 21 219.2343; 10.3502; 23.1652
90; 90; 90
2214.06Kyri, A. W.; Schnakenburg, G.; Streubel, R.
A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.
Chemical communications (Cambridge, England), 2016, 52, 8593-8595
7124799 CIFC49 H71 Br2 Fe3 N6 O SP -111.9958; 12.5852; 17.0913
104.697; 102.692; 91.2459
2426.6Lee, Yousoon; Abboud, Khalil A.; García-Serres, Ricardo; Murray, Leslie J.
A three-coordinate Fe(ii) center within a [3Fe-(μ3-S)] cluster that provides an accessible coordination site.
Chemical communications (Cambridge, England), 2016, 52, 9295-9298
7124800 CIFC50.88 H74.76 Br1.03 Fe3 N6 O1.47 SP -111.651; 12.6465; 17.0493
94.401; 95.909; 96.266
2473.99Lee, Yousoon; Abboud, Khalil A.; García-Serres, Ricardo; Murray, Leslie J.
A three-coordinate Fe(ii) center within a [3Fe-(μ3-S)] cluster that provides an accessible coordination site.
Chemical communications (Cambridge, England), 2016, 52, 9295-9298
7124801 CIFC31 H29 Br2 N O4P 4312.339; 12.339; 18.0683
90; 90; 90
2750.9Li, Meng; Lu, Hai-Yan; Zhang, Chao; Shi, Lin; Tang, Zhiyong; Chen, Chuan-Feng
Helical aromatic imide based enantiomers with full-color circularly polarized luminescence.
Chemical communications (Cambridge, England), 2016, 52, 9921-9924
7124802 CIFC31 H29 Br2 N O4P 4112.347; 12.347; 18.073
90; 90; 90
2755.2Li, Meng; Lu, Hai-Yan; Zhang, Chao; Shi, Lin; Tang, Zhiyong; Chen, Chuan-Feng
Helical aromatic imide based enantiomers with full-color circularly polarized luminescence.
Chemical communications (Cambridge, England), 2016, 52, 9921-9924
7124803 CIFC23 H19 N O SP 21 21 215.6327; 14.2928; 21.544
90; 90; 90
1734.4León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124804 CIFC22 H25 B O3P -19.7865; 12.5627; 16.1123
90.4912; 102.202; 93.6195
1931.82León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124805 CIFC26 H21 B N2 OP 1 21/c 119.3909; 10.1233; 20.4987
90; 95.235; 90
4007.1León, Thierry; Fernández, Elena
The Pauson-Khand reaction using alkynylboronic esters: solving a long-standing regioselectivity issue.
Chemical communications (Cambridge, England), 2016, 52, 9363-9366
7124806 CIFC8 H4 In O5I 41 2 215.4625; 15.4625; 12.337
90; 90; 90
2949.6Peralta, Ricardo A.; Campos-Reales-Pineda, Alberto; Pfeiffer, Heriberto; Álvarez, J Raziel; Zárate, J Antonio; Balmaseda, Jorge; González-Zamora, Eduardo; Martínez, Ana; Martínez-Otero, Diego; Jancik, Vojtech; Ibarra, Ilich A.
CO2 capture enhancement in InOF-1 via the bottleneck effect of confined ethanol.
Chemical communications (Cambridge, England), 2016, 52, 10273-10276
7124807 CIFC10 H10 In O6I 41 2 215.483; 15.483; 12.308
90; 90; 90
2950.5Peralta, Ricardo A.; Campos-Reales-Pineda, Alberto; Pfeiffer, Heriberto; Álvarez, J Raziel; Zárate, J Antonio; Balmaseda, Jorge; González-Zamora, Eduardo; Martínez, Ana; Martínez-Otero, Diego; Jancik, Vojtech; Ibarra, Ilich A.
CO2 capture enhancement in InOF-1 via the bottleneck effect of confined ethanol.
Chemical communications (Cambridge, England), 2016, 52, 10273-10276
7124808 CIFC60 H62 Au Cl P S3P 1 21 19.8334; 21.319; 12.7266
90; 95.59; 90
2655.3Aillard, Paul; Dova, Davide; Magné, Valentin; Retailleau, Pascal; Cauteruccio, Silvia; Licandro, Emanuela; Voituriez, Arnaud; Marinetti, Angela
The synthesis of substituted phosphathiahelicenes via regioselective bromination of a preformed helical scaffold: a new approach to modular ligands for enantioselective gold-catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10984-10987
7124809 CIFC12 H6 Cl2 Cu2 N2 O10 PdR -3 m :H18.899; 18.899; 31.69
90; 90; 120
9802Spanopoulos, I.; Bratsos, I.; Tampaxis, C.; Vourloumis, D.; Klontzas, E.; Froudakis, G. E.; Charalambopoulou, G.; Steriotis, T. A.; Trikalitis, P. N.
Exceptional gravimetric and volumetric CO2 uptake in a palladated NbO-type MOF utilizing cooperative acidic and basic, metal-CO2 interactions.
Chemical communications (Cambridge, England), 2016, 52, 10559-10562
7124810 CIFC16 H34 Mg N2 O2 P2 S2P 1 21/n 113.2446; 10.2823; 17.0713
90; 97.7952; 90
2303.37Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124811 CIFC20 H28 N2 P2 S2 SnP -18.5948; 9.7615; 14.7996
85.955; 87.786; 73.175
1185.33Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124812 CIFC96 H209 N16 Na17 O8 P16 S17P 4 c c23.7918; 23.7918; 37.5449
90; 90; 90
21252.3Benson, Callum G. M.; Plajer, Alex J.; García-Rodríguez, Raúl; Bond, Andrew D.; Singh, Sanjay; Gade, Lutz H.; Wright, Dominic S.
A versatile hard-soft N/S-ligand for metal coordination and cluster formation.
Chemical communications (Cambridge, England), 2016, 52, 9683-9686
7124813 CIFC11 H9 N OP 1 21/c 15.8141; 23.591; 6.8413
90; 114.257; 90
855.5Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124814 CIFC17 H14 Cl N O3P 1 21/c 115.84; 13.517; 7.047
90; 101.395; 90
1479.1Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124815 CIFC24 H24 N2P 1 21/c 112.648; 5.914; 13.125
90; 94.02; 90
979Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124816 CIFC10 H13 N O4P 1 21 14.8503; 17.114; 6.4411
90; 105.911; 90
514.2Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124817 CIFC10 H13 N O3P -16.69; 8.863; 9.115
107.219; 111.191; 92.478
474.4Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124818 CIFC22 H16 N2P 1 21/c 120.26; 5.434; 16.088
90; 110.528; 90
1658.7Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124819 CIFC26 H28 N2I 1 2/a 118.301; 6.133; 18.738
90; 94.032; 90
2098Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124820 CIFC10 H13 N O3P 1 21/c 16.8201; 16.879; 9.0566
90; 106.25; 90
1000.9Stephens, David E.; Lakey-Beitia, Johant; Burch, Jessica E.; Arman, Hadi D.; Larionov, Oleg V.
Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls.
Chemical communications (Cambridge, England), 2016, 52, 9945-9948
7124821 CIFC77 H66 B4 Cl6P -112.3724; 16.262; 18.3411
68.034; 76.109; 68.507
3161.58Zhang, Zuolun; Wang, Zheng; Haehnel, Martin; Eichhorn, Antonius; Edkins, Robert M.; Steffen, Andreas; Krueger, Anke; Lin, Zhenyang; Marder, Todd B.
Synthesis and fluxional behaviour of novel chloroborole dimers.
Chemical communications (Cambridge, England), 2016, 52, 9707-9710
7124822 CIFC38 H28 B2 Br4 Cl2P -110.7763; 11.4318; 15.5909
74.252; 81.811; 69.779
1732.1Zhang, Zuolun; Wang, Zheng; Haehnel, Martin; Eichhorn, Antonius; Edkins, Robert M.; Steffen, Andreas; Krueger, Anke; Lin, Zhenyang; Marder, Todd B.
Synthesis and fluxional behaviour of novel chloroborole dimers.
Chemical communications (Cambridge, England), 2016, 52, 9707-9710
7124823 CIFC14 H36 Cu N6 O8P -19.4885; 10.1789; 11.6397
85.237; 74.922; 77.744
1060.29Yu, Fengshou; Li, Fei; Hu, Jixiang; Bai, Lichen; Zhu, Yong; Sun, Licheng
Electrocatalytic water oxidation by a macrocyclic Cu(ii) complex in neutral phosphate buffer.
Chemical communications (Cambridge, England), 2016, 52, 10377-10380
7124824 CIFC41 H36 F16 N2P 1 21/c 112.7034; 15.8896; 29.1048
90; 94.795; 90
5854.3Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124825 CIFC45 H42 Au Cl F14 N2 OP 1 21/c 115.0816; 14.3924; 20.4104
90; 96.525; 90
4401.6Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124826 CIFC34 H41 F5 N2C 1 2/c 118.227; 17.04; 20.143
90; 101.779; 90
6124Kim, Youngsuk; Lee, Eunsung
Activation of C-F bonds in fluoroarenes by N-heterocyclic carbenes as an effective route to synthesize abnormal NHC complexes.
Chemical communications (Cambridge, England), 2016, 52, 10922-10925
7124827 CIFC29 H16P 1 21/c 111.856; 7.3071; 20.186
90; 96.412; 90
1737.8Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124828 CIFC30 H14 SP c a 219.2775; 26.8593; 7.3125
90; 90; 90
1822.18Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124829 CIFC29 H16 SP 1 21/n 114.111; 7.318; 18.169
90; 100.411; 90
1845.3Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124830 CIFC30 H19 NP 1 21/n 114.3543; 7.4826; 17.7472
90; 97.963; 90
1887.8Rajeshkumar, Venkatachalam; Stuparu, Mihaiela C.
A photochemical approach to aromatic extension of the corannulene nucleus.
Chemical communications (Cambridge, England), 2016, 52, 9957-9960
7124831 CIFC13 H12 Cd N2 O2I 41/a :224.583; 24.583; 10.8704
90; 90; 90
6569.2Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124832 CIFC13 H12 Cd N2 O2I 41/a :224.0666; 24.0666; 10.5856
90; 90; 90
6131.2Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124833 CIFC13 H12 Cd N2 O2I 41/a :224.6108; 24.6108; 10.76785
90; 90; 90
6521.99Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124834 CIFC13 H12 Cd N2 O2I 41/a :224.029; 24.029; 10.5501
90; 90; 90
6091.6Xiao, Qiong; Wu, Yuan; Li, Mian; O'Keeffe, Michael; Li, Dan
A metal-organic framework with rod secondary building unit based on the Boerdijk-Coxeter helix.
Chemical communications (Cambridge, England), 2016, 52, 11543-11546
7124835 CIFC15 H9 Cd2 N13 O12P c c n9.1873; 12.5692; 20.0824
90; 90; 90
2319.1Frost, Jamie M.; Kobera, Libor; Pialat, Amélie; Zhang, Yixin; Southern, Scott A.; Gabidullin, Bulat; Bryce, David L.; Murugesu, Muralee
From discrete molecule, to polymer, to MOF: mapping the coordination chemistry of Cd(II) using (113)Cd solid-state NMR.
Chemical communications (Cambridge, England), 2016, 52, 10680-10683
7124836 CIFC10 H6 Cd N4 O4I m -3 m30.1172; 30.1172; 30.1172
90; 90; 90
27317.7Frost, Jamie M.; Kobera, Libor; Pialat, Amélie; Zhang, Yixin; Southern, Scott A.; Gabidullin, Bulat; Bryce, David L.; Murugesu, Muralee
From discrete molecule, to polymer, to MOF: mapping the coordination chemistry of Cd(II) using (113)Cd solid-state NMR.
Chemical communications (Cambridge, England), 2016, 52, 10680-10683
7124837 CIFC45 H51.47 F12 Mo N3 O3 P4P 1 21/c 115.3031; 15.9629; 20.6295
90; 104.622; 90
4876.2Pal, Raja; Laureanti, Joseph A.; Groy, Thomas L.; Jones, Anne K.; Trovitch, Ryan J.
Hydrogen production from water using a bis(imino)pyridine molybdenum electrocatalyst.
Chemical communications (Cambridge, England), 2016, 52, 11555-11558
7124838 CIFC39 H41 Mo N3 O P2P 1 21/c 111.1519; 16.9788; 18.245
90; 105.844; 90
3323.4Pal, Raja; Laureanti, Joseph A.; Groy, Thomas L.; Jones, Anne K.; Trovitch, Ryan J.
Hydrogen production from water using a bis(imino)pyridine molybdenum electrocatalyst.
Chemical communications (Cambridge, England), 2016, 52, 11555-11558
7124839 CIFC15 H10 O5C 1 2/c 127.783; 4.6822; 20.212
90; 118.891; 90
2302Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124840 CIFC15 H10 O5P 1 21/n 116.4721; 3.6915; 19.4294
90; 96.188; 90
1174.56Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124841 CIFC15 H10 O5P 1 21/n 112.6343; 3.6437; 31.2026
90; 95.706; 90
1429.31Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124842 CIFC15 H10 O5P 1 21/n 116.6384; 3.6887; 19.406
90; 95.544; 90
1185.45Li, Meiqi; Zhang, Qi; Wang, Jian-Rong; Mei, Xuefeng
Mechanochromism triggered fluorescent color switching among polymorphs of a natural fluorescence pigment.
Chemical communications (Cambridge, England), 2016, 52, 11288-11291
7124843 CIFC44 H36 Cl F24 N7 P2P -112.175; 12.483; 18.276
75.34; 78.55; 71.31
2524.5Amendola, Valeria; Bergamaschi, Greta; Boiocchi, Massimo; Legnani, Laura; Presti, Eliana Lo; Miljkovic, Ana; Monzani, Enrico; Pancotti, Francesca
Chloride-binding in organic-water mixtures: the powerful synergy of C-H donor groups within a bowl-shaped cavity.
Chemical communications (Cambridge, England), 2016, 52, 10910-10913
7124844 CIFC44 H36 Br F24 N7 P2P -112.226; 12.514; 18.219
75.477; 78.586; 71.715
2540.5Amendola, Valeria; Bergamaschi, Greta; Boiocchi, Massimo; Legnani, Laura; Presti, Eliana Lo; Miljkovic, Ana; Monzani, Enrico; Pancotti, Francesca
Chloride-binding in organic-water mixtures: the powerful synergy of C-H donor groups within a bowl-shaped cavity.
Chemical communications (Cambridge, England), 2016, 52, 10910-10913
7124845 CIFC18 H17 Cl2 N O4 SP 1 21/c 113.725; 7.0845; 20.233
90; 108.593; 90
1864.7Xia, Dong; Li, Yang; Miao, Tao; Li, Pinhua; Wang, Lei
Direct synthesis of sulfonated dihydroisoquinolinones from N-allylbenzamide and arylsulfinic acids via TBHP-promoted cascade radical addition and cyclization.
Chemical communications (Cambridge, England), 2016, 52, 11559-11562
7124846 CIFC42 H40 Br2 N2 O6P 1 21 19.5936; 17.0134; 12.402
90; 111.095; 90
1888.6Li, Jun-Long; Yang, Kai-Chuan; Li, Yi; Li, Qiang; Zhu, Hong-Ping; Han, Bo; Peng, Cheng; Zhi, Yong-Gang; Gou, Xiao-Jun
Asymmetric synthesis of bicyclic dihydropyrans via organocatalytic inverse-electron-demand oxo-Diels-Alder reactions of enolizable aliphatic aldehydes.
Chemical communications (Cambridge, England), 2016, 52, 10617-10620
7124847 CIFC31 H27 I N2 O2 SP 1 21/c 19.6062; 11.1759; 25.6122
90; 92.1354; 90
2747.76Li, Honghe; Li, Xiaoxiao; Zhao, Zhigang; Ma, Ting; Sun, Chenyang; Yang, Bowen
Intermolecular iodofunctionalization of allenamides with indoles, pyrroles, and furans: synthesis of iodine-substituted Z-enamides.
Chemical communications (Cambridge, England), 2016, 52, 10167-10170
7124848 CIFC19 H18 I N3 O2 SP -18.421; 10; 11.8424
100.66; 103.744; 90.605
950.42Li, Honghe; Li, Xiaoxiao; Zhao, Zhigang; Ma, Ting; Sun, Chenyang; Yang, Bowen
Intermolecular iodofunctionalization of allenamides with indoles, pyrroles, and furans: synthesis of iodine-substituted Z-enamides.
Chemical communications (Cambridge, England), 2016, 52, 10167-10170
7124849 CIFC20 H13 F N4 SP -19.927; 13.059; 13.682
69.528; 89.026; 78.107
1623.1Yoshida, Suguru; Yano, Takahisa; Nishiyama, Yoshitake; Misawa, Yoshihiro; Kondo, Masakazu; Matsushita, Takeshi; Igawa, Kazunobu; Tomooka, Katsuhiko; Hosoya, Takamitsu
Thiazolobenzyne: a versatile intermediate for multisubstituted benzothiazoles.
Chemical communications (Cambridge, England), 2016, 52, 11199-11202
7124850 CIFC32 H64 B Li O8P 1 21/n 110.6111; 22.4729; 14.576
90; 92.676; 90
3472.03Basnet, Prakash; Thapa, Surendra; Dickie, Diane A.; Giri, Ramesh
The copper-catalysed Suzuki-Miyaura coupling of alkylboron reagents: disproportionation of anionic (alkyl)(alkoxy)borates to anionic dialkylborates prior to transmetalation.
Chemical communications (Cambridge, England), 2016, 52, 11072-11075
7124851 CIFC28 H56 B2 Li2 O6P -18.3308; 9.3831; 10.3351
98.43; 106.326; 90.671
765.74Basnet, Prakash; Thapa, Surendra; Dickie, Diane A.; Giri, Ramesh
The copper-catalysed Suzuki-Miyaura coupling of alkylboron reagents: disproportionation of anionic (alkyl)(alkoxy)borates to anionic dialkylborates prior to transmetalation.
Chemical communications (Cambridge, England), 2016, 52, 11072-11075
7124852 CIFC19 H27 N O9 ZnP -110.4273; 10.8211; 10.8805
85.208; 74.992; 67.508
1095.45Foster, Jonathan A.; Henke, Sebastian; Schneemann, Andreas; Fischer, Roland A.; Cheetham, Anthony K.
Liquid exfoliation of alkyl-ether functionalised layered metal-organic frameworks to nanosheets.
