Crystallography Open Database

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7117064 CIFC18 H18 N5 O10 P3 Zn3P -19.149; 11.202; 14.628
73.526; 88.045; 71.284
1358.9Wang, Chih-Min; Chang, Tsung-Yuan; Lee, Li-Wei; Lin, Hsiu-Mei; Lu, Kuang-Lieh; Lii, Kwang-Hwa
The first zinc phosphite with remarkable structural and functional transformations
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7824-7826
7117065 CIFC18 H16 N5 O9 P3 Zn3P -19.578; 11.517; 13.244
76.705; 88.391; 69.043
1325.4Wang, Chih-Min; Chang, Tsung-Yuan; Lee, Li-Wei; Lin, Hsiu-Mei; Lu, Kuang-Lieh; Lii, Kwang-Hwa
The first zinc phosphite with remarkable structural and functional transformations
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7824-7826
7117066 CIFC23 H18 N2 O SP 1 21/c 116.26; 8.0578; 16.7298
90; 118.216; 90
1931.47Xiaohan Ye; Jeffrey L. Petersen; Xiaodong Shi
Nickel-catalyzed directed sulfenylation of sp2 and sp3 C-H bonds
Chem.Commun., 2015, 51, 7863
7117067 CIFC22 H15 Cl N2 O SP 1 21/n 112.0459; 10.3781; 15.4051
90; 107.395; 90
1837.78Xiaohan Ye; Jeffrey L. Petersen; Xiaodong Shi
Nickel-catalyzed directed sulfenylation of sp2 and sp3 C-H bonds
Chem.Commun., 2015, 51, 7863
7117068 CIFC32 H47 Au N2 SP -19.6005; 11.3245; 15.2126
74.9336; 82.8296; 77.8418
1556.94Kazunori Miyamoto; Masaya Hirobe; Masanobu Uchiyama; Masahito Ochiai
Stereoselective synthesis and reaction of gold(I) (Z)-enethiolates
Chem.Commun., 2015, 51, 7962
7117069 CIFC8 H6 F3 I O6 SP -15.4618; 9.7781; 11.8765
98.2; 93.463; 91.657
626.19Akira Yoshimura; Khiem C. Nguyen; Scott C. Klasen; Akio Saito; Victor N. Nemykin; Viktor V. Zhdankin
Preparation, structure, and versatile reactivity of pseudocyclic benziodoxole triflate, new hypervalent iodine reagent
Chem.Commun., 2015, 51, 7835
7117071 CIFC40 H50 Cl2 Cu N2 O2C 1 2 113.608; 10.347; 14.528
90; 117.341; 90
1817.1Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117072 CIFC36 H42 Cl2 Cu N2 O2P 1 21 113.8568; 15.8847; 15.2073
90; 96.046; 90
3328.68Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117073 CIFC32 H34 Cl2 Cu N2C 1 2/c 125.878; 10.4574; 10.7037
90; 102.636; 90
2826.44Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117074 CIFC21 H45 Cu3 I6 N3P 2 21 218.52016; 31.2866; 13.2813
90; 90; 90
3540.35Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117075 CIFC18 H42 Cu3 I6 N3P 2 21 218.5342; 31.3102; 13.3245
90; 90; 90
3560.4Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117076 CIFC21 H45 Cu3.01 I6 N3P 2 21 218.5719; 13.4018; 31.305
90; 90; 90
3596.3Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117077 CIFC21 H45 Cu3 I6 N3P 2 21 218.6; 31.212; 13.5728
90; 90; 90
3643.3Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117078 CIFC21 H45 Cu2.99 I6 N3P 2 21 218.6034; 13.5945; 31.256
90; 90; 90
3655.7Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117079 CIFC21 H45 Cu3.01 I6 N3P 2 21 218.6312; 13.6767; 31.2048
90; 90; 90
3683.6Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117080 CIFC44 H32 Cd2 Cl2 N4 O8P -18.9041; 17.9362; 18.9879
100.842; 102.263; 103.409
2791.2Cheng Chen; Li-Xuan Cai; Bin Tan; Ya-Jun Zhang; Xiao-Dong Yang; Jie Zhang
Ammonia detection by using flexible Lewis acidic sites in luminescent porous frameworks constructed from a bipyridinium derivative
Chem.Commun., 2015, 51, 8189
7117081 CIFC44 H32 Br2 Cd2 N4 O8P -19.0867; 18.0356; 18.8207
102.462; 103.387; 100.625
2839.4Cheng Chen; Li-Xuan Cai; Bin Tan; Ya-Jun Zhang; Xiao-Dong Yang; Jie Zhang
Ammonia detection by using flexible Lewis acidic sites in luminescent porous frameworks constructed from a bipyridinium derivative
Chem.Commun., 2015, 51, 8189
7117082 CIFC20 H17 N O2 SP 1 21 15.7758; 20.087; 7.3139
90; 92.951; 90
847.42Li Lin; Yuhong Yang; Mei Wang; Luhao Lai; Yarong Guo; Rui Wang
Oxidative N-heterocyclic carbene catalyzed stereoselective annulation of simple aldehydes and 5-alkenyl thiazolones
Chem.Commun., 2015, 51, 8134
7117083 CIFC20 H17 N O2 SP 1 21 15.7825; 20.098; 7.311
90; 92.824; 90
848.6Li Lin; Yuhong Yang; Mei Wang; Luhao Lai; Yarong Guo; Rui Wang
Oxidative N-heterocyclic carbene catalyzed stereoselective annulation of simple aldehydes and 5-alkenyl thiazolones
Chem.Commun., 2015, 51, 8134
7117084 CIFC25 H21 Cl3 N2 SiP 1 21/c 110.681; 19.442; 11.152
90; 101.368; 90
2270.4Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117085 CIFC26 H24 N2 SiP 1 21/a 114.1331; 7.8144; 18.4958
90; 102.186; 90
1996.68Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117086 CIFC36 H28 N2 O0.5 SiC 1 2/c 121.767; 12.983; 19.854
90; 108.48; 90
5321.4Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117087 CIFC73 H58 Cl2 N4 Si2P 32 2 113.156; 13.156; 28.415
90; 90; 120
4259.2Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117088 CIFC22 H22 Cu4 N2 O18 S2F d d 224.748; 32.354; 21.712
90; 90; 90
17385Xing; Meng,ab; Shu-Yan Song; Xue-Zhi Song; Min Zhu; Shu-Na Zhao; Lan-Lan Wu; Hong-Jie Zhang
A tetranuclear copper cluster-based MOF with sulfonate-carboxylate ligands exhibiting high proton conduction properties
Chem.Commun., 2015, 51, 8150
7117089 CIFC40 H38 Cl2 Fe2 N2 O2P 1 21/n 110.271; 20.397; 17.702
90; 105.15; 90
3579.6Fabio Marchetti; Stefano Zacchini; Valerio Zanotti
Carbon monoxide-isocyanide coupling promoted by acetylide addition to a diiron complex
Chem.Commun., 2015, 51, 8101
7117090 CIFC42 H43 Fe2 N2 O2.5P 1 21/c 116.505; 14.661; 17.918
90; 111.59; 90
4031.6Fabio Marchetti; Stefano Zacchini; Valerio Zanotti
Carbon monoxide-isocyanide coupling promoted by acetylide addition to a diiron complex
Chem.Commun., 2015, 51, 8101
7117091 CIFC43 H39 Cu F12 N5 P2P 1 21/n 112.70025; 21.30927; 15.21998
90; 93.2975; 90
4112.21Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117092 CIFC90 H78 Cl2 Cu2 Fe N8 O8P 1 21/n 118.1611; 52.0625; 20.5495
90; 106.087; 90
18669Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117093 CIFC22 H15 Fe I N2P 1 21/c 15.8216; 15.604; 19.8079
90; 91.3; 90
1798.89Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117094 CIFC34 H22 Fe N4P 1 21/n 115.622; 9.169; 17.531
90; 102.084; 90
2455.5Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117095 CIFC22 H16 Fe N2P n a 2123.8585; 6.8313; 10.025
90; 90; 90
1633.92Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117096 CIFC18 H16 F6 Fe N PP 1 21 17.396; 10.9122; 11.2342
90; 104.382; 90
878.26Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117097 CIFC20 H19 BrP 1 n 16.0119; 15.806; 8.3765
90; 98.292; 90
787.65Xin-Xing Wu; Yi Shen; Wen-Long Chen; Si Chen; Xin-Hua Hao; Yu Xia; Peng-Fei Xu; Yong-Min Liang
Palladium-catalyzed ring opening of norbornene: efficient synthesis of methylenecyclopentane derivatives
Chem.Commun., 2015, 51, 8031
7117098 CIFC21 H22 OP 1 21/c 117.781; 15.3478; 6.0728
90; 99.114; 90
1636.34Xin-Xing Wu; Yi Shen; Wen-Long Chen; Si Chen; Xin-Hua Hao; Yu Xia; Peng-Fei Xu; Yong-Min Liang
Palladium-catalyzed ring opening of norbornene: efficient synthesis of methylenecyclopentane derivatives
Chem.Commun., 2015, 51, 8031
7117099 CIFC2 H11 Cl2 N3 O2 PtP -17.103; 9.028; 13.105
90.17; 94.67; 90.44
837.5Giorgio Pelosi; Mauro Ravera; Elisabetta Gabano; Federico Fregonese; Domenico Osella
Unprecedented one-pot synthesis of an unsymmetrical cisplatin-based Pt(IV)-acetamidato complex
Chem.Commun., 2015, 51, 8051
7117100 CIFC15 H21 N O4P 21 21 2110.9624; 11.2771; 12.2022
90; 90; 90
1508.49Alejandra Millan-Ortiz; German Lopez-Valdez; Fernando Cortez-Guzman; Luis D. Miranda
A novel carbamoyl radical based dearomatizing spiroacylation process
Chem.Commun., 2015, 51, 8345
7117101 CIFC15 H14 Br NP b c a19.318; 7.18486; 19.6634
90; 90; 90
2729.22Johannes F. Franz; Wolfgang B. Kraus; Kirsten Zeitler
No photocatalyst required – versatile, visible light mediated transformations with polyhalomethanes
Chem.Commun., 2015, 51, 8280
7117102 CIFC76 H28 F10 O2I 41/a28.7283; 28.7283; 12.1809
90; 90; 90
10053.1Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117103 CIFC46 H20 Cl6 F10 O4P 1 21/c 110.3234; 15.5838; 13.5017
90; 102.531; 90
2120.4Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117104 CIFC82 H9 F5 O2C 1 2/c 126.962; 13.616; 24.071
90; 97.746; 90
8756Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117105 CIFC78.25 H24 F10 O4.75P -115.928; 19.014; 20.624
101.456; 110.099; 108.543
5218.1Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117106 CIFC32 H10 F10 O4P 1 21/c 114.649; 10.269; 8.425
90; 99.012; 90
1251.7Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117107 CIFC106 H26 F10 O4P 1 21/c 127.439; 9.7293; 23.787
90; 97.272; 90
6299.2Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117108 CIFC8 H14 Cr Mn N O12P -3 1 c8.2865; 8.2865; 13.88
90; 90; 120
825.4Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117109 CIFC7 H12 Cr Mn N O12P -3 1 c8.2708; 8.2708; 14.088
90; 90; 120
834.6Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117110 CIFC8 H14 Al Mn N O12P -3 1 c8.2179; 8.2179; 13.646
90; 90; 120
798.1Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117111 CIFC8 H14 Cr Mg N O12P -3 1 c8.1565; 8.1565; 13.705
90; 90; 120
789.6Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117112 CIFC34 H53 Cu N2 O S SiC 1 2/c 128.986; 12.887; 19.067
90; 92.619; 90
7115Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117113 CIFC34 H53 Cu N2 O Se SiC 1 2/c 129.597; 12.842; 19.184
90; 93.196; 90
7280Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117114 CIFC30 H45 Cu N2 Si TeP 1 21/n 19.789; 21.443; 15.58
90; 100.673; 90
3214Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117115 CIFC58 H80 Cl8 Cu2 Hg N4 S2P 1 21/n 113.026; 16.803; 16.264
90; 106.93; 90
3405.5Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117116 CIFC26 H15 N O4 S ZnP -17.9902; 11.043; 13.43
105.463; 102.922; 107.508
1028Zhi-Qiang Shi; Zi-Jian Guo; He-Gen Zheng
Two luminescent Zn(II) metal-organic frameworks for exceptionally selective detection of picric acid explosives
Chem.Commun., 2015, 51, 8300
7117117 CIFC36 H24 N4 O4 S ZnP b c a18.379; 10.6606; 31.736
90; 90; 90
6218.1Zhi-Qiang Shi; Zi-Jian Guo; He-Gen Zheng
Two luminescent Zn(II) metal-organic frameworks for exceptionally selective detection of picric acid explosives
Chem.Commun., 2015, 51, 8300
7117118 CIFC48 H47 Co N3 O8P -112.848; 14.185; 15.785
114.87; 97.126; 109.338
2343.4Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117119 CIFC60 H65 Co N4 O11P -110.6129; 14.9365; 18.7658
108.987; 92.348; 106.134
2673.7Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117120 CIFC72 H64 Co3 N4 O14C 1 2/c 126.758; 10.635; 29.565
90; 116.906; 90
7503Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117121 CIFC46 H25 Cl3 F10 N6 O2P 4113.62; 13.62; 22.0245
90; 90; 90
4085.64Rafal Orlowski; Olena Vakuliuk; Maria Pia Gullo; Oksana Danylyuk; Barbara Ventura; Beata Koszarna; Anna Tarnowska; Nina Jaworska; Andrea Barbieri; Daniel T. Gryko
Self-assembling corroles
Chem.Commun., 2015, 51, 8284
7117122 CIFC44 H28 Cl3 F10 N5 O2P -111.084; 13.9124; 15.6917
95.169; 107.245; 111.916
2088.2Rafal Orlowski; Olena Vakuliuk; Maria Pia Gullo; Oksana Danylyuk; Barbara Ventura; Beata Koszarna; Anna Tarnowska; Nina Jaworska; Andrea Barbieri; Daniel T. Gryko
Self-assembling corroles
Chem.Commun., 2015, 51, 8284
7117123 CIFC30 H8 F10 N4P -15.996; 7.348; 13.198
87.325; 86.01; 71.49
549.9Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117124 CIFC30 H8 F10 N4 OP 1 21/c 128.021; 11.565; 7.319
