Crystallography Open Database

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7117822 CIFC21 H42 Si3P 1 21/n 18.5296; 22.691; 13.414
90; 105.992; 90
2495.7Marina Fukawa; Takayuki Sato; Yoshio Kabe
A hydrogen bonded molecular capsule versus a 3D network of tripodal organopolysilanols
Chem.Commun., 2015, 51, 14746
7117823 CIFC33 H66 Si3P 1 21/c 127.388; 9.4848; 27.972
90; 93.236; 90
7254.7Marina Fukawa; Takayuki Sato; Yoshio Kabe
A hydrogen bonded molecular capsule versus a 3D network of tripodal organopolysilanols
Chem.Commun., 2015, 51, 14746
7117824 CIFC54 H61 Si3P -113.138; 14.093; 14.255
70.5; 84.236; 70.66
2347.4Marina Fukawa; Takayuki Sato; Yoshio Kabe
A hydrogen bonded molecular capsule versus a 3D network of tripodal organopolysilanols
Chem.Commun., 2015, 51, 14746
7117825 CIFC21 H42 O3 Si3P 21 317.538; 17.538; 17.538
90; 90; 90
5394.4Marina Fukawa; Takayuki Sato; Yoshio Kabe
A hydrogen bonded molecular capsule versus a 3D network of tripodal organopolysilanols
Chem.Commun., 2015, 51, 14746
7117826 CIFC51 H56 O4 Si3P c a n19.2489; 19.7912; 23.545
90; 90; 90
8969.7Marina Fukawa; Takayuki Sato; Yoshio Kabe
A hydrogen bonded molecular capsule versus a 3D network of tripodal organopolysilanols
Chem.Commun., 2015, 51, 14746
7117827 CIFC44 H48 B2 F4 N4 S4P -18.3989; 14.2716; 18.5507
94.761; 96.451; 101.646
2151.23A. Mirloup; Q. Huaulme; N. Leclerc; P. Leveque; T. Heiser; P. Retailleau; R. Ziessel
Thienyl-BOPHY dyes as promising templates for bulk heterojunction solar cells
Chem.Commun., 2015, 51, 14742
7117828 CIFC27 H31 Br2 F6 I3 N6 O PP -110.9697; 14.1499; 16.42
93.11; 108.455; 112.057
2196.8Sourav Chakraborty; Ranjan Dutta; Pradyut Ghosh
Halogen bonding assisted selective removal of bromide
Chem.Commun., 2015, 51, 14793
7117829 CIFC27 H33 Cl2 F6 I3 N6 O PP -110.6955; 13.5915; 16.862
93.543; 107.602; 110.756
2145.2Sourav Chakraborty; Ranjan Dutta; Pradyut Ghosh
Halogen bonding assisted selective removal of bromide
Chem.Commun., 2015, 51, 14793
7117830 CIFC54 H72 Cl3 I6 N12C 1 2/c 129.993; 12.6135; 21.963
90; 109.059; 90
7853.5Sourav Chakraborty; Ranjan Dutta; Pradyut Ghosh
Halogen bonding assisted selective removal of bromide
Chem.Commun., 2015, 51, 14793
7117831 CIFC84 H60 N24 O40 V12I -4 3 m20.084; 20.084; 20.084
90; 90; 90
8101A. W. Augustyniak; M. Fandzloch; M. Domingo; I. Lakomsk; J. A. R. Navarro
A vanadium(IV) pyrazolate metal-organic polyhedron with permanent porosity and adsorption selectivity
Chem.Commun., 2015, 51, 14724
7117832 CIFC18 H21 Br O3P 1 21 19.2717; 5.6343; 15.8631
90; 100.448; 90
814.94Pradeep R. Nareddy; Christoph Schneider
A highly enantioselective, organocatalytic [3+2]-cycloannulation reaction towards the de novo-synthesis of 1-cyclopentenyl-alpha-keto esters
Chem.Commun., 2015, 51, 14797
7117833 CIFC28 H33 N2 O1.5C 1 2/c 125.482; 11.2723; 21.767
90; 124.839; 90
5131.7Qiang Dai; Yan Jiang; Songjin Guo; Jin-Tao Yu; Jiang Cheng
3-Aza pi-allyl palladium derived from imino migration in palladium-carbene: MCRs toward multiple substituted indole skeleton
Chem.Commun., 2015, 51, 14781
7117834 CIFC29 H32 N2 OP 1 21/c 18.225; 12.718; 24.068
90; 95.287; 90
2506.9Qiang Dai; Yan Jiang; Songjin Guo; Jin-Tao Yu; Jiang Cheng
3-Aza pi-allyl palladium derived from imino migration in palladium-carbene: MCRs toward multiple substituted indole skeleton
Chem.Commun., 2015, 51, 14781
7117835 CIFC80 H70 N2 O12P 1 21/c 116.978; 16.7517; 10.8751
90; 92.952; 90
3088.9Ping Li; Josef M. Maier; Jungwun Hwang; Mark D. Smith; Jeanette A. Krause; Brian T. Mullis; Sharon M. S. Strickland; Ken D. Shimizu
Solvent-induced reversible solid-state colour change of an intramolecular charge-transfer complex
Chem.Commun., 2015, 51, 14809
7117836 CIFC74 H58 Cl4 N2 O8P 1 21/n 117.1824; 10.3899; 17.8902
90; 113.491; 90
2929.1Ping Li; Josef M. Maier; Jungwun Hwang; Mark D. Smith; Jeanette A. Krause; Brian T. Mullis; Sharon M. S. Strickland; Ken D. Shimizu
Solvent-induced reversible solid-state colour change of an intramolecular charge-transfer complex
Chem.Commun., 2015, 51, 14809
7117837 CIFC76 H64 N4 O12P -110.3369; 17.108; 18.463
115.858; 90.538; 92.053
2935.1Ping Li; Josef M. Maier; Jungwun Hwang; Mark D. Smith; Jeanette A. Krause; Brian T. Mullis; Sharon M. S. Strickland; Ken D. Shimizu
Solvent-induced reversible solid-state colour change of an intramolecular charge-transfer complex
Chem.Commun., 2015, 51, 14809
7117838 CIFC74 H60 N4 O12P -110.0093; 10.5133; 16.3672
71.388; 89.742; 62.504
1426.83Ping Li; Josef M. Maier; Jungwun Hwang; Mark D. Smith; Jeanette A. Krause; Brian T. Mullis; Sharon M. S. Strickland; Ken D. Shimizu
Solvent-induced reversible solid-state colour change of an intramolecular charge-transfer complex
Chem.Commun., 2015, 51, 14809
7117839 CIFC72 H54 N2 O8P -18.4849; 12.661; 13.7331
108.388; 98.716; 104.328
1313.5Ping Li; Josef M. Maier; Jungwun Hwang; Mark D. Smith; Jeanette A. Krause; Brian T. Mullis; Sharon M. S. Strickland; Ken D. Shimizu
Solvent-induced reversible solid-state colour change of an intramolecular charge-transfer complex
Chem.Commun., 2015, 51, 14809
7117840 CIFC40 H38 N2 O8P 1 21/c 19.0743; 15.186; 12.46
90; 106.575; 90
1645.7Ping Li; Josef M. Maier; Jungwun Hwang; Mark D. Smith; Jeanette A. Krause; Brian T. Mullis; Sharon M. S. Strickland; Ken D. Shimizu
Solvent-induced reversible solid-state colour change of an intramolecular charge-transfer complex
Chem.Commun., 2015, 51, 14809
7117841 CIFC75.36 H59.36 Cl1.28 N3.36 O8P 1 21/n 117.132; 10.4771; 17.718
90; 113.969; 90
2906Ping Li; Josef M. Maier; Jungwun Hwang; Mark D. Smith; Jeanette A. Krause; Brian T. Mullis; Sharon M. S. Strickland; Ken D. Shimizu
Solvent-induced reversible solid-state colour change of an intramolecular charge-transfer complex
Chem.Commun., 2015, 51, 14809
7117842 CIFC32 H52 Au2 F12 N8 P2P -110.3753; 10.8525; 11.5698
113.079; 90.44; 115.08
1061.59V. Leich; T. P. Spaniol; J. Okuda
Formation of alpha-[KSiH3] by hydrogenolysis of potassium triphenylsilyl
Chem.Commun., 2015, 51, 14772
7117843 CIFC46 H32 F6 Ir N6 O PP -113.99; 15.425; 23.9686
104.571; 106.453; 93.491
4752.1Chaojie Xu; Aurelie Guenet; Nathalie Kyritsakas; Jean-Marc Planeix; Mir Wais Hosseini
Molecular tectonics: heterometallic (Ir,Cu) grid-type coordination networks based on cyclometallated Ir(III) chiral metallatectons
Chem.Commun., 2015, 51, 14785
7117844 CIFC60 H48 Cl Ir N6 OP 21 21 232.5454; 12.2814; 13.942
90; 90; 90
5572.66Chaojie Xu; Aurelie Guenet; Nathalie Kyritsakas; Jean-Marc Planeix; Mir Wais Hosseini
Molecular tectonics: heterometallic (Ir,Cu) grid-type coordination networks based on cyclometallated Ir(III) chiral metallatectons
Chem.Commun., 2015, 51, 14785
7117845 CIFC60 H48 Cl Ir N6 OP 21 21 232.7712; 12.3271; 13.9638
90; 90; 90
5641Chaojie Xu; Aurelie Guenet; Nathalie Kyritsakas; Jean-Marc Planeix; Mir Wais Hosseini
Molecular tectonics: heterometallic (Ir,Cu) grid-type coordination networks based on cyclometallated Ir(III) chiral metallatectons
Chem.Commun., 2015, 51, 14785
7117846 CIFC97 H68 B2 Cl12 Cu F20 Ir2 N12 O P2C 1 2/c 133.6718; 33.6481; 13.8979
90; 110.279; 90
14770.2Chaojie Xu; Aurelie Guenet; Nathalie Kyritsakas; Jean-Marc Planeix; Mir Wais Hosseini
Molecular tectonics: heterometallic (Ir,Cu) grid-type coordination networks based on cyclometallated Ir(III) chiral metallatectons
Chem.Commun., 2015, 51, 14785
7117847 CIFC74 H80 F2 N4 O12 S4P 21 21 2110.1404; 25.087; 27.663
90; 90; 90
7037.3Xianfu Shen; Yongyun Zhou; Yongkai Xi; Jingfeng Zhao; Hongbin Zhang
Copper catalyzed sequential arylation-oxidative dimerization of o-haloanilides: synthesis of dimeric HPI alkaloids
Chem.Commun., 2015, 51, 14873
7117848 CIFC28 H42 N4 S2 Si2P 1 21/n 18.5203; 15.4125; 11.7589
90; 99.3033; 90
1523.86Philipp Biegger; Manuel Schaffroth; Kerstin Brodner; Olena Tverskoy; Frank Rominger; Uwe H. F. Bunz
Bisalkynylated 3,6-diiminocyclohexa-1,4-diene-1,4-diamine
Chem.Commun., 2015, 51, 14844
7117849 CIFC28 H52 N4 Si2P -17.813; 12.886; 15.976
102.557; 96.908; 93.896
1551.2Philipp Biegger; Manuel Schaffroth; Kerstin Brodner; Olena Tverskoy; Frank Rominger; Uwe H. F. Bunz
Bisalkynylated 3,6-diiminocyclohexa-1,4-diene-1,4-diamine
Chem.Commun., 2015, 51, 14844
7117850 CIFC28 H48 N4 Si2C 1 2/c 119.958; 14.9301; 14.7268
90; 132.098; 90
3256.1Philipp Biegger; Manuel Schaffroth; Kerstin Brodner; Olena Tverskoy; Frank Rominger; Uwe H. F. Bunz
Bisalkynylated 3,6-diiminocyclohexa-1,4-diene-1,4-diamine
Chem.Commun., 2015, 51, 14844
7117851 CIFC19 H28 N4 SiC 1 2/c 137.446; 7.8246; 30.575
90; 116.744; 90
8000Philipp Biegger; Manuel Schaffroth; Kerstin Brodner; Olena Tverskoy; Frank Rominger; Uwe H. F. Bunz
Bisalkynylated 3,6-diiminocyclohexa-1,4-diene-1,4-diamine
Chem.Commun., 2015, 51, 14844
7117852 CIFC28 H48 N4 S Si2P 1 21/c 115.4408; 13.9268; 14.8221
90; 103.112; 90
3104.3Philipp Biegger; Manuel Schaffroth; Kerstin Brodner; Olena Tverskoy; Frank Rominger; Uwe H. F. Bunz
Bisalkynylated 3,6-diiminocyclohexa-1,4-diene-1,4-diamine
Chem.Commun., 2015, 51, 14844
7117853 CIFC56 H58 N4 O Si2C 1 2/c 137.073; 11.0554; 26.576
90; 118.358; 90
9585.2Philipp Biegger; Manuel Schaffroth; Kerstin Brodner; Olena Tverskoy; Frank Rominger; Uwe H. F. Bunz
Bisalkynylated 3,6-diiminocyclohexa-1,4-diene-1,4-diamine
Chem.Commun., 2015, 51, 14844
7117854 CIFC68 H66 Cl0 N4 Si2P 1 21/n 118.069; 24.9858; 29.3954
90; 101.471; 90
13006Philipp Biegger; Manuel Schaffroth; Kerstin Brodner; Olena Tverskoy; Frank Rominger; Uwe H. F. Bunz
Bisalkynylated 3,6-diiminocyclohexa-1,4-diene-1,4-diamine
Chem.Commun., 2015, 51, 14844
7117855 CIFC42 H48 N4 O7P 1 21 19.8877; 21.2513; 11.0106
90; 107.696; 90
2204.14Kunru Yu; Xiaohua Liu; Xiaobin Lin; Lili Lin; Xiaoming Feng
Organocatalytic dynamic kinetic resolution of azlactones to construct chiral N-acyl amino acid oxime esters
Chem.Commun., 2015, 51, 14897
7117856 CIFC124 H168P 4/n19.3824; 19.3824; 14.8604
90; 90; 90
5582.7Dominik Wendinger; Johanna A. Januszewski; Frank Hampel; Rik R. Tykwinski
Thermal dimerization of [n]cumulenes (n = 5, 7, 9)
Chem.Commun., 2015, 51, 14877
7117857 CIFC76 H56P 1 21/c 116.2177; 9.01016; 21.3998
90; 98.2323; 90
3094.8Dominik Wendinger; Johanna A. Januszewski; Frank Hampel; Rik R. Tykwinski
Thermal dimerization of [n]cumulenes (n = 5, 7, 9)
Chem.Commun., 2015, 51, 14877
7117858 CIFC74 H60 Cl4P -19.7822; 12.5174; 12.6361
104.011; 90.739; 104.207
1451.01Dominik Wendinger; Johanna A. Januszewski; Frank Hampel; Rik R. Tykwinski
Thermal dimerization of [n]cumulenes (n = 5, 7, 9)
Chem.Commun., 2015, 51, 14877
7117859 CIFC24 H16 Cr2 N4 Ni O7I 2 2 28.5465; 15.9683; 20.726
90; 90; 90
2828.5Hayley S. Scott; Alankriti Bajpai; Kai-Jie Chen; Tony Pham; Brian Space; John J. Perry,IV; Michael J. Zaworotko
Novel mode of 2-fold interpenetration observed in a primitive cubic network of formula [Ni(1,2-bis(4-pyridyl)acetylene)2(Cr2O7)]n
Chem.Commun., 2015, 51, 14832
7117860 CIFC41 H41 O2 P Ru S2 SiP -111.7262; 12.1957; 13.2281
87.934; 75.058; 82.308
1811.33Julia Weismann; Viktoria H. Gessner
Si-H activation by means of metal ligand cooperation in a methandiide derived carbene complex
Chem.Commun., 2015, 51, 14909
7117861 CIFC50.5 H49 O2 P Ru S2 SiP -19.3712; 13.5265; 17.6717
97.379; 97.74; 101.302
2148.8Julia Weismann; Viktoria H. Gessner
Si-H activation by means of metal ligand cooperation in a methandiide derived carbene complex
Chem.Commun., 2015, 51, 14909
7117862 CIFC35 H37 O2 P Ru S2 SiP 1 21/n 119.017; 8.552; 20.5995
90; 105.15; 90
3233.7Julia Weismann; Viktoria H. Gessner
Si-H activation by means of metal ligand cooperation in a methandiide derived carbene complex
Chem.Commun., 2015, 51, 14909
7117867 CIFC12 H6 Cu F3 O5R -3 m :H18.5283; 18.5283; 38.8075
90; 90; 120
11537.7Chang, Ganggang; Li, Bin; Wang, Hailong; Bao, Zongbi; Yildirim, Taner; Yao, Zizhu; Xiang, Shengchang; Zhou, Wei; Chen, Banglin
A microporous metal-organic framework with polarized trifluoromethyl groups for high methane storage.