Chemical communications (Cambridge, England), 2016, 52, 10474-10477
7124853 CIFC27 H24 Au F5 N2P 1 21/c 122.2207; 12.08219; 20.7776
90; 114.995; 90
5055.81Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124854 CIFC11 H8 Au F5 N2P 1 21/c 112.1492; 7.1342; 13.5219
90; 97.48; 90
1162.03Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124855 CIFC15 H16 Au F5 N2P -19.2638; 9.9251; 10.7976
104.458; 104.138; 114.79
801.05Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124856 CIFC29 H32 Au F5 N2P 1 21/c 116.6316; 6.73754; 23.1802
90; 107.797; 90
2473.18Johnson, Alice; Gimeno, M Concepción
An efficient and sustainable synthesis of NHC gold complexes.
Chemical communications (Cambridge, England), 2016, 52, 9664-9667
7124857 CIFC32 H20 F N3 OP 1 21/c 127.5965; 5.8463; 14.617
90; 93.918; 90
2352.76Yu, Ling; Wu, Zhongbin; Xie, Guohua; Zhong, Cheng; Zhu, Zece; Cong, Hengjiang; Ma, Dongge; Yang, Chuluo
Achieving a balance between small singlet-triplet energy splitting and high fluorescence radiative rate in a quinoxaline-based orange-red thermally activated delayed fluorescence emitter.
Chemical communications (Cambridge, England), 2016, 52, 11012-11015
7124858 CIFC55.18 H49.76 B2 Cl3.96 Cu2 F8 Mo4 N4.6 O8 P4P 31 2 113.2466; 13.2466; 38.4491
90; 90; 120
5842.9Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124859 CIFC28.2 H25.9 B Cl0.4 Cu F4 Mo2 N2.5 O4 P2P -112.15; 12.9837; 13.0995
112.581; 95.502; 112.579
1688.53Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124860 CIFC28.1 H22.2 B Cl0.2 Cu F4 Mo2 N2 O8 P2P -111.051; 12.9411; 14.5125
107.454; 109.734; 92.922
1836.64Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124861 CIFC57 H46 B2 Cl2 Cu2 F8 Mo4 N4 O16 P4C 1 2/c 123.3364; 15.9366; 20.1067
90; 116.735; 90
6678.3Elsayed Moussa, M.; Attenberger, B.; Peresypkina, E. V.; Fleischmann, M.; Balázs, G; Scheer, M.
Facile synthesis of one-dimensional organometallic-organic hybrid polymers based on a diphosphorus complex and flexible bipyridyl linkers.
Chemical communications (Cambridge, England), 2016, 52, 10004-10007
7124862 CIFC36 H17 B2 F20 NP 1 21/n 114.9491; 11.0572; 20.4604
90; 102.897; 90
3296.69Körte, Leif A; Blomeyer, Sebastian; Heidemeyer, Shari; Mix, Andreas; Neumann, Beate; Mitzel, Norbert W.
Intramolecular cooperativity in frustrated Lewis pairs.
Chemical communications (Cambridge, England), 2016, 52, 9949-9952
7124863 CIFC13 H22 B10 O2P -17.0022; 11.1149; 12.7151
72.088; 85.357; 77.321
918.58Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124864 CIFC14 H24 B10 O2P -16.9249; 11.0485; 13.4241
70.985; 82.699; 79.375
951.9Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124865 CIFC15 H27 B10 N O2P -17.3998; 11.4524; 12.796
101.746; 102.967; 101.723
998.81Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124866 CIFC13 H21 B10 Cl O2P 1 21/n 114.2465; 6.9536; 19.296
90; 103.257; 90
1860.6Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124867 CIFC13 H21 B10 Br O2P 1 21/n 114.3765; 6.99225; 19.7177
90; 105.687; 90
1908.28Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124868 CIFC19 H26 B10 O2P 1 21/c 115.59137; 7.11207; 20.7564
90; 106.786; 90
2203.55Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124869 CIFC17 H24 B10 O2P -17.5123; 11.5047; 13.1285
109.896; 91.522; 105.035
1022.13Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124870 CIFC18 H26 B10 O3C 1 2/c 126.4656; 8.57309; 20.8506
90; 111.965; 90
4387.43Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124871 CIFC11 H20 B10 O3P 1 21/n 122.1533; 6.78019; 23.3341
90; 100.05; 90
3451.09Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124872 CIFC11 H20 B10 O2 SP 1 21/n 114.009; 7.0087; 17.9756
90; 100.292; 90
1736.5Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124873 CIFC11 H20 B10 O2 SP 1 21/n 114.1171; 7.06182; 17.8292
90; 100.102; 90
1749.88Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124874 CIFC12 H21 B10 N O2C 1 2/c 122.0219; 6.88628; 24.2999
90; 104.579; 90
3566.4Zheng, Fangrui; Leung, Tsz-Fai; Chan, Ka-Wing; Sung, Herman H. Y.; Williams, Ian D.; Xie, Zuowei; Jia, Guochen
Phosphine-catalyzed cage carbon functionalization of o-carborane: facile synthesis of alkenylcarboranes.
Chemical communications (Cambridge, England), 2016, 52, 10767-10770
7124875 CIFC124 Cl12 N7 O73 Si2 Sn6 W18P 1 21 118.7517; 28.4384; 21.539
90; 115.122; 90
10399.6Suzuki, Kosuke; Hanaya, Takumi; Sato, Rinta; Minato, Takuo; Yamaguchi, Kazuya; Mizuno, Noritaka
Hexanuclear tin(ii) and mixed valence tin(ii,iv) oxide clusters within polyoxometalates.
Chemical communications (Cambridge, England), 2016, 52, 10688-10691
7124876 CIFC115 N10 O77 Si2 Sn6 W18P -117.6999; 18.7362; 29.8744
82.659; 88.278; 74.291
9458.9Suzuki, Kosuke; Hanaya, Takumi; Sato, Rinta; Minato, Takuo; Yamaguchi, Kazuya; Mizuno, Noritaka
Hexanuclear tin(ii) and mixed valence tin(ii,iv) oxide clusters within polyoxometalates.
Chemical communications (Cambridge, England), 2016, 52, 10688-10691
7124877 CIFC64 H36 F4 N2 O8 Zn2P -113.967; 15.48; 20.893
89.948; 83.096; 89.209
4484Wang, Fangming; Liu, Wei; Teat, Simon J.; Xu, Feng; Wang, Hao; Wang, Xinlong; An, Litao; Li, Jing
Chromophore-immobilized luminescent metal-organic frameworks as potential lighting phosphors and chemical sensors.
Chemical communications (Cambridge, England), 2016, 52, 10249-10252
7124878 CIFC66 H38 F4 N2 O8 Zn2P -116.317; 16.8197; 20.0452
89.982; 85.952; 85.919
5473.6Wang, Fangming; Liu, Wei; Teat, Simon J.; Xu, Feng; Wang, Hao; Wang, Xinlong; An, Litao; Li, Jing
Chromophore-immobilized luminescent metal-organic frameworks as potential lighting phosphors and chemical sensors.
Chemical communications (Cambridge, England), 2016, 52, 10249-10252
7124879 CIFC23 H22 S2P 1 21 110.023; 7.569; 13.421
90; 108.949; 90
963Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124880 CIFC15 H16 O S2P 1 21/c 115.567; 7.3046; 12.5049
90; 107.222; 90
1358.2Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124881 CIFC52 H40 O2 S4P 1 21 110.601; 19.272; 11.193
90; 117.501; 90
2028.4Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124882 CIFC26 H20 O S2C 1 2/c 122.945; 11.378; 16.575
90; 111.887; 90
4015Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124883 CIFC28 H38 Au F6 N O2 P SbP 1 21/n 112.9088; 13.5954; 18.3182
90; 93.268; 90
3209.6Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124884 CIFC26 H20 S2P 1 21/n 111.9307; 11.8029; 13.8044
90; 98.163; 90
1924.2Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124885 CIFC29 H20 S2P 1 21/c 115.8061; 6.3393; 21.023
90; 95.291; 90
2097.5Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124886 CIFC28 H24 O3 S2P -19.8628; 11.701; 12.236
108.538; 104.931; 90.24
1287.9Xu, Wei; Chen, Ming; Sun, Ning; Liu, Yuanhong
Gold-catalyzed cyclization of 1,6-diynyl dithioacetals via 1,7-carbene transfer and aromatic C-H functionalization.
Chemical communications (Cambridge, England), 2016, 52, 11000-11003
7124887 CIFC13 H11 Cl N4 OP 1 21 16.1447; 8.6445; 12.6178
90; 101.032; 90
657.84Vishwanath, Manjunatha; Sivamuthuraman, Koilpitchai; Kesavan, Venkitasamy
An efficient construction of N,N-bicyclic pyrazolidinones comprising enaminonitriles via asymmetric [3+2] cycloaddition.
Chemical communications (Cambridge, England), 2016, 52, 12314-12317
7124888 CIFC50 H96 Br8 Dy6 N14 O32P -111.225; 12.338; 18.269
72.433; 82.638; 89.18
2391.5Li, Xiao-Lei; Wu, Jianfeng; Tang, Jinkui; Le Guennic, Boris; Shi, Wei; Cheng, Peng
A planar triangular Dy3 + Dy3 single-molecule magnet with a toroidal magnetic moment.
Chemical communications (Cambridge, England), 2016, 52, 9570-9573
7124889 CIFC16 H16 Co Dy N8 O5P 1 21/m 16.897; 15.6685; 9.6096
90; 102.131; 90
1015.28Chorazy, Szymon; Wang, Junhao; Ohkoshi, Shin-Ichi
Yellow to greenish-blue colour-tunable photoluminescence and 4f-centered slow magnetic relaxation in a cyanido-bridged Dy(III)(4-hydroxypyridine)-Co(III) layered material.
Chemical communications (Cambridge, England), 2016, 52, 10795-10798
7124890 CIFC45 H62 Cl2 N4 O4 ZrP 1 21/n 112.9667; 18.0916; 18.8976
90; 95.342; 90
4413.9Schneider, Fabian; Zhao, Tiankun; Huhn, Thomas
Cytotoxic heteroleptic heptacoordinate salan zirconium(iv)-bis-chelates - synthesis, aqueous stability and X-ray structure analysis.
Chemical communications (Cambridge, England), 2016, 52, 10151-10154
7124891 CIFC29 H33 N3 O6 ZrP 1 21/n 19.4729; 22.863; 12.408
90; 93.774; 90
2681.5Schneider, Fabian; Zhao, Tiankun; Huhn, Thomas
Cytotoxic heteroleptic heptacoordinate salan zirconium(iv)-bis-chelates - synthesis, aqueous stability and X-ray structure analysis.
Chemical communications (Cambridge, England), 2016, 52, 10151-10154
7124892 CIFC31 H29 B2 F10 N O2P -19.8867; 10.3242; 16.1713
76.107; 86.224; 73.616
1537.3Fleige, Mirco; Möbus, Juri; Vom Stein, Thorsten; Glorius, Frank; Stephan, Douglas W.
Lewis acid catalysis: catalytic hydroboration of alkynes initiated by Piers' borane.
Chemical communications (Cambridge, England), 2016, 52, 10830-10833
7124893 CIFC20 H16 Br N2 O2P 1 21/n 121; 7.6152; 23.7899
90; 112.403; 90
3517.3Das, Tapas; Kayet, Anirban; Mishra, Ruchika; Singh, Vinod K.
Highly fluorescent 1,2-dihydropyrimido[1,6-α]indole: an efficient metal free synthesis and photophysical study.
Chemical communications (Cambridge, England), 2016, 52, 11231-11234
7124894 CIFC120 H101 B Cl6 N12 O5C m c 2126.6592; 23.6211; 19.6982
90; 90; 90
12404.3Zhang, Yuehong; Oh, Juwon; Wang, Kang; Shin, Dongju; Zhan, Xiaopeng; Zheng, Yingting; Kim, Dongho; Jiang, Jianzhuang
The first porphyrin-subphthalocyaninatoboron(iii)-fused hybrid with unique conformation and intramolecular charge transfer behavior.
Chemical communications (Cambridge, England), 2016, 52, 10517-10520
7124895 CIFC19 H16 O3P -17.0903; 10.2299; 11.0836
67.824; 77.107; 79.532
721.45Jiang, Chongguo; Xiong, Zhiling; Jin, Shengfei; Gao, Peng; Tang, Yingzhan; Wang, Yanshi; Du, Chuan; Wang, Xiaoyu; Liu, Yang; Lin, Bin; Liu, Yongxiang; Cheng, Maosheng
A Au(i)-catalyzed hydrogen bond-directed tandem strategy to synthesize indeno-chromen-4-one and indeno-quinolin-4-one derivatives.
Chemical communications (Cambridge, England), 2016, 52, 11516-11519
7124896 CIFC78 H66 Eu N7 O18P 21 320.898; 20.898; 20.898
90; 90; 90
9127Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124897 CIFC78 H60 Cd Eu N7.5 O26P 21 320.509; 20.509; 20.509
90; 90; 90
8626.48Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124898 CIFC26 H20 Cl4 Hg2 N2 O5C 1 2/c 120.25; 12.1502; 13.984
90; 123.951; 90
2854.1Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124899 CIFC52 H48 N8 O25 Pb2P 1 21/c 116.777; 12.3446; 13.27
90; 96.886; 90
2728.5Sun, Yan-Qiong; Wan, Fang; Li, Xin-Xiong; Lin, Jian; Wu, Tao; Zheng, Shou-Tian; Bu, Xianhui
A lanthanide complex for metal encapsulations and anion exchanges.
Chemical communications (Cambridge, England), 2016, 52, 10125-10128
7124900 CIFC14 H12P 1 21/c 118.222; 5.648; 20.014
90; 97.925; 90
2040.1Chen, Gen-Qiang; Fang, Wei; Wei, Yin; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed dehydrogenative cycloisomerization of 1,5-enynes.
Chemical communications (Cambridge, England), 2016, 52, 10799-10802
7124901 CIFC41 H30 B Cl3 N4 O2P -19.821; 12.383; 15.111
79.156; 84.922; 73.193
1726.7Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124902 CIFC61.5 H46.5 B Cl4.5 N4 O6P -113.411; 20.416; 21.32
75.181; 83.052; 88.03
5602Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124903 CIFC40.5 H30 B Cl N4 O2P 19.887; 11.839; 15.495
77.762; 80.071; 66.473
1617.3Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124904 CIFC60 H42 B2 N4 O6P 1 21 111.4322; 16.3704; 12.5755
90; 100.994; 90
2310.31Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124905 CIFC62 H44 B2 Cl6 N4 O6P 1 21/n 127.3653; 13.783; 31.7984
90; 114.516; 90
10912.3Saikawa, Makoto; Nakamura, Takashi; Uchida, Junji; Yamamura, Masaki; Nabeshima, Tatsuya
Synthesis of figure-of-eight helical bisBODIPY macrocycles and their chiroptical properties.
Chemical communications (Cambridge, England), 2016, 52, 10727-10730
7124906 CIFC33 H53 B K N3 O SiP 21 21 2111.5483; 15.6266; 19.1969
90; 90; 90
3464.3Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124907 CIFC47 H59 N O3 Si ZnP -4 21 c21.1923; 21.1923; 18.9615
90; 90; 90
8515.9Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124908 CIFC33 H53 B Br N3 O Si ZnP 1 21/c 115.203; 11.974; 19.965
90; 100.3; 90
3575.9Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124909 CIFC84 H98 N2 O2 Si2 Zn2P -113.39; 14.317; 20.067
80.79; 79.66; 71.54
3567.7Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124910 CIFC42 H48.98 Br0.02 N Si ZnP -114.0869; 15.8901; 17.1769
72.101; 81.448; 81.036
3593.29Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124911 CIFC45 H54 Br N O3 Si ZnI 41/a :220.9835; 20.9835; 37.613
90; 90; 90
16561.3Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124912 CIFC55.75 H62 N O2 Si ZnP n a 2127.289; 12.855; 28.084
90; 90; 90
9852Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124913 CIFC44 H53 N Si ZnP b c a18.699; 10.648; 37.755
90; 90; 90
7517Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124914 CIFC38 H41 N Si ZnP -19.9787; 11.6997; 14.992
88.8; 85.337; 72.292
1661.8Dawkins, Michael J. C.; Middleton, Ewart; Kefalidis, Christos E.; Dange, Deepak; Juckel, Martin M.; Maron, Laurent; Jones, Cameron
Two-coordinate terminal zinc hydride complexes: synthesis, structure and preliminary reactivity studies.
Chemical communications (Cambridge, England), 2016, 52, 10490-10492
7124915 CIFC28 H23 Br N2 O2P 1 21/c 18.1067; 15.997; 18.8373
90; 99.636; 90
2408.41Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124916 CIFC32 H23 N OP 1 21/n 113.2048; 9.7962; 36.3
90; 90.681; 90
4695.3Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124917 CIFC44 H31 N OP 1 21/n 19.7155; 11.1424; 33.67
90; 94.871; 90
3631.7Zhou, Xiaorong; Peng, Zhixing; Zhao, Hongyang; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang
Rh-Catalyzed annulations of N-methoxybenzamides with ketenimines: synthesis of 3-aminoisoindolinones and 3-diarylmethyleneisoindolinones with strong aggregation induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10676-10679
7124918 CIFC42 H90 Cl4 N6 O2 ReP -110.4031; 11.9265; 11.9819
64.8219; 75.0617; 82.2082
1299.34Feng, Xiaowen; Liu, Jun-Liang; Pedersen, Kasper S.; Nehrkorn, Joscha; Schnegg, Alexander; Holldack, Karsten; Bendix, Jesper; Sigrist, Marc; Mutka, Hannu; Samohvalov, Dumitru; Aguilà, David; Tong, Ming-Liang; Long, Jeffrey R.; Clérac, Rodolphe
Multifaceted magnetization dynamics in the mononuclear complex [Re<sup>IV</sup>Cl<sub>4</sub>(CN)<sub>2</sub>]<sup>2</sup>.
Chemical communications (Cambridge, England), 2016, 52, 12905-12908
7124919 CIFC13 H9 F3 N2 OP -15.617; 7.3899; 14.156
75.267; 80.383; 88.88
560.1Ragupathi, Ayyakkannu; Sagadevan, Arunachalam; Lin, Chun-Cheng; Hwu, Jih-Ru; Hwang, Kuo Chu
Copper(i)-catalysed oxidative C-N coupling of 2-aminopyridine with terminal alkynes featuring a C[triple bond, length as m-dash]C bond cleavage promoted by visible light.