90; 95.576; 90
2360.6Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117125 CIFC31 H10 F10 N4P 16.1461; 7.3648; 14.031
76.834; 82.082; 72.763
588.95Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117126 CIFC40 H72 Mo2 N32 O11 Zn4P c a 2114.7778; 14.8566; 31.0576
90; 90; 90
6818.6N. Bridonneau; J. Long; J.-L. Cantin; J. von Bardeleben; S. Pillet; E.-E. Bendeif; D. Aravena; E. Ruiz; V. Marvaud
First evidence of light-induced spin transition in molybdenum(IV)
Chem.Commun., 2015, 51, 8229
7117127 CIFC34 H42 N4 O11 SP 1 21/n 18.6053; 18.642; 12.19
90; 98.319; 90
1934.9M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117128 CIFC28 H28 N4 O10P 21 21 219.942; 14.412; 18.805
90; 90; 90
2694.5M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117129 CIFC28 H28 N4 O10P 21 21 219.9943; 14.47; 18.796
90; 90; 90
2718.2M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117130 CIFC27 H21 Br O5P 1 21/n 18.0879; 27.2026; 10.7134
90; 93.374; 90
2352.99Jieru Yang; Ao Mao; Zhenting Yue; Wenxuan Zhu; Xuewei Luo; Chuwei Zhu; Yuanjing Xiao; Junliang Zhang
A simple base-mediated synthesis of diverse functionalized ring-fluorinated 4H-pyrans via double direct C-F substitutions
Chem.Commun., 2015, 51, 8326
7117131 CIFC16 H13 F O2C 1 2/c 125.8977; 8.7711; 11.9279
90; 111.181; 90
2526.4Jieru Yang; Ao Mao; Zhenting Yue; Wenxuan Zhu; Xuewei Luo; Chuwei Zhu; Yuanjing Xiao; Junliang Zhang
A simple base-mediated synthesis of diverse functionalized ring-fluorinated 4H-pyrans via double direct C-F substitutions
Chem.Commun., 2015, 51, 8326
7117132 CIFC18 H12 Cl N O3P 21 21 219.3195; 10.8944; 14.3609
90; 90; 90
1458.07Lin, Youqiang; Yang, Limin; Deng, Yue; Zhong, Guofu
Cooperative catalysis of N-heterocyclic carbene and Brønsted acid for a highly enantioselective route to unprotected spiro-indoline-pyrans
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8330-8333
7117133 CIFC20 H16 Cl3 F2 N O Pt SP 1 21 15.897; 13.924; 12.852
90; 96.001; 90
1049.5Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117134 CIFC20 H18 F2 N P PtC 1 2/c 123.9938; 12.5106; 12.1687
90; 107.325; 90
3487.04Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117135 CIFC29 H36 Cl2 F2 N P PtP b c a14.9738; 15.8809; 24.6498
90; 90; 90
5861.7Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117136 CIFC29.5 H36.5 Cl3.5 F2 N P PtP 1 21/c 142.5003; 8.95573; 15.7762
90; 92.949; 90
5996.8Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117137 CIFC29 H36 Cl2 F2 N P PtP n a 2117.9634; 13.9987; 11.0698
90; 90; 90
2783.66Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117138 CIFC82 H20 Cl4P b c a17.0287; 18.1277; 29.437
90; 90; 90
9086.9Ran Tao; Tomokazu Umeyama; Tomohiro Higashino; Tomoyuki Koganezawa; Hiroshi Imahori
A single cis-2 regioisomer of ethylene-tethered indene dimer-fullerene adduct as an electron-acceptor in polymer solar cells
Chem.Commun., 2015, 51, 8233
7117139 CIFC44 H71 B2 F8 N4 Ni O6.5P 1 21 116.4359; 15.6364; 19.2398
90; 92.863; 90
4938.4Yulong Zhang; Na Yang; Xiaohua Liu; Jing Guo; Xiying Zhang; Lili Lin; Changwei Hu; Xiaoming Feng
Reversal of enantioselective Friedel-Crafts C3-alkylation of pyrrole by slightly tuning the amide units of N,N'-dioxide ligands
Chem.Commun., 2015, 51, 8432
7117140 CIFC55 H92 B2 F8 N4 Ni O8I 1 2 116.452; 8.8684; 22.2394
90; 110.682; 90
3035.68Yulong Zhang; Na Yang; Xiaohua Liu; Jing Guo; Xiying Zhang; Lili Lin; Changwei Hu; Xiaoming Feng
Reversal of enantioselective Friedel-Crafts C3-alkylation of pyrrole by slightly tuning the amide units of N,N'-dioxide ligands
Chem.Commun., 2015, 51, 8432
7117141 CIFC32 H24 B F15 Si2P -113.8787; 14.2041; 19.8693
101.859; 98.658; 117.694
3254.49Christina Eller; Gerald Kehr; Constantin G. Daniliuc; Gerhard Erker
Unusual product formation in a 1,1-carboboration reaction
Chem.Commun., 2015, 51, 8436
7117142 CIFC23 H20 Fe O4P 1 21/n 18.6879; 6.4163; 34.7054
90; 94.776; 90
1927.91Tatsuo Okauchi; Naoki Sata; Akihiro Urakawa; Mitsuru Kitamura
Unprecedented formation of eta^46-(vinylketene)iron complexes from eta^4^-(diene)iron complexes and aromatic compounds in the presence of a Lewis acid
Chem.Commun., 2015, 51, 8454
7117143 CIFC21 H33 Cu N3 O11.5R -3 m :H18.483; 18.483; 46.758
90; 90; 120
13833Chengling Song; Yajing Ling; Yunlong Feng; Wei Zhou; Taner Yildirim; Yabing He
A NbO-type metal-organic framework exhibiting high deliverable capacity for methane storage
Chem.Commun., 2015, 51, 8508
7117144 CIFC147 H182 N14 O56 Zn6P m n a19.7928; 17.7591; 28.543
90; 90; 90
10032.9Fei-Yan Yi; Hai-Long Jiang; Zhong-Ming Sun
Linearly bridging CO2 in a metal-organic framework
Chem.Commun., 2015, 51, 8446
7117145 CIFC24 H17 NP 1 21/c 113.0849; 9.1297; 13.5767
90; 93.893; 90
1618.15Sisir Lohar; Damir A. Safin; Archya Sengupta; Ansuman Chattopadhyay; Jesus Sanmartin Matalobos; Maria G. Babashkina; Koen Robeyns; Mariusz P. Mitoraj; Piotr Kubisiak; Yann Garcia; Debasis Das
Ratiometric sensing of lysine through the formation of the pyrene excimer: experimental and computational studies
Chem.Commun., 2015, 51, 8536
7117146 CIFC22 H17 NP 1 21/n 14.2713; 14.11; 25.725
90; 91.832; 90
1549.6Sisir Lohar; Damir A. Safin; Archya Sengupta; Ansuman Chattopadhyay; Jesus Sanmartin Matalobos; Maria G. Babashkina; Koen Robeyns; Mariusz P. Mitoraj; Piotr Kubisiak; Yann Garcia; Debasis Das
Ratiometric sensing of lysine through the formation of the pyrene excimer: experimental and computational studies
Chem.Commun., 2015, 51, 8536
7117147 CIFC31 H30 Al Cr F24 O7P 1 21/n 125.012; 13.9336; 25.099
90; 111.913; 90
8115.2Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117148 CIFC48 H33 Al Cr F36 O6 PP 1 21/n 119.1442; 34.536; 19.5979
90; 119.074; 90
11324.7Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117149 CIFC32 H33 Cr O2 PP -18.649; 9.593; 17.771
90.671; 99.551; 116.355
1296.8Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117150 CIFC18 H20 O2 SP 1 21 17.323; 12.346; 9.152
90; 108.447; 90
784.9Ryosuke Takechi; Takahiro Nishimura
Enantioselective 1,4-addition of cyclopropylboronic acid catalyzed by rhodium/chiral diene complexes
Chem.Commun., 2015, 51, 8528
7117151 CIFC51 H50 N2 O2 S6C 1 2/c 137.215; 14.101; 9.619
90; 96.595; 90
5014.3Minh T. Nguyen; Bradley J. Holliday
Direct insights into metal-induced conductivity enhancement in conducting metallopolymers
Chem.Commun., 2015, 51, 8610
7117152 CIFC18.86 H19 Ag I0.14 N3.86P 1 21/n 19.6546; 10.6457; 17.115
90; 90.385; 90
1759.04Rachael Heath; Helge Muller-Bunz; Martin Albrecht
Silver(I) NHC mediated C-C bond activation of alkyl nitriles and catalytic efficiency in oxazoline synthesis
Chem.Commun., 2015, 51, 8699
7117153 CIFC19 H19 Ag N4P 1 21/n 19.59019; 10.57651; 17.1999
90; 90.1567; 90
1744.59Rachael Heath; Helge Muller-Bunz; Martin Albrecht
Silver(I) NHC mediated C-C bond activation of alkyl nitriles and catalytic efficiency in oxazoline synthesis
Chem.Commun., 2015, 51, 8699
7117154 CIFC20 H16 Cl F3 N2 O2P 1 21 110.4449; 7.9864; 11.2224
90; 93.069; 90
934.8Mingxia Ma; Yuanyuan Zhu; Quantao Sun; Xiaoyuan Li; Jinhuan Su; Long Zhao; Yanyan Zhao; Shuai Qiu; Wenjin Yan; Kairong Wang; Rui Wang
The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2'-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Chem.Commun., 2015, 51, 8789
7117155 CIFC11 H8 Br F3 N2 OP 1 21/n 16.8291; 12.139; 14.882
90; 101.467; 90
1209.1Mingxia Ma; Yuanyuan Zhu; Quantao Sun; Xiaoyuan Li; Jinhuan Su; Long Zhao; Yanyan Zhao; Shuai Qiu; Wenjin Yan; Kairong Wang; Rui Wang
The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2'-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Chem.Commun., 2015, 51, 8789
7117156 CIFC15 H11 N O SP 1 21/c 116.112; 7.8274; 9.593
90; 101.081; 90
1187.27Bhaskar Garg; Yong-Chien Ling
A highly selective phenothiazine-based fluorescence 'turn-on' indicator based on cyanide-promoted novel protection/deprotection mechanism
Chem.Commun., 2015, 51, 8809
7117157 CIFC29 H23 Br O2P -19.845; 10.37; 12.763
89.509; 70.585; 71.497
1158.5Ya-Jing Chen; Tian-Jiao Hu; Chen-Guo Feng; Guo-Qiang Lin
Synthesis of chiral cyclobutanes via rhodium/diene-catalyzed asymmetric 1,4-addition: a dramatic ligand effect on the diastereoselectivity
Chem.Commun., 2015, 51, 8773
7117158 CIFC15 H4 F4 I NP -17.4665; 9.3784; 10.5061
85.468; 75.25; 67.203
655.7Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117159 CIFC15 H8 I NF d d 218.421; 7.6185; 17.387
90; 90; 90
2440.1Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117160 CIFC15 H4 Br F4 NP 1 21/c 113.2997; 9.7019; 19.917
90; 102.415; 90
2509.8Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117161 CIFC15 H6 Br F2 NP -15.7972; 8.6736; 12.715
73.612; 85.418; 86.061
610.7Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117162 CIFC15 H8 Br NF d d 217.893; 7.5409; 17.168
90; 90; 90
2316.5Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117163 CIFC15 H9 NP -19.404; 9.48; 13.047
94.412; 102.356; 103.038
1097.3Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117164 CIFC16 H12 F2 N O4P 1 21/c 122.639; 5.0207; 11.438
90; 93.54; 90
1297.6Rui Guo; Haodong Yang; Pingping Tang
Silver-catalyzed Meerwein arylation: intermolecular and intramolecular fluoroarylation of styrenes
Chem.Commun., 2015, 51, 8829
7117165 CIFC20 H36 Au Cl N8 O4P n a 2111.5632; 12.4279; 19.2238
90; 90; 90
2762.58Serebryanskaya, T. V.; Zolotarev, A. A.; Ott, I.
A novel aminotriazole-based NHC complex for the design of gold(i) anti-cancer agents: synthesis and biological evaluation
Med. Chem. Commun., 2015, 6, 1186
7117166 CIFC10 H16 N4 O4 SC 1 2/c 19.642; 15.986; 9.334
90; 92.708; 90
1437Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117167 CIFC14 H14 N4 O4 SF d d 214.6766; 18.8388; 11.8862
90; 90; 90
3286.4Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117168 CIFC16 H18 N4 O4 SC 1 2/c 117.398; 7.4436; 14.051
90; 105.38; 90
1754.5Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117169 CIFC28 H28 N4 O5 SP b c n16.62; 8.218; 19.159
90; 90; 90
2616.8Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117170 CIFC28 H30 N4 O6 SP b c n16.933; 8.0337; 19.688
90; 90; 90
2678.3Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117171 CIFC14 H14 N4 O4 SeP 43 21 218.5107; 18.5107; 18.953
90; 90; 90
6494.2Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117172 CIFC17 H23 N4 O5.5 SeC 1 2/c 125.917; 8.7717; 17.5915
90; 100.377; 90
3933.8Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117173 CIFC26 H22 N4 O4 SeP -19.611; 10.852; 11.918
83.339; 72.175; 88.808
1175.2Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117174 CIFC28 H30 N4 O6 SeP b c n17.3442; 8.0712; 19.5768
90; 90; 90
2740.5Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117175 CIFC30 H24 O2C 1 2/c 131.067; 13.835; 15.67
90; 93.254; 90
6724Suman Kalyan Samanta; Eduard Preis; Christian W. Lehmann; Richard Goddard; Saientan Bag; Prabal K. Maiti; Gunther Brunklaus; Ullrich Scherf
One-step synthesis of a cyclic 2,17-dioxo[3,3](4,4') biphenylophane and first preparation of a microporous polymer network from a macrocyclic precursor by cyclotrimerization
Chem.Commun., 2015, 51, 9046
7117176 CIFC18 H11 F3 O SP 1 21 15.593; 8.107; 17.57
90; 95.029; 90
793.6Amparo Sanz-Marco; Gonzalo Blay; M. Carmen Munoz; Jose R. Pedro
Highly enantioselective copper(I)-catalyzed conjugate addition of 1,3-diynes to alpha,beta-unsaturated trifluoromethyl ketones