Chemical communications (Cambridge, England), 2015, 51, 14789-14792
7117868 CIFC16 H17 N2 O10 ZnP -17.1095; 9.5924; 13.2708
83.938; 84.247; 86.754
894.47Wu, Bing; Zhang, Wen-Hua; Ren, Zhi-Gang; Lang, Jian-Ping
A 1D anionic coordination polymer showing superior Congo Red sorption and its dye composite exhibiting remarkably enhanced photocurrent response.
Chemical communications (Cambridge, England), 2015, 51, 14893-14896
7117869 CIFC58 H50 Br6 Cl2P -113.6; 14.111; 16.306
106.28; 94.05; 118.05
2574Majewski, Marcin A.; Lis, Tadeusz; Cybińska, Joanna; Stępień, Marcin
Chrysaorenes: assembling coronoid hydrocarbons via the fold-in synthesis.
Chemical communications (Cambridge, England), 2015, 51, 15094-15097
7117870 CIFC90 H80 Br8P b c n29.202; 17.637; 14.745
90; 90; 90
7594Majewski, Marcin A.; Lis, Tadeusz; Cybińska, Joanna; Stępień, Marcin
Chrysaorenes: assembling coronoid hydrocarbons via the fold-in synthesis.
Chemical communications (Cambridge, England), 2015, 51, 15094-15097
7117871 CIFC9 H16 Co N O5 PP 6318.3143; 18.3143; 6.1688
90; 90; 120
1791.9Liu, Xun-Gao; Bao, Song-Song; Huang, Jian; Otsubo, Kazuya; Feng, Jian-Shen; Ren, Min; Hu, Feng-Chun; Sun, Zhihu; Zheng, Li-Min; Wei, Shiqiang; Kitagawa, Hiroshi
Homochiral metal phosphonate nanotubes.
Chemical communications (Cambridge, England), 2015, 51, 15141-15144
7117872 CIFC9 H16 Co N O5 PP 6318.288; 18.288; 6.168
90; 90; 120
1786.5Liu, Xun-Gao; Bao, Song-Song; Huang, Jian; Otsubo, Kazuya; Feng, Jian-Shen; Ren, Min; Hu, Feng-Chun; Sun, Zhihu; Zheng, Li-Min; Wei, Shiqiang; Kitagawa, Hiroshi
Homochiral metal phosphonate nanotubes.
Chemical communications (Cambridge, England), 2015, 51, 15141-15144
7117873 CIFC9 H16 N Ni O5 PP 6318.0812; 18.0812; 6.1296
90; 90; 120
1735.5Liu, Xun-Gao; Bao, Song-Song; Huang, Jian; Otsubo, Kazuya; Feng, Jian-Shen; Ren, Min; Hu, Feng-Chun; Sun, Zhihu; Zheng, Li-Min; Wei, Shiqiang; Kitagawa, Hiroshi
Homochiral metal phosphonate nanotubes.
Chemical communications (Cambridge, England), 2015, 51, 15141-15144
7117874 CIFC9 H16 N Ni O5 PP 6318.1621; 18.1621; 6.168
90; 90; 120
1762Liu, Xun-Gao; Bao, Song-Song; Huang, Jian; Otsubo, Kazuya; Feng, Jian-Shen; Ren, Min; Hu, Feng-Chun; Sun, Zhihu; Zheng, Li-Min; Wei, Shiqiang; Kitagawa, Hiroshi
Homochiral metal phosphonate nanotubes.
Chemical communications (Cambridge, England), 2015, 51, 15141-15144
7117875 CIFC32 H39 Cl2 Ir N O2 P SP -110.16597; 10.5116; 15.531
76.518; 78.361; 80.796
1569.58Oldenhof, S.; Lutz, M.; van der Vlugt, J. I.; Reek, J. N. H.
Intermolecular C-H activation with an Ir-METAMORPhos piano-stool complex - multiple reaction steps at a reactive ligand.
Chemical communications (Cambridge, England), 2015, 51, 15200-15203
7117876 CIFC32 H38 Cl Ir N O2 P SP 1 21/n 114.3385; 14.6511; 15.2223
90; 107.913; 90
3042.8Oldenhof, S.; Lutz, M.; van der Vlugt, J. I.; Reek, J. N. H.
Intermolecular C-H activation with an Ir-METAMORPhos piano-stool complex - multiple reaction steps at a reactive ligand.
Chemical communications (Cambridge, England), 2015, 51, 15200-15203
7117877 CIFC40 H44 Cl Ir N O2 P SC 1 2/c 122.7439; 18.8669; 17.573
90; 106.106; 90
7244.7Oldenhof, S.; Lutz, M.; van der Vlugt, J. I.; Reek, J. N. H.
Intermolecular C-H activation with an Ir-METAMORPhos piano-stool complex - multiple reaction steps at a reactive ligand.
Chemical communications (Cambridge, England), 2015, 51, 15200-15203
7117878 CIFC54 H52 Cl2 O10P -112.0078; 19.6299; 20.8822
97.198; 98.706; 96.895
4778.4Wei, Peifa; Li, Debing; Shi, Bingbing; Wang, Qi; Huang, Feihe
An anthracene-appended 2:3 copillar[5]arene: synthesis, computational studies, and application in highly selective fluorescence sensing for Fe(iii) ions.
Chemical communications (Cambridge, England), 2015, 51, 15169-15172
7117879 CIFC17 H14 O4P 21 21 216.7978; 7.3605; 29.386
90; 90; 90
1470.3Shi, Taoda; Guo, Xin; Teng, Shenghan; Hu, Wenhao
Pd(ii)-catalyzed formal [4+1] cycloaddition reactions of diazoacetates and aryl propargyl alcohols to form 2,5-dihydrofurans.
Chemical communications (Cambridge, England), 2015, 51, 15204-15207
7117880 CIFC113.67 H108 Cl11 I12 N24 Pd6R -3 :H35.2807; 35.2807; 10.4598
90; 90; 120
11275.3Maity, Ramananda; Mekic, Amel; van der Meer, Margarethe; Verma, Amit; Sarkar, Biprajit
Triply cyclometalated trinuclear iridium(iii) and trinuclear palladium(ii) complexes with a tri-mesoionic carbene ligand.
Chemical communications (Cambridge, England), 2015, 51, 15106-15109
7117881 CIFC3 H8 Dy O10P 1 21/c 110.9675; 9.6145; 9.9881
90; 114.179; 90
960.8Zhang, Sheng; Ke, Hongshan; Liu, Xiangyu; Wei, Qing; Xie, Gang; Chen, Sanping
A nine-coordinated dysprosium(iii) compound with an oxalate-bridged dysprosium(iii) layer exhibiting two slow magnetic relaxation processes.
Chemical communications (Cambridge, England), 2015, 51, 15188-15191
7117882 CIFC27 H35 Cl5 N3 RhP -111.144; 11.7173; 13.5405
80.6465; 68.8848; 63.5599
1476.84Cajaraville, Ana; Suárez, Jaime; López, Susana; Varela, Jesús A; Saá, Carlos
Rh(iii)-catalyzed [5+1] oxidative cycloaddition of arylguanidines with alkynes: a novel access to C4-disubstituted 1,4-dihydroquinazolin-2-amines.
Chemical communications (Cambridge, England), 2015, 51, 15157-15160
7117883 CIFC31 H41 Cl N3 RhP 1 21/c 115.6033; 11.0447; 16.5835
90; 99.361; 90
2819.8Cajaraville, Ana; Suárez, Jaime; López, Susana; Varela, Jesús A; Saá, Carlos
Rh(iii)-catalyzed [5+1] oxidative cycloaddition of arylguanidines with alkynes: a novel access to C4-disubstituted 1,4-dihydroquinazolin-2-amines.
Chemical communications (Cambridge, England), 2015, 51, 15157-15160
7117884 CIFC24 H21 N2 O2C 1 2/c 129.479; 12.053; 11.6531
90; 108.029; 90
3937.17Chen, Xun; Xie, Ying; Xiao, Xinsheng; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Rh(iii)-catalyzed chelation-assisted intermolecular carbenoid functionalization of α-imino Csp(3)-H bonds.
Chemical communications (Cambridge, England), 2015, 51, 15328-15331
7117885 CIFC23 H20 N2 O2 SP 1 21/c 115.4468; 12.2137; 10.5709
90; 90.313; 90
1994.3Chen, Xun; Xie, Ying; Xiao, Xinsheng; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Rh(iii)-catalyzed chelation-assisted intermolecular carbenoid functionalization of α-imino Csp(3)-H bonds.
Chemical communications (Cambridge, England), 2015, 51, 15328-15331
7117886 CIFC111 H156 Cu6 N11 O50P 4/m n c26.582; 26.582; 39.19
90; 90; 90
27692Wang, Dongmei; Liu, Bing; Yao, Shuo; Wang, Tao; Li, Guanghua; Huo, Qisheng; Liu, Yunling
A polyhedral metal-organic framework based on the supermolecular building block strategy exhibiting high performance for carbon dioxide capture and separation of light hydrocarbons.
Chemical communications (Cambridge, England), 2015, 51, 15287-15289
7117887 CIFC10.17 H11.33 N1.33 O2C 1 2/c 148.4142; 11.8956; 22.5531
90; 94.643; 90
12946.1Zhang, Qian; Zhang, Chun-Hang; Yang, Jun-Hui; Xin, Peng-Yang; Xuan, Xiao-Peng; Wang, Jian-Ge; Ma, Na-Na; Guo, Hai-Ming; Qu, Gui-Rong
A four-unit [c2]daisy chain connected by hydrogen bonds.
Chemical communications (Cambridge, England), 2015, 51, 15253-15256
7117888 CIFC18 H30 Fe7 N2 O40P -16.8366; 10.967; 14.884
111.35; 97.42; 92.39
1025.9Wu, Qi-Long; Han, Song-De; Wang, Qing-Lun; Zhao, Jiong-Peng; Ma, Feng; Jiang, Xue; Liu, Fu-Chen; Bu, Xian-He
Divalent metal ions modulated strong frustrated M(ii)-Fe(iii)3O (M = Fe, Mn, Mg) chains with metamagnetism only in a mixed valence iron complex.
Chemical communications (Cambridge, England), 2015, 51, 15336-15339
7117889 CIFC18 H30 Fe6 Mn N2 O40P -16.8216; 10.968; 14.889
111.14; 97.28; 92.22
1026.3Wu, Qi-Long; Han, Song-De; Wang, Qing-Lun; Zhao, Jiong-Peng; Ma, Feng; Jiang, Xue; Liu, Fu-Chen; Bu, Xian-He
Divalent metal ions modulated strong frustrated M(ii)-Fe(iii)3O (M = Fe, Mn, Mg) chains with metamagnetism only in a mixed valence iron complex.
Chemical communications (Cambridge, England), 2015, 51, 15336-15339
7117890 CIFC18 H30 Fe6 Mg N2 O40P -16.8025; 10.887; 14.826
111.43; 97.52; 92.24
1008.8Wu, Qi-Long; Han, Song-De; Wang, Qing-Lun; Zhao, Jiong-Peng; Ma, Feng; Jiang, Xue; Liu, Fu-Chen; Bu, Xian-He
Divalent metal ions modulated strong frustrated M(ii)-Fe(iii)3O (M = Fe, Mn, Mg) chains with metamagnetism only in a mixed valence iron complex.
Chemical communications (Cambridge, England), 2015, 51, 15336-15339
7117891 CIFC28 H23 N O2 S2P -110.428; 14.031; 17.164
85.171; 80.935; 82.229
2452.1Dwivedi, Vikas; Hari Babu, Madala; Kant, Ruchir; Sridhar Reddy, Maddi
N-Substitution dependent stereoselectivity switch in palladium catalyzed hydroalkynylation of ynamides: a regio and stereoselective synthesis of ynenamides.
Chemical communications (Cambridge, England), 2015, 51, 14996-14999
7117892 CIFC20 H14 F3 N O2P 1 21/c 114.816; 7.625; 15.92
90; 108.298; 90
1707.6Dwivedi, Vikas; Hari Babu, Madala; Kant, Ruchir; Sridhar Reddy, Maddi
N-Substitution dependent stereoselectivity switch in palladium catalyzed hydroalkynylation of ynamides: a regio and stereoselective synthesis of ynenamides.
Chemical communications (Cambridge, England), 2015, 51, 14996-14999
7117893 CIFC27 H25 N O2 SP 21 21 217.9578; 10.706; 27.133
90; 90; 90
2311.6Dwivedi, Vikas; Hari Babu, Madala; Kant, Ruchir; Sridhar Reddy, Maddi
N-Substitution dependent stereoselectivity switch in palladium catalyzed hydroalkynylation of ynamides: a regio and stereoselective synthesis of ynenamides.
Chemical communications (Cambridge, England), 2015, 51, 14996-14999
7117894 CIFC25 H17 N OP -16.4707; 11.8959; 12.415
76.422; 87.715; 74.476
894.8Dwivedi, Vikas; Hari Babu, Madala; Kant, Ruchir; Sridhar Reddy, Maddi
N-Substitution dependent stereoselectivity switch in palladium catalyzed hydroalkynylation of ynamides: a regio and stereoselective synthesis of ynenamides.