Chemical communications (Cambridge, England), 2016, 52, 11756-11759
7124920 CIFC5 H16 Cl5 N2 SbP 21 21 217.662; 13.433; 13.883
90; 90; 90
1428.9Mei, Guang-Quan; Zhang, Han-Yue; Liao, Wei-Qiang
A symmetry breaking phase transition-triggered high-temperature solid-state quadratic nonlinear optical switch coupled with a switchable dielectric constant in an organic-inorganic hybrid compound.
Chemical communications (Cambridge, England), 2016, 52, 11135-11138
7124921 CIFC5 H16 Cl5 N2 SbP n m a13.514; 7.818; 13.8
90; 90; 90
1458Mei, Guang-Quan; Zhang, Han-Yue; Liao, Wei-Qiang
A symmetry breaking phase transition-triggered high-temperature solid-state quadratic nonlinear optical switch coupled with a switchable dielectric constant in an organic-inorganic hybrid compound.
Chemical communications (Cambridge, England), 2016, 52, 11135-11138
7124922 CIFC70 H78 N2 O2 Ti2P 1 21/c 111.09321; 22.0757; 28.1078
90; 92.8099; 90
6875.05Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124923 CIFC72 H83 N2 O2.5 Zr2P -111.3506; 15.5365; 19.1544
79.469; 79.993; 81.353
3245.81Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124924 CIFC73.5 H85.5 Hf2 N2 O2P 1 21/c 114.6909; 16.2174; 27.5623
90; 103.614; 90
6382.2Liu, Cham-Chuen; Chan, Michael C. W.; Lo, Po-Kam; Lau, Kai-Chung; Yiu, Shek-Man
Multifaceted chelating μ-(η(3):η(3)-antifacial)-(cis-C4R2H2) coordination motif in binuclear complexes.
Chemical communications (Cambridge, England), 2016, 52, 11056-11059
7124925 CIFC211 H82 Cl5 N6 Na2 O12 Sc6P 1 21/c 115.1344; 20.6079; 21.8351
90; 90.019; 90
6810.1Konarev, Dmitri V.; Zorina, Leokadiya V.; Khasanov, Salavat S.; Popov, Alexey A.; Otsuka, Akihiro; Yamochi, Hideki; Saito, Gunzi; Lyubovskaya, Rimma N.
A crystalline anionic complex of scandium nitride endometallofullerene: experimental observation of single-bonded (Sc3N@Ih-C80(-))2 dimers.
Chemical communications (Cambridge, England), 2016, 52, 10763-10766
7124926 CIFC67.5 H108 O13 S6 Zn4P -113.8362; 15.0709; 20.3113
89.161; 79.646; 73.544
3992.8Kelly, Rory P.; Kazeminejad, Neda; Lamsfus, Carlos A.; Maron, Laurent; Roesky, Peter W.
Activation of SO<sub>2</sub> by [Zn(Cp*)<sub>2</sub>] and [(Cp*)Zn<sup>I</sup>-Zn<sup>I</sup>(Cp*)].
Chemical communications (Cambridge, England), 2016, 52, 13090-13093
7124927 CIFC16 H40 N4 O8 S3 Zn2P 1 21/c 112.903; 15.8305; 13.4913
90; 103.699; 90
2677.4Kelly, Rory P.; Kazeminejad, Neda; Lamsfus, Carlos A.; Maron, Laurent; Roesky, Peter W.
Activation of SO<sub>2</sub> by [Zn(Cp*)<sub>2</sub>] and [(Cp*)Zn<sup>I</sup>-Zn<sup>I</sup>(Cp*)].
Chemical communications (Cambridge, England), 2016, 52, 13090-13093
7124928 CIFC29 H20 O2P -18.6037; 9.6242; 13.0214
79.03; 81.504; 74.717
1015.65Chen, Ling; Cui, Yu-Ming; Xu, Zheng; Cao, Jian; Zheng, Zhan-Jiang; Xu, Li-Wen
An efficient approach toward formation of polycyclic coumarin derivatives via carbocation-initiated [4+2] cycloaddition and atom-economical photo-irradiated cyclization.
Chemical communications (Cambridge, England), 2016, 52, 11131-11134
7124929 CIFC17 H14 O4P 1 21/n 18.1218; 27.7422; 12.2315
90; 95.062; 90
2745.2Ji, Wei; Liu, Guofeng; Wang, Fang; Zhu, Zhu; Feng, Chuanliang
Galactose-decorated light-responsive hydrogelator precursors for selectively killing cancer cells.
Chemical communications (Cambridge, England), 2016, 52, 12574-12577
7124930 CIFC29 H33 N3 O2P -19.6437; 11.6855; 12.1217
87.115; 71.784; 82.973
1287.7Quinodoz, P.; Wright, K.; Drouillat, B.; David, O.; Marrot, J.; Couty, F.
Synthesis of homopropargylamines from 2-cyanoazetidines.
Chemical communications (Cambridge, England), 2016, 52, 10072-10075
7124931 CIFC28 H26P c a 2120.325; 11.622; 8.52
90; 90; 90
2012.6Wang, Guohua; Chen, Chao; Peng, Jing
Copper-catalyzed intramolecular aryl-bicyclization of diynes with diaryliodonium salts via vinyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10277-10280
7124932 CIFC192 H240 Cl4 N36 Ni4 O16I 2 323.432; 23.432; 23.432
90; 90; 90
12865.5Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124933 CIFC192 H240 Cl4 N36 Ni4 O16I 2 323.4359; 23.4359; 23.4359
90; 90; 90
12872Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124934 CIFC204 H264 B6 F24 N36 Ni4 O12P 118.9274; 19.8289; 22.328
110.839; 102.662; 108.564
6881.7Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124935 CIFC240 H276 Cl4 N36 Ni4 O6F 41 3 239.2624; 39.2624; 39.2624
90; 90; 90
60524Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124936 CIFC241 H264 F3 N36 Ni4 O3 SP 119.222; 20.854; 22.254
106.518; 103.878; 112.172
7289.5Xi, Sai-Fei; Bao, Ling-Yu; Lin, Jian-Guo; Liu, Qing-Zhu; Qiu, Ling; Zhang, Feng-Li; Wang, Yu-Xia; Ding, Zheng-Dong; Li, Ke; Gu, Zhi-Guo
Enantiomers of tetrahedral metal-organic cages: a new class of highly efficient G-quadruplex ligands with potential anticancer activities.
Chemical communications (Cambridge, England), 2016, 52, 10261-10264
7124937 CIFC29 H28 F4 N2 O5P 1 21/c 112.4966; 9.7777; 22.6334
90; 100.263; 90
2721.3Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124938 CIFC24 H22 F2 N2 O3P b c a12.2175; 15.8782; 22.0697
90; 90; 90
4281.34Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124939 CIFC28 H25 Cl F4 N2 O5P 1 21/c 112.8985; 14.8772; 27.961
90; 97.992; 90
5313.4Hua, Hui-Liang; Zhang, Bo-Sheng; He, Yu-Tao; Qiu, Yi-Feng; Hu, Jing-Yuan; Yang, Yu-Chen; Liang, Yong-Min
Copper-catalyzed difluoromethylation of propargylamide-substituted indoles: synthesis of mono- and bis-difluoromethylated indoloazepinone derivatives.
Chemical communications (Cambridge, England), 2016, 52, 10396-10399
7124940 CIFC29 H28 N2 OP 1 21 18.118; 16.336; 8.515
90; 91.597; 90
1128.8Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124941 CIFC41 H38 N4 O2R -3 :H24.722; 24.722; 13.524
90; 90; 120
7158Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124942 CIFC28 H27 B F4 N4P 1 21/c 16.691; 29.96; 12.952
90; 104.2; 90
2517Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124943 CIFC29 H31 N3 O SP 1 21 113.438; 14.165; 13.5796
90; 93.657; 90
2579.6Wilkie, Ross P.; Neal, Andrew R.; Johnston, Craig A.; Voute, Nicholas; Lancefield, Christopher S.; Stell, Matthew D.; Medda, Federico; Makiyi, Edward F.; Turner, Emma M.; Stephen Ojo, O.; Slawin, Alexandra M. Z.; Lebl, Tomas; Mullen, Peter; Harrison, David J.; Ireland, Chris M.; Westwood, Nicholas J.
Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi-Sakurai reaction.
Chemical communications (Cambridge, England), 2016, 52, 10747-10750
7124944 CIFC56 H82 N4 Na4 O6P 1 2/c 118.372; 10.659; 28.255
90; 100.193; 90
5446Lichtenberg, C.; Krummenacher, I.
Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation.
Chemical communications (Cambridge, England), 2016, 52, 10044-10047
7124945 CIFC25 H39 Co N6 O4P 1 21/n 114.5396; 9.6307; 20.8295
90; 109.316; 90
2752.5Das, Debasree; Pattanayak, Santanu; Singh, Kundan K.; Garai, Bikash; Sen Gupta, Sayam
Electrocatalytic water oxidation by a molecular cobalt complex through a high valent cobalt oxo intermediate.
Chemical communications (Cambridge, England), 2016, 52, 11787-11790
7124946 CIFC167 H278 Al4 N8 O12I 1 2/a 129.9091; 11.0908; 25.9834
90; 108.075; 90
8193.8McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124947 CIFC33 H51 Al N2 O3P 1 21/c 112.1388; 19.0837; 14.1406
90; 102.663; 90
3196.04McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124948 CIFC38 H61 Al N2 O2P 1 21/c 113.8779; 13.002; 20.8532
90; 98.2288; 90
3724McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124949 CIFC43 H61 Al N2 O3P -110.9794; 14.2923; 15.1168
115.692; 100.605; 102.864
1974.85McKeown, Paul; Davidson, Matthew G.; Kociok-Köhn, Gabriele; Jones, Matthew D.
Aluminium salalens vs. salans: "Initiator Design" for the isoselective polymerisation of rac-lactide.
Chemical communications (Cambridge, England), 2016, 52, 10431-10434
7124950 CIFC23 H20 Br N O P TcC 1 2/c 122.001; 13.607; 17.541
90; 126.91; 90
4198.8Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124951 CIFC24 H20 B F4 N O2 P TcP 1 21/c 19.27; 17.374; 14.27
90; 100.29; 90
2261.3Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124952 CIFC29 H25 N O P TcP 1 21 19.179; 13.937; 10.048
90; 112.89; 90
1184.2Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124953 CIFC36.5 H31 Br3 Cl N O3 P2 TcP 1 21/c 112.551; 14.394; 44.488
90; 97.55; 90
7967.5Ackermann, J.; Hagenbach, A.; Abram, U.
{Tc(NO)(Cp)(PPh3)}(+) - a novel technetium(i) core.
Chemical communications (Cambridge, England), 2016, 52, 10285-10288
7124954 CIFC25 H28 N2 O4 SP 21 21 218.782; 10.8274; 26.0299
90; 90; 90
2475.08Rainoldi, G.; Faltracco, M.; Lo Presti, L.; Silvani, A.; Lesma, G.
Highly diastereoselective entry into chiral spirooxindole-based 4-methyleneazetidines via formal [2+2] annulation reaction.
Chemical communications (Cambridge, England), 2016, 52, 11575-11578
7124955 CIFC18 H12 Cu2 N0 O10 SiP 63/m m c18.5185; 18.5185; 19.1215
90; 90; 120
5678.9Gao, Chao-Ying; Tian, Hong-Rui; Ai, Jing; Li, Lei-Jiao; Dang, Song; Lan, Ya-Qian; Sun, Zhong-Ming
A microporous Cu-MOF with optimized open metal sites and pore spaces for high gas storage and active chemical fixation of CO2.
Chemical communications (Cambridge, England), 2016, 52, 11147-11150
7124956 CIFC8 H16 Cu F6 N4 O4 VP 4/n b m :29.7325; 9.7325; 8.2154
90; 90; 90
778.18Manson, Jamie L.; Schlueter, John A.; Garrett, Kerry E.; Goddard, Paul A.; Lancaster, Tom; Möller, Johannes S; Blundell, Stephen J.; Steele, Andrew J.; Franke, Isabel; Pratt, Francis L.; Singleton, John; Bendix, Jesper; Lapidus, Saul H.; Uhlarz, Marc; Ayala-Valenzuela, Oscar; McDonald, Ross D.; Gurak, Mary; Baines, Christopher
Bimetallic MOFs (H<sub>3</sub>O)<sub>x</sub>[Cu(MF<sub>6</sub>)(pyrazine)<sub>2</sub>]·(4 - x)H<sub>2</sub>O (M = V<sup>4+</sup>, x = 0; M = Ga<sup>3+</sup>, x = 1): co-existence of ordered and disordered quantum spins in the V<sup>4+</sup> system.
Chemical communications (Cambridge, England), 2016, 52, 12653-12656
7124957 CIFC8 H17 Cu F6 Ga N4 O4P 4/n b m :29.7134; 9.7134; 8.2415
90; 90; 90
777.59Manson, Jamie L.; Schlueter, John A.; Garrett, Kerry E.; Goddard, Paul A.; Lancaster, Tom; Möller, Johannes S; Blundell, Stephen J.; Steele, Andrew J.; Franke, Isabel; Pratt, Francis L.; Singleton, John; Bendix, Jesper; Lapidus, Saul H.; Uhlarz, Marc; Ayala-Valenzuela, Oscar; McDonald, Ross D.; Gurak, Mary; Baines, Christopher
Bimetallic MOFs (H<sub>3</sub>O)<sub>x</sub>[Cu(MF<sub>6</sub>)(pyrazine)<sub>2</sub>]·(4 - x)H<sub>2</sub>O (M = V<sup>4+</sup>, x = 0; M = Ga<sup>3+</sup>, x = 1): co-existence of ordered and disordered quantum spins in the V<sup>4+</sup> system.
Chemical communications (Cambridge, England), 2016, 52, 12653-12656
7124958 CIFC24 H20 N2 O2P 1 21/c 110.3006; 17.4826; 10.8631
90; 92.484; 90
1954.4Huo, Congde; Dong, Jie; Su, Yingpeng; Tang, Jing; Chen, Fengjuan
Iron-catalyzed oxidative sp<sup>3</sup> carbon-hydrogen bond functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones.
Chemical communications (Cambridge, England), 2016, 52, 13341-13344
7124959 CIFC19 H22 N2 O2 SP 1 21 19.5967; 9.265; 10.1709
90; 102.244; 90
883.76Zhao, Quan-Qing; Hu, Xiao-Qiang; Yang, Meng-Nan; Chen, Jia-Rong; Xiao, Wen-Jing
A visible-light photocatalytic N-radical cascade of hydrazones for the synthesis of dihydropyrazole-fused benzosultams.
Chemical communications (Cambridge, England), 2016, 52, 12749-12752
7124960 CIFC19 H20 N2 O2 SP -19.31; 13.2449; 14.8906
69.506; 77.927; 89.163
1678.5Zhao, Quan-Qing; Hu, Xiao-Qiang; Yang, Meng-Nan; Chen, Jia-Rong; Xiao, Wen-Jing
A visible-light photocatalytic N-radical cascade of hydrazones for the synthesis of dihydropyrazole-fused benzosultams.
Chemical communications (Cambridge, England), 2016, 52, 12749-12752
7124961 CIFC104 H92 Br8 Cl2 N4 OP -110.9254; 13.4449; 15.8457
95.9; 100.524; 95.947
2258.4Krzeszewski, Maciej; Swider, Paweł; Dobrzycki, Łukasz; Cyrański, Michał K; Danikiewicz, Witold; Gryko, Daniel T.
The role of steric hindrance in the intramolecular oxidative aromatic coupling of pyrrolo[3,2-b]pyrroles.
Chemical communications (Cambridge, England), 2016, 52, 11539-11542
7124962 CIFC46 H51 Ge N2 O PP 1 21/n 113.91699; 19.62321; 14.94628
90; 94.7717; 90
4067.62Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124963 CIFC46 H51 N2 O P SiP -19.4352; 12.6209; 17.8147
85.36; 78.369; 76.089
2015.71Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124964 CIFC46 H51 N2 O P SnP 1 21/n 114.0166; 19.8309; 14.945
90; 94.185; 90
4143.06Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124965 CIFC49 H61 N2 O P SnP -110.64809; 11.6076; 19.4163
91.4216; 92.8956; 110.289
2245.77Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124966 CIFC45 H51 Ge N2 PP 1 21/n 124.0628; 12.8152; 25.4632
90; 94.7933; 90
7824.62Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124967 CIFC160 H164 N8 O1.5 P4 Sn4P -113.0114; 17.0048; 18.7117
111.389; 94.838; 110.638
3498.2Li, Zhongshu; Chen, Xiaodan; Li, Yaqi; Su, Cheng-Yong; Grützmacher, Hansjörg
N-Heterocyclic carbene phosphaketene adducts as precursors to carbene-phosphinidene adducts and a rearranged π-system.
Chemical communications (Cambridge, England), 2016, 52, 11343-11346
7124968 CIFC51 H41 N7 O2P 1 21/c 111.998; 14.423; 21.871
90; 92.101; 90
3782Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124969 CIFC69 H52 N8 O4P 1 21/c 121.3761; 12.4047; 21.2424
90; 113.697; 90
5157.8Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124970 CIFC46 H38 Cl2 N6P -117.9422; 18.3629; 20.9128
107.088; 100.483; 116.305
5498.3Mosca, Lorenzo; Čejka, Jan; Dolenský, Bohumil; Havlík, Martin; Jakubek, Milan; Kaplánek, Robert; Král, Vladimír; Anzenbacher, Pavel
Bowl-shaped Tröger's bases and their recognition properties.
Chemical communications (Cambridge, England), 2016, 52, 10664-10667
7124971 CIFC17 H14 Ag N7 O4I 41/a :231.37; 31.37; 7.8467
90; 90; 90
7721.8Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124972 CIFC17 H15 Ag N7 O3.5I 41/a :231.065; 31.065; 8.0003
90; 90; 90
7720.6Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124973 CIFC19 H14 Ag F3 N6 O3P 42/n :222.8131; 22.8131; 7.7879
90; 90; 90
4053.1Li, Cheng-Peng; Wang, Si; Guo, Wei; Yan, Yan; Du, Miao
Dual structure evolution of a Ag(i) supramolecular framework triggered by anion-exchange: replacement of terminal ligand and switching of network interpenetration degree.