Chem.Commun., 2015, 51, 8958
7117177 CIFC29 H31 N3 O6P 1 21/c 119.2486; 10.9164; 12.4114
90; 93.117; 90
2604.09Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117178 CIFC116 H132 B4 F16 N12 O28 Pd2P -114.8562; 16.5839; 16.9982
117.401; 93.11; 114.691
3216.5Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117179 CIFC58 H62 Cl4 N6 O12 Pd2C 1 2/m 113.8958; 21.0537; 11.1192
90; 101.982; 90
3182.1Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117180 CIFC126 H150 N16 O38 Pd2 S4P 1 21/n 113.099; 17.179; 32.25
90; 91.566; 90
7254.4Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117181 CIFC24 H44 Cu7 I8 N8R -3 :H25.9051; 25.9051; 20.4603
90; 90; 120
11890.9Yao Kang; Wei-Hui Fang; Lei Zhang; Jian Zhang
A structure-directing method to prepare semiconductive zeolitic cluster-organic frameworks with Cu3I4 building units
Chem.Commun., 2015, 51, 8994
7117182 CIFC15 H29 Cu4 I4 N4I 4 2 218.5097; 18.5097; 36.1113
90; 90; 90
12372.1Yao Kang; Wei-Hui Fang; Lei Zhang; Jian Zhang
A structure-directing method to prepare semiconductive zeolitic cluster-organic frameworks with Cu3I4 building units
Chem.Commun., 2015, 51, 8994
7117183 CIFC26 H16 N2 O8 S UP 21 21 218.435; 12.595; 22.468
90; 90; 90
2387Shu-wen An; Lei Mei; Cong-zhi Wang; Chuan-qin Xia; Zhi-fang Chai; Wei-qun Shi
The first case of actinide triple helices: pH-dependent structural evolution and kinetically-controlled transformation of two supramolecular conformational isomers
Chem.Commun., 2015, 51, 8978
7117184 CIFC26 H18 N2 O9 S UP 1 21/c 114.395; 8.675; 20.368
90; 95.16; 90
2533.2Shu-wen An; Lei Mei; Cong-zhi Wang; Chuan-qin Xia; Zhi-fang Chai; Wei-qun Shi
The first case of actinide triple helices: pH-dependent structural evolution and kinetically-controlled transformation of two supramolecular conformational isomers
Chem.Commun., 2015, 51, 8978
7117185 CIFC11 H9 F3 N2 O3P -15.736; 7.686; 15.026
102.598; 92.769; 110.155
601.4Ai-Jie Cai; Yan Zheng; Jun-An Ma
Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols
Chem.Commun., 2015, 51, 8946
7117186 CIFC11 H9 Cl F3 N O2P 1 21/c 17.764; 22.824; 7.398
90; 112.915; 90
1207.5Ai-Jie Cai; Yan Zheng; Jun-An Ma
Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols
Chem.Commun., 2015, 51, 8946
7117187 CIFC11 H16 N3 O7P 21 21 215.438; 10.4231; 22.933
90; 90; 90
1299.9Tamborini, Lucia; Mastronardi, Federica; Dall'Oglio, Federica; De Micheli, Carlo; Nielsen, Birgitte; Lo Presti, Leonardo; Conti, Paola; Pinto, Andrea
Synthesis of unusual isoxazoline containingβandγ-dipeptides as potential glutamate receptor ligands
Med. Chem. Commun., 2015, 6, 1260
7117188 CIFC46 H43 Cl3 S6P b c a9.4165; 19.7949; 45.588
90; 90; 90
8497.5Shu-Wei Chang; Masaki Horie
A donor-acceptor conjugated block copolymer of poly(arylenevinylene)s by ring-opening metathesis polymerization
Chem.Commun., 2015, 51, 9113
7117189 CIFC16 H17.13 Cu2 O19.5 S2P -17.6226; 8.0332; 19.2709
89.772; 88.902; 76.322
1146.36Xiao-Qin Wu; Jian-Gong Ma; Han Li; Di-Ming Chen; Wen Gu; Guang-Ming Yang; Peng Cheng
Metal-organic framework biosensor with high stability and selectivity in a bio-mimic environment
Chem.Commun., 2015, 51, 9161
7117190 CIFC17 H21 F4 N O4 SP 21 21 217.7459; 9.8069; 25.602
90; 90; 90
1944.8Chen Xie; Yanling Dai; Haibo Mei; Jianlin Han; Vadim A. Soloshonok; Yi Pan
Asymmetric synthesis of quaternary alpha-fluoro-beta-keto-amines via detrifluoroacetylative Mannich reactions
Chem.Commun., 2015, 51, 9149
7117191 CIFC22 H19 Br Cl3 N2 O4P 21 21 2110.2175; 12.1386; 19.641
90; 90; 90
2436Wu-Lin Yang; Yang-Zi Liu; Shuai Luo; Xingxin Yu; John S. Fossey; Wei-Ping Deng
The copper-catalyzed asymmetric construction of a dispiropyrrolidine skeleton via 1,3-dipolar cycloaddition of azomethine ylides to alpha-alkylidene succinimides
Chem.Commun., 2015, 51, 9212
7117192 CIFC24 H18 F6 O6P -18.917; 11.888; 12.165
62.137; 81.719; 78.834
1116.3Jingbo Wu; Scott T. Iacono; Gregory T. McCandless; Dennis W. Smith; Bruce M. Novak
Utilization of a Meldrum's acid towards functionalized fluoropolymers possessing dual reactivity for thermal crosslinking and post-polymerization modification
Chem.Commun., 2015, 51, 9220
7117193 CIFC19 H14 B F2 N3 SP 1 21/c 113.4997; 13.9995; 10.1052
90; 111.458; 90
1777.4Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117194 CIFC23 H23 B F2 N3 SP 1 21/n 116.3271; 8.327; 16.9926
90; 109.759; 90
2174.2Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117195 CIFC20 H16 B F2 N3 O SP 1 21/c 110.5497; 19.995; 9.2865
90; 104.898; 90
1893.1Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117196 CIFC18 H11 B Cl F2 N3P 1 21/c 19.7361; 14.5464; 12.214
90; 111.146; 90
1613.33Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117197 CIFC90 H106 Cl4 N10 O92.75 V16P 1 21/a 121.2958; 21.33; 21.9581
90; 105.868; 90
9594.2Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117198 CIFC80 H80 Cl4 N4 O81.5 V16I 4/m m m14.9098; 14.9098; 38.069
90; 90; 90
8462.8Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117199 CIFC51.75 H64.75 Br4 Cl2 N7.25 O42.75 V8P -115.1975; 19.1532; 19.3115
103.817; 95.3294; 98.3478
5352.9Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117200 CIFC91 H119 Cl7 N9 O83.25 V16P -114.9214; 16.0334; 16.7794
79.476; 82.828; 81.284
3881.7Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117201 CIFC45 H109 Cr Mo6 N6 O29P -113.554; 13.7899; 21.0955
86.768; 88.944; 63.016
3508Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117202 CIFC62 H143 Br Cr Mo6 N5 O27P 1 21/c 124.0245; 13.9963; 26.7955
90; 94.54; 90
8981.8Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117203 CIFC69 H158 Br Cr Mo6 N8 O29P 113.2494; 14.7378; 14.8892
119.221; 103.752; 96.589
2371.5Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117204 CIFC46 H108 Cr Mo6 N5 O28P -113.6865; 13.7366; 21.5248
86.727; 83.692; 62.304
3561.4Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117205 CIFC67 H155 Br Mn Mo6 N9 O29P 113.2671; 14.756; 14.887
119.33; 103.729; 96.883
2370.4Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117206 CIFC8 H43 Cr Mo6 N2 O30P 1 21/n 115.0834; 11.5341; 23.0245
90; 98.122; 90
3965.47Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117207 CIFC62 H54 Cl6 P4 RuP -112.3129; 14.9215; 18.0053
67.588; 85.054; 78.028
2991.6Samantha G. Eaves; Sam J. Hart; Adrian C. Whitwood; Dmitry S. Yufit; Paul J. Low; Jason M. Lynam
Rapid Markovnikov addition of HCl to a pendant alkyne: evidence for a quinoidal cumulene
Chem.Commun., 2015, 51, 9362
7117208 CIFC63.5 H57 Cl5 P4 RuP -111.3506; 12.3819; 21.4222
80.7264; 74.684; 83.7147
2858.75Samantha G. Eaves; Sam J. Hart; Adrian C. Whitwood; Dmitry S. Yufit; Paul J. Low; Jason M. Lynam
Rapid Markovnikov addition of HCl to a pendant alkyne: evidence for a quinoidal cumulene
Chem.Commun., 2015, 51, 9362
7117209 CIFC25 H21 Br N2 O2P 1 21 110.912; 8.3793; 11.228
90; 93.81; 90
1024.4Gao, Zhong-Hua; Chen, Xiang-Yu; Cheng, Jin-Tang; Liao, Wei-Lin; Ye, Song
N-Heterocyclic carbene-catalyzed [2+3] cyclocondensation of α-chloroaldehydes with azomethine imines
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 9328-9331
7117210 CIFC67.99 H56.99 F11.99 N14 O P2 RuR -317.6408; 17.6408; 44.355
90; 90; 120
11953.9E. Rousset; D. Chartrand; I. Ciofini; V. Marvaud; G. S. Hanan
Red-light-driven photocatalytic hydrogen evolution using a ruthenium quaterpyridine complex
Chem.Commun., 2015, 51, 9261
7117211 CIFC60 H42 Cl2 N12 O5 RuP 41 3 221.1118; 21.1118; 21.1118
90; 90; 90
9409.7E. Rousset; D. Chartrand; I. Ciofini; V. Marvaud; G. S. Hanan
Red-light-driven photocatalytic hydrogen evolution using a ruthenium quaterpyridine complex
Chem.Commun., 2015, 51, 9261
7117212 CIFC17 H13 N3 OP 1 21/n 15.212; 17.471; 15.196
90; 92.267; 90
1382.6Liang Zhang; Mingzhu Zhao; Xiaoming Zhao
The synthesis of carbonyl 2-amino-pyrimidines via tandem regioselective heterocyclization of 1,3-diynes with guanidine and selective oxidation
Chem.Commun., 2015, 51, 9370
7117213 CIFAl4 H3 Na3 O19 P4P 1 21/m 17.537; 12.525; 9.7
90; 98.51; 90
905.6Yanjun Sun; Yan Yan; Yanyan Wang; Yi Li; Jiyang Li; Jihong Yu
High proton conduction in a new alkali metal-templated open-framework aluminophosphate
Chem.Commun., 2015, 51, 9317
7117214 CIFC96 H40 Cd5 O34R -3 c :H29.1653; 29.1653; 83.513
90; 90; 120
61520Hongming He; Yang Song; Chuanqi Zhang; Fuxing Sun; Rongrong Yuan; Zheng Bian; Lianxun Gao; Guangshan Zhu
A highly robust metal-organic framework based on an aromatic 12-carboxyl ligand with highly selective adsorption of CO2 over CH4
Chem.Commun., 2015, 51, 9463
7117215 CIFCl7 Cu10 O16 Pb2 Se4C 1 2/m 118.605; 6.204; 12.673
90; 109.869; 90
1376Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117216 CIFCl10 Cu12 O16 Pb2 Se4C 1 2/m 118.4956; 6.1454; 15.2985
90; 119.311; 90
1516.25Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117217 CIFCl11.6 Cu13.6 K1.6 O16 Pb0.4 Se4C 1 2/m 115.1158; 6.1853; 9.2672
90; 95.965; 90
861.75Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117218 CIFC15 H9 Ag Cl N9 O4I -4 3 d20.2313; 20.2313; 20.2313
90; 90; 90
8280.8Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117219 CIFC40 H27 Ag4 F12 N27 O12 S4P 1 21/n 110.6023; 18.0069; 33.316
90; 90.1374; 90
6360.5Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117220 CIFC24 H18 Ag2 F12 N18 P2P n m a10.6565; 16.8754; 19.1418
90; 90; 90
3442.3Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117221 CIFC30 H24 Cl2 N Ni O3 PP -110.2518; 11.9007; 13.0245
111.438; 97.586; 98.593
1432.11Wenfeng Lo; Chunhua Hu; Tyler Berenson; Nathaniel Tracer; Daniel Shlian; Michael Khaloo; Avraham Benhaim; Jianfeng Jiang
Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell
Chem.Commun., 2015, 51, 9432
7117222 CIFC20 H40 N4 Ni O2C 1 2/c 114.857; 10.303; 15.562
90; 99.009; 90
2352.7Wenfeng Lo; Chunhua Hu; Tyler Berenson; Nathaniel Tracer; Daniel Shlian; Michael Khaloo; Avraham Benhaim; Jianfeng Jiang
Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell
Chem.Commun., 2015, 51, 9432
7117223 CIFC62 H42 N6 Ni2 O18P 1 21/n 113.142; 12.337; 17.656
90; 108.519; 90
2714Jun Zhao; Yenan Wang; Wenwen Dong; Yapan Wu; Dongsheng Li; Bin Liu; Qichun Zhang
A new surfactant-introduction strategy for separating the pure single-phase of metal-organic frameworks
Chem.Commun., 2015, 51, 9479
7117224 CIFC36 H21 N4 Ni2 O8C m c a31.395; 13.702; 15.808
90; 90; 90
6800Jun Zhao; Yenan Wang; Wenwen Dong; Yapan Wu; Dongsheng Li; Bin Liu; Qichun Zhang
A new surfactant-introduction strategy for separating the pure single-phase of metal-organic frameworks
Chem.Commun., 2015, 51, 9479
7117225 CIFC18 H12 N2 O2P 1 21/n 17.72; 21.073; 8.161
90; 92.202; 90
1326.7David E. Stephens; Johant Lakey-Beitia; Gabriel Chavez; Carla Ilie; Hadi D. Arman; Oleg V. Larionov
Experimental and mechanistic analysis of the palladium-catalyzed oxidative C8-selective C-H homocoupling of quinoline N-oxides
Chem.Commun., 2015, 51, 9507
7117226 CIFC127 H224 In5 N29 O87P 1 21/c 115.3713; 37.512; 38.979
90; 105.255; 90
21684Song, Bai-Qiao; Wang, Xin-Long; Zhang, Yu-Teng; Wu, Xue-Song; Liu, Hong-Sheng; Shao, Kui-Zhan; Su, Zhong-Min
Periodic tiling of triangular and square nanotubes in a cationic metal-organic framework for selective anion exchange
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 9515-9518
7117227 CIFC28 H31 N3C 1 2/c 131.282; 8.8017; 19.4725
90; 121.27; 90
4582.6Qian Gao; Peng Zhou; Feng Liu; Wen-Juan Hao; Changsheng Yao; Bo Jiang; Shu-Jiang Tu