Chemical communications (Cambridge, England), 2015, 51, 14996-14999
7117895 CIFC16 H16 N2 S7P 1 21 15.1724; 11.6911; 31.9993
90; 91.346; 90
1934.5Amacher, Anneliese M.; Puigmartí-Luis, Josep; Geng, Yan; Lebedev, Victor; Laukhin, Vladimir; Krämer, Karl; Hauser, Jürg; Amabilino, David B.; Decurtins, Silvio; Liu, Shi-Xia
Coordination-directed self-assembly of a simple benzothiadiazole-fused tetrathiafulvalene to low-bandgap metallogels.
Chemical communications (Cambridge, England), 2015, 51, 15063-15066
7117896 CIFC60 H76 Ce N4 O6P 1 21/c 115.1376; 13.3253; 26.6562
90; 99.733; 90
5299.5Kim, Jee Eon; Carroll, Patrick J.; Schelter, Eric J.
Bidentate nitroxide ligands stable toward oxidative redox cycling and their complexes with cerium and lanthanum.
Chemical communications (Cambridge, England), 2015, 51, 15047-15050
7117897 CIFC30 H40 N2 O3P 1 21/c 110.0002; 9.8745; 27.4051
90; 96.384; 90
2689.39Kim, Jee Eon; Carroll, Patrick J.; Schelter, Eric J.
Bidentate nitroxide ligands stable toward oxidative redox cycling and their complexes with cerium and lanthanum.
Chemical communications (Cambridge, England), 2015, 51, 15047-15050
7117912 CIFC33 H34 Cl Ir N2P 21 21 2110.9592; 11.0891; 22.818
90; 90; 90
2773Kazuhiro Yoshida; Takumi Kamimura; Hiroshi Kuwabara; Akira Yanagisawa
Chiral bicyclic NHC/Ir complexes for catalytic asymmetric transfer hydrogenation of ketones
Chem.Commun., 2015, 51, 15442
7117913 CIFC40 H48 Cl3 Ir N2P 21 21 218.0761; 15.8222; 28.1212
90; 90; 90
3593.4Kazuhiro Yoshida; Takumi Kamimura; Hiroshi Kuwabara; Akira Yanagisawa
Chiral bicyclic NHC/Ir complexes for catalytic asymmetric transfer hydrogenation of ketones
Chem.Commun., 2015, 51, 15442
7117914 CIFF4 Mo Na2 O2P 1 21/c 15.48; 5.701; 16.319
90; 91.316; 90
509.7Hajime Ishikawa; Irene Munao; Bela E. Bode; Zenji Hiroi; Philip Lightfoot
Na2MoO2-deltaF4+delta - a perovskite with a unique combination of atomic orderings and octahedral tilts
Chem.Commun., 2015, 51, 15469
7117915 CIFC18 H16 O3P 1 21/c 112.9279; 7.923; 14.2519
90; 98.232; 90
1444.75Sachin Bhausahe Wagh; Rai-Shung Liu
Gold-catalyzed reactions of propargylic esters with vinylazides for the synthesis of Z- or E-configured buta-1,3-dien-2-yl esters
Chem.Commun., 2015, 51, 15462
7117916 CIFC64 H112 B2 Cr2 N14 O4P -19.552; 12.156; 17.626
77.672; 75.089; 66.894
1804.4Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117917 CIFC34 H55 B Cr N7P 1 21/n 110.976; 15.479; 21.013
90; 96.879; 90
3544.4Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117918 CIFC68 H124 B2 Cr2 N14 O2P -19.7601; 12.9429; 17.3259
75.376; 73.639; 68.607
1927.7Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117919 CIFC62 H108 B2 Cr2 N14 O2P 1 21/n 19.4997; 26.8005; 14.0071
90; 95.321; 90
3550.8Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117920 CIFC34 H58 B Cr N6 O5P -314.441; 14.441; 9.8961
90; 90; 120
1787.3Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117921 CIFC32 H58 B Cr N6 Si2P -113.129; 16.903; 17.292
97.804; 91.134; 90.927
3800.5Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117922 CIFC57 H95 B2 Cr2 N12 O4.5P -112.973; 14.797; 18.908
71.013; 74.824; 73.01
3226.1Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117923 CIFC50 H84 B2 Cr2 N12P -111.792; 13.394; 18.815
86.554; 87.189; 77.25
2891.2Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117924 CIFC28 H46 B Cr N6P 1 21/n 19.852; 19.085; 15.557
90; 90.209; 90
2925Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117925 CIFC49 H63 B Cr N6 OP 1 21/n 111.0663; 18.0587; 23.05
90; 96.87; 90
4573.3Eser S. Akturk; Glenn P. A. Yap; Klaus H. Theopold
Mechanism-based design of labile precursors for chromium(I) chemistry
Chem.Commun., 2015, 51, 15402
7117926 CIFC19 H31 B Cl Fe O3 P SiP 1 21/n 18.606; 18.251; 14.997
90; 91.994; 90
2354.1Holger Braunschweig; Rian D. Dewhurst; Krzysztof Radacki; Benedikt Wennemann; Qing Ye
1,2-Halosilane vs. 1,2-alkylborane elimination from (boryl)(silyl) complexes of iron: switching between borylenes and silylenes just by changing the alkyl group
Chem.Commun., 2015, 51, 15465
7117927 CIFC20 H38 Fe2 O6 P2 Si2P 1 21/n 110.1597; 12.9; 10.7901
90; 105.385; 90
1363.5Holger Braunschweig; Rian D. Dewhurst; Krzysztof Radacki; Benedikt Wennemann; Qing Ye
1,2-Halosilane vs. 1,2-alkylborane elimination from (boryl)(silyl) complexes of iron: switching between borylenes and silylenes just by changing the alkyl group
Chem.Commun., 2015, 51, 15465
7117928 CIFC19 H38 Fe2 O5 P2 Si2P 1 21 19.1382; 12.4474; 11.8729
90; 96.852; 90
1340.86Holger Braunschweig; Rian D. Dewhurst; Krzysztof Radacki; Benedikt Wennemann; Qing Ye
1,2-Halosilane vs. 1,2-alkylborane elimination from (boryl)(silyl) complexes of iron: switching between borylenes and silylenes just by changing the alkyl group
Chem.Commun., 2015, 51, 15465
7117929 CIFC19 H19 Br N2 O2P 21 21 215.5598; 16.478; 19.769
90; 90; 90
1811.1Liang Wei; Chun-Jiang Wang
The catalytic asymmetric synthesis of tetrahydropyridazines via inverse electron-demand aza-Diels-Alder reaction of enol ethers with azoalkenes
Chem.Commun., 2015, 51, 15374
7117930 CIFC32 H78 K N5 O8 Si6 UP 1 21/m 111.5823; 17.9907; 14.1292
90; 111.687; 90
2735.76Clement Camp; Lucile Chatelain; Christos E. Kefalidis; Jacques Pecaut; Laurent Maron; Marinella Mazzanti
CO2 conversion to isocyanate via multiple N-Si bond cleavage at a bulky uranium(III) complex
Chem.Commun., 2015, 51, 15454
7117931 CIFC36 H38 Dy N9 O13P 1 21/c 111.097; 22.1612; 16.3266
90; 90.525; 90
4014.9Long-Fei Wang; Jiang-Zhen Qiu; Jun-Liang Liu; Yan-Cong Chen; Jian-Hua Jia; Jesus Jover; Eliseo Ruiz; Ming-Liang Tong
Modulation of single-molecule magnet behaviour via photochemical [2+2] cycloaddition
Chem.Commun., 2015, 51, 15358
7117932 CIFC72 H76 Dy2 N18 O26P 1 21/c 111.039; 21.826; 16.5559
90; 93.732; 90
3980.47Long-Fei Wang; Jiang-Zhen Qiu; Jun-Liang Liu; Yan-Cong Chen; Jian-Hua Jia; Jesus Jover; Eliseo Ruiz; Ming-Liang Tong
Modulation of single-molecule magnet behaviour via photochemical [2+2] cycloaddition
Chem.Commun., 2015, 51, 15358
7117933 CIFC36 H38 Dy0.06 N9 O13 Y0.94P 1 21/c 111.0672; 22.1008; 16.3215
90; 90.754; 90
3991.79Long-Fei Wang; Jiang-Zhen Qiu; Jun-Liang Liu; Yan-Cong Chen; Jian-Hua Jia; Jesus Jover; Eliseo Ruiz; Ming-Liang Tong
Modulation of single-molecule magnet behaviour via photochemical [2+2] cycloaddition
Chem.Commun., 2015, 51, 15358
7117934 CIFC72 H76 Dy0.11 N18 O26 Y1.89P 1 21/c 111.0563; 21.8263; 16.5576
90; 93.631; 90
3987.6Long-Fei Wang; Jiang-Zhen Qiu; Jun-Liang Liu; Yan-Cong Chen; Jian-Hua Jia; Jesus Jover; Eliseo Ruiz; Ming-Liang Tong
Modulation of single-molecule magnet behaviour via photochemical [2+2] cycloaddition
Chem.Commun., 2015, 51, 15358
7117940 CIFC30 H36 F24 N4 P4I b a m23.95; 7.9241; 21.1235
90; 90; 90
4008.9Mathilde Berville; Lydia Karmazin; Jennifer A. Wytko; Jean Weiss
Viologen cyclophanes: redox controlled host-guest interactions
Chem.Commun., 2015, 51, 15772
7117941 CIFC37 H53 F18 N7 O6 P3C m c a24.2281; 16.2943; 25.5184
90; 90; 90
10074.2Mathilde Berville; Lydia Karmazin; Jennifer A. Wytko; Jean Weiss
Viologen cyclophanes: redox controlled host-guest interactions
Chem.Commun., 2015, 51, 15772
7117942 CIFC38 H50 F12 N6 P2P 21 21 2113.5413; 14.3275; 22.1621
90; 90; 90
4299.7Mathilde Berville; Lydia Karmazin; Jennifer A. Wytko; Jean Weiss
Viologen cyclophanes: redox controlled host-guest interactions
Chem.Commun., 2015, 51, 15772
7117943 CIFC58 H72 F30 N8 P5I b a m11.8988; 21.8945; 25.6947
90; 90; 90
6693.9Mathilde Berville; Lydia Karmazin; Jennifer A. Wytko; Jean Weiss
Viologen cyclophanes: redox controlled host-guest interactions
Chem.Commun., 2015, 51, 15772
7117944 CIFC44 H54 F24 N6 P4 S4P 1 21/c 110.0815; 13.6749; 23.3545
90; 115.451; 90
2907.3Mathilde Berville; Lydia Karmazin; Jennifer A. Wytko; Jean Weiss
Viologen cyclophanes: redox controlled host-guest interactions
Chem.Commun., 2015, 51, 15772
7117945 CIFC34 H44 F12 N5 O0.5 P2P 21 21 2115.7788; 17.1208; 28.0061
90; 90; 90
7565.7Mathilde Berville; Lydia Karmazin; Jennifer A. Wytko; Jean Weiss
Viologen cyclophanes: redox controlled host-guest interactions
Chem.Commun., 2015, 51, 15772
7117946 CIFC39 H47 F12 N5 P2P 21 21 2114.767; 15.632; 18.005
90; 90; 90
4156Mathilde Berville; Lydia Karmazin; Jennifer A. Wytko; Jean Weiss
Viologen cyclophanes: redox controlled host-guest interactions
Chem.Commun., 2015, 51, 15772
7117947 CIFC30 H24 Br N3 O3P 21 21 2110.8543; 13.163; 17.7406
90; 90; 90
2534.69Guodong Zhu; Baomin Wang; Xiaoze Bao; Huanrui Zhang; Qian Wei; Jingping Qu
Catalytic asymmetric construction of spiro[pyrrolidine-2,3'-oxindole] scaffolds through chiral phosphoric acid-catalyzed 1,3-dipolar cycloaddition involving 3-amino oxindoles
Chem.Commun., 2015, 51, 15510
7117948 CIFC3 H8 N2 O6 ZnP 21 21 217.29731; 7.94804; 13.8224
90; 90; 90
801.69Gregor Kieslich; Shohei Kumagai; Keith T. Butler; Takuro Okamura; Christopher H. Hendon; Shijing Sun; Masahiro Yamashita; Aron Walsh; Anthony K. Cheetham
Role of entropic effects in controlling the polymorphism in formate ABX3 metal-organic frameworks
Chem.Commun., 2015, 51, 15538
7117949 CIFC27 H34 N2 O4P 1 21/n 115.0493; 6.6839; 24.3241
90; 100.495; 90
2405.78Giovanna Parisi; Emanuela Capitanelli; Antonella Pierro; Giuseppe Romanazzi; Guy J. Clarkson; Leonardo Degennaro; Renzo Luisi
Easy access to constrained peptidomimetics and 2,2-disubstituted azetidines by the unexpected reactivity profile of alpha-lithiated N-Boc-azetidines
Chem.Commun., 2015, 51, 15588
7117950 CIFC27 H34 N2 O4P 1 21/n 110.0556; 23.0371; 10.8204
90; 106.221; 90
2406.78Giovanna Parisi; Emanuela Capitanelli; Antonella Pierro; Giuseppe Romanazzi; Guy J. Clarkson; Leonardo Degennaro; Renzo Luisi
Easy access to constrained peptidomimetics and 2,2-disubstituted azetidines by the unexpected reactivity profile of alpha-lithiated N-Boc-azetidines
Chem.Commun., 2015, 51, 15588
7117951 CIFC19 H29 N3 O6 SP 21 21 217.0964; 16.23; 19.1256
90; 90; 90
2202.8Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117952 CIFC12 H12 N2 O5 SP 1 21/c 114.99; 11.3156; 7.9
90; 95.96; 90
1333Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117953 CIFC12 H12 N2 O5 SP -15.309; 10.5807; 12.1499
76.377; 89.187; 77.195
646.28Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117954 CIFC12 H12 N2 O5 SP 1 21/n 18.464; 9.721; 16.137
90; 100.001; 90
1307.6Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117955 CIFC13 H13 N3 O5 SC 1 2/c 131.237; 5.1056; 20.362
90; 124.55; 90
2674.7Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117956 CIFC18 H18 N4 O6 SP 1 21/c 120.414; 6.5885; 14.747
90; 101.671; 90
1942.4Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117957 CIFC19 H21 N3 O6 SP 1 21/c 17.3848; 31.15; 8.9746
90; 90.676; 90
2064.3Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117958 CIFC19 H18 N5 O6 SP -15.0179; 11.3168; 18.156
95.966; 90.05; 95.469