Chemical communications (Cambridge, England), 2016, 52, 11060-11063
7124974 CIFC29 H41 F6 Fe N4 O2 PP 1 21/c 121.0286; 8.7204; 17.6555
90; 99.237; 90
3195.6Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124975 CIFC29.5 H41 Cl Fe N4 O2P 1 21/c 19.6385; 13.7609; 23.41
90; 92.164; 90
3102.8Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124976 CIFC29 H44 Br3 Fe N5P -110.0331; 13.3181; 14.1
64.813; 81.091; 81.046
1675.9Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124977 CIFC27 H40 F6 Fe N6 O2 PP -18.4876; 12.8367; 16.0181
112.855; 90.553; 99.918
1578.52Kwon, Yubin M.; Delgado, Mayra; Zakharov, Lev N.; Seda, Takele; Gilbertson, John D.
Nitrite reduction by a pyridinediimine complex with a proton-responsive secondary coordination sphere.
Chemical communications (Cambridge, England), 2016, 52, 11016-11019
7124978 CIFC25 H25 Cl Hg N2 O3P -19.4629; 11.35; 12.3473
103.843; 109.616; 99.745
1166.87Hong, Jung-Ho; Kurapati, Sathish; Jo, Yunhee; Shin, June-Ho; Cho, Dong-Gyu
Accelerated hydration reaction of an unsymmetrical tolan evidenced by a Hg(ii)-trapped macrocycle and its application as a Hg(ii)-selective indicator.
Chemical communications (Cambridge, England), 2016, 52, 10759-10762
7124979 CIFC127 H139 Cd2 Cr4 N8 Na5 O42F 2 2 240.623; 41.321; 51.868
90; 90; 90
87065Xia, Qingchun; Liu, Yan; Li, Zijian; Gong, Wei; Cui, Yong
A Cr(salen)-based metal-organic framework as a versatile catalyst for efficient asymmetric transformations.
Chemical communications (Cambridge, England), 2016, 52, 13167-13170
7124980 CIFC8 H8 N2 O4P 1 21/c 14.7242; 12.369; 13.831
90; 82.466; 90
801.2Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124981 CIFC12 H16 N2 O5P 1 21/c 122.309; 19.1478; 9.01
90; 91.398; 90
3847.6Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124982 CIFC10 H11 N3 O4P -113.3689; 15.143; 18.786
77.079; 74.563; 63.839
3265.5Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124983 CIFC11 H14 N2 O5P 1 21/n 114.6759; 31.285; 15.9269
90; 99.324; 90
7216Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124984 CIFC12.2 H11.5 N2.7 O5.4P -4 21 c17.707; 17.707; 7.3732
90; 90; 90
2311.8Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124985 CIFC20 H22 N4 O4P -14.5668; 20.531; 20.9009
76.149; 88.228; 88.156
1901.2Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124986 CIFC8 H10 N2 O5P 21 21 214.5426; 10.729; 18.692
90; 90; 90
911Kennedy, Stuart R.; Miquelot, Adeline; Aguilar, Juan A.; Steed, Jonathan W.
Trimeric cyclamers: solution aggregation and high Z' crystals based on guest structure and basicity.
Chemical communications (Cambridge, England), 2016, 52, 11846-11849
7124987 CIFC28 H24 N4 O4 Pd2P 1 21/c 113.9426; 18.5793; 18.8456
90; 146.18; 90
2717.16Monas, Andrea; Užarević, Krunoslav; Halasz, Ivan; Kulcsár, Marina Juribašić; Ćurić, Manda
Vapour-induced solid-state C-H bond activation for the clean synthesis of an organopalladium biothiol sensor.
Chemical communications (Cambridge, England), 2016, 52, 12960-12963
7124988 CIFC28 H24 N4 O4 Pd2P b c a15.7028; 12.1884; 27.7307
90; 90; 90
5307.4Monas, Andrea; Užarević, Krunoslav; Halasz, Ivan; Kulcsár, Marina Juribašić; Ćurić, Manda
Vapour-induced solid-state C-H bond activation for the clean synthesis of an organopalladium biothiol sensor.
Chemical communications (Cambridge, England), 2016, 52, 12960-12963
7124989 CIFC30 H36 B2 Br4 Fe N6 O6C 1 2/c 126.14; 8.4019; 18.4972
90; 117.658; 90
3598.3Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124990 CIFC50 H52 B2 Fe N10 O6P 1 21/c 18.84673; 38.91135; 14.15673
90; 105.312; 90
4700.3Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124991 CIFC408 H368 B8 F48 Fe4 N40 O72 P16 Pt8 S16P -128.3614; 28.8276; 41.0379
101.861; 92.914; 104.12
31663Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124992 CIFC24 H24 B2 Br4 Fe N6 O6I 1 2/a 114.7088; 12.8848; 18.6454
90; 102.859; 90
3445.05Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124993 CIFC44 H40 B2 Fe N10 O6P 1 21/c 19.4866; 10.6979; 47.959
90; 94.425; 90
4852.7Cecot, Giacomo; Alameddine, Bassam; Prior, Stéphanie; Zorzi, Rita De; Geremia, Silvano; Scopelliti, Rosario; Fadaei, Farzaneh T.; Solari, Euro; Severin, Kay
Large heterometallic coordination cages with gyrobifastigium-like geometry.
Chemical communications (Cambridge, England), 2016, 52, 11243-11246
7124994 CIFC95 H34 O2P 1 21/c 110.8278; 30.7175; 16.9665
90; 102.171; 90
5516.3Vidal, Sara; Izquierdo, Marta; Law, Wai Kit; Jiang, Kui; Filippone, Salvatore; Perles, Josefina; Yan, He; Martín, Nazario
Photochemical site-selective synthesis of [70]methanofullerenes.
Chemical communications (Cambridge, England), 2016, 52, 12733-12736
7124995 CIFC140 H136 K4 O11P -113.3928; 15.4263; 15.9182
72.759; 71.007; 66.158
2792.2Sumy, Daniel P.; Finke, Aaron D.; Whalley, Adam C.
The reductive aromatization of tridecacyclene.
Chemical communications (Cambridge, England), 2016, 52, 12368-12371
7124996 CIFC93 H128.56 O3 UP 1 21/c 116.6756; 37.752; 12.3496
90; 93.136; 90
7762.9Hoerger, Christopher J.; La Pierre, Henry S.; Maron, Laurent; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Reductive disproportionation of nitric oxide mediated by low-valent uranium.
Chemical communications (Cambridge, England), 2016, 52, 10854-10857
7124997 CIFC81 H105 O4 UP 1 21/c 121.4453; 13.7404; 25.313
90; 119.622; 90
6484.1Hoerger, Christopher J.; La Pierre, Henry S.; Maron, Laurent; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Reductive disproportionation of nitric oxide mediated by low-valent uranium.
Chemical communications (Cambridge, England), 2016, 52, 10854-10857
7124998 CIFC9 H20 B N O2I b a 210.1195; 29.385; 7.4892
90; 90; 90
2227Romero, Erik A.; Peltier, Jesse L.; Jazzar, Rodolphe; Bertrand, Guy
Catalyst-free dehydrocoupling of amines, alcohols, and thiols with pinacol borane and 9-borabicyclononane (9-BBN).
Chemical communications (Cambridge, England), 2016, 52, 10563-10565
7124999 CIFC24 H18 Br PP 1 21/n 110.9091; 8.4128; 20.1396
90; 94.569; 90
1842.46Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125000 CIFC24 H18 As BrP 1 21/n 110.8919; 8.4344; 20.3175
90; 94.242; 90
1861.39Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125001 CIFC24 H18 Br SbP 1 21/n 110.9265; 8.5022; 20.5734
90; 93.534; 90
1907.62Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125002 CIFC33 H29 As TeP 1 21/n 112.0462; 8.7352; 25.0693
90; 98.504; 90
2608.94Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125003 CIFC33 H29 Sb TeP -18.7261; 11.7875; 14.189
79.576; 74.286; 75.358
1349.35Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125004 CIFC28 H26 Cl O P TeP 1 21/c 18.7067; 12.5095; 22.0558
90; 94.318; 90
2395.42Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125005 CIFC25 H20 Cl3 P TeP -18.5366; 11.678; 12.597
89.5; 87.76; 85.74
1251.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125006 CIFC48 H36 P2 TeP -111.7394; 12.5066; 14.3469
91.146; 101.003; 117.065
1827.45Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125007 CIFC18 H22 Cl P TeP 1 21/c 114.502; 8.33; 14.464
90; 91.826; 90
1746.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125008 CIFC18 H22 Br P TeP 1 21/n 17.786; 13.9267; 16.4054
90; 97.078; 90
1765.3Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125009 CIFC18 H22 I P TeP 1 21/n 17.9634; 14.047; 16.871
90; 99.976; 90
1858.7Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125010 CIFC38 H48 Cl4 I6 P2 Te3C 1 2/c 122.509; 11.4213; 22.101
90; 110.786; 90
5312Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125011 CIFC18 H22 I3 P TeP 1 21/n 19.8954; 15.5322; 14.5588
90; 93.366; 90
2233.8Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125012 CIFC25 H18 F3 O3 P S TeP 1 21/n 18.5859; 13.5523; 20.3142
90; 99.133; 90
2333.77Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125013 CIFC25 H18 As F3 O3 S TeP 1 21/n 18.6484; 13.5162; 20.5103
90; 99.069; 90
2367.55Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125014 CIFC28 H24 F3 O3 S Sb TeC 1 2/c 122.9864; 12.573; 20.1946
90; 115.397; 90
5272.4Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125015 CIFC40 H26 B F15 Na O7 PP 1 21/c 110.0891; 18.9802; 20.8742
90; 93.041; 90
3991.6Kather, Ralf; Rychagova, Elena; Sanz Camacho, Paula; Ashbrook, Sharon E.; Woollins, J. Derek; Robben, Lars; Lork, Enno; Ketkov, Sergey; Beckmann, Jens
Increasing the Brønsted acidity of Ph2PO2H by the Lewis acid B(C6F5)3. Formation of an eight-membered boraphosphinate ring [Ph2POB(C6F5)2O]2.
Chemical communications (Cambridge, England), 2016, 52, 10992-10995
7125016 CIFC440 H572 Au92 S44C 1 2/c 145.325; 28.1243; 88.076
90; 91.544; 90
112233Liao, Lingwen; Chen, Jishi; Wang, Chengming; Zhuang, Shengli; Yan, Nan; Yao, Chuanhao; Xia, Nan; Li, Lingling; Bao, Xiaoli; Wu, Zhikun
Transition-sized Au<sub>92</sub> nanoparticle bridging non-fcc-structured gold nanoclusters and fcc-structured gold nanocrystals.
Chemical communications (Cambridge, England), 2016, 52, 12036-12039
7125017 CIFC15 H20 N2 O2 SP -16.2192; 9.1506; 13.4968
98.63; 96.96; 92.679
752.15Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125018 CIFC18 H24 N2 O2 SP 1 21/n 110.79743; 13.38129; 11.85342
90; 96.5156; 90
1701.56Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125019 CIFC19 H20 N2 O2 SP 1 21/c 115.7933; 8.92836; 12.9799
90; 110.209; 90
1717.6Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125020 CIFC30 H40 N4 O4 S2P 1 21/n 118.0343; 7.581; 23.5816
90; 109.174; 90
3045.18Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125021 CIFC12 H16 N2 O2 S2P 1 21/c 114.6626; 5.3944; 18.2386
90; 113.435; 90
1323.6Meyer, Andreas Uwe; Berger, Anna Lucia; König, Burkhard
Metal-free C-H sulfonamidation of pyrroles by visible light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 10918-10921
7125022 CIFC29 H21 Br N2 O4P 21 21 217.08473; 16.7619; 22.085
90; 90; 90
2622.67Wang, Kai-Kai; Wang, Pan; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
Substrate-controlled switchable asymmetric annulations to access polyheterocyclic skeletons.
Chemical communications (Cambridge, England), 2016, 52, 11104-11107
7125023 CIFC23 H17 N3 O2P 21 21 2110.06732; 10.59058; 22.9703
90; 90; 90
2449.06Wang, Kai-Kai; Wang, Pan; Ouyang, Qin; Du, Wei; Chen, Ying-Chun
Substrate-controlled switchable asymmetric annulations to access polyheterocyclic skeletons.
Chemical communications (Cambridge, England), 2016, 52, 11104-11107
7125024 CIFC40 H38.4 Cl4 Cr2 F8 N4 O21.2 Tb2P -19.6481; 11.3861; 13.3598
67.617; 78.339; 87.41
1328.23Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125025 CIFC40 H37.2 Cl4 Cr2 Dy2 F8 N4 O20.6P -19.543; 11.414; 13.306
67.56; 77.95; 87.25
1309.3Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125026 CIFC40 H37.67 Cl4 Cr2 F8 Ho2 N4 O20.83P -19.667; 11.331; 13.316
67.54; 78.27; 87.69
1318.7Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125027 CIFC70 H114 Cr2 Dy2 N4 O23P -111.164; 11.907; 16.534
70.77; 73.76; 82.43
1990.5Langley, Stuart K.; Wielechowski, Daniel P.; Moubaraki, Boujemaa; Murray, Keith S.
Enhancing the magnetic blocking temperature and magnetic coercivity of {CrLn} single-molecule magnets via bridging ligand modification.
Chemical communications (Cambridge, England), 2016, 52, 10976-10979
7125028 CIFC12 H24 B10 O8P 1 21/n 111.7899; 13.5842; 13.728
90; 104.058; 90
2132.78Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125029 CIFC20 H32 B10 O8P -112.7205; 13.3454; 16.395
98.928; 92.479; 90.262
2746.7Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125030 CIFC6 H18 B10 O2P -17.3484; 7.6219; 12.005
83.262; 88.589; 88.161
667.2Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125031 CIFC6 H18 B10 O2P 1 21/n 17.7915; 21.7; 8.0127
90; 94.885; 90
1349.83Cao, Ke; Xu, Tao-Tao; Wu, Ji; Jiang, Linhai; Yang, Junxiao
Palladium catalyzed/silver tuned selective mono-/tetra-acetoxylation of o-carboranes via B-H activation.
Chemical communications (Cambridge, England), 2016, 52, 11446-11449
7125032 CIFC25 H28 F6 N4 O2 P RuC 1 2/c 130.6243; 19.9078; 11.5863
90; 102.813; 90
6887.83Xie, Jianhui; Lo, Po-Kam; Lam, William W. Y.; Man, Wai-Lun; Ma, Li; Yiu, Shek-Man; Lau, Kai-Chung; Lau, Tai-Chu
Oxidation of hydroquinones by a (salen)ruthenium(vi) nitrido complex.
Chemical communications (Cambridge, England), 2016, 52, 11430-11433
7125033 CIFC22 H16 Br Cl N2 OP 21 21 218.048; 9.69; 25.348
90; 90; 90
1976.8Bao, Xiaoze; Wei, Shiqiang; Zou, Liwei; He, Yuli; Xue, Fuzhao; Qu, Jingping; Wang, Baomin
Asymmetric chlorination of 4-substituted pyrazolones catalyzed by natural cinchona alkaloid.
Chemical communications (Cambridge, England), 2016, 52, 11426-11429
7125034 CIFC5.5 H12 F6 N2 O0.5 PC 1 2/c 116.155; 6.7318; 19.587
90; 109.09; 90
2013Regnier, Vianney; Molton, Florian; Philouze, Christian; Martin, David
An air-persistent oxyallyl radical cation with simple di(methyl)amino substituents.
Chemical communications (Cambridge, England), 2016, 52, 11422-11425
7125035 CIFC24 H17 N OP n a 2115.3015; 12.1976; 9.6252
90; 90; 90
1796.5Liu, Ren-Rong; Xu, Teng-Fei; Wang, Yong-Gang; Xiang, Bin; Gao, Jian-Rong; Jia, Yi-Xia
Palladium-catalyzed dearomative arylalkynylation of indoles.
Chemical communications (Cambridge, England), 2016, 52, 13664-13667
7125036 CIFC31 H30 Cl3 F6 N6 O P RuP -110.63; 12.402; 14.118
77.336; 74.113; 79.124
1730.1Ng, Chee Koon; Wu, Jie; Hor, T. S. Andy; Luo, He-Kuan
A binary catalyst system of a cationic Ru-CNC pincer complex with an alkali metal salt for selective hydroboration of carbon dioxide.
Chemical communications (Cambridge, England), 2016, 52, 11842-11845
7125037 CIFC31 H30 Cl4 F6 N5 O2 P RuP b c a16.6675; 11.1422; 38.2172
90; 90; 90
7097.4Ng, Chee Koon; Wu, Jie; Hor, T. S. Andy; Luo, He-Kuan
A binary catalyst system of a cationic Ru-CNC pincer complex with an alkali metal salt for selective hydroboration of carbon dioxide.
Chemical communications (Cambridge, England), 2016, 52, 11842-11845
7125038 CIFC27 H32 Br N3 O6 SP 1 21/n 113.4851; 8.5343; 25.6709
90; 103.401; 90
2873.9Fuentes de Arriba, Ángel L; Simón, Luis; Rubio, Omayra H.; Monleón, Laura M; Alcázar, Victoria; Sanz, Francisca; Raposo, César A; Morán, Joaquín R
A bio-inspired enantioselective small-molecule artificial receptor for β adrenergic agonists and antagonists and its application for enantioselective extraction.
Chemical communications (Cambridge, England), 2016, 52, 12582-12585
7125039 CIFC92 H108 Br2 N10 O15 S2P 1 21 18.3467; 25.1787; 22.297
90; 92.223; 90
4682.4Fuentes de Arriba, Ángel L; Simón, Luis; Rubio, Omayra H.; Monleón, Laura M; Alcázar, Victoria; Sanz, Francisca; Raposo, César A; Morán, Joaquín R
A bio-inspired enantioselective small-molecule artificial receptor for β adrenergic agonists and antagonists and its application for enantioselective extraction.
Chemical communications (Cambridge, England), 2016, 52, 12582-12585
7125040 CIFC44.16 N8 O76 Zr12C 1 2/m 121.28954; 14.55846; 8.10658
90; 84.173; 90
2499.59Waitschat, S.; Reinsch, H.; Stock, N.
Water-based synthesis and characterisation of a new Zr-MOF with a unique inorganic building unit.
Chemical communications (Cambridge, England), 2016, 52, 12698-12701
7125041 CIFC28 H21 Br O3P -17.336; 11.8041; 13.6969
104.265; 98.881; 96.225
1122.36Wu, Ya-Nan; Xu, Ting; Fu, Rong; Wang, Nan-Nan; Hao, Wen-Juan; Wang, Shu-Liang; Li, Guigen; Tu, Shu-Jiang; Jiang, Bo
Dual rhodium/copper catalysis: synthesis of benzo[b]fluorenes and 2-naphthalenylmethanones via de-diazotized cycloadditions.