Cobalt(II)/silver relay catalytic isocyanide insertion/cycloaddition cascades: a new access to pyrrolo[2,3-b]indoles
Chem.Commun., 2015, 51, 9519
7117228 CIFC23 H18 N2 O4P 1 21/c 110.8247; 12.1491; 14.009
90; 96.356; 90
1831Subrata Mukherjee; Santigopal Mondal; Atanu Patra; Rajesh G. Gonnade; Akkattu T. Biju
N-Heterocyclic carbene-catalyzed diastereoselective synthesis of beta-lactone-fused cyclopentanes using homoenolate annulation reaction
Chem.Commun., 2015, 51, 9559
7117229 CIFC24 H20 Cl3 N O3P 1 21/c 115.3285; 11.4221; 12.7961
90; 95.471; 90
2230.2Subrata Mukherjee; Santigopal Mondal; Atanu Patra; Rajesh G. Gonnade; Akkattu T. Biju
N-Heterocyclic carbene-catalyzed diastereoselective synthesis of beta-lactone-fused cyclopentanes using homoenolate annulation reaction
Chem.Commun., 2015, 51, 9559
7117230 CIFC50 H60 B F24 Na P6P 1 21/c 118.4514; 13.2631; 26.133
90; 90.826; 90
6394.7Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117231 CIFC62 H60 B F24 Na P6P -112.5084; 16.4798; 17.5637
79.047; 78.403; 81.625
3460.2Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117232 CIFC46 H48 Al F36 Li O4 P6P n a 2115.092; 27.737; 15.405
90; 90; 90
6448.6Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117233 CIFC48 H68 Cl Fe In N2 O4P 21 21 2110.3658; 18.6942; 23.794
90; 90; 90
4610.8Stephanie M. Quan; Paula L. Diaconescu
High activity of an indium alkoxide complex toward ring opening polymerization of cyclic esters
Chem.Commun., 2015, 51, 9643
7117234 CIFC27 H18 Br N3 OP 1 21 18.1413; 13.747; 10.606
90; 108.05; 90
1128.6Tianyou Qin; Lu Cheng; Sean Xiao-An Zhang; Weiwei Liao
Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction
Chem.Commun., 2015, 51, 9714
7117235 CIFC32 H24 N2 O SP -19.4724; 12.292; 12.563
104; 109.97; 102.72
1258.3Tianyou Qin; Lu Cheng; Sean Xiao-An Zhang; Weiwei Liao
Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction
Chem.Commun., 2015, 51, 9714
7117236 CIFC33 H15 Cu6 N6 O19F m -3 m44.588; 44.588; 44.588
90; 90; 90
88645Wen-Yang Gao; Tony Pham; Katherine A. Forrest; Brian Space; Lukasz Wojtas; Yu-Sheng Chen; Shengqian Ma
The local electric field favours more than exposed nitrogen atoms on CO2 capture: a case study on the rht-type MOF platform
Chem.Commun., 2015, 51, 9636
7117237 CIFC69 H65 Au2 F6 N P SbP 1 21/c 116.83401; 18.4515; 19.639
90; 100.054; 90
6006.44Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117238 CIFC58.01 H55.02 Au2 F6 N P SbP b c n24.291; 17.933; 24.334
90; 90; 90
10600Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117239 CIFC66 H64 Au3 F6 N2 SbP 1 21/c 116.33309; 18.64797; 18.79354
90; 91.0581; 90
5723.14Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117240 CIFC32 H42 Cl3 N3 PdP 1 21/c 19.2943; 21.212; 18.121
90; 114.171; 90
3259.4Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117241 CIFC26 H30 Cl3 N3 PtP 21 21 235.0384; 9.1217; 16.6331
90; 90; 90
5316.1Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117242 CIFC32 H42 Cl3 N3 PtP 1 21/c 19.3227; 21.1418; 18.1068
90; 115.162; 90
3230.18Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117243 CIFC32 H41 Cl2 N3 PdP 1 21/c 19.7411; 22.3057; 14.8046
90; 98.163; 90
3184.2Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117244 CIFC33 H43 Cl4 N3 PdI 41/a :233.4882; 33.4882; 12.9635
90; 90; 90
14538Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117245 CIFC39 H49 Cl2 N3 PdP 1 21/c 114.8545; 17.1043; 14.8749
90; 102.243; 90
3693.4Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117246 CIFC22 H21 Cl2 N3 PdP 1 21/c 19.0414; 25.274; 10.5618
90; 120.856; 90
2071.9Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117247 CIFC44 H42 Br1.81 Cl2.18 N6 Pd2C 1 c 114.907; 15.9956; 18.4249
90; 99.438; 90
4333.9Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117248 CIFC26 H29 Cl2 N3 PdP 1 21/c 111.5869; 14.0962; 15.7142
90; 100.524; 90
2523.45Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117249 CIFC27 H31 Cl4 N3 PtP 1 21/c 116.5349; 11.8855; 14.5488
90; 91.162; 90
2858.62Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117250 CIFC22 H21 Cl2 N3 PtP 1 21/c 19.0255; 25.338; 10.5412
90; 120.716; 90
2072.5Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117251 CIFC79 H21 Cl2 NP 1 21/c 110.4764; 25.5317; 16.5265
90; 102.296; 90
4319.1Bolong Zhang; Jegadesan Subbiah; Yu-Ying Lai; Jonathan M. White; David J. Jones; Wallace W. H. Wong
One-pot selective synthesis of a fullerene bisadduct for organic solar cell applications
Chem.Commun., 2015, 51, 9837
7117252 CIFC21 H19 Cl N2 O3P 21 21 216.1999; 13.2765; 23.277
90; 90; 90
1916Santosh Agrawal; Nagaraju Molleti; Vinod K. Singh
Organocatalytic enantio- and diastereoselective synthesis of highly substituted ?-lactones via a Michael-cyclization cascade
Chem.Commun., 2015, 51, 9793
7117253 CIFC116 H150 Ag24 F12 N2 O16P 1 21/n 123.5527; 20.9694; 29.346
90; 95.231; 90
14433.2Kuan-Guan Liu; Su-Kun Chen; Yu-Mei Lin; Quan-Ming Wang
An organic anion template: a 24-nucleus silver cluster encapsulating a squarate dimer
Chem.Commun., 2015, 51, 9896
7117254 CIFC12 H18P -15.246; 6.1956; 7.9824
103.859; 98.602; 100.131
242.93Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117255 CIFC12 H18P -15.2512; 6.2279; 7.9892
103.846; 98.464; 99.919
245Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117256 CIFC12 H18P -15.2639; 6.2567; 8.0155
103.858; 98.504; 99.75
247.65Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117257 CIFC12 H18P -15.2748; 6.2602; 8.0316
103.949; 98.651; 99.531
248.77Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117258 CIFC12 H18P -15.2944; 6.2771; 8.0612
104.026; 98.839; 99.456
251.09Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117259 CIFC9 H9 Br3P -17.6628; 9.0535; 9.0675
119.828; 106.926; 95.17
500.73Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117260 CIFC9 H9 Br3P -17.6795; 9.0494; 9.0657
119.817; 106.887; 95.081
502.02Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117261 CIFC9 H9 Br3P -17.7114; 9.0669; 9.0829
119.802; 106.864; 95.034
506.39Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117262 CIFC9 H9 Br3P -17.7305; 9.0698; 9.0855
119.773; 106.867; 95.034
508.12Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117263 CIFC9 H9 Br3P -17.7631; 9.0805; 9.0999
119.76; 106.811; 95.019
512.06Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117264 CIFC9 H9 Cl3P -17.5031; 8.7681; 8.7862
119.731; 106.219; 95.51
462.5Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117265 CIFC9 H9 Cl3P -17.6629; 8.7822; 8.7994
119.644; 107.474; 96.23
466.72Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117266 CIFC9 H9 Cl3P -17.6799; 8.7893; 8.8083
119.651; 107.294; 96.335
469.01Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117267 CIFC9 H9 Cl3P -17.7076; 8.801; 8.8248
119.644; 107.231; 96.278
472.73Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117268 CIFC9 H9 Cl3P -17.7324; 8.8179; 8.8415
119.64; 107.114; 96.298
476.54Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117269 CIFC9 H9 I3P -17.9189; 9.5531; 9.5594
60.255; 66.67; 85.526
570.15Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117270 CIFC9 H9 I3P -17.9431; 9.5681; 9.5753
60.225; 66.662; 85.52
573.51Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117271 CIFC9 H9 I3P -17.97; 9.5781; 9.5874
60.223; 66.693; 85.452
577.07Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117272 CIFC9 H9 I3P -17.9901; 9.5851; 9.5953
60.221; 66.709; 85.445
579.51Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117273 CIFC9 H9 I3P -18.0247; 9.6025; 9.6148
60.183; 66.729; 85.377
584.24Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829
7117274 CIFC35 H44 B2 N2 O2P 1 21/c 112.8272; 21.122; 14.0969
90; 93.392; 90
3812.7Marc-Andre Courtemanche; Alexander P. Pulis; Etienne Rochette; Marc-Andre Legare; Douglas W. Stephan; Frederic-Georges Fontaine
Intramolecular B/N frustrated Lewis pairs and the hydrogenation of carbon dioxide
Chem.Commun., 2015, 51, 9797
7117275 CIFC56 H78 B2 Cl4 F8 Ir2 N4C 1 2/c 119.338; 16.601; 18.949
90; 95.101; 90
6059.1Laura Rubio-Perez; Manuel Iglesias; Julen Munarriz; Victor Polo; Pablo J. Sanz Miguel; Jesus J. Perez-Torrente; Luis A. Oro
A bimetallic iridium(II) catalyst: [{Ir(IDipp)(H)}2][BF4]2 (IDipp = 1,3-bis(2,6-diisopropylphenylimidazol-2-ylidene))
Chem.Commun., 2015, 51, 9860
7117276 CIFC30 H34 N2 O2 SP 1 21/c 111.426; 16.485; 15.147
90; 100.185; 90
2808.1Stephanie Norsikian; Margaux Beretta; Alexandre Cannillo; Amelie Martin; Pascal Retailleau; Jean-Marie Beau
Synthesis of enantioenriched 1,2-trans-diamines using the borono-Mannich reaction with N-protected alpha-amino aldehydes
Chem.Commun., 2015, 51, 9991
7117277 CIFC38 H28 Co N4 O4P 1 21/n 19.3634; 21.379; 15.2
90; 101.912; 90
2977.2Sk Amanullah; Pradip Kumar Das; Subhra Samanta; Abhishek Dey
Tuning the thermodynamic onset potential of electrocatalytic O2 reduction reaction by synthetic iron-porphyrin complexes
Chem.Commun., 2015, 51, 10010
7117278 CIFC39 H42 Cl2 N O6 PP 1 21 19.921; 16.32; 11.549
90; 97.356; 90
1854.5Taichi Kano; Hiroki Maruyama; Ryu Sakamoto; Keiji Maruoka
Regioselectivity switch in chiral amine-catalysed asymmetric addition of aldehydes to reactive enals
Chem.Commun., 2015, 51, 10062
7117279 CIFC21 H19 N O4P 21 21 219.7332; 12.3327; 15.1571
90; 90; 90
1819.41Weiwei Luo; Jiannan Zhao; Jie Ji; Lili Lin; Xiaohua Liu; Hongjiang Mei; Xiaoming Feng
A catalytic asymmetric carbonyl-ene reaction of beta,gamma-unsaturated alpha-ketoesters with 5-methyleneoxazolines
Chem.Commun., 2015, 51, 10042
7117280 CIFC22 H19 N O4P 21 21 219.8442; 12.3537; 16.5313
90; 90; 90
2010.41Weiwei Luo; Jiannan Zhao; Jie Ji; Lili Lin; Xiaohua Liu; Hongjiang Mei; Xiaoming Feng
A catalytic asymmetric carbonyl-ene reaction of beta,gamma-unsaturated alpha-ketoesters with 5-methyleneoxazolines
Chem.Commun., 2015, 51, 10042
7117281 CIFC15 H21 N O3 SP 21 21 217.89498; 11.4535; 16.5401
90; 90; 90
1495.64Jin-Miao Tian; Yong-Hai Yuan; Yong-Qiang Tu; Fu-Min Zhang; Xiao-Bo Zhang; Shi-Heng Zhang; Shao-Hua Wang; Xiao-Ming Zhang
The design of a spiro-pyrrolidine organocatalyst and its application to catalytic asymmetric Michael addition for the construction of all-carbon quaternary centers
Chem.Commun., 2015, 51, 9979
7117283 CIFC48 H51 B F4 Ir N5P -110.3919; 13.6438; 15.4722
95.673; 95.753; 98.925
2141.59Mewis, Ryan E.; Fekete, Marianna; Green, Gary G. R.; Whitwood, Adrian C.; Duckett, Simon B.
Deactivation of signal amplification by reversible exchange catalysis, progress towards in vivo application.
Chemical communications (Cambridge, England), 2015, 51, 9857-9859
7117285 CIFC44 H34 Cl2 F9 N12 O10 S3 W2P 1 21/n 113.377; 15.6886; 25.1243
90; 102.402; 90
5149.7Brogden, David W.; Berry, John F.
Not all density functionals are created equal: the case of the missing electron in the oxidized [W-W[triple bond, length as m-dash]O](7+) core.
Chemical communications (Cambridge, England), 2015, 51, 9153-9156
7117286 CIFC90 H189 N30 Na5 O162 S10 U20 V20P c c n32.023; 27.232; 28.774
90; 90; 90
25092G. A. Senchyk; E. M. Wylie; S. Prizio; J. E. S. Szymanowski; G. E. Sigmon; P. C. Burns
Hybrid uranyl-vanadium nano-wheels
Chem.Commun., 2015, 51, 10134
7117287 CIFC48 H90 N16 O51 U2 V16C 1 2/c 123.656; 14.981; 27.97
90; 112.886; 90
9132G. A. Senchyk; E. M. Wylie; S. Prizio; J. E. S. Szymanowski; G. E. Sigmon; P. C. Burns
Hybrid uranyl-vanadium nano-wheels