1020.7Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117959 CIFC18 H18 N4 O6 SP 1 21/c 119.7594; 5.25798; 20.2747
90; 117.924; 90
1861.18Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117960 CIFC19 H20 N4 O6 SP 1 21/c 18.2357; 26.102; 9.2781
90; 98.283; 90
1973.7Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117961 CIFC32 H34 N6 O13 S2C 1 c 113.2514; 7.0517; 38.1412
90; 91.962; 90
3562.01Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117962 CIFC19 H21 N3 O8 SP 1 21/n 16.95437; 12.7192; 23.9115
90; 92.737; 90
2112.66Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117963 CIFC13 H13 N3 O5 SP 1 21/n 110.2113; 8.085; 17.663
90; 92.033; 90
1457.3Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117964 CIFC19 H20 N4 O6 SP 1 21/c 111.5333; 7.91065; 22.4905
90; 100.021; 90
2020.64Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117965 CIFC12 H16 N2 O5 SP -18.2121; 9.3439; 10.6539
112.237; 106.403; 95.743
705.92Geetha Bolla; Ashwini Nangia
Multicomponent ternary cocrystals of the sulfonamide group with pyridine-amides and lactams
Chem.Commun., 2015, 51, 15578
7117966 CIFC83.7 H97.7 Cl0.6 N11.7 O12P -111.6914; 13.3995; 13.6649
105.227; 99.554; 102.607
1958.27Guobao Huang; Zhenfeng He; Chen-Xi Cai; Fangfang Pan; Dingqiao Yang; Kari Rissanen; Wei Jiang
Bis-urea macrocycles with a deep cavity
Chem.Commun., 2015, 51, 15490
7117967 CIFC79 H93 Cl2 N9 O12P n m a23.8532; 16.58652; 19.13712
90; 90; 90
7571.44Guobao Huang; Zhenfeng He; Chen-Xi Cai; Fangfang Pan; Dingqiao Yang; Kari Rissanen; Wei Jiang
Bis-urea macrocycles with a deep cavity
Chem.Commun., 2015, 51, 15490
7117968 CIFC74 H82 Cl6 N4 O12P -111.992; 12.642; 13.39
78.03; 69.89; 65.52
1729.8Guobao Huang; Zhenfeng He; Chen-Xi Cai; Fangfang Pan; Dingqiao Yang; Kari Rissanen; Wei Jiang
Bis-urea macrocycles with a deep cavity
Chem.Commun., 2015, 51, 15490
7117969 CIFC79.8 H95.6 Cl2.8 N4 O15.2P 1 2/n 112.4884; 17.1551; 17.3844
90; 96.545; 90
3700.2Guobao Huang; Zhenfeng He; Chen-Xi Cai; Fangfang Pan; Dingqiao Yang; Kari Rissanen; Wei Jiang
Bis-urea macrocycles with a deep cavity
Chem.Commun., 2015, 51, 15490
7117970 CIFC18 H27 B O2P 1 21/c 112.301; 6.124; 24.187
90; 94.165; 90
1817.2Hye Ryung Kim; Jaesook Yun
Correction: Highly regio- and stereoselective synthesis of alkenylboronic esters by copper-catalyzed boron additions to disubstituted alkynes
Chem.Commun., 2015, 51, 15600
7117972 CIFC20 H22 N4 O6P 1 21/n 118.938; 5.258; 20.517
90; 108.76; 90
1934.5Aleksandr Grisin; Samuel Oliver; Michael D. Ganton; John Bacsa; P. Andrew Evans
Diastereoselective construction of anti-4,5-disubstituted-1,3-dioxolanes via a bismuth-mediated two-component hemiacetal oxa-conjugate addition of gamma-hydroxy-alpha,beta-unsaturated ketones with paraformaldehyde
Chem.Commun., 2015, 51, 15681
7117973 CIFC60 H50 B Cl8 F4 N2 O2 P2 RhP 1 21/c 132.934; 14.4798; 52.282
90; 103.448; 90
24249G. Storch; M. Siebert; F. Rominger; O. Trapp
5,5'-Diamino-BIPHEP ligands bearing small selector units for non-covalent binding of chiral analytes in solution
Chem.Commun., 2015, 51, 15665
7117975 CIFC3 H10 Cd N10P 1 21/c 18.6061; 9.3656; 13.016
90; 105.803; 90
1009.45Zi-Yi Du; Yu-Zhi Sun; Shao-Li Chen; Bo Huang; Yu-Jun Su; Ting-Ting Xu; Wei-Xiong Zhang; Xiao-Ming Chen
Insight into the molecular dynamics of guest cations confined in deformable azido coordination frameworks
Chem.Commun., 2015, 51, 15641
7117976 CIFC3 H10 Cd N10C 1 2/c 18.6276; 9.4066; 13.0569
90; 105.504; 90
1021.09Zi-Yi Du; Yu-Zhi Sun; Shao-Li Chen; Bo Huang; Yu-Jun Su; Ting-Ting Xu; Wei-Xiong Zhang; Xiao-Ming Chen
Insight into the molecular dynamics of guest cations confined in deformable azido coordination frameworks
Chem.Commun., 2015, 51, 15641
7117977 CIFC37 H38 B N O10P 1 21 18.877; 13.3291; 14.6644
90; 98.596; 90
1715.64Lawrence W-Y. Wong; Jack W-H. Kan; Thanh-ha Nguyen; Herman H-Y. Sung; Dang Li; Alex S-F. Au-Yeung; Rajpal Sharma; Zhenyang Lin; Ian D. Williams
Bis(mandelato)borate: an effective, inexpensive spiroborate anion for chiral resolution
Chem.Commun., 2015, 51, 15760
7117978 CIFC36 H40 B2 N2 O13P 1 21 112.7917; 8.7742; 16.8769
90; 103.527; 90
1841.67Lawrence W-Y. Wong; Jack W-H. Kan; Thanh-ha Nguyen; Herman H-Y. Sung; Dang Li; Alex S-F. Au-Yeung; Rajpal Sharma; Zhenyang Lin; Ian D. Williams
Bis(mandelato)borate: an effective, inexpensive spiroborate anion for chiral resolution
Chem.Commun., 2015, 51, 15760
7117979 CIFC84 H60 B3 Co N6 O18P 21 21 222.7598; 74.1769; 13.0562
90; 90; 90
22042.1Lawrence W-Y. Wong; Jack W-H. Kan; Thanh-ha Nguyen; Herman H-Y. Sung; Dang Li; Alex S-F. Au-Yeung; Rajpal Sharma; Zhenyang Lin; Ian D. Williams
Bis(mandelato)borate: an effective, inexpensive spiroborate anion for chiral resolution
Chem.Commun., 2015, 51, 15760
7117980 CIFC18 H18 B Na O7P 19.2739; 13.4321; 14.8221
87.1166; 88.9874; 81.7319
1824.75Lawrence W-Y. Wong; Jack W-H. Kan; Thanh-ha Nguyen; Herman H-Y. Sung; Dang Li; Alex S-F. Au-Yeung; Rajpal Sharma; Zhenyang Lin; Ian D. Williams
Bis(mandelato)borate: an effective, inexpensive spiroborate anion for chiral resolution
Chem.Commun., 2015, 51, 15760
7117981 CIFC30 H32 Au B2 N O5P 1 21/c 116.224; 13.4035; 13.0086
90; 98.365; 90
2798.7Amberle R. Browne; Nihal Deligonul; Bryce L. Anderson; Matthias Zeller; Allen D. Hunter; Thomas G. Gray
Cyclometalated (boroxinato)gold(III) complexes from arrested transmetalation
Chem.Commun., 2015, 51, 15800
7117982 CIFC71 H64 Au2 B4 Fe4 N2 O6P 1 21/c 120.8526; 7.7561; 21.4691
90; 118.283; 90
3057.8Amberle R. Browne; Nihal Deligonul; Bryce L. Anderson; Matthias Zeller; Allen D. Hunter; Thomas G. Gray
Cyclometalated (boroxinato)gold(III) complexes from arrested transmetalation
Chem.Commun., 2015, 51, 15800
7117983 CIFC28.5 H25 Au B2 Cl N O3P -18.007; 17.734; 20.141
66.28; 89.959; 77.147
2540Amberle R. Browne; Nihal Deligonul; Bryce L. Anderson; Matthias Zeller; Allen D. Hunter; Thomas G. Gray
Cyclometalated (boroxinato)gold(III) complexes from arrested transmetalation
Chem.Commun., 2015, 51, 15800
7117984 CIFC57 H50 Au2 B4 Cl2 N2 O10P -18.6237; 11.2419; 14.8115
73.806; 85.564; 72.674
1316.36Amberle R. Browne; Nihal Deligonul; Bryce L. Anderson; Matthias Zeller; Allen D. Hunter; Thomas G. Gray
Cyclometalated (boroxinato)gold(III) complexes from arrested transmetalation
Chem.Commun., 2015, 51, 15800
7117985 CIFC46 N6 Ni2 O2 S10P 1 21/n 110.877; 19.073; 13.93
90; 94.607; 90
2880.5Mikihiro Hayashi; Kazuya Otsubo; Tatsuhisa Kato; Kunihisa Sugimoto; Akihiko Fujiwara; Hiroshi Kitagawa
A compact planar low-energy-gap molecule with a donor-acceptor-donor nature based on a bimetal dithiolene complex
Chem.Commun., 2015, 51, 15796
7117986 CIFC46 N6 Ni2 O2 S10P 1 21/n 110.895; 19.189; 13.957
90; 94.674; 90
2908.2Mikihiro Hayashi; Kazuya Otsubo; Tatsuhisa Kato; Kunihisa Sugimoto; Akihiko Fujiwara; Hiroshi Kitagawa
A compact planar low-energy-gap molecule with a donor-acceptor-donor nature based on a bimetal dithiolene complex
Chem.Commun., 2015, 51, 15796
7117987 CIFC46 N6 Ni2 O2 S10P 1 21/n 110.885; 19.278; 13.961
90; 94.81; 90
2919.3Mikihiro Hayashi; Kazuya Otsubo; Tatsuhisa Kato; Kunihisa Sugimoto; Akihiko Fujiwara; Hiroshi Kitagawa
A compact planar low-energy-gap molecule with a donor-acceptor-donor nature based on a bimetal dithiolene complex
Chem.Commun., 2015, 51, 15796
7117988 CIFC46 N6 Ni2 O2 S10P 1 21/n 110.7705; 19.924; 13.848
90; 96.499; 90
2952.6Mikihiro Hayashi; Kazuya Otsubo; Tatsuhisa Kato; Kunihisa Sugimoto; Akihiko Fujiwara; Hiroshi Kitagawa
A compact planar low-energy-gap molecule with a donor-acceptor-donor nature based on a bimetal dithiolene complex
Chem.Commun., 2015, 51, 15796
7117989 CIFC46 N6 Ni2 O2 S10P 1 21/n 110.7047; 20.555; 13.8324
90; 98.106; 90
3013.2Mikihiro Hayashi; Kazuya Otsubo; Tatsuhisa Kato; Kunihisa Sugimoto; Akihiko Fujiwara; Hiroshi Kitagawa
A compact planar low-energy-gap molecule with a donor-acceptor-donor nature based on a bimetal dithiolene complex
Chem.Commun., 2015, 51, 15796
7117990 CIFC46 N6 Ni2 O2 S10P 1 21/n 110.6962; 20.721; 13.8764
90; 98.222; 90
3043.9Mikihiro Hayashi; Kazuya Otsubo; Tatsuhisa Kato; Kunihisa Sugimoto; Akihiko Fujiwara; Hiroshi Kitagawa
A compact planar low-energy-gap molecule with a donor-acceptor-donor nature based on a bimetal dithiolene complex
Chem.Commun., 2015, 51, 15796
7117991 CIFC40 N6 Ni S4P 1 21/n 17.7723; 20.4416; 14.1183
90; 96.37; 90
2229.2Mikihiro Hayashi; Kazuya Otsubo; Tatsuhisa Kato; Kunihisa Sugimoto; Akihiko Fujiwara; Hiroshi Kitagawa
A compact planar low-energy-gap molecule with a donor-acceptor-donor nature based on a bimetal dithiolene complex
Chem.Commun., 2015, 51, 15796
7117992 CIFC22 H17 N O3 SC 1 2 120.9821; 6.438; 15.242
90; 111.466; 90
1916.11Zhen-Hua Wang; Zhi-Jun Wu; Xue-Qun Huang; Deng-Feng Yue; Yong You; Xiao-Ying Xu; Xiao-Mei Zhang; Wei-Cheng Yuan
Diastereo- and enantioselective direct vinylogous Michael addition of gamma-substituted butenolides to 2-enoylpyridines catalyzed by chiral bifunctional amine-squaramides
Chem.Commun., 2015, 51, 15835
7117993 CIFC42 H46 N2 P2 Si2 ZnP 1 21 19.3979; 16.24; 13.49
90; 100.87; 90
2021.9Genette I. McGrew; Pathik A. Khatri; William E. Geiger; Richard A. Kemp; Rory Waterman
Unexpected formal insertion of CO2 into the C-Si bonds of a zinc compound
Chem.Commun., 2015, 51, 15804
7117994 CIFC32 H54 N2 O4 P2 Si2 ZnP -19.3607; 14.583; 15.9704
63.857; 81.986; 78.518
1914.6Genette I. McGrew; Pathik A. Khatri; William E. Geiger; Richard A. Kemp; Rory Waterman
Unexpected formal insertion of CO2 into the C-Si bonds of a zinc compound
Chem.Commun., 2015, 51, 15804
7118003 CIFC50 H44 B2 Cd F8 N12 O2P 43 21 215.9333; 15.9333; 21.1312
90; 90; 90
5364.6Chao-Wei Zhao; Yan-An Li; Xue-Ru Wang; Gong-Jun Chen; Qi-Kui Liu; Jian-Ping Ma; Yu-Bin Dong
Fabrication of Cd(II)-MOF-based ternary photocatalytic composite materials for H2 production via a gel-to-crystal approach
Chem.Commun., 2015, 51, 15906
7118004 CIFC36 H32 N2P -17.9415; 15.4054; 21.5716
102.614; 95.363; 97.396
2533.8Timothy D. Lash; Deyaa I. AbuSalim; Gregory M. Ferrence
adj-Dicarbachlorin, the first free base carbaporphyrinoid system with an internal methylene unit
Chem.Commun., 2015, 51, 15952
7118005 CIFC28 H30 N2P -19.6391; 11.5516; 19.4951
80.562; 85.708; 85.426
2130.3Timothy D. Lash; Deyaa I. AbuSalim; Gregory M. Ferrence
adj-Dicarbachlorin, the first free base carbaporphyrinoid system with an internal methylene unit
Chem.Commun., 2015, 51, 15952
7118006 CIFC24 H38 B2 P2P 1 21/c 19.367; 15.172; 17.348
90; 96.96; 90
2447.3Philipp Bissinger; Holger Braunschweig; Mehmet Ali Celik; Christina Claes; Rian D. Dewhurst; Sebastian Endres; Hauke Kelch; Thomas Kramer; Ivo Krummenacher; Christoph Schneider
Synthesis of cyclic diborenes with unprecedented cis-configuration
Chem.Commun., 2015, 51, 15917
7118007 CIFC46 H47 B2 P2P -114.4599; 16.0807; 16.867
79.939; 86.355; 78.644