Chemical communications (Cambridge, England), 2016, 52, 11943-11946
7125042 CIFC52 H42 B F2 Fe2 N3 O4P -112.567; 13.2195; 14.1831
114.172; 93.299; 97.933
2112Didukh, Natalia O.; Zatsikha, Yuriy V.; Rohde, Gregory T.; Blesener, Tanner S.; Yakubovskyi, Viktor P.; Kovtun, Yuriy P.; Nemykin, Victor N.
NIR absorbing diferrocene-containing meso-cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin.
Chemical communications (Cambridge, England), 2016, 52, 11563-11566
7125043 CIFC29 H21 Br Cl3 F3 N2 O3P 21 21 2112.0262; 13.8263; 17.009
90; 90; 90
2828.2Wang, Zhen-Hua; Wu, Zhi-Jun; Yue, Deng-Feng; Hu, Wen-Fei; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng
Organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with 3-alkenyl-5-arylfuran-2(3H)-ones.
Chemical communications (Cambridge, England), 2016, 52, 11708-11711
7125044 CIFC31 H30 Bi F6 Mn N3 O12 S2P -19.6023; 12.8674; 15.9332
96.095; 105.256; 104.605
1806.25Pearson, Tyler J.; Fataftah, Majed S.; Freedman, Danna E.
Enhancement of magnetic anisotropy in a Mn-Bi heterobimetallic complex.
Chemical communications (Cambridge, England), 2016, 52, 11394-11397
7125045 CIFC23 H31 BrC 1 2/c 122.7174; 6.5055; 25.667
90; 94.802; 90
3780Christopher Braddock, D.; Mahtey, Areeb; Rzepa, Henry S.; White, Andrew J. P.
Stable bromoallene oxides.
Chemical communications (Cambridge, England), 2016, 52, 11219-11222
7125046 CIFC17 H25 Br OP 1 21/n 110.8427; 6.8117; 21.255
90; 94.932; 90
1564.02Christopher Braddock, D.; Mahtey, Areeb; Rzepa, Henry S.; White, Andrew J. P.
Stable bromoallene oxides.
Chemical communications (Cambridge, England), 2016, 52, 11219-11222
7125047 CIFC19 H24 N2 O5P 1 21/c 112.59; 8.3056; 17.163
90; 97.211; 90
1780.5Cheng, Jian; Xu, Pan; Li, Weipeng; Cheng, Yixiang; Zhu, Chengjian
The functionalization of a cascade of C(sp(2))-H/C(sp(3))-H bonds: synthesis of fused dihydropyrazoles via visible-light photoredox catalysis.
Chemical communications (Cambridge, England), 2016, 52, 11901-11904
7125048 CIFC48 H64 B4 N4 O8P 1 21/n 16.4277; 10.233; 18.9139
90; 94.954; 90
1239.41Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125049 CIFC40 H26 N2P -13.9995; 9.9251; 17.4542
106.27; 91.672; 92.388
663.92Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125050 CIFC40 H26 N2P 1 21/c 111.0512; 14.4682; 8.5519
90; 91.007; 90
1367.2Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125051 CIFC52 H26 N2P 1 21/c 19.1494; 8.9306; 20.285
90; 92.501; 90
1655.9Barbero, Héctor; Ferrero, Sergio; Álvarez-Miguel, Lucía; Gómez-Iglesias, Patricia; Miguel, Daniel; Álvarez, Celedonio M
Affinity modulation of photoresponsive hosts for fullerenes: light-gated corannulene tweezers.
Chemical communications (Cambridge, England), 2016, 52, 12964-12967
7125052 CIFC18 H19 Br O3P 21 21 218.7409; 12.0555; 16.4217
90; 90; 90
1730.45Liu, Yangbin; Hu, Haipeng; Lin, Lili; Hao, Xiaoyu; Liu, Xiaohua; Feng, Xiaoming
Enantioselective construction of branched 1,3-dienyl substituted quaternary carbon stereocenters by asymmetric allenyl Claisen rearrangement.
Chemical communications (Cambridge, England), 2016, 52, 11963-11966
7125053 CIFC16 H13 Br I O3P 21 21 217.5432; 12.7924; 17.2791
90; 90; 90
1667.36Liu, Yangbin; Hu, Haipeng; Lin, Lili; Hao, Xiaoyu; Liu, Xiaohua; Feng, Xiaoming
Enantioselective construction of branched 1,3-dienyl substituted quaternary carbon stereocenters by asymmetric allenyl Claisen rearrangement.
Chemical communications (Cambridge, England), 2016, 52, 11963-11966
7125054 CIFC46 H29.41 Ba3.99 Br0 N2 O20 P6C 1 2/c 143.611; 8.549; 34.589
90; 103.59; 90
12535Fard, Z. H.; Kalinovskyy, Y.; Spasyuk, D. M.; Blight, B. A.; Shimizu, G. K. H.
Alkaline-earth phosphonate MOFs with reversible hydration-dependent fluorescence.
Chemical communications (Cambridge, England), 2016, 52, 12865-12868
7125055 CIFC52 H41 N3C 1 2/c 127.2441; 12.2005; 23.5008
90; 103.574; 90
7593.3Norouzi-Arasi, Hassan; Pal, Amlan K.; Nag, Samik; Chartrand, Daniel; Hanan, Garry S.
Synthesis and photophysical properties of C<sub>3</sub>-symmetric tris(pyridyl)truxene scaffolds of Ru(ii) and Re(i).
Chemical communications (Cambridge, England), 2016, 52, 12159-12162
7125056 CIFC68 H53 Cl60 F6 N3 O3 P ReR -3 :H13.4468; 13.4468; 53.0891
90; 90; 120
8313.3Norouzi-Arasi, Hassan; Pal, Amlan K.; Nag, Samik; Chartrand, Daniel; Hanan, Garry S.
Synthesis and photophysical properties of C<sub>3</sub>-symmetric tris(pyridyl)truxene scaffolds of Ru(ii) and Re(i).
Chemical communications (Cambridge, England), 2016, 52, 12159-12162
7125057 CIFC176 H532 N135 O209 Pd20P -125.125; 25.841; 36.446
71.625; 74.386; 67.204
20408Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125058 CIFC204 H351 N130 O191 Pd20C 1 2/c 148.457; 27.761; 37.941
90; 108.713; 90
48341Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125059 CIFC196 H357 N118.5 O119.5 Pd20 Si3P 1 21/c 146.603; 25.734; 37.303
90; 113.398; 90
41058Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125060 CIFC108 H166 N55 O59.5 Pd8 Si4P 1 21/n 124.8071; 18.2127; 40.556
90; 96.472; 90
18207Wang, Shitao; Sawada, Tomohisa; Fujita, Makoto
Capsule-bowl conversion triggered by a guest reaction.
Chemical communications (Cambridge, England), 2016, 52, 11653-11656
7125061 CIFC20 H16 F2 N6 O4P -15.502; 8.865; 10.409
107.757; 97.878; 93.199
476.4Duncan, Andrew J. E.; Dudovitz, Roxanne L.; Dudovitz, Shawna J.; Stojaković, Jelena; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Quantitative and regiocontrolled cross-photocycloaddition of the anticancer drug 5-fluorouracil achieved in a cocrystal.
Chemical communications (Cambridge, England), 2016, 52, 13109-13111
7125062 CIFC16 H13 F N4 O2P -17.8358; 12.4452; 15.629
98.513; 102.02; 101.749
1430.3Duncan, Andrew J. E.; Dudovitz, Roxanne L.; Dudovitz, Shawna J.; Stojaković, Jelena; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Quantitative and regiocontrolled cross-photocycloaddition of the anticancer drug 5-fluorouracil achieved in a cocrystal.
Chemical communications (Cambridge, England), 2016, 52, 13109-13111
7125063 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.802; 20.7715; 18.8547
90; 100.48; 90
5315.3El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125064 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.869; 20.739; 18.963
90; 100.223; 90
5368El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125065 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 113.935; 20.745; 19.086
90; 100.55; 90
5424El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125066 CIFC102 H88 Cl0 Cu4 F12 N2 P10P 1 21/n 114.023; 20.778; 19.191
90; 100.733; 90
5494El Sayed Moussa, M.; Evariste, S.; Wong, H.-L.; Le Bras, L.; Roiland, C.; Le Polles, L.; Le Guennic, B.; Costuas, K.; Yam, V. W.-W.; Lescop, C.
A solid state highly emissive Cu(i) metallacycle: promotion of cuprophilic interactions at the excited states.
Chemical communications (Cambridge, England), 2016, 52, 11370-11373
7125067 CIFC4 H4 N2 O2.5 S0.5P 1 21/c 18.533; 13.0141; 9.6918
90; 92.131; 90
1075.5Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125068 CIFC8 H8 N4 O5.4 S0.6P 1 21/c 18.4569; 12.94; 9.5593
90; 92.626; 90
1045Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125069 CIFC8 H8 N4 O5.2 S0.8P 1 21/c 18.4662; 12.9681; 9.6819
90; 92.49; 90
1062Shemchuk, O.; Braga, D.; Grepioni, F.
Alloying barbituric and thiobarbituric acids: from solid solutions to a highly stable keto co-crystal form.
Chemical communications (Cambridge, England), 2016, 52, 11815-11818
7125070 CIFC5 H12 O P2P n m a18.159; 7.4484; 6.3101
90; 90; 90
853.5Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125071 CIFC18 H39 N7 O2 P2P 1 21/c 111.8762; 15.7545; 13.6079
90; 94.012; 90
2539.8Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125072 CIFC5 H12 N O PP 1 21/m 15.941; 7.4092; 8.8324
90; 99.184; 90
383.8Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125073 CIFC39 H90 P3 Sb11C 1 c 131.443; 11.2133; 21.6617
90; 123.21; 90
6390Jost, Maximilian; Finger, Lars H.; Sundermeyer, Jörg; von Hänisch, Carsten
Simple access to ionic liquids and organic salts containing the phosphaethynolate (PCO(-)) and Zintl (Sb11(3-)) anions.
Chemical communications (Cambridge, England), 2016, 52, 11646-11648
7125074 CIFC26 H19 Cl O4P -18.8081; 9.9881; 12.6194
79.9048; 82.4837; 80.2931
1071.49Gao, Wen-Chao; Hu, Fei; Tian, Jun; Li, Xing; Wei, Wen-Long; Chang, Hong-Hong
Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes.
Chemical communications (Cambridge, England), 2016, 52, 13097-13100
7125075 CIFC26 H22 O4P 1 21/n 18.5852; 15.905; 15.6721
90; 95.176; 90
2131.3Gao, Wen-Chao; Hu, Fei; Tian, Jun; Li, Xing; Wei, Wen-Long; Chang, Hong-Hong
Hypoiodite-catalysed oxidative cyclisation of Michael adducts of chalcones with 1,3-dicarbonyl compounds: a facile and versatile approach to substituted furans and cyclopropanes.
Chemical communications (Cambridge, England), 2016, 52, 13097-13100
7125076 CIFC27 H30 F2 N4 O6P -19.423; 12.742; 12.89
62.717; 70.16; 76.407
1288Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125077 CIFC29 H34 F2 N4 O6P -17.9588; 10.3333; 17.8484
80.749; 87.489; 72.019
1377.99Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125078 CIFC28 H32 F2 N4 O6P -19.5457; 12.8769; 13.338
62.8916; 71.3599; 77.1301
1377.05Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125079 CIFC30 H36 F2 N4 O6P -19.5693; 9.7134; 17.7964
74.767; 76.025; 69.597
1475.24Gunnam, Anilkumar; Suresh, Kuthuru; Ganduri, Ramesh; Nangia, Ashwini
Crystal engineering of a zwitterionic drug to neutral cocrystals: a general solution for floxacins.
Chemical communications (Cambridge, England), 2016, 52, 12610-12613
7125080 CIFC27 H28 Cl2 N6 Ni O8P 1 21/c 19.5286; 17.004; 17.9431
90; 96.744; 90
2887.1Kankanamalage, Pavithra H. A.; Mazumder, Shivnath; Tiwari, Vishwas; Kpogo, Kenneth K.; Bernhard Schlegel, H.; Verani, Cláudio N
Efficient electro/photocatalytic water reduction using a [Ni<sup>II</sup>(N<sub>2</sub>Py<sub>3</sub>)]<sup>2+</sup> complex.
Chemical communications (Cambridge, England), 2016, 52, 13357-13360
7125081 CIFC22 H28 O3P -17.8366; 8.8547; 14.3134
84.725; 88.103; 87.621
987.73Tharra, Prabhakararao; Baire, Beeraiah
The Z-enoate assisted, Meyer-Schuster rearrangement cascade: unconventional synthesis of α-arylenone esters.
Chemical communications (Cambridge, England), 2016, 52, 12147-12150
7125082 CIFC144 H126 Br12 Mn18 N24 Na6 O66R -3 c :H44.3099; 44.3099; 21.2242
90; 90; 120
36088Manoli, Maria; Inglis, Ross; Piligkos, Stergios; Yanhua, Lan; Wernsdorfer, Wolfgang; Brechin, Euan K.; Tasiopoulos, Anastasios J.
A hexameric [MnNa<sub>6</sub>] wheel based on [MnO]<sup>7+</sup> sub-units.
Chemical communications (Cambridge, England), 2016, 52, 12829-12832
7125083 CIFC20 H20 As F6 S12P -16.6588; 8.4075; 15.219
83.79; 77.405; 67.799
769.6Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125084 CIFC20 H20 As F6 S12P 16.6849; 8.3964; 15.203
86.78; 77.306; 68.018
771.63Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125085 CIFC20 H20 F6 S12 SbP -16.6221; 8.485; 15.3114
87.078; 77.556; 68.221
779.75Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125086 CIFC20 H20 F6 S12 SbP 16.6529; 8.4663; 15.2766
87.151; 77.495; 68.478
781.06Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125087 CIFC20 H20 As2 F12 S12P 1 21 18.0663; 16.177; 14.023
90; 100.231; 90
1800.7Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125088 CIFC20 H20 As2 F12 S12P 1 21 18.0746; 16.1837; 14.0446
90; 100.159; 90
1806.53Pop, Flavia; Auban-Senzier, Pascale; Canadell, Enric; Avarvari, Narcis
Anion size control of the packing in the metallic versus semiconducting chiral radical cation salts (DM-EDT-TTF)<sub>2</sub>XF<sub>6</sub> (X = P, As, Sb).
Chemical communications (Cambridge, England), 2016, 52, 12438-12441
7125089 CIFC26 H16 N2 O8 Zn2P -110.887; 10.896; 14.07
91.252; 92.588; 104.43
1613.8Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125090 CIFC13 H8 N O4 ZnP -17.9917; 9.4227; 10.5835
65.314; 86.464; 76.513
703.6Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125091 CIFC26.87 H16 N2 O9.73 Zn2P 1 21/c 114.099; 10.997; 21.865
90; 93.971; 90
3382Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125092 CIFC13 H8 N O4 ZnP -17.871; 9.34; 10.629
65.253; 86.362; 77.446
692.3Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125093 CIFC26 H16 N2 O8 Zn2P 1 21/c 114.065; 10.949; 21.771
90; 94.319; 90
3343Bhatt, Prashant M.; Batisai, Eustina; Smith, Vincent J.; Barbour, Leonard J.
Creation of new guest accessible space under gas pressure in a flexible MOF: multidimensional insight through combination of in situ techniques.
Chemical communications (Cambridge, England), 2016, 52, 11374-11377
7125094 CIFC30 Cu2 N2 O12F m -3 m46.542; 46.542; 46.542
90; 90; 90
100817Zheng, Baishu; Wang, Hang; Wang, Zhaoxu; Ozaki, Noriaki; Hang, Cheng; Luo, Xin; Huang, Lu; Zeng, Wenjiang; Yang, Ming; Duan, Jingui
A highly porous rht-type acylamide-functionalized metal-organic framework exhibiting large CO<sub>2</sub> uptake capabilities.
Chemical communications (Cambridge, England), 2016, 52, 12988-12991
7125095 CIFC20 H26 N O4P 1 21/n 16.1031; 11.4651; 26.396
90; 95.114; 90
1839.6Zhang, Hang; Wang, Bo; Yi, Heng; Sun, Tong; Zhang, Yan; Wang, Jianbo
Transition-metal-free three-component reaction of cyclopropenes, aldehydes and amines.
Chemical communications (Cambridge, England), 2016, 52, 13285-13287
7125096 CIFC144 H232 Sn10P -114.287; 15.4; 16.699
102.618; 97.963; 99.865
3472.7Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125097 CIFC44 H64 Mg N2P 21 21 219.0942; 20.5821; 21.2116
90; 90; 90
3970.3Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125098 CIFC38 H52 Mg N2P 21 21 2111.2579; 16.4458; 18.2926
90; 90; 90
3386.79Wiederkehr, J.; Wölper, C; Schulz, S.
Synthesis and solid state structure of a metalloid tin cluster [Sn<sub>10</sub>(trip<sub>8</sub>)].
Chemical communications (Cambridge, England), 2016, 52, 12282-12285
7125099 CIFC15 H24 O3P 1 21 19.9792; 6.6848; 10.2099
90; 96.735; 90
676.39Li, Fu-Zhuo; Li, Shuang; Zhang, Peng-Peng; Huang, Zhi-Hui; Zhang, Wei-Bin; Gong, Jianxian; Yang, Zhen
A chiral pool approach for asymmetric syntheses of (-)-antrocin, (+)-asperolide C, and (-)-trans-ozic acid.
Chemical communications (Cambridge, England), 2016, 52, 12426-12429
7125100 CIFC54 H64 B2 Mg O8P 1 21/n 111.3567; 12.2346; 18.4353
90; 108.188; 90
2433.5Mukherjee, Debabrata; Shirase, Satoru; Spaniol, Thomas P.; Mashima, Kazushi; Okuda, Jun
Magnesium hydridotriphenylborate [Mg(thf)<sub>6</sub>][HBPh<sub>3</sub>]<sub>2</sub>: a versatile hydroboration catalyst.
Chemical communications (Cambridge, England), 2016, 52, 13155-13158
7125101 CIFC15 H25 N O3P 1 21/n 111.3879; 10.6012; 12.1055
90; 98.506; 90
1445.37Ho, Guo-Ming; Li, Yu-Jang
Stereoselective synthesis of 2,3,4-highly substituted oxetanes by intramolecular C-C bond forming Michael addition.