Chem.Commun., 2015, 51, 10134
7117288 CIFC28 H24 O2P 1 21 19.6751; 10.2214; 10.6522
90; 96.993; 90
1045.6Meng Zhang; Xianpeng Yin; Tian Tian; Yun Liang; Weina Li; Yue Lan; Jian Li; Meimei Zhou; Yong Ju; Guangtao Li
AIE-induced fluorescent vesicles containing amphiphilic binding pockets and the FRET triggered by host-guest chemistry
Chem.Commun., 2015, 51, 10210
7117289 CIFC60 H51 P10P -110.102; 13.842; 19.518
90.19; 93.99; 93.2
2718.3Heidi Schneider; David Schmidt; Udo Radius
The reductive P-P coupling of primary and secondary phosphines mediated by N-heterocyclic carbenes
Chem.Commun., 2015, 51, 10138
7117290 CIFC42 H42 P6R -3 :H13.896; 13.896; 20.034
90; 90; 120
3350.3Heidi Schneider; David Schmidt; Udo Radius
The reductive P-P coupling of primary and secondary phosphines mediated by N-heterocyclic carbenes
Chem.Commun., 2015, 51, 10138
7117291 CIFC90 H111 B Cl F15 Ge P4 Pt2P -113.4568; 18.179; 18.421
92.687; 105.972; 96.846
4286.5Norio Nakata; Noriko Sekizawa; Akihiko Ishii
Cationic dinuclear platinum and palladium complexes with bridging hydrogermylene and hydrido ligands
Chem.Commun., 2015, 51, 10111
7117292 CIFC90 H112 B F15 Ge P4 Pt2P -113.4434; 18.197; 18.3865
92.576; 106.152; 97.311
4269.9Norio Nakata; Noriko Sekizawa; Akihiko Ishii
Cationic dinuclear platinum and palladium complexes with bridging hydrogermylene and hydrido ligands
Chem.Commun., 2015, 51, 10111
7117293 CIFC96 H116 B Cl F16 Ge P4 Pd2P n a 2124.942; 32.139; 11.1842
90; 90; 90
8965Norio Nakata; Noriko Sekizawa; Akihiko Ishii
Cationic dinuclear platinum and palladium complexes with bridging hydrogermylene and hydrido ligands
Chem.Commun., 2015, 51, 10111
7117294 CIFC33 H48 B F4 P2 RhP 1 21 110.6347; 29.6678; 10.7567
90; 105.968; 90
3262.88E. Louise Hazeland; Andy M. Chapman; Paul G. Pringle; Hazel A. Sparkes
A one-step, modular route to optically-active diphos ligands
Chem.Commun., 2015, 51, 10206
7117295 CIFC30 H34 Cl4 O2 P2 PtP 21 21 219.8749; 10.7553; 29.0217
90; 90; 90
3082.3E. Louise Hazeland; Andy M. Chapman; Paul G. Pringle; Hazel A. Sparkes
A one-step, modular route to optically-active diphos ligands
Chem.Commun., 2015, 51, 10206
7117296 CIFC6 H7 Cu2 N9 O2.5C 1 2/c 124.258; 9.4877; 16.473
90; 118.79; 90
3322.7Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117297 CIFC6 H8 Cu2 N9 O3C 1 2/c 124.321; 9.4098; 16.628
90; 119.24; 90
3320.5Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117298 CIFC6 H4 Cu2 N9 O1.5C 1 2/c 124.338; 9.4877; 16.502
90; 119.89; 90
3303.6Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117299 CIFC12 H19 Cu2 N10 OC 1 2/c 124.225; 9.6254; 16.37
90; 118.54; 90
3353.2Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117300 CIFC12 H18 Cu2 N10 O0.5C 1 c 124.349; 9.2334; 16.959
90; 119.41; 90
3321.4Chao Huang; Jie Wu; Chuanjun Song; Ran Ding; Yan Qiao; Hongwei Hou; Junbiao Chang; Yaoting Fan
Reversible conversion of valence-tautomeric copper metal-organic frameworks dependent single-crystal-to-single-crystal oxidation/reduction: a redox-switchable catalyst for C-H bonds activation reaction
Chem.Commun., 2015, 51, 10353
7117301 CIFC81 H49 O20 Tb3P 1 2/c 110.8511; 28.8803; 19.155
90; 123.902; 90
4982.3Hang Xu; Chun-Shuai Cao; Bin Zhao
A water-stable lanthanide-organic framework as a recyclable luminescent probe for detecting pollutant phosphorus anions
Chem.Commun., 2015, 51, 10280
7117302 CIFC20 H18 O2P b c a15.2594; 10.4298; 19.4355
90; 90; 90
3093.2Kegong Ji; Xiang Liu; Bowen Du; Fang Yang; Jinming Gao
Gold-catalyzed selective oxidation of 4-oxahepta-1,6-diynes to 2H-pyran-3(6H)-ones and chromen-3(4H)-ones via beta-gold vinyl cation intermediates
Chem.Commun., 2015, 51, 10318
7117303 CIFC164 H261 Cu31 N64 O35 PP -120.4153; 22.91; 25.8662
103.685; 94.975; 110.593
10809.7Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117304 CIFC145 H227 As Cu31 N64 O35P -120.4878; 22.9195; 25.7171
103.64; 95.22; 110.663
10777.1Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117305 CIFC117 H196 Cu30 N61 O42 PP 1 21/c 119.9142; 28.2823; 33.9811
90; 106.132; 90
18385.2Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117306 CIFC104 H149 Br1.5 Cu15 N39.5 O19 P2P 1 21/c 117.1774; 24.4; 33.549
90; 103.254; 90
13686.8Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117307 CIFC110 H154 As2 Br2 Cu15 N40 O20C 1 2/c 117.3262; 25.319; 31.9199
90; 102.256; 90
13683.6Gellert Mezei
Incarceration of one or two phosphate or arsenate species within nanojars, capped nanojars and nanohelicages: helical chirality from two closely-spaced, head-to-head PO4^3-^ or AsO4^3-^ ions
Chem.Commun., 2015, 51, 10341
7117308 CIFC16 H13 Cl Fe SP -15.7825; 8.6085; 14.043
99.114; 99.532; 94.734
676.43Zongjun Qiao; Nanyang Ge; Xuefeng Jiang
CO2-promoted oxidative cross-coupling reaction for C-S bond formation via masked strategy in an odourless way
Chem.Commun., 2015, 51, 10295
7117309 CIFC22 H40 Cu F2 N4 O8 S4P -17.5312; 8.2038; 13.344
92.852; 93.152; 107.116
784.9Zongjun Qiao; Nanyang Ge; Xuefeng Jiang
CO2-promoted oxidative cross-coupling reaction for C-S bond formation via masked strategy in an odourless way
Chem.Commun., 2015, 51, 10295
7117310 CIFC17.75 H24 N2 O3.5 PtC 1 2/c 133.626; 12.052; 24.064
90; 134.007; 90
7014Mohamed E. Moustafa; Paul D. Boyle; Richard J. Puddephatt
A biomimetic phenol substituent effect on the reaction of a dimethylplatinum(II) complex with oxygen: proton coupled electron transfer and multiple proton relay
Chem.Commun., 2015, 51, 10334
7117311 CIFC75 H72 F9 N16 O21 S3 Yb Zn4P 4/n c c23.3111; 23.3111; 19.866
90; 90; 90
10795.3Quan-Wen Li; Jun-Liang Liu; Jian-Hua Jia; Yan-Cong Chen; Jiang Liu; Long-Fei Wang; Ming-Liang Tong
'Half-sandwich' Yb^III^ single-ion magnets with metallacrowns
Chem.Commun., 2015, 51, 10291
7117312 CIFC100 H100 F9 N19 O24 S3 Yb Zn4P 1 21/c 116.1341; 42.5371; 18.4653
90; 93.131; 90
12653.8Quan-Wen Li; Jun-Liang Liu; Jian-Hua Jia; Yan-Cong Chen; Jiang Liu; Long-Fei Wang; Ming-Liang Tong
'Half-sandwich' Yb^III^ single-ion magnets with metallacrowns
Chem.Commun., 2015, 51, 10291
7117313 CIFC23 H16 N2 O3C 1 2/c 126.382; 8.7432; 15.937
90; 97.035; 90
3648.4Ahmed Kamal; Chada Narsimha Reddy; Malasala Satyaveni; D. Chandrasekhar; Jagadeesh Babu Nanubolu; Kiran Kumar Singarapud; Ram Awatar Maurya
Cu(OAc)2-Et3N mediated oxidative coupling of alpha-azido ketones with pyridinium ylides: utilizing in situ generated imines for regioselective synthesis of imidazo[1,2-a]pyridines
Chem.Commun., 2015, 51, 10475
7117314 CIFC45 H36 O4C 1 2/c 120.81; 13.789; 12.317
90; 90.752; 90
3534Zhaozhong Yi; Hitoshi Okuda; Yasuhito Koyama; Ryota Seto; Satoshi Uchida; Hiromitsu Sogawa; Shigeki Kuwata; Toshikazu Takata
Exact helical polymer synthesis by a two-point-covalent-linking protocol between C2-chiral spirobifluorene and C2- or Cs-symmetric anthraquinone monomers
Chem.Commun., 2015, 51, 10423
7117315 CIFC46 H56 Cu2 N22 O10 Tb2P 19.6495; 11.9679; 12.5126
78.879; 85.44; 79.309
1391.83Xing-Cai Huang; Veacheslav Vieru; Liviu F. Chibotaru; Wolfgang Wernsdorfer; Shang-Da Jiang; Xin-Yi Wang
Determination of magnetic anisotropy in a multinuclear Tb^III^-based single-molecule magnet
Chem.Commun., 2015, 51, 10373
7117316 CIFC46 H56 Cu2 N22 O10 Tb2P 19.6455; 11.9723; 12.5139
78.864; 85.397; 79.256
1391.56Xing-Cai Huang; Veacheslav Vieru; Liviu F. Chibotaru; Wolfgang Wernsdorfer; Shang-Da Jiang; Xin-Yi Wang
Determination of magnetic anisotropy in a multinuclear Tb^III^-based single-molecule magnet
Chem.Commun., 2015, 51, 10373
7117317 CIFC30 H30 N2 O4I 4117.4485; 17.4485; 16.711
90; 90; 90
5087.67Jianlin Zhang; Yulong Zhang; Lili Lin; Qian Yao; Xiaohua Liu; Xiaoming Feng
Catalytic asymmetric desymmetrization of N-arylmaleimides: efficient construction of both atom chirality and axial chirality
Chem.Commun., 2015, 51, 10554
7117318 CIFC65 H115 N2 O6 P5 Re6 S2 Se8P 1 21 112.8853; 12.9302; 25.069
90; 92.4338; 90
4173Jessica L. Durham; Wade B. Wilson; Daniel N. Huh; Robert McDonald; Lisa F. Szczepura
Organometallic rhenium(III) chalcogenide clusters: coordination of N-heterocyclic carbenes
Chem.Commun., 2015, 51, 10536
7117319 CIFC55 H80 Cl4 N4 P2 Re6 S8P 1 21/c 116.6282; 16.7446; 25.1262
90; 92.1776; 90
6990.9Jessica L. Durham; Wade B. Wilson; Daniel N. Huh; Robert McDonald; Lisa F. Szczepura
Organometallic rhenium(III) chalcogenide clusters: coordination of N-heterocyclic carbenes
Chem.Commun., 2015, 51, 10536
7117320 CIFC19 H13 N OP 1 21/c 18.3956; 21.0394; 8.2906
90; 105.859; 90
1408.7Pengchong Xue; Jiabao Sun; Peng Chen; Panpan Wang; Boqi Yao; Peng Gong; Zhenqi Zhang; Ran Lu
Luminescence switching of a persistent room-temperature phosphorescent pure organic molecule in response to external stimuli
Chem.Commun., 2015, 51, 10381
7117321 CIFC14 H17 N3 O3P -19.212; 12.624; 12.927
94.78; 109.99; 105.42
1336.5Lingliang Long; Yanjun Wu; Lin Wang; Aihua Gong; Feilong Hu; Chi Zhang
A fluorescent probe for hypochlorite based on the modulation of the unique rotation of the N-N single bond in acetohydrazide
Chem.Commun., 2015, 51, 10435
7117322 CIFC20 H21 N3 O3P 1 21/c 113.1553; 6.9401; 21.0792
90; 109.629; 90
1812.67Lingliang Long; Yanjun Wu; Lin Wang; Aihua Gong; Feilong Hu; Chi Zhang
A fluorescent probe for hypochlorite based on the modulation of the unique rotation of the N-N single bond in acetohydrazide
Chem.Commun., 2015, 51, 10435
7117323 CIFC29 H29 Br N2 O3P 1 21/c 113.077; 12.197; 16.687
90; 114.69; 90
2418.3Kalia, Dimpy; K. S., Anil Kumar; Meena, Gajanand; Sethi, Kashmir Prasad; Sharma, Rohit; Trivedi, Priyanka; Khan, Shaheb Raj; Verma, Ajay Singh; Singh, Shyam; Sharma, Sandeep; Roy, Kuldeep K.; Kant, Ruchir; Krishnan, Manju Yasodha; Singh, Bhupendra N.; Sinha, Sudhir; Chaturvedi, Vinita; Saxena, Anil K.; Dikshit, Dinesh K.
Synthesis and anti-tubercular activity of conformationally-constrained and bisquinoline analogs of TMC207
Med. Chem. Commun., 2015, 6, 1554
7117324 CIFC29 H29 Br N2 O3P 1 21/c 110.747; 10.565; 23.94
90; 111.837; 90
2523.2Kalia, Dimpy; K. S., Anil Kumar; Meena, Gajanand; Sethi, Kashmir Prasad; Sharma, Rohit; Trivedi, Priyanka; Khan, Shaheb Raj; Verma, Ajay Singh; Singh, Shyam; Sharma, Sandeep; Roy, Kuldeep K.; Kant, Ruchir; Krishnan, Manju Yasodha; Singh, Bhupendra N.; Sinha, Sudhir; Chaturvedi, Vinita; Saxena, Anil K.; Dikshit, Dinesh K.
Synthesis and anti-tubercular activity of conformationally-constrained and bisquinoline analogs of TMC207
Med. Chem. Commun., 2015, 6, 1554
7117325 CIFC30 H30 Br Cl N2 O3P -17.799; 13.077; 14.674
102.019; 102.584; 105.196
1352.4Kalia, Dimpy; K. S., Anil Kumar; Meena, Gajanand; Sethi, Kashmir Prasad; Sharma, Rohit; Trivedi, Priyanka; Khan, Shaheb Raj; Verma, Ajay Singh; Singh, Shyam; Sharma, Sandeep; Roy, Kuldeep K.; Kant, Ruchir; Krishnan, Manju Yasodha; Singh, Bhupendra N.; Sinha, Sudhir; Chaturvedi, Vinita; Saxena, Anil K.; Dikshit, Dinesh K.
Synthesis and anti-tubercular activity of conformationally-constrained and bisquinoline analogs of TMC207
Med. Chem. Commun., 2015, 6, 1554
7117326 CIFC31 H33 Cl N2 O4P -110.198; 12.405; 12.423
79.72; 70.82; 72.77
1412Kalia, Dimpy; K. S., Anil Kumar; Meena, Gajanand; Sethi, Kashmir Prasad; Sharma, Rohit; Trivedi, Priyanka; Khan, Shaheb Raj; Verma, Ajay Singh; Singh, Shyam; Sharma, Sandeep; Roy, Kuldeep K.; Kant, Ruchir; Krishnan, Manju Yasodha; Singh, Bhupendra N.; Sinha, Sudhir; Chaturvedi, Vinita; Saxena, Anil K.; Dikshit, Dinesh K.