3784.4Philipp Bissinger; Holger Braunschweig; Mehmet Ali Celik; Christina Claes; Rian D. Dewhurst; Sebastian Endres; Hauke Kelch; Thomas Kramer; Ivo Krummenacher; Christoph Schneider
Synthesis of cyclic diborenes with unprecedented cis-configuration
Chem.Commun., 2015, 51, 15917
7118008 CIFC24 H40 B2 P2P 1 21/c 19.4899; 13.6443; 9.7286
90; 99.393; 90
1242.8Philipp Bissinger; Holger Braunschweig; Mehmet Ali Celik; Christina Claes; Rian D. Dewhurst; Sebastian Endres; Hauke Kelch; Thomas Kramer; Ivo Krummenacher; Christoph Schneider
Synthesis of cyclic diborenes with unprecedented cis-configuration
Chem.Commun., 2015, 51, 15917
7118009 CIFC35 H41 Al F6 N2P 1 21/c 122.5345; 17.93193; 26.6666
90; 110.278; 90
10107.8Mark R. Crimmin; Michael J. Butler; Andrew J. P. White
Oxidative addition of carbon-fluorine and carbon-oxygen bonds to Al(I)
Chem.Commun., 2015, 51, 15994
7118010 CIFC37 H47 Al N2 OP n a 2116.8019; 12.4929; 15.8089
90; 90; 90
3318.36Mark R. Crimmin; Michael J. Butler; Andrew J. P. White
Oxidative addition of carbon-fluorine and carbon-oxygen bonds to Al(I)
Chem.Commun., 2015, 51, 15994
7118011 CIFC26 H22 Br N O3P 16.2811; 7.9645; 11.2853
71.701; 89.752; 81.716
529.91Keiji Mori; Ayaka Miyake; Takahiko Akiyama
Enantioselective synthesis of fused heterocycles with contiguous stereogenic centers by chiral phosphoric acid catalyzed symmetry breaking
Chem.Commun., 2015, 51, 16107
7118012 CIFC54 H64 Au PP 1 21/c 112.8975; 12.5051; 28.706
90; 90.438; 90
4629.7Michael Stollenz; Deeb Taher; Nattamai Bhuvanesh; Joseph H. Reibenspies; Zuzana Baranova; John A. Gladysz
Steric control of the in/out sense of bridgehead substituents in macrobicyclic compounds: isolation of new 'crossed chain' variants of in/out isomers
Chem.Commun., 2015, 51, 16053
7118013 CIFC118 H192 Au2 O P2P n a 2147.793; 13.1566; 17.5594
90; 90; 90
11041.2Michael Stollenz; Deeb Taher; Nattamai Bhuvanesh; Joseph H. Reibenspies; Zuzana Baranova; John A. Gladysz
Steric control of the in/out sense of bridgehead substituents in macrobicyclic compounds: isolation of new 'crossed chain' variants of in/out isomers
Chem.Commun., 2015, 51, 16053
7118014 CIFC114 H182 Au2 P2P 1 21/c 113.0821; 24.554; 17.7022
90; 108.761; 90
5384.1Michael Stollenz; Deeb Taher; Nattamai Bhuvanesh; Joseph H. Reibenspies; Zuzana Baranova; John A. Gladysz
Steric control of the in/out sense of bridgehead substituents in macrobicyclic compounds: isolation of new 'crossed chain' variants of in/out isomers
Chem.Commun., 2015, 51, 16053
7118015 CIFC29 H25 B N2P 1 21/n 117.3899; 10.3122; 26.5129
90; 108.487; 90
4509.16Aslam C. Shaikh; Dnyanesh S. Ranade; Shridhar Thorat; Arunava Maity; Prasad P. Kulkarni; Rajesh G. Gonnade; Parthapratim Munshi; Nitin T. Patil
Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons
Chem.Commun., 2015, 51, 16115
7118016 CIFC27 H20 B NP 1 21/c 18.898; 7.0675; 30.362
90; 98; 90
1890.78Aslam C. Shaikh; Dnyanesh S. Ranade; Shridhar Thorat; Arunava Maity; Prasad P. Kulkarni; Rajesh G. Gonnade; Parthapratim Munshi; Nitin T. Patil
Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons
Chem.Commun., 2015, 51, 16115
7118017 CIFC29 H23 B N2P -19.3145; 9.7778; 12.5665
83.55; 84.896; 76.744
1104.59Aslam C. Shaikh; Dnyanesh S. Ranade; Shridhar Thorat; Arunava Maity; Prasad P. Kulkarni; Rajesh G. Gonnade; Parthapratim Munshi; Nitin T. Patil
Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons
Chem.Commun., 2015, 51, 16115
7118018 CIFC25 H20 B NP 1 21/n 113.9351; 9.0239; 14.1194
90; 92.128; 90
1774.28Aslam C. Shaikh; Dnyanesh S. Ranade; Shridhar Thorat; Arunava Maity; Prasad P. Kulkarni; Rajesh G. Gonnade; Parthapratim Munshi; Nitin T. Patil
Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons
Chem.Commun., 2015, 51, 16115
7118019 CIFC21 H25 B N2P -17.9636; 8.8054; 14.8492
106.476; 90.57; 116.512
882.12Aslam C. Shaikh; Dnyanesh S. Ranade; Shridhar Thorat; Arunava Maity; Prasad P. Kulkarni; Rajesh G. Gonnade; Parthapratim Munshi; Nitin T. Patil
Highly emissive organic solids with remarkably broad color tunability based on N,C-chelate, four-coordinate organoborons
Chem.Commun., 2015, 51, 16115
7118021 CIFC20 H14 N2 OP 1 21/c 110.9292; 16.0839; 8.704
90; 103.591; 90
1487.2Huan-Wei Tseng; Ta-Chun Lin; Chi-Lin Chen; Tzu-Chieh Lin; Yi-An Chen; Jun-Qi Liu; Cheng-Hsien Hung; Chi-Min Chao; Kuan-Miao Liu; Pi-Tai Chou
A new class of N-H proton transfer molecules: wide tautomer emission tuning from 590 nm to 770 nm via a facile, single site amino derivatization in 10-aminobenzo[h]quinoline
Chem.Commun., 2015, 51, 16099
7118022 CIFC6 H12 N2 SP 1 21/n 18.6023; 7.671; 12.76
90; 107.862; 90
801.42L. H. Finger; F. Wohde; E. I. Grigoryev; A.-K. Hansmann; R. Berger; B. Roling; J. Sundermeyer
Access to pure and highly volatile hydrochalcogenide ionic liquids
Chem.Commun., 2015, 51, 16169
7118023 CIFC9 H21 N SP 42/m b c15.6635; 15.6635; 8.9408
90; 90; 90
2193.58L. H. Finger; F. Wohde; E. I. Grigoryev; A.-K. Hansmann; R. Berger; B. Roling; J. Sundermeyer
Access to pure and highly volatile hydrochalcogenide ionic liquids
Chem.Commun., 2015, 51, 16169
7118024 CIFC18 H39 Fe N O3 P2P 1 21/n 19.8949; 17.1226; 13.9266
90; 105.661; 90
2271.9Liam S. Sharninghausen; Brandon Q. Mercado; Robert H. Crabtree; Nilay Hazari
Selective conversion of glycerol to lactic acid with iron pincer precatalysts
Chem.Commun., 2015, 51, 16201
7118025 CIFC21 H16 Cl N O2 S2P 21 21 218.7074; 12.6241; 18.0261
90; 90; 90
1981.48Kui Liao; Feng Zhou; Jin-Sheng Yu; Wei-Ming Gao; Jian Zhou
Catalytic asymmetric sulfenylation to structurally diverse dithioketals
Chem.Commun., 2015, 51, 16255
7118026 CIFC21 H14 Cl2 O S2P 16.8482; 7.9264; 8.7986
92.069; 99.774; 96.704
466.69Kui Liao; Feng Zhou; Jin-Sheng Yu; Wei-Ming Gao; Jian Zhou
Catalytic asymmetric sulfenylation to structurally diverse dithioketals
Chem.Commun., 2015, 51, 16255
7118027 CIFC18 H15 F3 O3 S2P 21 21 213.1691; 38.663; 7.1029
90; 90; 90
3616.5Kui Liao; Feng Zhou; Jin-Sheng Yu; Wei-Ming Gao; Jian Zhou
Catalytic asymmetric sulfenylation to structurally diverse dithioketals
Chem.Commun., 2015, 51, 16255
7118028 CIFC40 H72 Bi2 N8 P4P 1 21/c 123.3993; 10.7452; 21.7187
90; 114.212; 90
4980.4Minggang Zhao; Lixia Wang; Pangpang Li; Xiang Zhang; Ying Yang; Wenjun Zheng
Paddlewheel 1,2,4-diazaphospholide dibismuthanes with very short bismuth-bismuth single bonds
Chem.Commun., 2015, 51, 16184
7118029 CIFC32 H56 Bi2 N8 P4P -110.5121; 13.7719; 15.2443
90.269; 101.428; 93.926
2157.74Minggang Zhao; Lixia Wang; Pangpang Li; Xiang Zhang; Ying Yang; Wenjun Zheng
Paddlewheel 1,2,4-diazaphospholide dibismuthanes with very short bismuth-bismuth single bonds
Chem.Commun., 2015, 51, 16184
7118030 CIFC28 H20 Bi N4 P2P 1 21/n 19.4968; 20.3504; 13.5884
90; 97.027; 90
2606.42Minggang Zhao; Lixia Wang; Pangpang Li; Xiang Zhang; Ying Yang; Wenjun Zheng
Paddlewheel 1,2,4-diazaphospholide dibismuthanes with very short bismuth-bismuth single bonds
Chem.Commun., 2015, 51, 16184
7118031 CIFC24 H28 N4 O6P 21 21 216.1328; 16.7206; 22.9284
90; 90; 90
2351.17Chang Won Kang; Matthew P. Sarnowski; Sujeewa Ranatunga; Lukasz Wojtas; Rainer S. Metcalf; Wayne C. Guida; Juan R. Del Valle
Beta-Strand mimics based on tetrahydropyridazinedione (tpd) peptide stitching
Chem.Commun., 2015, 51, 16259
7118032 CIFC32 H34 N4 O5P 21 21 2111.0349; 14.8582; 17.2323
90; 90; 90
2825.39Chang Won Kang; Matthew P. Sarnowski; Sujeewa Ranatunga; Lukasz Wojtas; Rainer S. Metcalf; Wayne C. Guida; Juan R. Del Valle
Beta-Strand mimics based on tetrahydropyridazinedione (tpd) peptide stitching
Chem.Commun., 2015, 51, 16259
7118034 CIFC14.5 H29.5 N6.5 Nd O5 S8P 42/n n m16.3046; 16.3046; 6.6306
90; 90; 90
1762.7Xu, Jin; Liu, Ting; Han, Xiaohui; Wang, Shanshan; Liu, Dan; Wang, Cheng
Construction of a porous three dimensional rare earth metal-sulfur-ligand open framework.
Chemical communications (Cambridge, England), 2015, 51, 15819-15822
7118035 CIFC14.5 H29.5 N6.5 Nd O5 S8P 42/n n m16.2525; 16.2525; 6.5933
90; 90; 90
1741.6Xu, Jin; Liu, Ting; Han, Xiaohui; Wang, Shanshan; Liu, Dan; Wang, Cheng
Construction of a porous three dimensional rare earth metal-sulfur-ligand open framework.
Chemical communications (Cambridge, England), 2015, 51, 15819-15822
7118036 CIFC28 H37 Cl O5P 1 21/c 113.459; 10.509; 20.134
90; 105.46; 90
2744.7Gai, Kuo; Fang, Xinxin; Li, Xuanyi; Xu, Jinyi; Wu, Xiaoming; Lin, Aijun; Yao, Hequan
Synthesis of spiro[2.5]octa-4,7-dien-6-one with consecutive quaternary centers via 1,6-conjugate addition induced dearomatization of para-quinone methides.
Chemical communications (Cambridge, England), 2015, 51, 15831-15834
7118037 CIFC25 H18 O2P -19.284; 9.32; 11.404
77.278; 70.928; 88.102
908.9Pan, Xiaolin; Luo, Yong; Xia, Hong-Guang; Wu, Jie
A palladium-catalyzed tandem reaction of 2-(2-bromobenzylidene)cyclobutanone with 2-alkynylphenol.
Chemical communications (Cambridge, England), 2015, 51, 16483-16485
7118038 CIFC19 H24 B Mn N2 O3P 1 21/c 16.0538; 22.484; 14.589
90; 101.902; 90
1943.1Braunschweig, Holger; Jimenez-Halla, J Oscar C; Radacki, Krzysztof; Shang, Rong
A metal-mediated boron-centred isomerisation reaction via C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 16569-16572
7118039 CIFC40 H28 F12 N16 O4P n m a11.427; 6.76; 14.006
90; 90; 90
1081.9Chen, Zhen; Fan, Shuang-Qing; Zheng, Yan; Ma, Jun-An
Silver-catalyzed regioselective [3+2] cycloaddition of arene-diazonium salts with 2,2,2-trifluorodiazoethane (CF3CHN2): a facile access to 2-aryl-5-trifluoromethyltetrazoles.
Chemical communications (Cambridge, England), 2015, 51, 16545-16548
7118040 CIFC8 H5 F3 N4 OP n m a9.5762; 7.0422; 14.1082
90; 90; 90
951.42Chen, Zhen; Fan, Shuang-Qing; Zheng, Yan; Ma, Jun-An
Silver-catalyzed regioselective [3+2] cycloaddition of arene-diazonium salts with 2,2,2-trifluorodiazoethane (CF3CHN2): a facile access to 2-aryl-5-trifluoromethyltetrazoles.
Chemical communications (Cambridge, England), 2015, 51, 16545-16548
7118041 CIFC21 H42 N7 P4 Se4P -110.546; 12.3897; 14.0003
78.264; 70.648; 75.644
1657.28Shi, Yan X.; Liang, Rong Z.; Martin, Katherine A.; Star, Daniel G.; Díaz, Jesús; Li, Xin Y.; Ganguly, Rakesh; García, Felipe
Steric C-N bond activation on the dimeric macrocycle [{P(μ-NR)}2(μ-NR)]2.
Chemical communications (Cambridge, England), 2015, 51, 16468-16471
7118042 CIFC24 H54 N6 P4C 1 2/m 128.4547; 16.8252; 9.7507
90; 94.991; 90
4650.5Shi, Yan X.; Liang, Rong Z.; Martin, Katherine A.; Star, Daniel G.; Díaz, Jesús; Li, Xin Y.; Ganguly, Rakesh; García, Felipe
Steric C-N bond activation on the dimeric macrocycle [{P(μ-NR)}2(μ-NR)]2.
Chemical communications (Cambridge, England), 2015, 51, 16468-16471
7118043 CIFC18 H42 N6 P4P 1 21/n 18.9073; 15.7025; 9.9032
90; 113.061; 90
1274.4Shi, Yan X.; Liang, Rong Z.; Martin, Katherine A.; Star, Daniel G.; Díaz, Jesús; Li, Xin Y.; Ganguly, Rakesh; García, Felipe
Steric C-N bond activation on the dimeric macrocycle [{P(μ-NR)}2(μ-NR)]2.