Chemical communications (Cambridge, England), 2016, 52, 12108-12111
7125102 CIFC13 H39 N24 O13P -111.1811; 11.6175; 14.5096
70.505; 78.122; 74.189
1695.7Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125103 CIFC19 H13 N O4P 1 21/n 110.7549; 7.0492; 19.1664
90; 102.5; 90
1418.63Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125104 CIFC23 H21 N O3P -18.6755; 10.6916; 11.439
69.968; 73.363; 72.428
930.3Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125105 CIFC20 H16 Br N O3P 1 21/c 14.288; 27.2739; 14.6976
90; 90.213; 90
1718.9Zhang, Cheng; Chang, Sailan; Qiu, Lihua; Xu, Xinfang
Chemodivergent synthesis of multi-substituted/fused pyrroles via copper-catalyzed carbene cascade reaction of propargyl α-iminodiazoacetates.
Chemical communications (Cambridge, England), 2016, 52, 12470-12473
7125106 CIFC31 H55 Co Fe P5 SiP -110.1595; 12.5137; 15.7867
100.375; 100.066; 108.045
1819.16Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125107 CIFC29 H50 Co Fe N P5P 1 21/n 112.73; 15.579; 17.3044
90; 108.258; 90
3259.05Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125108 CIFC29 H50 Fe N Ni P5P 1 21/n 112.7483; 15.4746; 17.3699
90; 107.71; 90
3264.25Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125109 CIFC29 H50 Fe2 N P5P 1 21/c 117.2557; 12.4359; 16.6796
90; 114.972; 90
3244.67Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125110 CIFC31 H55 Cr Fe P5 SiP 1 21/c 119.9256; 11.6275; 16.4157
90; 106.491; 90
3646.82Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125111 CIFC31 H55 Co F6 Fe P6 SiP 1 21/n 114.9545; 16.8539; 15.7381
90; 98.016; 90
3927.9Mädl, Eric; Peresypkina, Eugenia; Timoshkin, Alexey Y.; Scheer, Manfred
Triple-decker sandwich complexes with a bent cyclo-P<sub>5</sub> middle-deck.
Chemical communications (Cambridge, England), 2016, 52, 12298-12301
7125112 CIFC50 H60 B2 N2P b c n12.89; 9.6595; 16.653
90; 90; 90
2073.5Yuan, Ningning; Wang, Wenqing; Wu, Ziye; Chen, Sheng; Tan, Gengwen; Sui, Yunxia; Wang, Xinping; Jiang, Jun; Power, Philip P.
A boron-centered radical: a potassium-crown ether stabilized boryl radical anion.
Chemical communications (Cambridge, England), 2016, 52, 12714-12716
7125113 CIFC41 H62 B K N O7P 1 21 18.243; 20.22; 12.5726
90; 101.097; 90
2056.3Yuan, Ningning; Wang, Wenqing; Wu, Ziye; Chen, Sheng; Tan, Gengwen; Sui, Yunxia; Wang, Xinping; Jiang, Jun; Power, Philip P.
A boron-centered radical: a potassium-crown ether stabilized boryl radical anion.
Chemical communications (Cambridge, England), 2016, 52, 12714-12716
7125114 CIFC60 H93 Cd3 Ce I6 N6 O11 P2P 1 21/c 126.1665; 15.2608; 23.2073
90; 114.863; 90
8408.3Li, Quan-Wen; Wan, Rui-Chen; Chen, Yan-Cong; Liu, Jun-Liang; Wang, Long-Fei; Jia, Jian-Hua; Chilton, Nicholas F.; Tong, Ming-Liang
Unprecedented hexagonal bipyramidal single-ion magnets based on metallacrowns.
Chemical communications (Cambridge, England), 2016, 52, 13365-13368
7125115 CIFC60 H93 Cd3 I6 N6 Nd O11 P2P 1 21/c 126.2751; 15.2788; 23.1448
90; 114.769; 90
8436.7Li, Quan-Wen; Wan, Rui-Chen; Chen, Yan-Cong; Liu, Jun-Liang; Wang, Long-Fei; Jia, Jian-Hua; Chilton, Nicholas F.; Tong, Ming-Liang
Unprecedented hexagonal bipyramidal single-ion magnets based on metallacrowns.
Chemical communications (Cambridge, England), 2016, 52, 13365-13368
7125116 CIFC12 H8 F2 O SP -16.924; 8.665; 8.772
108.778; 94.634; 90.55
496.3Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125117 CIFC37 H12 B F21 O SP n a 2114.6347; 9.785; 23.547
90; 90; 90
3371.9Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125118 CIFC36 H10 B F21 O SP b c a15.099; 18.8792; 23.143
90; 90; 90
6597.1Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125119 CIFC24 H8 B0.5 F11 O SC 1 2/c 125.433; 8.7969; 18.856
90; 97.15; 90
4185.9Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125120 CIFC12 H8 B F5 O SP 1 21/n 16.9113; 10.7857; 16.5078
90; 99.049; 90
1215.2Tsao, Fu An; Waked, Alexander E.; Cao, Levy; Hofmann, Jordan; Liu, Lei; Grimme, Stefan; Stephan, Douglas W.
S(vi) Lewis acids: fluorosulfoxonium cations.
Chemical communications (Cambridge, England), 2016, 52, 12418-12421
7125121 CIFC30 H55 Au3 Co2 N6 O18 S6 ZnI 2 2 210.307; 18.544; 27.144
90; 90; 90
5188Surinwong, Sireenart; Yoshinari, Nobuto; Kojima, Tatsuhiro; Konno, Takumi
A drastic change in the superhydrophilic crystal porosities of metallosupramolecular structures via a slight change in pH.
Chemical communications (Cambridge, England), 2016, 52, 12893-12896
7125122 CIFC94 H168 Au9 Co6 N18 Na2 O50 S18 ZnP 61 2 244.2485; 44.2485; 28.4446
90; 90; 120
48231.1Surinwong, Sireenart; Yoshinari, Nobuto; Kojima, Tatsuhiro; Konno, Takumi
A drastic change in the superhydrophilic crystal porosities of metallosupramolecular structures via a slight change in pH.
Chemical communications (Cambridge, England), 2016, 52, 12893-12896
7125123 CIFC29 H80 B20 Cl2 N4 O P2P -111.8867; 12.3732; 16.807
92.305; 91.809; 98.884
2438.5Wong, Yuen Onn; Smith, Mark D.; Peryshkov, Dmitry V.
Reversible water activation driven by contraction and expansion of a 12-vertex-closo-12-vertex-nido biscarborane cluster.
Chemical communications (Cambridge, England), 2016, 52, 12710-12713
7125124 CIFC30 H81 B20 N5 O P2P n a 2144.006; 9.8902; 22.5051
90; 90; 90
9794.9Wong, Yuen Onn; Smith, Mark D.; Peryshkov, Dmitry V.
Reversible water activation driven by contraction and expansion of a 12-vertex-closo-12-vertex-nido biscarborane cluster.
Chemical communications (Cambridge, England), 2016, 52, 12710-12713
7125125 CIFC62 H80 O2 Sn2P 1 21/n 113.542; 13.931; 14.562
90; 97.201; 90
2725.5Erickson, Jeremy D.; Lai, Ting Yi; Liptrot, David J.; Olmstead, Marilyn M.; Power, Philip P.
Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride.
Chemical communications (Cambridge, England), 2016, 52, 13656-13659
7125126 CIFC59 H69 N Sn2C 1 2/c 125.5341; 22.081; 21.1566
90; 122.336; 90
10078.7Erickson, Jeremy D.; Lai, Ting Yi; Liptrot, David J.; Olmstead, Marilyn M.; Power, Philip P.
Catalytic dehydrocoupling of amines and boranes by an incipient tin(ii) hydride.
Chemical communications (Cambridge, England), 2016, 52, 13656-13659
7125127 CIFC40 H40 B P3 PdP 1 21/c 110.6783; 18.823; 17.516
90; 97.699; 90
3488.9Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125128 CIFC32 H30 Cl2 I2 N P PdP -19.0882; 10.5044; 16.7224
82.47; 80.174; 86.84
1558.56Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125129 CIFC46 H45 B I N P2 PdP 1 21/c 18.8638; 22.432; 19.469
90; 94.012; 90
3861.6Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125130 CIFC36 H28 B I P2 PdF d d 218.47; 31.893; 10.3482
90; 90; 90
6095.7Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125131 CIFC66 H55 B I N O2 P2 PdP 1 21/c 115.188; 20.733; 18.38
90; 109.077; 90
5469.9Schuhknecht, Danny; Ritter, Florian; Tauchert, Michael E.
Isolation and properties of a palladium PBP pincer complex featuring an ambiphilic boryl site.
Chemical communications (Cambridge, England), 2016, 52, 11823-11826
7125132 CIFC24 H42 B O6 P Si2 WC 1 2/c 119.042; 9.093; 35.451
90; 94.657; 90
6118Kyri, A. W.; Kunzmann, R.; Schnakenburg, G.; Qu, Z.-W.; Grimme, S.; Streubel, R.
Synthesis of a monomolecular anionic FLP complex.
Chemical communications (Cambridge, England), 2016, 52, 13361-13364
7125133 CIFC14 H23 O6 P Si2 WP 21 21 219.7786; 9.9521; 21.9977
90; 90; 90
2140.76Kyri, A. W.; Kunzmann, R.; Schnakenburg, G.; Qu, Z.-W.; Grimme, S.; Streubel, R.
Synthesis of a monomolecular anionic FLP complex.
Chemical communications (Cambridge, England), 2016, 52, 13361-13364
7125134 CIFC22 H24 B10P -19.52; 13.825; 17.646
88.713; 88.594; 79.932
2285.6Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125135 CIFC23 H26 B10P 1 21/n 17.684; 23.434; 12.637
90; 94.433; 90
2268.7Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125136 CIFC H BP 1 21/c 115.683; 13.493; 11.675
90; 108.429; 90
2343.9Tu, Deshuang; Leong, Pakkin; Li, Zhihong; Hu, Rongrong; Shi, Chao; Zhang, Kenneth Yin; Yan, Hong; Zhao, Qiang
A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence.
Chemical communications (Cambridge, England), 2016, 52, 12494-12497
7125137 CIFC25 H15 Cl O4P 21 21 216.3385; 15.072; 20.735
90; 90; 90
1980.9Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125138 CIFC26 H18 O5P 1 21 19.903; 6.3446; 16.4435
90; 94.703; 90
1029.68Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125139 CIFC31 H20 O4P 1 21 111.1942; 6.6554; 16.7572
90; 108.366; 90
1184.85Liu, Yang; Li, Jiangtao; Ye, Xinyi; Zhao, Xiaowei; Jiang, Zhiyong
Organocatalytic asymmetric formal arylation of benzofuran-2(3H)-ones with cooperative visible light photocatalysis.
Chemical communications (Cambridge, England), 2016, 52, 13955-13958
7125140 CIFC84 H114 Cl3 Ir3 N12 Si3P 1 21/c 120.9974; 14.9781; 31.1032
90; 94.152; 90
9756.3Olaru, Alexandra M.; Burt, Alister; Rayner, Peter J.; Hart, Sam J.; Whitwood, Adrian C.; Green, Gary G. R.; Duckett, Simon B.
Using signal amplification by reversible exchange (SABRE) to hyperpolarise <sup>119</sup>Sn and <sup>29</sup>Si NMR nuclei.
Chemical communications (Cambridge, England), 2016, 52, 14482-14485
7125141 CIFC89.42 H141.68 Cl3 Ir3 N12 O5.42 Si3P a -327.98535; 27.98535; 27.98535
90; 90; 90
21917.6Olaru, Alexandra M.; Burt, Alister; Rayner, Peter J.; Hart, Sam J.; Whitwood, Adrian C.; Green, Gary G. R.; Duckett, Simon B.
Using signal amplification by reversible exchange (SABRE) to hyperpolarise <sup>119</sup>Sn and <sup>29</sup>Si NMR nuclei.
Chemical communications (Cambridge, England), 2016, 52, 14482-14485
7125142 CIFC22 H30 O2 SiP 1 21/c 111.8899; 39.592; 9.1681
90; 94.087; 90
4304.9Akram, Manjur O.; Bera, Saibal; Patil, Nitin T.
A facile strategy for accessing 3-alkynylchromones through gold-catalyzed alkynylation/cyclization of o-hydroxyarylenaminones.
Chemical communications (Cambridge, England), 2016, 52, 12306-12309
7125143 CIFC10.5 H6 Br0.5 Mn0.5 N2 O2C 1 2/m 123.4756; 12.4761; 7.29758
90; 97.067; 90
2121.11Coogan, M. P.; Platts, J. A.
Blue rhenium tricarbonyl DPPZ complexes - low energy charge-transfer absorption at tissue-penetrating wavelengths.
Chemical communications (Cambridge, England), 2016, 52, 12498-12501
7125144 CIFC7 H5 I N3 Se4P -4 21 m16.3764; 16.3764; 4.1533
90; 90; 90
1113.86Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125145 CIFC7 H5 I N3 Se4P -4 21 m16.2024; 16.2024; 4.004
90; 90; 90
1051.1Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125146 CIFC7 H5 I N3 Se4P -4 21 m16.0383; 16.0383; 3.8839
90; 90; 90
999Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125147 CIFC7 H5 I N3 Se4P -4 21 m15.9987; 15.9987; 3.87
90; 90; 90
990.6Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125148 CIFC7 H5 I N3 Se4P -4 21 m15.9908; 15.9908; 3.8382
90; 90; 90
981.4Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125149 CIFC7 H5 I N3 Se4P -4 21 m15.9014; 15.9014; 3.784
90; 90; 90
956.8Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125150 CIFC7 H5 I N3 Se4P -4 21 m15.8651; 15.8651; 3.765
90; 90; 90
947.7Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125151 CIFC7 H5 I N3 Se4P -4 21 m15.7336; 15.7336; 3.7167
90; 90; 90
920.1Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125152 CIFC7 H5 I N3 Se4P -4 21 m15.7128; 15.7128; 3.6914
90; 90; 90
911.4Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125153 CIFC7 H5 I N3 Se4P -4 21 m15.6976; 15.6976; 3.6631
90; 90; 90
902.6Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125154 CIFC7 H5 I N3 Se4P -4 21 m15.6831; 15.6831; 3.6436
90; 90; 90
896.2Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125155 CIFC7 H5 I N3 Se4P -4 21 m16.4704; 16.4704; 4.2345
90; 90; 90
1148.71Lekin, Kristina; Ogata, Kazuma; Maclean, Adrian; Mailman, Aaron; Winter, Stephen M.; Assoud, Abdeljalil; Mito, Masaki; Tse, John S.; Desgreniers, Serge; Hirao, Naohisa; Dube, Paul A.; Oakley, Richard T.
Pushing T<sub>C</sub> to 27.5 K in a heavy atom radical ferromagnet.
Chemical communications (Cambridge, England), 2016, 52, 13877-13880
7125156 CIFC19 H18 Br N O4P 3115.6261; 15.6261; 6.58142
90; 90; 120
1391.72Donslund, Bjarke S.; Jessen, Nicolaj Inunnguaq; Jakobsen, Joakim Bøgelund; Monleón, Alicia; Nielsen, Rune Pagh; Jørgensen, Karl Anker
Enantioselective formation of cyclopropane spiroindenes from benzofulvenes by phase transfer catalysis.
Chemical communications (Cambridge, England), 2016, 52, 12474-12477
7125157 CIFC44 H60 K2 N2 O3P 1 21/c 121.3422; 9.8659; 19.6135
90; 103.086; 90
4022.57Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125158 CIFC48 H68 Li2 N2 O4P 1 21/n 110.6922; 15.3289; 12.9982
90; 90.058; 90
2130.4Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125159 CIFC44 H60 N2 Na2 O3P 1 21/n 110.30734; 27.6447; 14.8943
90; 105.588; 90
4087.94Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125160 CIFC40 H52 N2 Na2 O2C 1 c 110.2275; 35.0736; 19.991
90; 90.758; 90
7170.4Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125161 CIFC128 H144 N8 Na8P b c n19.8237; 19.6671; 32.4878
90; 90; 90
12666.2Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125162 CIFC72 H88 K4 N4 O2P -110.4694; 16.0165; 20.7659
109.148; 102.765; 92.213
3184.74Fuentes, M Ángeles; Martínez-Martínez, Antonio J; Kennedy, Alan R.; Mulvey, Robert E.
Revealing the remarkable structural diversity of the alkali metal transfer agents of the trans-calix[2]benzene[2]pyrrolide ligand.
Chemical communications (Cambridge, England), 2016, 52, 12199-12201
7125168 CIFC9 H8 N2 OP 21 21 215.7785; 9.7172; 14.76
90; 90; 90
828.8Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125169 CIFC9 H7 F N2 OP 21 21 213.7769; 10.7326; 19.387
90; 90; 90
785.87Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125170 CIFC10 H10 N2 O2P 21 21 215.6704; 10.076; 16.296
90; 90; 90
931.1Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125171 CIFC10 H10 N2 OP 1 21/c 17.769; 11.243; 10.244
90; 100.15; 90
880.8Tang, Baolei; Zhang, Houyu; Ye, Kaiqi; Zhang, Hongyu; Wang, Yue
Highly efficient blue solid emitters and tautomerization-induced ON/OFF fluorescence switching based on structurally simple 3(5)-phenol-1H-pyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 13128-13131
7125172 CIFC14 H24 O P2 S2P 21 21 216.4559; 12.3783; 22.5131
90; 90; 90
1799.09Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125173 CIFC16 H20 P2 S2P 1 21/c 19.3474; 7.1672; 13.3103
90; 101.49; 90
873.85Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125174 CIFC15 H18 P2 S2P b c a9.1542; 16.965; 10.682
90; 90; 90
1658.9Arisawa, Mieko; Yamada, Tomoki; Tanii, Saori; Kawada, Yuta; Hashimoto, Hisako; Yamaguchi, Masahiko
Rhodium-catalyzed P-P bond exchange reaction of diphosphine disulfides.
Chemical communications (Cambridge, England), 2016, 52, 13580-13583
7125175 CIFC17 H24 O2P 1 21/n 112.7728; 8.2427; 14.1842
90; 103.024; 90
1454.93Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125176 CIFC17 H22 O2P -18.9679; 11.9038; 14.801
91.758; 94.311; 110.931
1468.8Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125177 CIFC27 H51 O Si4 SmC m c 2111.6326; 13.777; 21.1559
90; 90; 90
3390.5Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125178 CIFC32 H66 O Si6 SmP 1 21/n 111.287; 22.3415; 16.921
90; 97.974; 90
4225.7Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125179 CIFC44 H50 O2 Si2 SmI -413.1871; 13.1871; 11.4268
90; 90; 90
1987.12Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125180 CIFC54 H54 O2 Si2 SmC 1 c 117.123; 9.6421; 27.6291
90; 99.283; 90
4501.9Plesniak, Mateusz P.; Just-Baringo, Xavier; Ortu, Fabrizio; Mills, David P.; Procter, David J.