Synthesis and anti-tubercular activity of conformationally-constrained and bisquinoline analogs of TMC207
Med. Chem. Commun., 2015, 6, 1554
7117327 CIFC24 H23 N O4P -19.9379; 10.0008; 10.8276
96.918; 104.753; 99.92
1009.72Min Tang; Dong Xing; Haoxi Huang; Wenhao Hu
Divergent synthesis of chiral heterocycles via sequencing of enantioselective three-component reactions and one-pot subsequent cyclization reactions
Chem.Commun., 2015, 51, 10612
7117328 CIFC25 H22 Br N O5P -19.6542; 10.7705; 12.1323
87.694; 71.902; 69.127
1116.89Min Tang; Dong Xing; Haoxi Huang; Wenhao Hu
Divergent synthesis of chiral heterocycles via sequencing of enantioselective three-component reactions and one-pot subsequent cyclization reactions
Chem.Commun., 2015, 51, 10612
7117329 CIFC28 H25 N O7P -19.1316; 11.5658; 12.884
87.471; 84.937; 78.96
1329.8Min Tang; Dong Xing; Haoxi Huang; Wenhao Hu
Divergent synthesis of chiral heterocycles via sequencing of enantioselective three-component reactions and one-pot subsequent cyclization reactions
Chem.Commun., 2015, 51, 10612
7117333 CIFC24 H256 Cl14 Gd24 O217 Zn4F m -3 m37.4763; 37.4763; 37.4763
90; 90; 90
52634.5Xiu-Ying Zheng; Shi-Qiang Wang; Wen Tang; Gui-Lin Zhuang; Xiang-Jian Kong; Yan-Ping Ren; La-Sheng Long; Lan-Sun Zheng
Two nanosized 3d-4f clusters featuring four Ln6 octahedra encapsulating a Zn4 tetrahedron
Chem.Commun., 2015, 51, 10687
7117334 CIFC24 H216 Cl14 O197 Sm24 Zn4F m -3 m37.8651; 37.8651; 37.8651
90; 90; 90
54289.7Xiu-Ying Zheng; Shi-Qiang Wang; Wen Tang; Gui-Lin Zhuang; Xiang-Jian Kong; Yan-Ping Ren; La-Sheng Long; Lan-Sun Zheng
Two nanosized 3d-4f clusters featuring four Ln6 octahedra encapsulating a Zn4 tetrahedron
Chem.Commun., 2015, 51, 10687
7117337 CIFC12 H9 N3 O2 SP 1 21/n 18.412; 15.9905; 8.469
90; 91.55; 90
1138.8Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117338 CIFC12 H9 N3 O2 SP 1 21/n 18.337; 15.8027; 8.4626
90; 91.44; 90
1114.6Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117339 CIFC12 H9 N3 O2 SP 1 21/n 18.2031; 15.4235; 8.4569
90; 90.851; 90
1069.9Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117340 CIFC12 H9 N3 O2 SP 1 21/n 18.116; 15.121; 8.4699
90; 90.38; 90
1039.4Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117341 CIFC12 H9 N3 O2 SP 1 21/n 18.0755; 14.874; 8.4734
90; 89.76; 90
1017.8Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117342 CIFC12 H9 N3 O2 SP 1 21/n 18.0025; 14.448; 8.4923
90; 89.15; 90
981.8Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117343 CIFC12 H9 N3 O2 SP 1 21/n 18.45062; 15.9403; 8.46555
90; 91.0663; 90
1140.16Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117344 CIFC12 H9 N3 O2 SP 1 21/n 17.9246; 14.028; 8.4897
90; 88.75; 90
943.5Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117345 CIFC12 H9 N3 O2 SP 1 21/n 17.8626; 13.721; 8.4707
90; 88.55; 90
913.5Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117346 CIFC12 H9 N3 O2 SP 1 21/n 18.5322; 16.412; 8.4958
90; 91.78; 90
1189.1Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117347 CIFC12 H9 N3 O2 SP 1 21/n 18.546; 16.42; 8.5053
90; 91.78; 90
1192.9Elena L. Harty; Alex R. Ha; Mark R. Warren; Amber L. Thompson; David R. Allan; Andrew L. Goodwin; Nicholas P. Funnell
Reversible piezochromism in a molecular wine-rack
Chem.Commun., 2015, 51, 10608
7117348 CIFC34 H50 Br2 Cl2 N3 PP 1 21/c 112.1055; 25.0614; 14.662
90; 123.958; 90
3689.5Thomas Simler; Andreas A. Danopoulos; Pierre Braunstein
N-Heterocyclic carbene-phosphino-picolines as precursors of anionic 'pincer' ligands with dearomatised pyridine backbones; transmetallation from potassium to chromium
Chem.Commun., 2015, 51, 10699
7117349 CIFC148 H220 K4 N12 O4 P4P -112.9906; 14.5542; 21.8297
72.803; 78.663; 70.389
3692.3Thomas Simler; Andreas A. Danopoulos; Pierre Braunstein
N-Heterocyclic carbene-phosphino-picolines as precursors of anionic 'pincer' ligands with dearomatised pyridine backbones; transmetallation from potassium to chromium
Chem.Commun., 2015, 51, 10699
7117350 CIFC29 H41 Cl Cr N3 PP 1 21/c 18.37; 23.052; 17.18
90; 116.249; 90
2973Thomas Simler; Andreas A. Danopoulos; Pierre Braunstein
N-Heterocyclic carbene-phosphino-picolines as precursors of anionic 'pincer' ligands with dearomatised pyridine backbones; transmetallation from potassium to chromium
Chem.Commun., 2015, 51, 10699
7117354 CIFC44 H50 N4 S Si2P -17.6707; 15.0819; 18.167
105.557; 94.548; 95.487
2003.3A. Belen Marco; Diego Cortizo-Lacalle; Cristian Gozalvez; Mikel Olano; Ainhoa Atxabal; Xiangnan Sun; Manuel Melle-Franco; Luis E. Hueso; Aurelio Mateo-Alonso
An electron-conducting pyrene-fused phenazinothiadiazole
Chem.Commun., 2015, 51, 10754
7117355 CIFC37 H30 Al Cl6 P3P -110.7482; 11.7146; 16.2326
108.178; 100.829; 99.8863
1848.28Chitra Gurnani; Nemanja Dordevic; Senthilkumar Muthaiah; Dusan Dimic; Rakesh Ganguly; Milena Petkovic; Dragoslav Vidovic
Extending the chemistry of carbones: P-N bond cleavage via an SN2'-like mechanism
Chem.Commun., 2015, 51, 10762
7117356 CIFC19 H20 Cl2 F6 N4 P SbP b c a11.63; 19.1931; 21.194
90; 90; 90
4730.8Chitra Gurnani; Nemanja Dordevic; Senthilkumar Muthaiah; Dusan Dimic; Rakesh Ganguly; Milena Petkovic; Dragoslav Vidovic
Extending the chemistry of carbones: P-N bond cleavage via an SN2'-like mechanism
Chem.Commun., 2015, 51, 10762
7117357 CIFC24 H26 Br N O4P 1 21 110.7238; 7.4576; 13.759
90; 93.502; 90
1098.3Shutao Sun; Ying Mao; Hongxiang Lou; Lei Liu
Copper(II)/amine synergistically catalyzed enantioselective alkylation of cyclic N-acyl hemiaminals with aldehydes
Chem.Commun., 2015, 51, 10691
7117358 CIFC23 H24 Br N O4P 21 21 215.1792; 11.1118; 36.24
90; 90; 90
2085.6Shutao Sun; Ying Mao; Hongxiang Lou; Lei Liu
Copper(II)/amine synergistically catalyzed enantioselective alkylation of cyclic N-acyl hemiaminals with aldehydes
Chem.Commun., 2015, 51, 10691
7117359 CIFC19 H22 Cl NP n a 217.4474; 16.4971; 12.9089
90; 90; 90
1585.99YoungKu Kang; Matthew T. Richers; Conrad H. Sawicki; Daniel Seidel
C-H functionalization of cyclic amines: redox-annulations with alpha,beta-unsaturated carbonyl compounds
Chem.Commun., 2015, 51, 10648
7117360 CIFC20 H23 Br NP 1 21/c 113.9903; 6.5457; 19.158
90; 103.355; 90
1706.97YoungKu Kang; Matthew T. Richers; Conrad H. Sawicki; Daniel Seidel
C-H functionalization of cyclic amines: redox-annulations with alpha,beta-unsaturated carbonyl compounds
Chem.Commun., 2015, 51, 10648
7117361 CIFC444 H1061 Cl9 In84 Mn23 N148 O7 Se150R -3 c :H34.7264; 34.7264; 155.851
90; 90; 120
162765Yu-Hong Wang; Jing Wu; Xiao-Wei Zhao; Li-Wen Qian; Qin-Yu Zhu; Jie Dai
A nano-scale triangular ring cluster of indium-selenide: the structure and templating effect
Chem.Commun., 2015, 51, 10668
7117362 CIFC46 H98 O Si10P -19.4329; 11.2567; 29.197
85.049; 83.862; 67.021
2834.5Tomoyuki Kosai; Shintaro Ishida; Takeaki Iwamoto
Transformation of azulenes to bicyclic [4]dendralene and heptafulvene derivatives via photochemical cycloaddition of dialkylsilylene
Chem.Commun., 2015, 51, 10707
7117363 CIFC31 H58 Si5P -19.5864; 10.9534; 18.638
105.877; 92.815; 110.499
1740.2Tomoyuki Kosai; Shintaro Ishida; Takeaki Iwamoto
Transformation of azulenes to bicyclic [4]dendralene and heptafulvene derivatives via photochemical cycloaddition of dialkylsilylene
Chem.Commun., 2015, 51, 10707
7117364 CIFC66 H43 N5P -19.45; 16.69; 19.57
82.49; 88.39; 74.9
2954.4Chenglong Li; Shipan Wang; Weiping Chen; Jinbei Wei; Guochun Yang; Kaiqi Ye; Yu Liu; Yue Wang
High performance full color OLEDs based on a class of molecules with dual carrier transport channels and small singlet-triplet splitting
Chem.Commun., 2015, 51, 10632
7117365 CIFC40 H41 N3 O12P 1 21/c 110.8958; 17.3981; 19.868
90; 91.143; 90
3765.6Qi-Lin Wang; Tian Cai; Jing Zhou; Fang Tian; Xiao-Ying Xu; Li-Xin Wang
An unprecedented base-promoted domino reaction of methyleneindolinones and N-tosyloxycarbamates for the construction of bispirooxindoles and spiroaziridine oxindoles
Chem.Commun., 2015, 51, 10726
7117366 CIFC24 H24 N2 O7P -16.647; 12.469; 14.173
87.147; 79.429; 89.31
1153Qi-Lin Wang; Tian Cai; Jing Zhou; Fang Tian; Xiao-Ying Xu; Li-Xin Wang
An unprecedented base-promoted domino reaction of methyleneindolinones and N-tosyloxycarbamates for the construction of bispirooxindoles and spiroaziridine oxindoles
Chem.Commun., 2015, 51, 10726
7117367 CIFC25 H30 B F4 Fe N3P -18.5466; 9.9789; 14.7438
104.047; 91.109; 101.147
1193.92Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117368 CIFC24 H27 Fe N3F d d 221.0171; 49.949; 7.7045
90; 90; 90
8088.1Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117369 CIFC21 H21 Fe N3P 1 21/n 17.2798; 16.749; 14.796
90; 103.923; 90
1751.1Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117370 CIFC22 H24 B F4 Fe N3P b c a9.213; 9.618; 47.215
90; 90; 90
4184Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117371 CIFC25 H29 Au Cl Fe N3C 1 2/c 129.3929; 9.2832; 17.3954
90; 90.428; 90
4746.4Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117372 CIFC22 H23 Au Cl Fe N3P 1 21/c 124.435; 7.515; 11.492
90; 93.546; 90
2106.2Lara Hettmanczyk; Sinja Manck; Carolin Hoyer; Stephan Hohloch; Biprajit Sarkar
Heterobimetallic complexes with redox-active mesoionic carbenes as metalloligands: electrochemical properties, electronic structures and catalysis
Chem.Commun., 2015, 51, 10949
7117373 CIFC12 H78 La4 N4 O53 P12P 1 21/c 114.274; 18.624; 12.53
90; 115.14; 90
3015.4Ricardo F. Mendes; Patricia Silva; Margarida M. Antunes; Anabela A. Valente; Filipe A. Almeida Paz
Sustainable synthesis of a catalytic active one-dimensional lanthanide-organic coordination polymer
Chem.Commun., 2015, 51, 10807
7117374 CIFC30 H22 F18 N2 O10 TbP 1 21/c 111.7995; 15.2788; 24.2492
90; 116.868; 90
3899.77Leilei Li; Shuang Liu; Han Li; Wei Shi; Peng Cheng
Influence of external magnetic field and magnetic-site dilution on the magnetic dynamics of a one-dimensional Tb(III)-radical complex
Chem.Commun., 2015, 51, 10933
7117375 CIFC21 H44 O2 P2 PdP c a 2115.9351; 14.7211; 21.273
90; 90; 90
4990.3S. Chantal E. Stieber; Nuria Huguet; Takeharu Kageyama; Ivana Jevtovikj; Piyal Ariyananda; Alvaro Gordillo; Stephan A. Schunk; Frank Rominger; Peter Hofmann; Michael Limbach
Acrylate formation from CO2 and ethylene: catalysis with palladium and mechanistic insight
Chem.Commun., 2015, 51, 10907
7117376 CIFC30 H58 P2 PdC 1 c 111.1923; 16.4379; 16.7601
90; 101.082; 90
3026S. Chantal E. Stieber; Nuria Huguet; Takeharu Kageyama; Ivana Jevtovikj; Piyal Ariyananda; Alvaro Gordillo; Stephan A. Schunk; Frank Rominger; Peter Hofmann; Michael Limbach
Acrylate formation from CO2 and ethylene: catalysis with palladium and mechanistic insight
Chem.Commun., 2015, 51, 10907
7117377 CIFC31.5 H56 O2 P2 PdC 1 2/c 128.266; 13.8216; 18.2436
90; 118.016; 90
6292.2S. Chantal E. Stieber; Nuria Huguet; Takeharu Kageyama; Ivana Jevtovikj; Piyal Ariyananda; Alvaro Gordillo; Stephan A. Schunk; Frank Rominger; Peter Hofmann; Michael Limbach
Acrylate formation from CO2 and ethylene: catalysis with palladium and mechanistic insight
Chem.Commun., 2015, 51, 10907
7117378 CIFC39 H56 F2 O4 P2 PdP 1 21/n 117.3557; 17.2752; 27.49
90; 106.717; 90
7893.8S. Chantal E. Stieber; Nuria Huguet; Takeharu Kageyama; Ivana Jevtovikj; Piyal Ariyananda; Alvaro Gordillo; Stephan A. Schunk; Frank Rominger; Peter Hofmann; Michael Limbach
Acrylate formation from CO2 and ethylene: catalysis with palladium and mechanistic insight
Chem.Commun., 2015, 51, 10907
7117379 CIFC19 H18 O2P 1 21 19.8399; 7.9143; 10.7479
90; 112.006; 90
776.02Naoya Kanbayashi; Kazuki Hosoda; Masanori Kato; Koichiro Takii; Taka-aki Okamura; Kiyotaka Onitsuka
Enantio- and diastereoselective asymmetric allylic alkylation catalyzed by a planar-chiral cyclopentadienyl ruthenium complex
Chem.Commun., 2015, 51, 10895
7117380 CIFC18 H12 Br Cl O3C 1 2/c 113.884; 10.515; 22.936
90; 96.166; 90
3329.1Dattatraya H. Dethe; Ganesh M. Murhade
FeCl3 mediated synthesis of substituted indenones by a formal [2+2] cycloaddition/ring opening cascade of o-keto-cinnamates
Chem.Commun., 2015, 51, 10891
7117381 CIFC37 H35 B3 F20 N2 OP 1 21/c 115.3212; 15.0201; 17.8636
90; 98.982; 90
4060.5Liam D. Curless; Ewan R. Clark; Jessica Cid; Alessandro Del Grosso; Michael J. Ingleson
Complete reductive cleavage of CO facilitated by highly electrophilic borocations
Chem.Commun., 2015, 51, 10903
7117382 CIFC36 H32 B2 F20 N2P -18.7661; 13.7257; 15.8543
82.373; 83.288; 81.661
1861.44Liam D. Curless; Ewan R. Clark; Jessica Cid; Alessandro Del Grosso; Michael J. Ingleson
Complete reductive cleavage of CO facilitated by highly electrophilic borocations
Chem.Commun., 2015, 51, 10903
7117383 CIFC16 H24 Gd3 Mn2 N48 O16P n -3 n17.1065; 17.1065; 17.1065
90; 90; 90
5005.9Huan-Cheng Hu; Xiao-Min Kang; Chun-Shuai Cao; Peng Cheng; Bin Zhao
First tetrazole-bridged d-f heterometallic MOFs with a large magnetic entropy change
Chem.Commun., 2015, 51, 10850
7117384 CIFC27 H21 Cl2 I N P2 PdP 1 21 19.2622; 18.511; 9.5911
90; 112.413; 90
1520.2Chen Tan; Peng Wang; Huan Liu; Xiao-Li Zhao; Yong Lu; Ye Liu
Bifunctional ligands in combination with phosphines and Lewis acidic phospheniums for the carbonylative Sonogashira reaction
Chem.Commun., 2015, 51, 10871
7117385 CIFC34 H32 Au Cl F3 N O3 P2 SP b c a17.0157; 15.2244; 27.1217
90; 90; 90
7026Chen Tan; Peng Wang; Huan Liu; Xiao-Li Zhao; Yong Lu; Ye Liu
Bifunctional ligands in combination with phosphines and Lewis acidic phospheniums for the carbonylative Sonogashira reaction
Chem.Commun., 2015, 51, 10871
7117386 CIFC29 H30 Au Cl F3 N O4 P2 SP 1 21/c 118.0468; 13.1909; 14.8731
90; 112.083; 90
3280.86Chen Tan; Peng Wang; Huan Liu; Xiao-Li Zhao; Yong Lu; Ye Liu
Bifunctional ligands in combination with phosphines and Lewis acidic phospheniums for the carbonylative Sonogashira reaction
Chem.Commun., 2015, 51, 10871
7117387 CIFC134.75 H221 N32 O23.75P 1 21 116.51; 27.312; 17.957
90; 96.33; 90
8048E. Prigorchenko; M. Oeren; S. Kaabel; M. Fomitsenko; I. Reile; I. Jarving; T. Tamm; F. Topic; K. Rissanen; R. Aav
Template-controlled synthesis of chiral cyclohexylhemicucurbit[8]uril
Chem.Commun., 2015, 51, 10921
7117388 CIFC95 H156 Cr6 F8 N2 O30 Zn2P 1 21/c 123.6326; 22.5386; 37.8111
90; 126.954; 90
16094.2Antonio Fernandez; Eufemio Moreno Pineda; Jesus Ferrando-Soria; Eric J. L. McInnes; Grigore A. Timco; Richard E. P. Winpenny
A hybrid organic-inorganic molecular daisy chain
Chem.Commun., 2015, 51, 11126
7117389 CIFC21 H25 Cl Cu N5 SP 1 21/n 111.2265; 14.264; 12.7921
90; 97.221; 90
2032.2B. N. Sanchez-Eguia; M. Flores-Alamo; M. Orio; I. Castillo
Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM
Chem.Commun., 2015, 51, 11134
7117390 CIFC52 H66 Cu2 F6 N10 O8 S4C 1 2/c 147.532; 11.8821; 29.711
90; 135.477; 90
11766B. N. Sanchez-Eguia; M. Flores-Alamo; M. Orio; I. Castillo
Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM
Chem.Commun., 2015, 51, 11134
7117391 CIFC42 H50 Br Cl3 Cu2 N10 O8 S2P 1 21/c 18.1746; 23.0559; 13.4166
90; 103.092; 90
2462.94B. N. Sanchez-Eguia; M. Flores-Alamo; M. Orio; I. Castillo
Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM
Chem.Commun., 2015, 51, 11134
7117392 CIFC58 H64 Cu2 F6 N10 O8 S4P 1 21/n 111.6838; 26.1913; 15.5908
90; 111.737; 90
4431.8B. N. Sanchez-Eguia; M. Flores-Alamo; M. Orio; I. Castillo
Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM
Chem.Commun., 2015, 51, 11134
7117393 CIFC27 H27 N3 O2 SP 1 21/c 19.0312; 13.3378; 19.5264
90; 99.689; 90
2318.53Guorong Sheng; Kai Huang; Shicong Ma; Jing Qian; Ping Lu; Yanguang Wang
Preparation of 3-aryl-2-aminoindoles, 3-allyl-3-amino-2-iminoindolines, and tetrahydro-[1,4]diazepino[2,3-b]indoles from 3-diazoindolin-2-imines
Chem.Commun., 2015, 51, 11056
7117394 CIFC22 H40 Cu2 F6 N6 O9 S2P 21 21 2112.6647; 15.6022; 17.2534
90; 90; 90
3409.2Mohammad S. Askari; MaylisOriob; Xavier Ottenwaelder
Controlled nitrene transfer from a tyrosinase-like arylnitroso-copper complex
Chem.Commun., 2015, 51, 11206
7117395 CIFC29 H44 Cl2 Cu F3 N4 O6 SP b c n34.9331; 10.1199; 20.5135
90; 90; 90
7251.9Mohammad S. Askari; MaylisOriob; Xavier Ottenwaelder
Controlled nitrene transfer from a tyrosinase-like arylnitroso-copper complex
Chem.Commun., 2015, 51, 11206
7117396 CIFC39 H41 Mn N8 O7 UI 1 2/a 125.9044; 13.2058; 23.7598
90; 99.772; 90
8010Lucile Chatelain; Floriana Tuna; Jacques Pecaut; Marinella Mazzanti
A zig-zag uranyl(V)-Mn(II) single chain magnet with a high relaxation barrier
Chem.Commun., 2015, 51, 11309
7117397 CIFC44 H56 Co N4 O4 UP 4215.8348; 15.8348; 16.3777
90; 90; 90
4106.56Lucile Chatelain; Floriana Tuna; Jacques Pecaut; Marinella Mazzanti
A zig-zag uranyl(V)-Mn(II) single chain magnet with a high relaxation barrier
Chem.Commun., 2015, 51, 11309
7117398 CIFC13 H12 N3 O2.5P b c n23.2307; 11.1515; 9.2568
90; 90; 90
2398.04Hai Qian; Ivan Aprahamian
An emissive and pH switchable hydrazone-based hydrogel
Chem.Commun., 2015, 51, 11158
7117399 CIFC14 H12 N2 O2P -15.032; 9.7091; 12.6168
89.6; 89.102; 79.669
606.34Hai Qian; Ivan Aprahamian
An emissive and pH switchable hydrazone-based hydrogel
Chem.Commun., 2015, 51, 11158
7117400 CIFC18 H76 Cu9 N36 O88 P2 W18P 63/m20.64; 20.64; 14.742
90; 90; 120
5439Yan-Qing Jiao; Hong-Ying Zang; Xin-Long Wang; En-Long Zhou; Bai-Qiao Song; Chun-Gang Wang; Kui-Zhan Shao; Zhong-Min Su
Self-assembled arrays of polyoxometalate-based metal-organic nanotubes for proton conduction and magnetism
Chem.Commun., 2015, 51, 11313
7117401 CIFC18 H23 N O7 SP 1 21 19.5125; 13.887; 14.68
90; 90.249; 90
1939.2Shizhou Liu; Mengchao Tong; Yang Yu; Hexin Xie; Hao Li; Wei Wang
Construction of an all-carbon quaternary stereocenter by organocatalytic enantioselective alpha-functionalization of alpha-substituted beta-ketocarbonyls with electron deficient vinylarenes
Chem.Commun., 2015, 51, 11221
7117402 CIFC20 H18 OP -19.39; 15.536; 17.758
64.69; 79.19; 85.9
2300Pérez, Manuel; Mahdi, Tayseer; Hounjet, Lindsay J.; Stephan, Douglas W.