Chemical communications (Cambridge, England), 2015, 51, 16468-16471
7118044 CIFC15 H36 N6 P4 Se4P 1 21/c 113.8909; 15.9194; 13.2049
90; 90.007; 90
2920.1Shi, Yan X.; Liang, Rong Z.; Martin, Katherine A.; Star, Daniel G.; Díaz, Jesús; Li, Xin Y.; Ganguly, Rakesh; García, Felipe
Steric C-N bond activation on the dimeric macrocycle [{P(μ-NR)}2(μ-NR)]2.
Chemical communications (Cambridge, England), 2015, 51, 16468-16471
7118045 CIFC39 H53 B Cl Co N S3P -111.5577; 18.1837; 18.2006
97.507; 92.728; 92.84
3782Shao, Feng; Cahier, Benjamin; Guihéry, Nathalie; Rivière, Eric; Guillot, Régis; Barra, Anne-Laure; Lan, Yanhua; Wernsdorfer, Wolfgang; Campbell, Victoria E.; Mallah, Talal
Tuning the Ising-type anisotropy in trigonal bipyramidal Co(ii) complexes.
Chemical communications (Cambridge, England), 2015, 51, 16475-16478
7118046 CIFC38 H37 F24 N13 P4 Ru2P 1 21/n 115.831; 16.614; 21.526
90; 109.97; 90
5321.3Albani, B. A.; Peña, B; Saha, S.; White, J. K.; Schaeffer, A. M.; Dunbar, K. R.; Turro, C.
A dinuclear Ru(ii) complex capable of photoinduced ligand exchange at both metal centers.
Chemical communications (Cambridge, England), 2015, 51, 16522-16525
7118047 CIFC18 H15 N3 SP 1 21/c 19.3536; 17.701; 9.8752
90; 111.505; 90
1521.2Vincent-Rocan, Jean-François; Derasp, Joshua S.; Beauchemin, André M
Diversity-oriented heterocyclic synthesis using divergent reactivity of N-substituted iso(thio)cyanates.
Chemical communications (Cambridge, England), 2015, 51, 16405-16408
7118050 CIFC21 H20 F3 N O5P 1 21/c 114.1742; 11.9882; 11.3206
90; 90.796; 90
1923.4Yamamoto, Y.; Kurohara, T.; Shibuya, M.
CF3-Substituted semisquarate: a pluripotent building block for the divergent synthesis of trifluoromethylated functional molecules.
Chemical communications (Cambridge, England), 2015, 51, 16357-16360
7118051 CIFC76 H92 N2 O12P 1 21/n 111.966; 12.944; 21.641
90; 90.39; 90
3351.9Yuan, Mao-Sen; Chen, Huanqing; Du, Xianchao; Li, Jian; Wang, Jinyi; Jia, Xueshun; Li, Chunju
Host-guest complexation of pillar[6]arenes towards neutral nitrile guests.
Chemical communications (Cambridge, England), 2015, 51, 16361-16364
7118053 CIFC17 H20 O2P -16.7321; 9.372; 11.4758
95.498; 99.49; 104.725
683.45Banerjee, Arghya; Santra, Sourav Kumar; Khatun, Nilufa; Ali, Wajid; Patel, Bhisma K.
Oxidant controlled regioselective mono- and di-functionalization reactions of coumarins.
Chemical communications (Cambridge, England), 2015, 51, 15422-15425
7118054 CIFC22 H15 I N4 OA e a 222.3839; 36.433; 10.0332
90; 90; 90
8182.2Hu, Yancheng; Yi, Ruxia; Yu, Xinzhang; Xin, Xiaoyi; Wang, Chunxiang; Wan, Boshun
O-Transfer-facilitated cyclizations of propargylamides with TMSN3: selective synthesis of tetrazoles and dihydroimidazoles.
Chemical communications (Cambridge, England), 2015, 51, 15398-15401
7118055 CIFC17 H16 I2 N2 O3 SP -17.2509; 11.487; 12.2569
97.897; 91.846; 103.895
979.4Hu, Yancheng; Yi, Ruxia; Yu, Xinzhang; Xin, Xiaoyi; Wang, Chunxiang; Wan, Boshun
O-Transfer-facilitated cyclizations of propargylamides with TMSN3: selective synthesis of tetrazoles and dihydroimidazoles.
Chemical communications (Cambridge, England), 2015, 51, 15398-15401
7118056 CIFC20 H16 Cu N10 O4P b n b17.7157; 22.1231; 25.3814
90; 90; 90
9947.6Manna, Biplab; Mukherjee, Soumya; Desai, Aamod V.; Sharma, Shivani; Krishna, Rajamani; Ghosh, Sujit K.
A π-electron deficient diaminotriazine functionalized MOF for selective sorption of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2015, 51, 15386-15389
7118057 CIFC10 H18 O5C 1 2 18.897; 6.768; 18.304
90; 90.365; 90
1102.2Cuyamendous, C.; Leung, K. S.; Durand, T.; Lee, J. C.-Y.; Oger, C.; Galano, J.-M.
Synthesis and discovery of phytofurans: metabolites of α-linolenic acid peroxidation.
Chemical communications (Cambridge, England), 2015, 51, 15696-15699
7118061 CIFC35 H34 Cl2 N2 O4C 1 c 126.271; 5.9202; 21.057
90; 108.458; 90
3106.5Yin Zheng; Youming Wang; Zhenghong Zhou
Organocatalytic multicomponent synthesis of polysubstituted pyrroles from 1,2-diones, aldehydes and arylamines
Chem.Commun., 2015, 51, 16652
7118062 CIFC62 H30 Al2 Cl2 F72 O10 S2P 1 21/n 111.7515; 24.273; 30.087
90; 99.776; 90
8457.5Ningning Yuan; Zaichao Zhang; Xingyong Wang; Xinping Wang
Isolation and crystal structure of a dithiophene dication: controlling covalent connection and disconnection with temperature and phase
Chem.Commun., 2015, 51, 16714
7118063 CIFC18 H20 N2 OP 1 21/c 18.471; 18.936; 9.695
90; 99.546; 90
1533.6Qiang Dai; Yan Jiang; Jin-Tao Yu; Jiang Cheng
Palladium-catalyzed three-component reaction of N-tosyl hydrazones, isonitriles and amines leading to amidines
Chem.Commun., 2015, 51, 16645
7118064 CIFC99.5 H133 B Cl2 N4 O3 Si UP -116.1844; 17.476; 19.116
94.215; 95.92; 111.501
4967.3Henry S. La Pierre; Michael Rosenzweig; Boris Kosog; Christina Hauser; Frank W. Heinemann; Stephen T. Liddle; Karsten Meyer
Charge control of the inverse trans-influence
Chem.Commun., 2015, 51, 16671
7118065 CIFC92.5 H132 F6 N4 O3 Sb Si UP 1 21/c 119.293; 16.638; 28.095
90; 101.198; 90
8847Henry S. La Pierre; Michael Rosenzweig; Boris Kosog; Christina Hauser; Frank W. Heinemann; Stephen T. Liddle; Karsten Meyer
Charge control of the inverse trans-influence
Chem.Commun., 2015, 51, 16671
7118066 CIFC132 H234 F18 N8 Na O18 Sb3 Si2 U2R 3 :H14.9276; 14.9276; 63.398
90; 90; 120
12234Henry S. La Pierre; Michael Rosenzweig; Boris Kosog; Christina Hauser; Frank W. Heinemann; Stephen T. Liddle; Karsten Meyer
Charge control of the inverse trans-influence
Chem.Commun., 2015, 51, 16671
7118067 CIFC24 H26 Au Cl N2P b c n15.6786; 18.9401; 7.1383
90; 90; 90
2119.75Julio Fernandez-Cestau; Benoit Bertrand; Maria Blaya; Garth A. Jones; Thomas J. Penfold; Manfred Bochmann
Synthesis and luminescence modulation of pyrazine-based gold(III) pincer complexes
Chem.Commun., 2015, 51, 16629
7118068 CIFC29 H33 Au N4P 1 21/c 110.4846; 21.4472; 11.2718
90; 94.619; 90
2526.4Julio Fernandez-Cestau; Benoit Bertrand; Maria Blaya; Garth A. Jones; Thomas J. Penfold; Manfred Bochmann
Synthesis and luminescence modulation of pyrazine-based gold(III) pincer complexes
Chem.Commun., 2015, 51, 16629
7118069 CIFC32 H31 Au N2P 1 21/a 18.404; 13.1184; 23.6
90; 90; 90
2601.83Julio Fernandez-Cestau; Benoit Bertrand; Maria Blaya; Garth A. Jones; Thomas J. Penfold; Manfred Bochmann
Synthesis and luminescence modulation of pyrazine-based gold(III) pincer complexes
Chem.Commun., 2015, 51, 16629
7118070 CIFC30 H35 Au N2P 1 21/c 112.37; 12.3194; 18.1788
90; 104.68; 90
2679.9Julio Fernandez-Cestau; Benoit Bertrand; Maria Blaya; Garth A. Jones; Thomas J. Penfold; Manfred Bochmann
Synthesis and luminescence modulation of pyrazine-based gold(III) pincer complexes
Chem.Commun., 2015, 51, 16629
7118073 CIFC15 H14 O2P 1 21/n 112.4961; 6.0394; 16.0699
90; 104.082; 90
1176.33Shivakrishna Kallepu; Krishna Kumar Gollapelli; Jagadeesh Babu Nanubolu; Rambabu Chegondi
Synthesis of highly strained bicyclic[3.n.1]alkenes by a metal-catalyzed Conia-ene reaction
Chem.Commun., 2015, 51, 16840
7118074 CIFC19 H37 B10 NP 1 21/n 110.5147; 20.272; 12.1906
90; 108.022; 90
2471Hao Wang; Jiji Zhang; Zhenyang Lin; Zuowei Xie
The synthesis and structure of a carbene-stabilized iminocarboranyl-boron(I) compound
Chem.Commun., 2015, 51, 16817
7118075 CIFC22.5 H40 B11 Br2 NP 1 21/c 18.8893; 16.193; 21.266
90; 94.996; 90
3049.5Hao Wang; Jiji Zhang; Zhenyang Lin; Zuowei Xie
The synthesis and structure of a carbene-stabilized iminocarboranyl-boron(I) compound
Chem.Commun., 2015, 51, 16817
7118076 CIFC30 H56 B11 N3P 1 21/c 19.9902; 23.386; 18.285
90; 96.636; 90
4243.3Hao Wang; Jiji Zhang; Zhenyang Lin; Zuowei Xie
The synthesis and structure of a carbene-stabilized iminocarboranyl-boron(I) compound
Chem.Commun., 2015, 51, 16817
7118077 CIFC24.5 H45.5 B11 N O4P -19.8557; 17.2485; 19.2849
97.064; 93.413; 102.491
3163.89Hao Wang; Jiji Zhang; Zhenyang Lin; Zuowei Xie
The synthesis and structure of a carbene-stabilized iminocarboranyl-boron(I) compound
Chem.Commun., 2015, 51, 16817
7118078 CIFC66.5 H77 Au4 Cl5 Fe4 N4 O4P 41 21 219.7785; 19.7785; 35.613
90; 90; 90
13931.4Marta Ayerbe Garcia; Wolfgang Frey; Mark R. Ringenberg; Max Schwilk; Rene Peters
Dinuclear planar chiral ferrocenyl gold(I) & gold(II) complexes
Chem.Commun., 2015, 51, 16806
7118079 CIFC32 H36 Au2 Cl2 Fe2 N2 O2P 21 21 210.8177; 18.8289; 7.6272
90; 90; 90
1553.55Marta Ayerbe Garcia; Wolfgang Frey; Mark R. Ringenberg; Max Schwilk; Rene Peters
Dinuclear planar chiral ferrocenyl gold(I) & gold(II) complexes
Chem.Commun., 2015, 51, 16806
7118080 CIFC32 H36 Au2 Cl2 Fe2 N2 O2P 21 21 2110.0819; 15.295; 20.4679
90; 90; 90
3156.2Marta Ayerbe Garcia; Wolfgang Frey; Mark R. Ringenberg; Max Schwilk; Rene Peters
Dinuclear planar chiral ferrocenyl gold(I) & gold(II) complexes
Chem.Commun., 2015, 51, 16806
7118081 CIFC280 H312 Cl24 Fe4 I12 N16P n m a23.387; 17.301; 18.913
90; 90; 90
7653Dipankar Sahoo; Sankar Prasad Rath
Controlled generation of highly saddled (porphyrinato)iron(III) iodide, tri-iodide and one-electron oxidized complexes
Chem.Commun., 2015, 51, 16790
7118082 CIFC68.25 H76.5 Cl0.5 Fe I N4P b c a19.736; 24.456; 31.304
90; 90; 90
15109Dipankar Sahoo; Sankar Prasad Rath
Controlled generation of highly saddled (porphyrinato)iron(III) iodide, tri-iodide and one-electron oxidized complexes
Chem.Commun., 2015, 51, 16790
7118083 CIFC29 H34 B2 F4 N4C 1 2/c 126.145; 7.697; 14.341
90; 101.917; 90
2823.8Changjiang Yu; Lijuan Jiao; Tingting Li; Qinghua Wu; Wei Miao; Jun Wang; Yun Wei; Xiaolong Mu; Erhong Hao
Fusion and planarization of bisBODIPY: a new family of photostable near infrared dyes
Chem.Commun., 2015, 51, 16852
7118084 CIFC29 H32 B2 F4 N4C m c 2123.035; 17.8506; 7.0291
90; 90; 90
2890.3Changjiang Yu; Lijuan Jiao; Tingting Li; Qinghua Wu; Wei Miao; Jun Wang; Yun Wei; Xiaolong Mu; Erhong Hao
Fusion and planarization of bisBODIPY: a new family of photostable near infrared dyes
Chem.Commun., 2015, 51, 16852
7118085 CIFC128 H104 N17 O7 Pd2C 1 2 113.798; 32.546; 13.7267
90; 100.33; 90
6064.3Li-Peng Zhou; Qing-Fu Sun
A self-assembled Pd2L4 cage that selectively encapsulates nitrate
Chem.Commun., 2015, 51, 16767
7118086 CIFC18 H17 NP 1 21/c 17.7592; 21.8617; 8.2702
90; 113.794; 90
1283.6Xin-Xing Wu; Yi Shen; Wen-Long Chen; Si Chen; Peng-Fei Xu; Yong-Min Liang
Palladium-catalyzed dearomative cyclization by a norbornene-mediated sequence: a route to spiroindolenine derivatives
Chem.Commun., 2015, 51, 16798
7118087 CIFC22 H25 NP b c a8.363; 16.4293; 25.672
90; 90; 90
3527.3Xin-Xing Wu; Yi Shen; Wen-Long Chen; Si Chen; Peng-Fei Xu; Yong-Min Liang