SmCp<sup>R</sup><sub>2</sub>-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols.
Chemical communications (Cambridge, England), 2016, 52, 13503-13506
7125181 CIFC48 H75 N3 O9P 112.0223; 15.7744; 15.908
61.685; 76.21; 82.022
2578.18Caumes, Xavier; Baldi, Arianna; Gontard, Geoffrey; Brocorens, Patrick; Lazzaroni, Roberto; Vanthuyne, Nicolas; Troufflard, Claire; Raynal, Matthieu; Bouteiller, Laurent
Tuning the structure of 1,3,5-benzene tricarboxamide self-assemblies through stereochemistry.
Chemical communications (Cambridge, England), 2016, 52, 13369-13372
7125182 CIFC45.5 H70.75 N3.25 O9.5P 111.5502; 15.7414; 15.8302
61.491; 83.352; 79.502
2485.47Caumes, Xavier; Baldi, Arianna; Gontard, Geoffrey; Brocorens, Patrick; Lazzaroni, Roberto; Vanthuyne, Nicolas; Troufflard, Claire; Raynal, Matthieu; Bouteiller, Laurent
Tuning the structure of 1,3,5-benzene tricarboxamide self-assemblies through stereochemistry.
Chemical communications (Cambridge, England), 2016, 52, 13369-13372
7125183 CIFC62 H44 Mo4 N22 Ni S2C 1 2/c 117.6253; 13.6069; 24.0534
90; 101.343; 90
5655.9Hung, Wei-Chieh; Sigrist, Marc; Hua, Shao-An; Wu, Lai-Chin; Liu, Tsai-Jung; Jin, Bih-Yaw; Lee, Gene-Hsiang; Peng, Shie-Ming
A heteropentanuclear metal string complex [Mo<sub>2</sub>NiMo<sub>2</sub>(tpda)<sub>4</sub>(NCS)<sub>2</sub>] with two linearly aligned quadruply bonded Mo<sub>2</sub> units connected by a Ni ion and a meso configuration of the complex.
Chemical communications (Cambridge, England), 2016, 52, 12380-12382
7125184 CIFC59 H88 N5 O SmP -112.769; 13.1625; 20.932
76.406; 80.735; 63.678
3058.5Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125185 CIFC125 H187 As5 Fe N8 O2 Sm2P -113.1985; 20.5277; 24.6698
108.733; 93.697; 93.654
6291.4Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125186 CIFC125 H187 Fe N8 O2 P5 Sm2P -113.12; 20.386; 24.637
109.26; 93.54; 93.97
6181Schoo, Christoph; Bestgen, Sebastian; Schmidt, Monika; Konchenko, Sergey N.; Scheer, Manfred; Roesky, Peter W.
Sterically induced reductive linkage of iron polypnictides with bulky lanthanide complexes by ring-opening of THF.
Chemical communications (Cambridge, England), 2016, 52, 13217-13220
7125187 CIFC30 H16 Br4 N2C 1 2/c 128.8213; 3.9568; 22.0852
90; 101.2; 90
2470.6Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125188 CIFC30 H16 Br4 N2C 1 2/c 128.561; 3.8983; 22.009
90; 100.956; 90
2405.8Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125189 CIFC30 H16 Br4 N2C 1 2/c 128.6436; 3.9085; 22.0408
90; 101.063; 90
2421.7Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125190 CIFC30 H16 Br4 N2C 1 2/c 128.6762; 3.9157; 22.0307
90; 101.079; 90
2427.67Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125191 CIFC30 H16 Br4 N2C 1 2/c 128.708; 3.9259; 22.0256
90; 101.117; 90
2435.8Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125192 CIFC30 H16 Br4 N2C 1 2/c 128.7391; 3.9377; 22.0251
90; 101.118; 90
2445.7Colin-Molina, Abraham; Pérez-Estrada, Salvador; Roa, Arian E.; Villagrana-Garcia, Alvin; Hernández-Ortega, Simón; Rodríguez, Mario; Brown, Stuart E.; Rodríguez-Molina, Braulio
Isotropic rotation in amphidynamic crystals of stacked carbazole-based rotors featuring halogen-bonded stators.
Chemical communications (Cambridge, England), 2016, 52, 12833-12836
7125193 CIFC25 H18 F3 N3C 1 2/c 121.381; 12.571; 16.69
90; 117.251; 90
3988Yu, Liu-Zhu; Wei, Yin; Shi, Min
Copper-catalyzed cascade cyclization of 1,5-enynes via consecutive trifluoromethylazidation/diazidation and click reaction: self-assembly of triazole fused isoindolines.
Chemical communications (Cambridge, England), 2016, 52, 13163-13166
7125194 CIFC44 H32 N12P -18.1858; 10.1508; 22.15
89.88; 83.44; 78.898
1793.9Yu, Liu-Zhu; Wei, Yin; Shi, Min
Copper-catalyzed cascade cyclization of 1,5-enynes via consecutive trifluoromethylazidation/diazidation and click reaction: self-assembly of triazole fused isoindolines.
Chemical communications (Cambridge, England), 2016, 52, 13163-13166
7125195 CIFC149 H168 Cl16 N6 PdP -112.4144; 17.9604; 33.3206
97.426; 96.076; 105.19
7033.5Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125196 CIFC142 H130 Cl2 N6 PdP 1 21/c 122.053; 39.391; 14.3467
90; 99.711; 90
12284.3Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125197 CIFC168 H166 Br4 N10 Pd2P -114.6518; 16.6609; 33.4649
97.604; 92.496; 92.487
8079.7Wright, James R.; Crowley, James D.; Lucas, Nigel T.
Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.
Chemical communications (Cambridge, England), 2016, 52, 12976-12979
7125198 CIFC23 H27 N3P 1 21/c 112.0143; 8.3594; 19.0526
90; 90.316; 90
1913.47Saya, Jordy M.; Oppelaar, Barry; Cioc, Răzvan C; van der Heijden, Gydo; Vande Velde, Christophe M. L.; Orru, Romano V. A.; Ruijter, Eelco
Synthesis of polycyclic spiroindolines by highly diastereoselective interrupted Ugi cascade reactions of 3-(2-isocyanoethyl)indoles.
Chemical communications (Cambridge, England), 2016, 52, 12482-12485
7125199 CIFC9 H16 F3 Li O7 SP 1 21/n 17.0179; 13.5605; 14.8661
90; 96.427; 90
1405.86Reuter, Kirsten; Thiele, Günther; Hafner, Thomas; Uhlig, Frank; von Hänisch, Carsten
Synthesis and coordination ability of a partially silicon based crown ether.
Chemical communications (Cambridge, England), 2016, 52, 13265-13268
7125200 CIFC14 H34 Cl2 F3 Li O7 S Si4P b c a14.6745; 24.0048; 32.5952
90; 90; 90
11481.9Reuter, Kirsten; Thiele, Günther; Hafner, Thomas; Uhlig, Frank; von Hänisch, Carsten
Synthesis and coordination ability of a partially silicon based crown ether.
Chemical communications (Cambridge, England), 2016, 52, 13265-13268
7125201 CIFC25 H32 Cl N5 O4 SP 1 21 16.26161; 25.924; 8.62429
90; 102.226; 90
1368.19Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125202 CIFC12 H11 N3 O3 SP -15.8245; 7.5038; 13.8162
94.785; 94.97; 95.755
595.96Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125203 CIFC23 H28 Cl N5 O4 SP 15.94757; 9.5911; 11.4509
83.8975; 82.015; 71.9997
613.81Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125204 CIFC24 H30 Cl N5 O4 SP 1 21 16.11235; 28.1898; 7.71338
90; 92.9285; 90
1327.33Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125205 CIFC22 H27 Cl N4 O4 S2P 1 21 15.99452; 23.7139; 9.33438
90; 108.528; 90
1258.14Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125206 CIFC24 H31 N5 O4 SP 1 21 16.191; 26.0113; 8.06978
90; 102.689; 90
1267.79Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125207 CIFC24 H30 N4 O5 SP 1 21 16.06973; 23.5497; 9.2011
90; 108.609; 90
1246.45Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125208 CIFC24 H29 Cl N4 O5 SP 1 21 16.00155; 26.1427; 8.40735
90; 105.247; 90
1272.66Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125209 CIFC25 H33 N5 O4 SP 1 21 16.21672; 26.581; 7.98985
90; 99.504; 90
1302.17Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125210 CIFC20 H21 Cl N4 O3 SP 1 21 17.3493; 6.04446; 23.3114
90; 94.695; 90
1032.08Miyano, Tetsuya; Sakai, Tatsuya; Hisaki, Ichiro; Ichida, Hideki; Kanematsu, Yasuo; Tohnai, Norimitsu
Hierarchical construction of SHG-active polar crystals by using multi-component crystals.
Chemical communications (Cambridge, England), 2016, 52, 13710-13713
7125211 CIFC16 H26 Cu N4 O9 ZnP 1 2/n 110.95; 6.53; 13.61
90; 92.58; 90
972.2Albalad, Jorge; Aríñez-Soriano, Javier; Vidal-Gancedo, José; Lloveras, Vega; Juanhuix, Jordi; Imaz, Inhar; Aliaga-Alcalde, Núria; Maspoch, Daniel
Hetero-bimetallic paddlewheel clusters in coordination polymers formed by a water-induced single-crystal-to-single-crystal transformation.
Chemical communications (Cambridge, England), 2016, 52, 13397-13400
7125212 CIFC32 H48 Cu3 N8 O26 ZnP 1 21/c 111.56; 16.83; 12.92
90; 110.97; 90
2347.2Albalad, Jorge; Aríñez-Soriano, Javier; Vidal-Gancedo, José; Lloveras, Vega; Juanhuix, Jordi; Imaz, Inhar; Aliaga-Alcalde, Núria; Maspoch, Daniel
Hetero-bimetallic paddlewheel clusters in coordination polymers formed by a water-induced single-crystal-to-single-crystal transformation.
Chemical communications (Cambridge, England), 2016, 52, 13397-13400
7125213 CIFC12 H14 N2 O7P 21 21 215.8274; 9.9168; 23.1227
90; 90; 90
1336.24Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125214 CIFC18 H20 N4 O8P 1 2 18.934; 5.1587; 43.225
90; 93; 90
1989.4Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125215 CIFC24 H28 N4 O14P 15.0886; 7.2518; 17.1681
93.324; 93.952; 97.338
625.42Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125216 CIFC24 H26 N6 O9P 1 21 15.074; 29.696; 8.498
90; 103.16; 90
1246.8Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125217 CIFC13 H18 N2 O8P 15.0892; 7.5329; 19.7851
84.757; 85.752; 81.727
746.03Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125218 CIFC7 H7 N2 O3P b c a7.2149; 12.4451; 15.6775
90; 90; 90
1407.69Wang, Jian-Rong; Bao, Junjie; Fan, Xiaowu; Dai, Wenjuan; Mei, Xuefeng
pH-Switchable vitamin B<sub>9</sub> gels for stoichiometry-controlled spherical co-crystallization.
Chemical communications (Cambridge, England), 2016, 52, 13452-13455
7125219 CIFC4 H13 B F3 NP b c m5.577; 11.436; 11.447
90; 90; 90
730.1Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125220 CIFC6 H24 B11 F2 NP 1 21 110.452; 13.828; 10.773
90; 90.102; 90
1557Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125221 CIFC6 H22 B11 F2 I2 NP -112.4538; 13.5015; 13.544
60.759; 72.3; 86.331
1883.28Duda, Katharina; Himmelspach, Alexander; Landmann, Johannes; Kraus, Florian; Finze, Maik
Synthesis of the fluorohydridoborate anions [BHF<sub>3</sub>]<sup>-</sup> and [1-HF<sub>2</sub>B-9,12-X<sub>2</sub>-closo-1,2-C<sub>2</sub>B<sub>10</sub>H<sub>9</sub>]<sup>-</sup> (X = H, I): deboronation of 1,2- and 1,7-dicarba-closo-dodecaboranes with anhydrous [Me<sub>4</sub>N]F.
Chemical communications (Cambridge, England), 2016, 52, 13241-13244
7125222 CIFC20 H23 N O3 SP 21 21 218.3041; 10.2744; 22.465
90; 90; 90
1916.7Huang, Wei; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Diastereoselective synthesis of 2-methoxyimidoyloxiranes via dimethyl phosphite-mediated coupling of α-keto N-sulfinyl imidates with aldehydes.
Chemical communications (Cambridge, England), 2016, 52, 13592-13595
7125223 CIFC28 H26 O4P 1 2/c 131.22; 10.5893; 13.5925
90; 89.984; 90
4493.7Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125224 CIFC25 H26 O4P 1 21 18.8392; 12.746; 9.5979
90; 99.664; 90
1066Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125225 CIFC24 H24 O5P 1 21/c 112.7888; 15.597; 11.0139
90; 110.204; 90
2061.73Lu, Danyang; Wan, Yimei; Kong, Lichun; Zhu, Gangguo
Copper-catalyzed cascade annulation between α-bromocarbonyls and biaryl or (Z)-arylvinylacetylenes enabling a direct synthesis of dibenzocycloheptanes and related compounds.
Chemical communications (Cambridge, England), 2016, 52, 13971-13974
7125226 CIFC16 H52 B20 Co N2 S4P n a 2136.4636; 9.9056; 9.921
90; 90; 90
3583.4Tu, Deshuang; Shao, Dong; Yan, Hong; Lu, Changsheng
A carborane-incorporated mononuclear Co(ii) complex showing zero-field slow magnetic relaxation.
Chemical communications (Cambridge, England), 2016, 52, 14326-14329
7125227 CIFC26 H46 Cl2 N4 SnC 1 c 110.291; 21.844; 12.742
90; 106.679; 90
2743.8Bertermann, Rüdiger; Braunschweig, Holger; Celik, Mehmet Ali; Dellermann, Theresa; Kelch, Hauke
Cyclisation of biscarbenoids - a novel mode of cyclobutadiene stabilisation.
Chemical communications (Cambridge, England), 2016, 52, 13249-13252
7125228 CIFC92 H56 N8 Zn2P 1 2/c 110.8018; 17.3515; 26.7953
90; 97.145; 90
4983.2Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125229 CIFC53 H38 N4 NiP 1 2/n 110.7748; 11.5828; 35.9716
90; 93.971; 90
4478.6Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125230 CIFC46 H28 N4 NiP c a 2118.03; 11.0785; 16.251
90; 90; 90
3246.1Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125231 CIFC46 H30 N4C 1 2/c 126.2435; 13.5308; 9.407
90; 99.357; 90
3295.9Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125232 CIFC136 H110 Ag4 F12 N16 O15 S4 Zn4P 1 21/n 19.4384; 34.9486; 20.3325
90; 101.347; 90
6575.8Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125233 CIFC63 H40 Ag3 F9 N8 O9 S3 Zn2P 1 21/n 111.3487; 18.6122; 33.9443
90; 95.1; 90
7141.5Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125234 CIFC216 H172 Ag4 F12 N16 O17 S4 Zn4P -115.4217; 16.4469; 22.1055
69.989; 69.909; 73.752
4863.4Baudron, Stéphane A; Hosseini, Mir Wais
Pre-organization of clefts for Ag-π interactions in Zn(ii) bisdipyrrin helicates for the construction of heterometallic networks.
Chemical communications (Cambridge, England), 2016, 52, 13000-13003
7125235 CIFC17 H16 N2 O3P 1 21/n 18.5064; 17.8133; 9.4824
90; 99.126; 90
1418.7Zhou, Tao; Li, Bin; Wang, Baiquan
Rhodium-catalyzed C-H activation of 3-(indolin-1-yl)-3-oxopropanenitriles with diazo compounds and tandem cyclization leading to hydrogenated azepino[3,2,1-hi]indoles.
Chemical communications (Cambridge, England), 2016, 52, 14117-14120
7125236 CIFC21 H20 N2 O4P -19.2814; 10.273; 11.8447
79.305; 79.574; 83.084
1087Zhou, Tao; Li, Bin; Wang, Baiquan
Rhodium-catalyzed C-H activation of 3-(indolin-1-yl)-3-oxopropanenitriles with diazo compounds and tandem cyclization leading to hydrogenated azepino[3,2,1-hi]indoles.
Chemical communications (Cambridge, England), 2016, 52, 14117-14120
7125237 CIFC16 H16 O4 S4P -17.6541; 9.3183; 12.9177
106.268; 100.626; 91.743
865.98Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125238 CIFC32 H30 O8 S8C 1 2/c 117.3602; 9.8696; 20.8727
90; 96.315; 90
3554.6Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125239 CIFC68 H102 Au2 Cl8 O8 S8P -19.062; 10.7865; 22.897
84.698; 80.375; 70.592
2079.6Adows, Hadeel; Zhao, Yuming
Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media.
Chemical communications (Cambridge, England), 2016, 52, 13101-13104
7125240 CIFC60 H60 Cl2 Cu N12 O14C 1 2/c 136.068; 14.096; 16.023
90; 109.397; 90
7684Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125241 CIFC60 H60 B2 Cu F8 N12 O6C 1 2/c 135.729; 13.9528; 15.8889
90; 109.211; 90
7479.8Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125242 CIFC60 H60 Cu N14 O12C 1 2/c 135.509; 14.304; 15.395
90; 108.369; 90
7421Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125243 CIFC264 H300 Cl6 Cu6 N54 O48P -124.331; 24.388; 24.415
118.745; 91.861; 118.748
10460Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125244 CIFC264 H290 Br12 Cu6 N48 O24C 1 2/c 134.915; 33.412; 34.291
90; 90.352; 90
40002Sarkar, Koushik; Paul, Mithun; Dastidar, Parthasarathi
Multifunctional single-layered vesicles derived from Cu(ii)-metal-organic-polyhedra.
Chemical communications (Cambridge, England), 2016, 52, 13124-13127
7125245 CIFC14 H20 F N O2 SP 1 21/c 17.9327; 9.5312; 19.6547
90; 100.885; 90
1459.32Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125246 CIFC16 H18 F N O2 SP 21 21 218.2947; 9.5293; 18.8749
90; 90; 90
1491.92Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125247 CIFC16 H17 N O2 SP 1 21 17.3082; 12.667; 7.9739
90; 102.802; 90
719.82Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125248 CIFC26 H36 F2 N2 O6 S2P -16.3281; 12.8693; 17.8671
105.544; 93.657; 100.435
1368.94Okoromoba, Otome E.; Li, Zhou; Robertson, Nicole; Mashuta, Mark S.; Couto, Uenifer R.; Tormena, Cláudio F; Xu, Bo; Hammond, Gerald B.