Electrophilic phosphonium cations catalyze hydroarylation and hydrothiolation of olefins
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11301-11304
7117403 CIFC23 H31 NP -19.3731; 9.7689; 11.5285
85.605; 74.318; 69.692
952.97Yuya Suzuki; Masato Kageyama; Ryuichi Morisawa; Yasuo Dobashi; Hiroshi Hasegawa; Satoshi Yokojima; Osamu Kitagawa
The synthesis of optically active N-C axially chiral tetrahydroquinoline and its response to an acid-accelerated molecular rotor
Chem.Commun., 2015, 51, 11229
7117404 CIFC29 H24 Cl N O5P 21 21 216.6033; 13.917; 27.99
90; 90; 90
2572.2Guofeng Li; Wangsheng Sun; Jingyi Li; Fengjing Jia; Liang Hong; Rui Wang
Organocatalytic enantioselective formal arylation of azlactones using quinones as the aromatic partner
Chem.Commun., 2015, 51, 11280
7117405 CIFC H8 I3 N O PbP 1 21/m 110.469; 4.6557; 11.214
90; 101.251; 90
536.07Gregory H. Imler; Xia Li; Bolei Xu; Graham E. Dobereiner; Hai-Lung Dai; Yi Rao; Bradford B. Wayland
Solid state transformation of the crystalline monohydrate (CH3NH3)PbI3(H2O) to the (CH3NH3)PbI3 perovskite
Chem.Commun., 2015, 51, 11290
7117406 CIFC93.14 H86.24 Br11.98 Cl1.87 N24 O3.42 Zn5.99C 1 2 133.964; 14.5897; 33.787
90; 104.936; 90
16177Timothy R. Ramadhar; Shao-Liang Zheng; Yu-Sheng Chen; Jon Clardy
The crystalline sponge method: MOF terminal ligand effects
Chem.Commun., 2015, 51, 11252
7117407 CIFC95.1 H90 Cl13.31 N24 O3.78 Zn6C 1 2 133.391; 14.3975; 33.897
90; 105.272; 90
15720.4Timothy R. Ramadhar; Shao-Liang Zheng; Yu-Sheng Chen; Jon Clardy
The crystalline sponge method: MOF terminal ligand effects
Chem.Commun., 2015, 51, 11252
7117408 CIFC26 H41 N2 O5 P Si3 WP n a 2120.7398; 9.2018; 17.6394
90; 90; 90
3366.36Nora C. Breit; Tibor Szilvasi; Shigeyoshi Inoue
Facile rotation around a silicon-phosphorus double bond enabled through coordination to tungsten
Chem.Commun., 2015, 51, 11272
7117409 CIFC52 H82 N4 O10 P2 Si6 W2I 1 2/a 118.8405; 10.1491; 34.9207
90; 92.318; 90
6671.87Nora C. Breit; Tibor Szilvasi; Shigeyoshi Inoue
Facile rotation around a silicon-phosphorus double bond enabled through coordination to tungsten
Chem.Commun., 2015, 51, 11272
7117410 CIFC12 H13 N O2P 1 21/c 19.1916; 12.6389; 9.1878
90; 100.21; 90
1050.5Yanxin Yang; Maotong Xu; Datong Song
Organocatalysts with carbon-centered activity for CO2 reduction with boranes
Chem.Commun., 2015, 51, 11293
7117411 CIFC52 H45 N5 O3 ZnC 1 2/c 124.4775; 12.968; 26.5412
90; 94.383; 90
8400.2MiLosz Pawlicki; Karolina Hurej; Katarzyna Kwiecinska; Ludmila Szterenberg; Lechoslaw Latos-Grazynski
A fused meso-aminoporphyrin: a switchable near-IR chromophore
Chem.Commun., 2015, 51, 11362
7117412 CIFC26 H22 N3 O4P 21 21 216.9776; 12.8353; 25.7684
90; 90; 90
2307.81Tianyu Huang; Lili Lin; Xiaolei Hu; Jianfeng Zheng; Xiaohua Liu; Xiaoming Feng
Kinetic resolution of 2,3-epoxy 3-aryl ketones via catalytic asymmetric ring-opening with pyrazole derivatives
Chem.Commun., 2015, 51, 11374
7117413 CIFC26 H21 N OC 1 2/c 128.0546; 9.681; 15.0716
90; 109.781; 90
3851.9Ghosh, Abhijit; Sengupta, Archya; Chattopadhyay, Ansuman; Das, Debasis
Lysine triggered ratiometric conversion of dynamic to static excimer of a pyrene derivative: aggregation-induced emission, nanomolar detection and human breast cancer cell (MCF7) imaging
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11455-11458
7117414 CIFC16 H37 Fe N10 Ni O6C 1 2/m 113.863; 12.502; 10.093
90; 133.02; 90
1278.92Beata Nowicka; Mateusz Reczynski; Michal Rams; Wojciech Nitek; Jan Zukrowski; Czeslaw Kapusta; Barbara Sieklucka
Hydration-switchable charge transfer in the first bimetallic assembly based on the [Ni(cyclam)]^3+^ - magnetic CN-bridged chain {(H3O)[Ni^III^(cyclam)][Fe^II^(CN)6]^.^5H2O}n
Chem.Commun., 2015, 51, 11485
7117415 CIFC91 H136 N4 Pt2 Sn2P 1 21/c 115.6296; 19.9002; 30.4007
90; 100.5; 90
9297.3Christian P. Sindlinger; Lars Wesemann
Dimeric platinum-stannylene complexes by twofold ligand transfer from an NHC adduct to an organotin(II) hydride
Chem.Commun., 2015, 51, 11421
7117416 CIFC18 H22 F6 N3 P PtP 1 21/c 110.9042; 12.0936; 15.9712
90; 93.73; 90
2101.68Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117417 CIFC19 H22 F6 N3 O P PtP -19.141; 9.5731; 13.2139
108.296; 97.486; 95.712
1076.33Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117418 CIFC21 H26 F6 N3 O2 P PtP 1 21/n 110.94969; 14.36; 15.746
90; 96.7748; 90
2458.57Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117419 CIFC15 H21 I N2 O2 PtP 1 21/n 111.1595; 11.6084; 13.5382
90; 103.102; 90
1708.1Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117420 CIFC21 H24 N2 O2 Pt SP 1 21/c 114.3479; 9.0481; 16.1964
90; 109.574; 90
1981.12Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117421 CIFC25 H27 N2 O6 Pt SP -17.2201; 13.2276; 14.0336
70.675; 80.551; 84.13
1245.94Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts
Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications
Chem.Commun., 2015, 51, 11441
7117422 CIFC118 H143 Mg3 N12P 63/m15.9267; 15.9267; 24.086
90; 90; 120
5291.1Jani O. Moilanen; Benjamin M. Day; Thomas Pugh; Richard A. Layfield
Open-shell doublet character in a hexaazatrinaphthylene trianion complex
Chem.Commun., 2015, 51, 11478
7117423 CIFC22 H19 Cl2 F6 N O3 S2 SbP -19.106; 10.58; 15.856
102.819; 97.906; 112.771
1330.3S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi
Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches
Chem.Commun., 2015, 51, 11452
7117424 CIFC21 H17 N O3 S2P b c a10.641; 14.807; 23.076
90; 90; 90
3635.9S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi
Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches
Chem.Commun., 2015, 51, 11452
7117425 CIFC21 H17 F6 N S2 SbP 1 21/n 18.543; 15.622; 16.383
90; 94.989; 90
2178.2S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi
Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches
Chem.Commun., 2015, 51, 11452
7117426 CIFC24 H22 O SiP 1 c 18.624; 15.417; 7.309
90; 104.681; 90
940.1Ryo Shintani; Hiroki Kurata; Kyoko Nozaki
Rhodium-catalyzed intramolecular alkynylsilylation of alkynes
Chem.Commun., 2015, 51, 11378
7117427 CIFC58 H64 Cl Mg N2 O SbP 1 21/n 113.7235; 16.6434; 23.277
90; 106.733; 90
5091.5Alexander Hinz; Axel Schulz; Alexander Villinger
Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3
Chem.Commun., 2015, 51, 11437
7117428 CIFC58 H64 Bi Cl Mg N2 OP 1 21/n 113.7359; 16.6363; 23.257
90; 106.645; 90
5091.9Alexander Hinz; Axel Schulz; Alexander Villinger
Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3
Chem.Commun., 2015, 51, 11437
7117429 CIFC48 H50 Bi Cl2 N2 SbP b c a14.6206; 15.5222; 18.7038
90; 90; 90
4244.7Alexander Hinz; Axel Schulz; Alexander Villinger
Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3
Chem.Commun., 2015, 51, 11437
7117432 CIFCu O4 P RbP c 21 n8.5261; 5.3562; 8.9064
90; 90; 90
406.733Henry, P.F.; Hughes, R.W.; Weller, M.T.; Ward, S.C.
Rb Cu P O4 - a maximum copper tetrahedral framework adopting the zeotype ABW structure
Chemical Communications, 2000, 2000, 1959-1960
7117433 CIFAl12 O50.7 Si12 Zn8.9P m -3 m11.9061; 11.9061; 11.9061
90; 90; 90
1687.75Readman, J.E.; Gameson, I.; Hriljac, J.A.; Anderson, P.A.; Edwards, P.P.
Synthesis and structure of zinc oxide clusters encapsulated in zeolite LTA
Chemical Communications, 2000, 2000, 595-596
7117434 CIFLi O8 Sb3P 1 21/a 110.2578; 4.7063; 5.6017
90; 96.467; 90
268.708Lopes, M.E.; Kirk, C.A.; Blake, S.M.; Marr, J.; West, A.R.
Li Sb3 O8: the first tetrarutile structure
Chemical Communications, 2000, 2000, 1951-1952
7117435 CIFC13 H10 N2 OC 1 2/c 117.9438; 6.3301; 19.758
90; 113.492; 90
2058.2Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117436 CIFC13 H12 N2 OC 1 2/c 118.9282; 6.0959; 20.6755
90; 116.768; 90
2130Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117437 CIFC13 H11 Cl N2 OP 1 21 113.4732; 9.5123; 19.795
90; 109.801; 90
2386.95Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117438 CIFC14 H14 N2 O SC 1 2/c 120.924; 5.7267; 23.879
90; 112.393; 90
2645.5Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117439 CIFC17 H15 Fe N3C 1 2/c 135.793; 5.7087; 13.346
90; 99.709; 90
2687.9Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit
KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones.
Chemical communications (Cambridge, England), 2015, 51, 11658-11661
7117440 CIFC22 H17 N O4P -17.3977; 11.6656; 20.3981
76.247; 83.564; 88.301
1699.07Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K.
A supramolecular approach for designing emissive solid-state carbazole arrays.
Chemical communications (Cambridge, England), 2015, 51, 11603-11606
7117441 CIFC46.67 H42 Co2 N3.34 O12P 1 21/n 110.148; 14.9006; 28.1544
90; 92.505; 90
4253.2Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K.
A supramolecular approach for designing emissive solid-state carbazole arrays.
Chemical communications (Cambridge, England), 2015, 51, 11603-11606
7117442 CIFC25 H20 Cu N2 O5C 1 2/c 127.7412; 11.114; 15.0069
90; 102.921; 90
4509.7Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K.
A supramolecular approach for designing emissive solid-state carbazole arrays.