Palladium-catalyzed dearomative cyclization by a norbornene-mediated sequence: a route to spiroindolenine derivatives
Chem.Commun., 2015, 51, 16798
7118088 CIFC23 H18 N2 O3 SP -19.4496; 10.255; 11.237
102.651; 93.971; 114.471
951.23Hong-Wen Liang; Kun Jiang; Wei Ding; Yi Yuan; Li Shuai; Ying-Chun Chen; Ye Wei
Selective remote C-H sulfonylation of aminoquinolines with arylsulfonyl chlorides via copper catalysis
Chem.Commun., 2015, 51, 16928
7118089 CIFC24 H20 N2 O4 SP -17.261; 9.44; 15.434
92.805; 95.279; 96.848
1044Hong-Wen Liang; Kun Jiang; Wei Ding; Yi Yuan; Li Shuai; Ying-Chun Chen; Ye Wei
Selective remote C-H sulfonylation of aminoquinolines with arylsulfonyl chlorides via copper catalysis
Chem.Commun., 2015, 51, 16928
7118090 CIFC33 H63 F12 Fe N7 Ni P2 S2P b c a24.9779; 15.3332; 25.33735
90; 90; 90
9703.98Carlo U. Perotto; George Marshall; Graham J. Jones; E. Stephen Davies; William Lewis; Jonathan McMaster; Martin Schroder
A Ni(I)Fe(II) analogue of the Ni-L state of the active site of the [NiFe] hydrogenases
Chem.Commun., 2015, 51, 16988
7118091 CIFC36 Eu2 N6 O17P 1 21/c 126.238; 14.1876; 16.8586
90; 98.014; 90
6214.4Xinping Lin; Yahui Hong; Chao Zhang; Ruiyun Huang; Cheng Wang; Wenbin Lin
Pre-concentration and energy transfer enable the efficient luminescence sensing of transition metal ions by metal-organic frameworks
Chem.Commun., 2015, 51, 16996
7118092 CIFC36 Cu1.02 Eu2 N7 O15P 1 21/c 126.531; 13.617; 16.4067
90; 98.04; 90
5869Xinping Lin; Yahui Hong; Chao Zhang; Ruiyun Huang; Cheng Wang; Wenbin Lin
Pre-concentration and energy transfer enable the efficient luminescence sensing of transition metal ions by metal-organic frameworks
Chem.Commun., 2015, 51, 16996
7118093 CIFC20 H42 Cl2 N2 ZnP 21 21 217.7915; 14.3961; 23.6463
90; 90; 90
2652.3Jezabel Praz; Julien Graff; Leo Egger; Laure Guenee; Simon Wagschal; E. Peter Kundig; Alexandre Alexakis
Asymmetric bromine-lithium exchange: on the importance of both the diamine ligand and the organolithium reagent
Chem.Commun., 2015, 51, 16912
7118094 CIFC140 H170.52 Cl9.78 S4C 1 2/c 142.616; 17.397; 18.769
90; 98.476; 90
13763Shohei Kato; Yuma Serizawa; Daisuke Sakamaki; Shu Seki; Yoshihiro Miyake; Hiroshi Shinokubo
Diversity-oriented synthesis of tetrathia[8]circulenes by sequential C-H borylation and annulation
Chem.Commun., 2015, 51, 16944
7118095 CIFC40 H40 S4P -14.7699; 13.122; 14.121
68.2; 74.332; 85.09
790Shohei Kato; Yuma Serizawa; Daisuke Sakamaki; Shu Seki; Yoshihiro Miyake; Hiroshi Shinokubo
Diversity-oriented synthesis of tetrathia[8]circulenes by sequential C-H borylation and annulation
Chem.Commun., 2015, 51, 16944
7118096 CIFC15.5 H9 Cl S2P c a 2125.926; 10.268; 9.738
90; 90; 90
2592.3Shohei Kato; Yuma Serizawa; Daisuke Sakamaki; Shu Seki; Yoshihiro Miyake; Hiroshi Shinokubo
Diversity-oriented synthesis of tetrathia[8]circulenes by sequential C-H borylation and annulation
Chem.Commun., 2015, 51, 16944
7118097 CIFC47 H67 B4 O8 S4P -112.2323; 13.9489; 16.2345
76.272; 81.959; 78.768
2626.6Shohei Kato; Yuma Serizawa; Daisuke Sakamaki; Shu Seki; Yoshihiro Miyake; Hiroshi Shinokubo
Diversity-oriented synthesis of tetrathia[8]circulenes by sequential C-H borylation and annulation
Chem.Commun., 2015, 51, 16944
7118098 CIFC54 H34 Cl8 F12 Ir2 N12 P2P -115.504; 16.732; 17.196
82.46; 65.65; 68.98
3792.9Guangfu Li; Wei Guan; Shuang Du; Dongxia Zhu; Guogang Shan; Xiaojuan Zhu; Likai Yan; Zhongmin Su; Martin R. Bryce; Andrew P. Monkmand
Anion-specific aggregation induced phosphorescence emission (AIPE) in an ionic iridium complex in aqueous media
Chem.Commun., 2015, 51, 16924
7118099 CIFC64 H51 Cl10 Ir2 N16 O8.5P -116.263; 16.337; 17.18
99.21; 117.64; 103.45
3738Guangfu Li; Wei Guan; Shuang Du; Dongxia Zhu; Guogang Shan; Xiaojuan Zhu; Likai Yan; Zhongmin Su; Martin R. Bryce; Andrew P. Monkmand
Anion-specific aggregation induced phosphorescence emission (AIPE) in an ionic iridium complex in aqueous media
Chem.Commun., 2015, 51, 16924
7118100 CIFC60 H45 Cl10 Ir2 N14 O8.5P -111.0662; 18.0408; 18.1054
78.903; 80.228; 75.744
3409.2Guangfu Li; Wei Guan; Shuang Du; Dongxia Zhu; Guogang Shan; Xiaojuan Zhu; Likai Yan; Zhongmin Su; Martin R. Bryce; Andrew P. Monkmand
Anion-specific aggregation induced phosphorescence emission (AIPE) in an ionic iridium complex in aqueous media
Chem.Commun., 2015, 51, 16924
7118101 CIFC36 H51 P PtP 1 21/c 113.7573; 11.3705; 20.9159
90; 98.182; 90
3238.52Laura Ortega-Moreno; Riccardo Peloso; Celia Maya; Andres Suarez; Ernesto Carmona
Platinum(0) olefin complexes of a bulky terphenylphosphine ligand. Synthetic, structural and reactivity studies
Chem.Commun., 2015, 51, 17008
7118102 CIFC38 H55 P PtP -19.9449; 12.8244; 14.3077
82.197; 86.808; 72.959
1728.25Laura Ortega-Moreno; Riccardo Peloso; Celia Maya; Andres Suarez; Ernesto Carmona
Platinum(0) olefin complexes of a bulky terphenylphosphine ligand. Synthetic, structural and reactivity studies
Chem.Commun., 2015, 51, 17008
7118103 CIFC99 H129 O3 P3 Pt3P 63/m18.9177; 18.9177; 17.466
90; 90; 120
5413.3Laura Ortega-Moreno; Riccardo Peloso; Celia Maya; Andres Suarez; Ernesto Carmona
Platinum(0) olefin complexes of a bulky terphenylphosphine ligand. Synthetic, structural and reactivity studies
Chem.Commun., 2015, 51, 17008
7118104 CIFC29 H25 B F2 N2 O2P -110.4699; 10.9521; 12.2593
108.143; 95.509; 106.047
1258.03Firoj Ali; Anila H. A.; Nandaraj Taye; Rajesh G. Gonnade; Samit Chattopadhyay; Amitava Das
A fluorescent probe for specific detection of cysteine in the lipid dense region of cells
Chem.Commun., 2015, 51, 16932
7118105 CIFC22 H20 Br2 N2 S2C 1 2/c 121.883; 5.8646; 17.6
90; 109.12; 90
2134.1Yu Jiang; Run Sun; Qiang Wang; Xiang-Ying Tang; Min Shi
Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines
Chem.Commun., 2015, 51, 16968
7118106 CIFC12 H13 N SP 1 21 15.9732; 7.2898; 11.9181
90; 100.646; 90
510.02Yu Jiang; Run Sun; Qiang Wang; Xiang-Ying Tang; Min Shi
Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines
Chem.Commun., 2015, 51, 16968
7118107 CIFC23 H21 N O2 S2C 1 2/c 132.732; 9.3213; 12.9047
90; 92.347; 90
3934Yu Jiang; Run Sun; Qiang Wang; Xiang-Ying Tang; Min Shi
Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines
Chem.Commun., 2015, 51, 16968
7118108 CIFC29 H26 N2 O2 SP 1 21/c 113.134; 15.776; 12.1965
90; 106.946; 90
2417.4Yu Jiang; Run Sun; Qiang Wang; Xiang-Ying Tang; Min Shi
Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines
Chem.Commun., 2015, 51, 16968
7118109 CIFC27 H20 N2P 1 21 19.9297; 9.6354; 10.6037
90; 90.08; 90
1014.53Sayani Mukherjee; P. S. Salini; A. Srinivasan; S Peruncheralathan
AIEE phenomenon: tetraaryl vs. triaryl pyrazoles
Chem.Commun., 2015, 51, 17148
7118110 CIFC26 H19 N3P 1 21 19.7331; 9.7771; 10.5392
90; 90.204; 90
1002.92Sayani Mukherjee; P. S. Salini; A. Srinivasan; S Peruncheralathan
AIEE phenomenon: tetraaryl vs. triaryl pyrazoles
Chem.Commun., 2015, 51, 17148
7118111 CIFC21 H16 N2F d d 229.627; 36.79; 5.865
90; 90; 90
6393Sayani Mukherjee; P. S. Salini; A. Srinivasan; S Peruncheralathan
AIEE phenomenon: tetraaryl vs. triaryl pyrazoles
Chem.Commun., 2015, 51, 17148
7118112 CIFC23 H17 F7 O2P -113.635; 13.766; 14.405
108.215; 105.015; 110.595
2187.4Can Xue; Xin Huang; Shangze Wu; Jing Zhou; Jianxin Dai; Chunling Fu; Shengming Ma
TfOH-catalyzed domino cycloisomerization/hydrolytic defluorination of 2,3-allenyl perfluoroalkyl ketones
Chem.Commun., 2015, 51, 17112
7118113 CIFC48 H32 Br8 Cu10 N4 O9F d d d :27.9878; 33.9352; 39.1992
90; 90; 90
10625.6Wei-Hui Fang; Lei Zhang; Jian Zhang; Guo-Yu Yang
A highly stable face-extended diamondoid cluster-organic framework incorporating infinite inorganic guests
Chem.Commun., 2015, 51, 17174
7118114 CIFC26 H32 O6P 21 21 217.7711; 11.0137; 12.6885
90; 90; 90
1085.99Gaoyuan Zhao; Min He; Huilin Li; Shuangshuang Duan; Ziyun Yuan; Xingang Xie; Xuegong She
Domino intramolecular Diels-Alder reactions to construct a 6/6/5/5 fused tetracyclic framework
Chem.Commun., 2015, 51, 17321
7118115 CIFC14 H20 O3P 1 21 115.8905; 6.1745; 19.186
90; 104.581; 90
1821.8Gaoyuan Zhao; Min He; Huilin Li; Shuangshuang Duan; Ziyun Yuan; Xingang Xie; Xuegong She
Domino intramolecular Diels-Alder reactions to construct a 6/6/5/5 fused tetracyclic framework
Chem.Commun., 2015, 51, 17321
7118116 CIFC22 H18 Co N4 O4P -18.665; 8.683; 9.769
80.53; 76.38; 76.01
688.6Yukun Zhao; Junqi Lin; Yongdong Liu; Baochun Ma; Yong Ding; Mindong Chen
Efficient light-driven water oxidation catalyzed by a mononuclear cobalt(III) complex
Chem.Commun., 2015, 51, 17309
7118117 CIFC40 H46 N2 S2P -19.4905; 13.4085; 15.1433
77.19; 87.743; 74.954
1814.32Daisuke Sakamaki; Daisuke Kumano; Eiji Yashim; Shu Seki
A double hetero[4]helicene composed of two phenothiazines: synthesis, structural properties, and cationic states
Chem.Commun., 2015, 51, 17237
7118118 CIFC41 H48 Cl8 N2 S2 SbP 1 21/c 111.982; 15.925; 24.598
90; 90.15; 90
4694Daisuke Sakamaki; Daisuke Kumano; Eiji Yashim; Shu Seki
A double hetero[4]helicene composed of two phenothiazines: synthesis, structural properties, and cationic states
Chem.Commun., 2015, 51, 17237
7118119 CIFC41 H52 N2 O S2C 1 2/c 123.0126; 29.0068; 22.0641
90; 104.716; 90
14245.1Daisuke Sakamaki; Daisuke Kumano; Eiji Yashim; Shu Seki
A double hetero[4]helicene composed of two phenothiazines: synthesis, structural properties, and cationic states
Chem.Commun., 2015, 51, 17237
7118120 CIFC46 H62 Cl12 N2 S2 Sb2P -116.337; 20.1317; 20.3767
103.182; 91.496; 112.226
5993.2Daisuke Sakamaki; Daisuke Kumano; Eiji Yashim; Shu Seki
A double hetero[4]helicene composed of two phenothiazines: synthesis, structural properties, and cationic states
Chem.Commun., 2015, 51, 17237
7118121 CIFC84 H132 Cl12 Cu4 Dy4 N28 O48P m m n19.3834; 27.657; 15.3958
90; 90; 90
8253.5Jianfeng Wu; Lang Zhao; Mei Guo; Jinkui Tang
Constructing supramolecular grids: from 4f square to 3d-4f grid
Chem.Commun., 2015, 51, 17317
7118122 CIFC80 H76 Dy4 F12 N28 O44 S4I 41/a m d21.384; 21.384; 38.507
90; 90; 90
17608Jianfeng Wu; Lang Zhao; Mei Guo; Jinkui Tang
Constructing supramolecular grids: from 4f square to 3d-4f grid
Chem.Commun., 2015, 51, 17317
7118123 CIFC76 H76 Cl12 Dy4 N28 O16P 42/n21.9388; 21.9388; 16.335
90; 90; 90
7862.2Jianfeng Wu; Lang Zhao; Mei Guo; Jinkui Tang
Constructing supramolecular grids: from 4f square to 3d-4f grid
Chem.Commun., 2015, 51, 17317
7118124 CIFC14 H4 N O9 Zn2I -4 3 m28.122; 28.122; 28.122
90; 90; 90
22240Jia, Yan-Yuan; Zhang, Ying-Hui; Xu, Jian; Feng, Rui; Zhang, Ming-Shi; Bu, Xian-He
A high-performance "sweeper" for toxic cationic herbicides: an anionic metal-organic framework with a tetrapodal cage.