Achieving regio- and stereo-control in the fluorination of aziridines under acidic conditions.
Chemical communications (Cambridge, England), 2016, 52, 13353-13356
7125249 CIFC12 H7 N O4 ZnP b c a7.1952; 19.7441; 20.4254
90; 90; 90
2901.7Zhang, Ling; Jiang, Ke; Jiang, Mengdie; Yue, Dan; Wan, Yating; Xing, Huabin; Yang, Yu; Cui, Yuanjing; Chen, Banglin; Qian, Guodong
A highly stable amino-coordinated MOF for unprecedented block off N<sub>2</sub> adsorption and extraordinary CO<sub>2</sub>/N<sub>2</sub> separation.
Chemical communications (Cambridge, England), 2016, 52, 13568-13571
7125250 CIFC21 H24 N2 O SiP -110.08; 11.8813; 16.5509
88.653; 86.499; 89.381
1977.86Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125251 CIFC20 H30 N2 O Si2P 1 21/c 117.5738; 10.3894; 12.0069
90; 100.934; 90
2152.44Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125252 CIFC26 H29 N3 O3 SiC 1 2 140.8407; 11.72; 10.659
90; 102.731; 90
4976.53Pan, Jin-Long; Li, Quan-Zhe; Zhang, Ting-Yu; Hou, Si-Hua; Kang, Jun-Cheng; Zhang, Shu-Yu
Palladium-catalyzed direct intermolecular silylation of remote unactivated C(sp<sup>3</sup>)-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 13151-13154
7125253 CIFC39 H21 Au Cl7 F2 N O4 PP 1 21/n 18.7297; 28.9112; 15.5735
90; 103.822; 90
3816.7Hattori, Yohei; Kusamoto, Tetsuro; Sato, Tohru; Nishihara, Hiroshi
Synergistic luminescence enhancement of a pyridyl-substituted triarylmethyl radical based on fluorine substitution and coordination to gold.
Chemical communications (Cambridge, England), 2016, 52, 13393-13396
7125254 CIFC47 H43 Cl6 F6 Ir N7 O2 PP b c a22.1254; 16.4448; 28.2843
90; 90; 90
10291.2Yellol, Jyoti; Pérez, Sergio A; Yellol, Gorakh; Zajac, Juraj; Donaire, Antonio; Vigueras, Gloria; Novohradsky, Vojtech; Janiak, Christoph; Brabec, Viktor; Ruiz, José
Highly potent extranuclear-targeted luminescent iridium(iii) antitumor agents containing benzimidazole-based ligands with a handle for functionalization.
Chemical communications (Cambridge, England), 2016, 52, 14165-14168
7125255 CIFC35.5 H30.5 Cl F6 Ir N7 O2 PC 1 2/c 124.4157; 16.5559; 23.3462
90; 113.79; 90
8635.2Yellol, Jyoti; Pérez, Sergio A; Yellol, Gorakh; Zajac, Juraj; Donaire, Antonio; Vigueras, Gloria; Novohradsky, Vojtech; Janiak, Christoph; Brabec, Viktor; Ruiz, José
Highly potent extranuclear-targeted luminescent iridium(iii) antitumor agents containing benzimidazole-based ligands with a handle for functionalization.
Chemical communications (Cambridge, England), 2016, 52, 14165-14168
7125256 CIFC15 H18 O2P 1 21/n 16.3004; 8.2192; 25.844
90; 94.486; 90
1334.2Ma, Dengke; Fu, Chunling; Ma, Shengming
Diastereoselective construction of cyclopent-2-enone-4-ols from aldehydes and 1,2-allenones catalyzed by N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2016, 52, 14426-14429
7125257 CIFC36 H28 O2 P2 Pd SP -19.0944; 11.4218; 15.9032
95.9441; 103.474; 102.049
1550.8Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125258 CIFC24 H36 O2 P2 Pd SP -18.7065; 11.0937; 15.13
73.3056; 80.9582; 74.899
1346.1Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125259 CIFC28 H44 O2 P2 Pd SP -18.6167; 11.5992; 16.4263
77.1791; 79.8629; 73.9166
1526.6Ma, Qiang-Qiang; Liu, Ting; Li, Shujun; Zhang, Jie; Chen, Xuenian; Guan, Hairong
Highly efficient reduction of carbon dioxide with a borane catalyzed by bis(phosphinite) pincer ligated palladium thiolate complexes.
Chemical communications (Cambridge, England), 2016, 52, 14262-14265
7125260 CIFC216 H310 Mn10 N12 O40P -114.9101; 17.9438; 22.3792
69.512; 75.796; 81.501
5424.6Coletta, Marco; McLellan, Ross; Waddington, Amy; Sanz, Sergio; Gagnon, Kevin J.; Teat, Simon J.; Brechin, Euan K.; Dalgarno, Scott J.
Core expansion of bis-calix[4]arene-supported clusters.
Chemical communications (Cambridge, England), 2016, 52, 14246-14249
7125261 CIFC206 H280 Gd2 Mn8 N10 O44P 1 21/n 122.096; 19.157; 27.0764
90; 105.149; 90
11063Coletta, Marco; McLellan, Ross; Waddington, Amy; Sanz, Sergio; Gagnon, Kevin J.; Teat, Simon J.; Brechin, Euan K.; Dalgarno, Scott J.
Core expansion of bis-calix[4]arene-supported clusters.
Chemical communications (Cambridge, England), 2016, 52, 14246-14249
7125262 CIFC20 H24 N2 O5P -18.9003; 9.3364; 11.3581
83.515; 76.869; 82.053
907.1Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125263 CIFC19 H21 N O6P -17.787; 9.08; 12.994
106.14; 91.08; 94.96
878.4Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125264 CIFC19 H21 N O6P c a 2110.2; 12.903; 14.787
90; 90; 90
1946.1Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125265 CIFC18 H19 N O5P 1 21/c 17.3465; 12.3261; 18.1727
90; 95.772; 90
1637.3Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125266 CIFC18 H18 F N O5P 1 21/c 118.99; 5.418; 17.32
90; 113.9; 90
1629.2Mallo, Neil; Brown, Patrick T.; Iranmanesh, Hasti; MacDonald, Thomas S. C.; Teusner, Matthew J.; Harper, Jason B.; Ball, Graham E.; Beves, Jonathon E.
Photochromic switching behaviour of donor-acceptor Stenhouse adducts in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 13576-13579
7125267 CIFC25 H30 N2 O3 SP 1 21/n 115.6911; 7.8759; 19.8219
90; 106.907; 90
2343.7Kumar, Ravi; Thorat, Shridhar H.; Reddy, Maddi Sridhar
Cu-Catalyzed iminative hydroolefination of unactivated alkynes en route to 4-imino-tetrahydropyridines and 4-aminopyridines.
Chemical communications (Cambridge, England), 2016, 52, 13475-13478
7125268 CIFC72 H110 Cl4 N7 O10P 1 21/n 114.6718; 22.9104; 23.5888
90; 104.564; 90
7674.3Lavendomme, Roy; Marcélis, Lionel; Wouters, Johan; Luhmer, Michel; Jabin, Ivan
A nano-sized container for specific encapsulation of isolated water molecules.
Chemical communications (Cambridge, England), 2016, 52, 14109-14112
7125269 CIFC27 H36 N3 UP 1 21/c 114.318; 11.54; 14.975
90; 93.52; 90
2469.6Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125270 CIFC27 H35 Cl0 N3 ThP -19.59; 11.143; 11.619
88.275; 77.613; 87.316
1211.1Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125271 CIFC111 H116 O S8 ThP 1 21/c 114.983; 25.115; 27.353
90; 92.488; 90
10283Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125272 CIFC118 H124 O S8 UP 1 21/c 115.004; 25.0884; 27.253
90; 92.527; 90
10248.8Behrle, Andrew C.; Myers, Alexander J.; Rungthanaphatsophon, Pokpong; Lukens, Wayne W.; Barnes, Charles L.; Walensky, Justin R.
Uranium(iii) and thorium(iv) alkyl complexes as potential starting materials.
Chemical communications (Cambridge, England), 2016, 52, 14373-14375
7125273 CIFC180 H200 Cl18 N17 O12 PC 1 2/c 130.3787; 19.6365; 32.742
90; 109.719; 90
18386Qiao, Bo; Liu, Yun; Lee, Semin; Pink, Maren; Flood, Amar H.
A high-yield synthesis and acid-base response of phosphate-templated [3]rotaxanes.
Chemical communications (Cambridge, England), 2016, 52, 13675-13678
7125274 CIFC130 H130 N10P 43 3 236.9585; 36.9585; 36.9585
90; 90; 90
50483Qiao, Bo; Liu, Yun; Lee, Semin; Pink, Maren; Flood, Amar H.
A high-yield synthesis and acid-base response of phosphate-templated [3]rotaxanes.
Chemical communications (Cambridge, England), 2016, 52, 13675-13678
7125275 CIFC26 H24 O3P 1 21/n 18.9587; 8.4815; 27.445
90; 92.802; 90
2082.9Tharra, Prabhakararao; Baire, Beeraiah
Regioselective, cascade [3+2] annulation of β-naphthols (resorcinols) with Z-enoate propargylic alcohols: a novel entry for the synthesis of complex naphtho(benzo)furans.
Chemical communications (Cambridge, England), 2016, 52, 14290-14293
7125276 CIFC47 H54 N O2 S2P 1 21/n 116.9652; 13.3015; 18.3142
90; 108.16; 90
3927Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125277 CIFC50 H66 Au2 Cl3 F6 P2 SbP -113.279; 14.462; 15.6401
100.277; 96.426; 115.812
2598.8Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125278 CIFC42.5 H42 Cl F2 N O2P -111.0496; 12.2287; 14.2619
64.774; 82.424; 88.269
1727.4Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125279 CIFC36 H35 N O2P 1 21/n 110.8442; 13.8546; 18.575
90; 92.116; 90
2788.8Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125280 CIFC38 H39 N O4P 1 21/n 112.6921; 17.3656; 14.0302
90; 99.986; 90
3045.5Ruch, Aaron A.; Kong, Fanji; Nesterov, Vladimir N.; Slaughter, LeGrande M
Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.
Chemical communications (Cambridge, England), 2016, 52, 14133-14136
7125281 CIFC39 H53 Ge N2 OP -110.7269; 11.206; 14.4819
86.134; 88.938; 81.551
1717.93Wu, Yile; Shan, Changkai; Sun, Ying; Chen, Peng; Ying, Jianxi; Zhu, Jun; Liu, Liu Leo; Zhao, Yufen
Main group metal-ligand cooperation of N-heterocyclic germylene: an efficient catalyst for hydroboration of carbonyl compounds.
Chemical communications (Cambridge, England), 2016, 52, 13799-13802
7125282 CIFC28 H24 O4P -15.6126; 8.3452; 12.339
88.55; 78.74; 87.54
566.2Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125283 CIFC28 H24 O6P -110.4453; 10.599; 10.8669
86.506; 84.424; 71.57
1135.4Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125284 CIFC26 H20 O3P 1 21/c 110.2062; 19.416; 10.5696
90; 109.487; 90
1974.5Zhou, Yuefeng; Ma, Jun; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa
Selectivity-switchable oxidation of tetraarylethylenes to fused polycyclic compounds.
Chemical communications (Cambridge, England), 2016, 52, 13345-13348
7125285 CIFC30 H30 O6 Te3P 1 21/n 115.5616; 24.9422; 15.8574
90; 104.681; 90
5954Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125286 CIFC30 H32 O6 Te2P 1 21/n 18.3225; 15.076; 23.2305
90; 95.2; 90
2902.7Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125287 CIFC30 H36 Br6 O9 Te3P -110.889; 10.89; 18.299
86.12; 86.29; 71.19
2047.2Wang, Shitao; Li, Xuexiang; Hou, Xueqing; Sun, Yantao; Shao, Xiangfeng
Tritellurasumanene: ultrasound assisted one-pot synthesis and extended valence adducts with bromine.
Chemical communications (Cambridge, England), 2016, 52, 14486-14489
7125288 CIFC23 H27 N3 O2P -18.2014; 10.9469; 12.241
99.951; 94.49; 103.679
1043.58El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125289 CIFC26 H31 N3 O2P -19.3834; 11.8498; 22.2318
87.603; 82.452; 71.9
2329.3El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125290 CIFC25 H27 N4 O5 PC 1 2/c 129.5009; 7.6614; 21.6674
90; 92.924; 90
4890.85El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent
Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
Chemical communications (Cambridge, England), 2016, 52, 14490-14493
7125291 CIFC24 H24 Cu4 I4 N4 O16 Zr3I 4/m m m17.5411; 17.5411; 34.6975
90; 90; 90
10676.1Tan, Yan-Xi; Yang, Xue; Li, Bei-Bei; Yuan, Daqiang
Rational design of a flu-type heterometallic cluster-based Zr-MOF.
Chemical communications (Cambridge, England), 2016, 52, 13671-13674
7125292 CIFC20 H18 Br N O5 SP -17.88851; 8.9545; 14.9033
92.1745; 99.8465; 107.839
982.77Modak, Atanu; Mondal, Anirban; Watile, Rahul; Mukherjee, Semanti; Maiti, Debabrata
Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives.
Chemical communications (Cambridge, England), 2016, 52, 13916-13919
7125293 CIFC25 H26 N2 O6 SP -18.3702; 12.3731; 13.2427
108.688; 105.715; 98.948
1205.6Modak, Atanu; Mondal, Anirban; Watile, Rahul; Mukherjee, Semanti; Maiti, Debabrata
Remote meta C-H bond functionalization of 2-phenethylsulphonic acid and 3-phenylpropanoic acid derivatives.
Chemical communications (Cambridge, England), 2016, 52, 13916-13919
7125294 CIFC21 H23 Br F3 N O6P 21 21 218.6647; 15.3884; 17.0772
90; 90; 90
2277Zhi, Ying; Zhao, Kun; Liu, Qiang; Wang, Ai; Enders, Dieter
Asymmetric synthesis of functionalized trifluoromethyl-substituted pyrrolidines via an organocatalytic domino Michael/Mannich [3+2] cycloaddition.
Chemical communications (Cambridge, England), 2016, 52, 14011-14014
7125295 CIFC26 H19 N OP 1 21/c 127.556; 7.4414; 19.1328
90; 109.435; 90
3699.7Bagle, Pradip N.; Mane, Manoj V.; Vanka, K.; Shinde, Dinesh R.; Shaikh, Samir R.; Gonnade, Rajesh G.; Patil, Nitin T.
Au(i)/Ag(i) co-operative catalysis: interception of Ag-bound carbocations with α-gold(i) enals in the imino-alkyne cyclizations with N-allenamides.
Chemical communications (Cambridge, England), 2016, 52, 14462-14465
7125296 CIFC56 H46 Br Cl2 F4 O3 P3 Pd SP -112.108; 12.5; 18.24
76.07; 74.442; 82.349
2574.3Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125297 CIFC63 H53 Br F2 P3 PdP -112.225; 12.671; 19.4112
98.543; 90.489; 118.142
2611.3Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125298 CIFC57.5 H47 Br Cl3 F4 O4 P3 Pd SP 1 21/c 114.2329; 20.4798; 19.1729
90; 96.688; 90
5550.6Firth, Kelly F.; Möbus, Juri; Stephan, Douglas W.
A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
Chemical communications (Cambridge, England), 2016, 52, 13967-13970
7125299 CIFC22 H54 N8 Ni2 O10.01 P2P -110.3977; 14.1488; 22.4532
90.093; 90.531; 90.097
3303.05Neri, Gaia; Forster, Mark; Walsh, James J.; Robertson, C. M.; Whittles, T. J.; Farràs, Pau; Cowan, Alexander J.
Photochemical CO<sub>2</sub> reduction in water using a co-immobilised nickel catalyst and a visible light sensitiser.
Chemical communications (Cambridge, England), 2016, 52, 14200-14203
7125300 CIFC15 H10 N2P b c a13.936; 7.077; 22.807
90; 90; 90
2249.3Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125301 CIFC19 H16 N2 O2 SP 1 21/c 19.3811; 20.8484; 8.6963
90; 99.098; 90
1679.43Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125302 CIFC16 H12 N2 O2 SP 1 21/c 19.0829; 10.2351; 15.664
90; 97.384; 90
1444.1Liao, Zhen-Yuan; Liao, Pen-Yuan; Chien, Tun-Cheng
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu-vinylidene intermediates.
Chemical communications (Cambridge, England), 2016, 52, 14404-14407
7125303 CIFC45 H21 Dy F18 N2 O6P 21 21 2111.111; 17.6697; 22.6965
90; 90; 90
4456Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125304 CIFC45 H21 Dy F18 N2 O6P 21 21 2111.1191; 17.6604; 22.693
90; 90; 90
4456.2Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125305 CIFC48 H28 Dy F18 N2 O6P -113.216; 13.9132; 14.5959
67.984; 72.454; 84.724
2371.71Ou-Yang, J-K; Saleh, N.; Fernandez Garcia, G.; Norel, L.; Pointillart, F.; Guizouarn, T.; Cador, O.; Totti, F.; Ouahab, L.; Crassous, J.; Le Guennic, B.
Improved slow magnetic relaxation in optically pure helicene-based Dy<sup>III</sup> single molecule magnets.
Chemical communications (Cambridge, England), 2016, 52, 14474-14477
7125306 CIFC28 H19 N OP 1 21 113.0425; 10.2377; 16.1011
90; 109.601; 90
2025.32Hornillos, Valentín; Ros, Abel; Ramírez-López, Pedro; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M
Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation.
Chemical communications (Cambridge, England), 2016, 52, 14121-14124
7125307 CIFC32 H21 N OP 1 21 17.6244; 7.9489; 18.4283
90; 93.193; 90
1115.12Hornillos, Valentín; Ros, Abel; Ramírez-López, Pedro; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M
Synthesis of axially chiral heterobiaryl alkynes via dynamic kinetic asymmetric alkynylation.
Chemical communications (Cambridge, England), 2016, 52, 14121-14124
7125308 CIFC22 H25 N O5P 1 21/n 16.2373; 36.3214; 8.6667
90; 94.598; 90
1957.1Fuentes de Arriba, Angel L.; Urbitsch, Felix; Dixon, Darren J.
Umpolung synthesis of branched α-functionalized amines from imines via photocatalytic three-component reductive coupling reactions.
Chemical communications (Cambridge, England), 2016, 52, 14434-14437

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