Chemical communications (Cambridge, England), 2015, 51, 17439-17442
7118125 CIFC72.5 H101.76 N12 O7.38I 1 2 121.656; 19.8282; 22.267
90; 106.048; 90
9188.8Briggs, Michael E.; Slater, Anna G.; Lunt, Neil; Jiang, Shan; Little, Marc A.; Greenaway, Rebecca L.; Hasell, Tom; Battilocchio, Claudio; Ley, Steven V.; Cooper, Andrew I.
Dynamic flow synthesis of porous organic cages.
Chemical communications (Cambridge, England), 2015, 51, 17390-17393
7118126 CIFC17 H18 N2 Na4 O12P 1 21 111.8894; 5.2299; 17.4663
90; 97.279; 90
1077.31Siman, Peter; Trickett, Christopher A.; Furukawa, Hiroyasu; Yaghi, Omar M.
l-Aspartate links for stable sodium metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 17463-17466
7118127 CIFC16.54 H16.85 N2 Na4 O12.85P 1 21 124.0448; 5.2432; 16.9833
90; 103.366; 90
2083.1Siman, Peter; Trickett, Christopher A.; Furukawa, Hiroyasu; Yaghi, Omar M.
l-Aspartate links for stable sodium metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 17463-17466
7118128 CIFC22.5 H20.5 N2 Na4 O13P 1 21 112.079; 5.2419; 21.254
90; 103.886; 90
1306.4Siman, Peter; Trickett, Christopher A.; Furukawa, Hiroyasu; Yaghi, Omar M.
l-Aspartate links for stable sodium metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 17463-17466
7118129 CIFC22.25 H19.25 N2 Na4 O11.5P 1 21 111.9807; 5.2345; 21.796
90; 99.274; 90
1349Siman, Peter; Trickett, Christopher A.; Furukawa, Hiroyasu; Yaghi, Omar M.
l-Aspartate links for stable sodium metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 17463-17466
7118130 CIFC120 H130 Cu4 N10 O46 S4P 115.722; 15.738; 18.629
104.9; 114.87; 91.3
3996.1Boer, Stephanie A.; Turner, David R.
Self-selecting homochiral quadruple-stranded helicates and control of supramolecular chirality.
Chemical communications (Cambridge, England), 2015, 51, 17375-17378
7118131 CIFC131.5 H156 Cu4 N12.5 O47.5 S4P 115.702; 15.714; 18.656
113.62; 107.65; 90.7
3971.6Boer, Stephanie A.; Turner, David R.
Self-selecting homochiral quadruple-stranded helicates and control of supramolecular chirality.
Chemical communications (Cambridge, England), 2015, 51, 17375-17378
7118132 CIFC120 H108 Cu4 D24 N8 O46 S8P 115.638; 15.832; 18.482
72.648; 65.229; 89.532
3929.5Boer, Stephanie A.; Turner, David R.
Self-selecting homochiral quadruple-stranded helicates and control of supramolecular chirality.
Chemical communications (Cambridge, England), 2015, 51, 17375-17378
7118133 CIFC118 H125 Cu4 N9 O45 S4C 1 2/c 133.892; 15.712; 62.235
90; 104.151; 90
32135Boer, Stephanie A.; Turner, David R.
Self-selecting homochiral quadruple-stranded helicates and control of supramolecular chirality.
Chemical communications (Cambridge, England), 2015, 51, 17375-17378
7118134 CIFC122 H134 Cu4 N10 O46 S4P -114.751; 17.672; 19.46
102.82; 107.63; 106.68
4358Boer, Stephanie A.; Turner, David R.
Self-selecting homochiral quadruple-stranded helicates and control of supramolecular chirality.
Chemical communications (Cambridge, England), 2015, 51, 17375-17378
7118135 CIFC98.5 H91.5 Cu4 N11.5 O49 S4P 1 21/n 116.094; 20.448; 20.371
90; 101.2; 90
6576Boer, Stephanie A.; Turner, David R.
Self-selecting homochiral quadruple-stranded helicates and control of supramolecular chirality.
Chemical communications (Cambridge, England), 2015, 51, 17375-17378
7118136 CIFC30 H27 Br N4 O3P -18.1126; 18.8402; 19.4228
88.825; 88.363; 84.224
2951.9Hernández-Melo, Denhy; Tiburcio, Jorge
Coupled molecular motions driven by light or chemical inputs: spiropyran to merocyanine isomerisation followed by pseudorotaxane formation.
Chemical communications (Cambridge, England), 2015, 51, 17564-17567
7118137 CIFC46 H25 N2.5 O16 Zn4P 1 21/c 124.736; 21.701; 25.337
90; 109.956; 90
12784Hu, Xiao-Li; Qin, Chao; Wang, Xin-Long; Shao, Kui-Zhan; Su, Zhong-Min
A luminescent dye@MOF as a dual-emitting platform for sensing explosives.
Chemical communications (Cambridge, England), 2015, 51, 17521-17524
7118138 CIFC24 H24 Cl4 F6 Mn N5 O6 S2P -19.7733; 11.0266; 15.5654
101.301; 100.49; 101.672
1567.37Fitzpatrick, Anthony J.; Trzop, Eliza; Müller-Bunz, Helge; Dîrtu, Marinela M; Garcia, Yann; Collet, Eric; Morgan, Grace G.
Electronic vs. structural ordering in a manganese(iii) spin crossover complex.
Chemical communications (Cambridge, England), 2015, 51, 17540-17543
7118139 CIFC24 H24 Cl4 F6 Mn N5 O6 S2P -19.9211; 11.2426; 15.4284
102.26; 100.491; 100.192
1611.34Fitzpatrick, Anthony J.; Trzop, Eliza; Müller-Bunz, Helge; Dîrtu, Marinela M; Garcia, Yann; Collet, Eric; Morgan, Grace G.
Electronic vs. structural ordering in a manganese(iii) spin crossover complex.
Chemical communications (Cambridge, England), 2015, 51, 17540-17543
7118140 CIFC24 H24 Cl4 F6 Mn N5 O6 S2P -19.9196; 20.8595; 16.9831
107.737; 106.146; 87.684
3211.27Fitzpatrick, Anthony J.; Trzop, Eliza; Müller-Bunz, Helge; Dîrtu, Marinela M; Garcia, Yann; Collet, Eric; Morgan, Grace G.
Electronic vs. structural ordering in a manganese(iii) spin crossover complex.
Chemical communications (Cambridge, England), 2015, 51, 17540-17543
7118141 CIFC24 H24 Cl4 F6 Mn N5 O6 S2P -19.9941; 11.2766; 15.4647
102.353; 100.671; 100.272
1629.38Fitzpatrick, Anthony J.; Trzop, Eliza; Müller-Bunz, Helge; Dîrtu, Marinela M; Garcia, Yann; Collet, Eric; Morgan, Grace G.
Electronic vs. structural ordering in a manganese(iii) spin crossover complex.
Chemical communications (Cambridge, England), 2015, 51, 17540-17543
7118142 CIFC12 H20 B O2 PP 21 21 2110.596; 11.039; 11.6053
90; 90; 90
1357.46Orgué, Sílvia; Flores-Gaspar, Areli; Biosca, Maria; Pàmies, Oscar; Diéguez, Montserrat; Riera, Antoni; Verdaguer, Xavier
Stereospecific SN2@P reactions: novel access to bulky P-stereogenic ligands.
Chemical communications (Cambridge, England), 2015, 51, 17548-17551
7118143 CIFC14 H11 N3 O3P 1 21/n 110.342; 6.841; 17.218
90; 102.267; 90
1190.4Maeda, Hiromitsu; Fukui, Ayaka; Yamakado, Ryohei; Yasuda, Nobuhiro
Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations.
Chemical communications (Cambridge, England), 2015, 51, 17572-17575
7118144 CIFC30 H46 N4 O3P 1 21/c 118.1094; 8.5397; 19.1583
90; 105.39; 90
2856.6Maeda, Hiromitsu; Fukui, Ayaka; Yamakado, Ryohei; Yasuda, Nobuhiro
Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations.
Chemical communications (Cambridge, England), 2015, 51, 17572-17575
7118145 CIFC26 H38 N4 O3P 1 21/c 116.8579; 8.6583; 18.4879
90; 111.416; 90
2512.18Maeda, Hiromitsu; Fukui, Ayaka; Yamakado, Ryohei; Yasuda, Nobuhiro
Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations.
Chemical communications (Cambridge, England), 2015, 51, 17572-17575
7118146 CIFC24 H30 N3 Na O8P 1 21/c 17.916; 16.599; 18.426
90; 94.92; 90
2412.2Maeda, Hiromitsu; Fukui, Ayaka; Yamakado, Ryohei; Yasuda, Nobuhiro
Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations.
Chemical communications (Cambridge, England), 2015, 51, 17572-17575
7118147 CIFC26 H36 K N3 O10P -110.778; 10.915; 14.506
82.963; 86.231; 63.226
1512Maeda, Hiromitsu; Fukui, Ayaka; Yamakado, Ryohei; Yasuda, Nobuhiro
Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations.
Chemical communications (Cambridge, England), 2015, 51, 17572-17575
7118148 CIFC21 H21 N5 O3P 1 21/a 19.516; 16.738; 12.25
90; 107.8; 90
1857.8Maeda, Hiromitsu; Fukui, Ayaka; Yamakado, Ryohei; Yasuda, Nobuhiro
Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations.
Chemical communications (Cambridge, England), 2015, 51, 17572-17575
7118149 CIFC29 H36 Br O SiP -19.5769; 15.5585; 18.7701
98.447; 95.244; 94.691
2741.97Aurora Lopez; Alejandro Parra; Carlos Jarava-Barrera; Mariola Tortosa
Copper-catalyzed silylation of p-quinone methides: new entry to dibenzylic silanes
Chem.Commun., 2015, 51, 17684
7118150 CIFC46 H46 Co3 F6 N14 O2 ReP 4/n c c13.6578; 13.6578; 25.5535
90; 90; 90
4766.6Vladimir Bulicanu; Kasper S. Pedersen; Mathieu Rouzieres; Jesper Bendix; Pierre Dechambenoit; Rodolphe Clerac; Elizabeth A. Hillard
One-dimensional coordination polymers of [Co3(dpa)4]^2+^ and [MF6]^2-^ (M = ReIV, ZrIV and SnIV)
Chem.Commun., 2015, 51, 17748
7118151 CIFC46 H46 Co3 F6 N14 O2 ZrP 4/n c c13.6527; 13.6527; 25.7947
90; 90; 90
4808Vladimir Bulicanu; Kasper S. Pedersen; Mathieu Rouzieres; Jesper Bendix; Pierre Dechambenoit; Rodolphe Clerac; Elizabeth A. Hillard
One-dimensional coordination polymers of [Co3(dpa)4]^2+^ and [MF6]^2-^ (M = ReIV, ZrIV and SnIV)
Chem.Commun., 2015, 51, 17748
7118152 CIFC46 H46 Co3 F6 N14 O2 SnP 4/n c c13.6633; 13.6633; 25.701
90; 90; 90
4798Vladimir Bulicanu; Kasper S. Pedersen; Mathieu Rouzieres; Jesper Bendix; Pierre Dechambenoit; Rodolphe Clerac; Elizabeth A. Hillard
One-dimensional coordination polymers of [Co3(dpa)4]^2+^ and [MF6]^2-^ (M = ReIV, ZrIV and SnIV)
Chem.Commun., 2015, 51, 17748
7118153 CIFC50 H43 F6 N P2 ReP -19.9941; 10.9876; 21.1474
104.686; 92.005; 106.919
2134.23Vladimir Bulicanu; Kasper S. Pedersen; Mathieu Rouzieres; Jesper Bendix; Pierre Dechambenoit; Rodolphe Clerac; Elizabeth A. Hillard
One-dimensional coordination polymers of [Co3(dpa)4]^2+^ and [MF6]^2-^ (M = ReIV, ZrIV and SnIV)
Chem.Commun., 2015, 51, 17748
7118154 CIFC22 H46 Cr N4 Si4P -110.972; 11.699; 13.519
99.28; 95.81; 115.672
1515Yi-Fei Deng; Tian Han; Zhenxing Wang; Zhongwen Ouyang; Bing Yin; Zhiping Zheng; J. Krzystek; Yan-Zhen Zheng
Uniaxial magnetic anisotropy of square-planar chromium(II) complexes revealed by magnetic and HF-EPR studies
Chem.Commun., 2015, 51, 17688
7118155 CIFC29 H41 F3 N O3 P Pt S SiP 1 21/c 19.8511; 20.837; 15.443
90; 99.5203; 90
3126.3Jun Takaya; Shisei Ito; Hironori Nomoto; Narumasa Saito; Naohiro Kirai; Nobuharu Iwasawa
Fluorine-controlled C-H borylation of arenes catalyzed by a PSiN-pincer platinum complex
Chem.Commun., 2015, 51, 17662
7118156 CIFC61.5 H64.5 N3.5 O13.5 Zn2I -415.6925; 15.6925; 19.1379
90; 90; 90
4712.8Alexandr V. Vinogradov; Haldor Zaake-Hertling; Andrey S. Drozdov; Peter Lonnecke; Gulaim A. Seisenbaeva; Vadim G. Kessler; Vladimir V. Vinogradov; Evamarie Hey-Hawkins
Anomalous adsorption of biomolecules on a Zn-based metal-organic framework obtained via a facile room-temperature route
Chem.Commun., 2015, 51, 17764
7118157 CIFC28 H38 Ag F3 N2 O3 SP 21 21 2112.981; 13.4443; 17.5825
90; 90; 90
3068.51Valerie H. L. Wong; Andrew J. P. White; T. S. Andy Hor; King Kuok (Mimi) Hii
Structure and bonding of [(SIPr)AgX] (X = Cl, Br, I and OTf
Chem.Commun., 2015, 51, 17752
7118158 CIFC56.5 H79 Ag2 Cl4 F3 N4 O3 SP 1 21/n 120.2292; 16.3318; 20.2255
90; 111.277; 90
6226.6Valerie H. L. Wong; Andrew J. P. White; T. S. Andy Hor; King Kuok (Mimi) Hii
Structure and bonding of [(SIPr)AgX] (X = Cl, Br, I and OTf
Chem.Commun., 2015, 51, 17752
7118159 CIFC27 H38 Ag Br N2P c c n10.94396; 12.5589; 19.9805
90; 90; 90
2746.2Valerie H. L. Wong; Andrew J. P. White; T. S. Andy Hor; King Kuok (Mimi) Hii
Structure and bonding of [(SIPr)AgX] (X = Cl, Br, I and OTf
Chem.Commun., 2015, 51, 17752
7118160 CIFC28 H40 Ag Cl2 I N2P 1 21/c 110.7195; 19.0287; 16.2788
90; 106.154; 90
3189.4Valerie H. L. Wong; Andrew J. P. White; T. S. Andy Hor; King Kuok (Mimi) Hii
Structure and bonding of [(SIPr)AgX] (X = Cl, Br, I and OTf
Chem.Commun., 2015, 51, 17752

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