Chemical communications (Cambridge, England), 2015, 51, 11603-11606
7117443 CIFC50 H47 N5 O12 Zn2P 21 21 2110.2867; 17.0328; 26.8808
90; 90; 90
4709.8Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K.
A supramolecular approach for designing emissive solid-state carbazole arrays.
Chemical communications (Cambridge, England), 2015, 51, 11603-11606
7117444 CIFC39 H37 Cl N2 O5 SiP -19.8459; 10.5371; 19.8151
94.748; 98.528; 110.714
1881.2Kim, Sooyeon; Fujitsuka, Mamoru; Tohnai, Norimitsu; Tachikawa, Takashi; Hisaki, Ichiro; Miyata, Mikiji; Majima, Tetsuro
The unprecedented J-aggregate formation of rhodamine moieties induced by 9-phenylanthracenyl substitution.
Chemical communications (Cambridge, England), 2015, 51, 11580-11583
7117445 CIFC30 H34 N6 O8P -19.0281; 11.3963; 16.9166
109.458; 90.63; 102.206
1597.7Li, Yi-Jin; Li, Xue; Zhang, Shao-Xiao; Zhao, Yu-Long; Liu, Qun
Copper(ii)-catalyzed oxidative [3+2] cycloaddition reactions of secondary amines with α-diazo compounds: a facile and efficient synthesis of 1,2,3-triazoles.
Chemical communications (Cambridge, England), 2015, 51, 11564-11567
7117446 CIFC22 H18 O3P 1 21/c 18.6642; 20.3575; 10.1977
90; 115.123; 90
1628.53Khoobi, Mehdi; Molaverdi, Fatemeh; Jafarpour, Farnaz; Abbasnia, Masoumeh; Kubicki, Maciej; Shafiee, Abbas
A one-pot domino C-H, C-C activation in coumarins: a fast track to 2,3-diaryl benzo[b]furans.
Chemical communications (Cambridge, England), 2015, 51, 11713-11716
7117447 CIFC22 H29 N O6P 21 21 218.4147; 11.96874; 21.5473
90; 90; 90
2170.1Zhou, Yuhang; Lin, Lili; Yin, Chengkai; Wang, Zhengmeng; Liu, Xiaohua; Feng, Xiaoming
The N,N'-dioxide/Ni(ii)-catalyzed asymmetric inverse-electron-demand hetero-Diels-Alder reaction of methyleneindolinones with hetero-substituted alkenes.
Chemical communications (Cambridge, England), 2015, 51, 11689-11692
7117448 CIFC30 H49 N O Si2P -112.502; 15.8137; 17.4136
74.497; 75.487; 76.75
3162.7Liu, Yan-Hua; Liu, Yue-Jin; Yan, Sheng-Yi; Shi, Bing-Feng
Ni(ii)-catalyzed dehydrative alkynylation of unactivated (hetero)aryl C-H bonds using oxygen: a user-friendly approach.
Chemical communications (Cambridge, England), 2015, 51, 11650-11653
7117449 CIFC54 H50 Cl0 Cu2 F0 N6 P2C 1 2/c 126.589; 17.564; 29.171
90; 106.352; 90
13072.1Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117450 CIFC144 H124 B4 Cl0 Cu4 F16 N12 O0 P4P -115.189; 15.957; 23.446
107.923; 101.304; 104.447
5001.1Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117451 CIFC172 H140 B0 Cl0 Cu4 F0 N12 P4P -115.705; 17.816; 21.535
107.871; 104.457; 97.386
5413.8Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117452 CIFC176 H148 B4 Cl0 Cu4 F16 N12 P4P -115.582; 17.047; 22.619
102.262; 104.435; 102.171
5460.5Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117453 CIFC146 H128 B4 Cl12 Cu4 F16 N12 P4P -113.887; 15.375; 18.799
101.562; 105.589; 101.967
3639.7Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117454 CIFC108 H102 B0 Cl0 Cu4 F0 N12 P4C 1 2/c 125.7551; 20.5086; 24.6987
90; 95.409; 90
12987.8Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C.
Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers.
Chemical communications (Cambridge, England), 2015, 51, 11560-11563
7117455 CIFC17 H20 N2 O2P -19.074; 9.586; 10.271
105.491; 97.554; 108.975
790.5García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D.
Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles.
Chemical communications (Cambridge, England), 2015, 51, 11669-11672
7117456 CIFC18 H22 N2 O2P 1 21/c 19.1496; 9.3085; 19.945
90; 95.325; 90
1691.4García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D.
Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles.
Chemical communications (Cambridge, England), 2015, 51, 11669-11672
7117457 CIFC21 H22 N2 O2P -19.2332; 10.3088; 10.7141
105.017; 100.269; 102.043
933.7García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D.
Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles.
Chemical communications (Cambridge, England), 2015, 51, 11669-11672
7117458 CIFC27 H18 O6P 131.1904; 31.2132; 51.976
72.71; 77.555; 60.912
42068Zentner, Cassandra A.; Lai, Holden W. H.; Greenfield, Joshua T.; Wiscons, Ren A.; Zeller, Matthias; Campana, Charles F.; Talu, Orhan; FitzGerald, Stephen A.; Rowsell, Jesse L. C.
High surface area and Z' in a thermally stable 8-fold polycatenated hydrogen-bonded framework.
Chemical communications (Cambridge, England), 2015, 51, 11642-11645
7117459 CIFC27 H18 O6I 1 2 131.419; 30.116; 45.32
90; 90.412; 90
42881Zentner, Cassandra A.; Lai, Holden W. H.; Greenfield, Joshua T.; Wiscons, Ren A.; Zeller, Matthias; Campana, Charles F.; Talu, Orhan; FitzGerald, Stephen A.; Rowsell, Jesse L. C.
High surface area and Z' in a thermally stable 8-fold polycatenated hydrogen-bonded framework.
Chemical communications (Cambridge, England), 2015, 51, 11642-11645
7117460 CIFC21 H26 O3P 21 21 215.7682; 7.7444; 39.9505
90; 90; 90
1784.64Akira Matsumoto; Keisuke Asano; Seijiro Matsubara
A chiral phosphoric acid catalyst for asymmetric construction of 1,3-dioxanes
Chem.Commun., 2015, 51, 11693
7117461 CIFC13 Co4 Ge O13P -115.853; 8.855; 8.096
110.45; 104.77; 80.64
1026.29Boese, R.; Schmid, G.
Germanium analogue of the well known methylidyne cobalt clusters: X-ray crystal structure of (C O)9 C O Ge Co (C O)4
Journal of the Chemical Society. Chemical Communications (1972-), 1979, 1979, 349-350
7117462 CIFC12 H2 O12 Os4 Se2P -110.004; 12.764; 9.711
98.14; 113.36; 100.73
1086.1Johnson, B. F. G.; Lewis, J.; Lodge, P. G.; Raithby, P. R.; Henrick, K.; McPartlin, M.
Reaction of [M~3~(CO)~12~](M = Ru or Os) with the chalconide elements; X-ray crystal and molecular structure of [Os~4~(CO)~12~H~2~Se~2~]
Journal of the Chemical Society. Chemical Communications (1972-), 1979, 1979, 719-720
7117463 CIFC11 H18 N2 OP 21 21 217.3992; 9.2492; 18.3176
90; 90; 90
1253.6Su, Wei; Gong, Tian-Jun; Xiao, Bin; Fu, Yao
Rhodium(III)-catalyzed cyanation of vinylic C–H bonds: N-cyano-N-phenyl-p-toluenesulfonamide as a cyanation reagent
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11848-11851
7117464 CIFC26 H18P 1 21/c 117.973; 7.352; 6.245
90; 90.646; 90
825.1Liu, Jie; Dong, Huanli; Wang, Zongrui; Ji, Deyang; Cheng, Changli; Geng, Hua; Zhang, Hantang; Zhen, Yonggang; Jiang, Lang; Fu, Hongbing; Bo, Zhishan; Chen, Wei; Shuai, Zhigang; Hu, Wenping
Thin film field-effect transistors of 2,6-diphenyl anthracene (DPA)
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11777-11779
7117465 CIFC48 H88 N12 O12P 21 21 219.4643; 19.6586; 31.9809
90; 90; 90
5950.2Julien Maury; Bryden A. F. Le Bailly; James Raftery; Jonathan Clayden
Conformational cooperativity between helical domains of differing geometry in oligoamide-oligourea foldamer chimeras
Chem.Commun., 2015, 51, 11802
7117466 CIFC27 H27 N3 O9 SP -18.3006; 9.3862; 17.717
86.352; 87.532; 77.772
1345.68Cong-Shuai Wang; Ren-Yi Zhu; Yu-Chen Zhang; Feng Shi
Catalytic chemoselective [3+3] cycloadditions of azomethine ylides with quinone monoimides leading to the construction of a dihydrobenzoxazine scaffold
Chem.Commun., 2015, 51, 11798
7117467 CIFC28 H21 Cl2 N3 O7 SP -18.4575; 12.5061; 13.4396
80.3987; 85.8752; 78.3825
1371.8Cong-Shuai Wang; Ren-Yi Zhu; Yu-Chen Zhang; Feng Shi
Catalytic chemoselective [3+3] cycloadditions of azomethine ylides with quinone monoimides leading to the construction of a dihydrobenzoxazine scaffold
Chem.Commun., 2015, 51, 11798
7117468 CIFC35 H36 Br N3 O3 SP 1 21 19.4805; 15.3417; 11.8162
90; 111.93; 90
1594.3Chao-You Liu; Fu-She Han
Organocatalytic asymmetric reaction of indol-2-yl carbinols with enamides: synthesis of chiral 2-indole-substituted 1,1-diarylalkanes
Chem.Commun., 2015, 51, 11844
7117469 CIFC31 H10 Al F36 N O4 SP 1 21/c 114.2945; 19.666; 19.9786
90; 134.333; 90
4017.3Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang
Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures
Chem.Commun., 2015, 51, 11822
7117470 CIFC69.8 H27.6 Al2 Cl3.61 F72 N2 O8 S2P 1 21/n 113.604; 20.135; 16.634
90; 93.113; 90
4549.6Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang
Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures
Chem.Commun., 2015, 51, 11822
7117471 CIFC71.56 H27.11 Al2 Cl3.11 F72 N2 O8 S2P 1 21/c 110.415; 15.3696; 28.611
90; 93.362; 90
4572Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang
Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures
Chem.Commun., 2015, 51, 11822
7117472 CIFC62 H24 Al2 F72 N2 O8P 1 21/c 127.656; 11.298; 25.57
90; 94.846; 90
7961Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang
Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures
Chem.Commun., 2015, 51, 11822
7117473 CIFC96 H109 Cl Li N4 O6 P4 Pd YP -113.4049; 15.2317; 22.79
99.348; 98.546; 99.455
4455Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117474 CIFC96 H109 Cl Li Lu N4 O6 P4 PdP 1 21/n 113.559; 28.87; 22.627
90; 90.84; 90
8856Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117475 CIFC96 H109 Cl Li Lu N4 O6 P4 PdP -113.332; 15.349; 21.771
88.53; 80.9; 83.96
4374.4Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117476 CIFC94.4 H105.8 Cl Li Lu N4 O5.6 P4 PdP -113.414; 15.386; 22.048
88.38; 80.4; 84.17
4463.2Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117477 CIFC124 H124 Li N6 O4 P6 Pd2 YP 1 21/c 128.427; 14.576; 29.04
90; 106.14; 90
11559Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117478 CIFC124 H124 Li Lu N6 O4 P6 Pd2P 1 21/c 128.3174; 14.561; 29.0288
90; 105.984; 90
11506.7Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117479 CIFC100 H116 Li N4 O7 P4 YP 1 21/c 114.911; 24.635; 26.155
90; 104.1; 90
9318Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky
Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides
Chem.Commun., 2015, 51, 11761
7117480 CIFC16 H24 TiP 1 21/n 19.5686; 10.0906; 15.5541
90; 97.1528; 90
1490.11Robert T. Cooper; F. Mark Chadwick; Andrew E. Ashley; Dermot O'Hare
Double CO2 activation by 14-electron eta^8^-permethylpentalene titanium dialkyl complexes
Chem.Commun., 2015, 51, 11856
7117481 CIFC28 H32 TiP -19.4641; 10.4852; 13.112
72.5421; 79.0295; 64.7729
1119.89Robert T. Cooper; F. Mark Chadwick; Andrew E. Ashley; Dermot O'Hare
Double CO2 activation by 14-electron eta^8^-permethylpentalene titanium dialkyl complexes
Chem.Commun., 2015, 51, 11856
7117482 CIFC18 H24 O4 TiP -18.0338; 9.4658; 11.9668
78.479; 88.7238; 75.3323
862.25Robert T. Cooper; F. Mark Chadwick; Andrew E. Ashley; Dermot O'Hare
Double CO2 activation by 14-electron eta^8^-permethylpentalene titanium dialkyl complexes
Chem.Commun., 2015, 51, 11856
7117483 CIFC30 H32 O4 TiC 1 2/c 134.424; 8.8424; 19.0704
90; 119.263; 90
5064.08Robert T. Cooper; F. Mark Chadwick; Andrew E. Ashley; Dermot O'Hare
Double CO2 activation by 14-electron eta^8^-permethylpentalene titanium dialkyl complexes
Chem.Commun., 2015, 51, 11856
7117484 CIFC34 H30 N5 Nb O13P -18.934; 11.3774; 17.883
78.587; 78.363; 70.115
1657.6Willian X. C. Oliveira; Cynthia L. M. Pereira; Carlos B. Pinheiro; Joan Cano; Francesc Lloret; Miguel Julve
Relatively strong intramolecular antiferromagnetic coupling in a neutral CrIII2NbV2 heterobimetallic molecular square
Chem.Commun., 2015, 51, 11806
7117485 CIFC28 H60 Cr2 Nb2 O30 S10P -111.4285; 12.1741; 12.185
98.122; 116.838; 94.962
1475.7Willian X. C. Oliveira; Cynthia L. M. Pereira; Carlos B. Pinheiro; Joan Cano; Francesc Lloret; Miguel Julve
Relatively strong intramolecular antiferromagnetic coupling in a neutral CrIII2NbV2 heterobimetallic molecular square
Chem.Commun., 2015, 51, 11806
7117486 CIFC76 H92 Cu4 N8 SP -4 3 n21.82156; 21.82156; 21.82156
90; 90; 90
10391Johnson, Brittany J.; Antholine, William E.; Lindeman, Sergey V.; Mankad, Neal P.
A Cu4S model for the nitrous oxide reductase active sites supported only by nitrogen ligands
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11860-11863
7117487 CIFCl16 O36 Sn6P c c n10.251; 16.429; 24.659
90; 90; 90
4152.91Belin, C.; Potier, J.; Chaabouni, M.; Pascal, J.L.; Roziere, J.
Synthesis and Crystal Structure of a New Oxo Perchlorato Complex of Tin(IV): (Sn3 O2 Cl4 (Cl O4)4)2
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 105-106
7117488 CIFC6 I6 O6 Re3R -3 :H6.915; 6.915; 36.939
90; 90; 120
1529.68Calderazzo, F.; Vitali, D.; Marchetti, F.; Poli, R.; Zanazzi, P.F.
Synthesis and molecular structure of mixed-valence compounds of rhenium obtained by di-diodine oxidation of rhenium(I) carbonyl complexes; X-Ray crystal structure of Re3 I6 (C O)6
Journal of the Chemical Society. Chemical Communications (1972-), 1981, 1981, 893-894
7117489 CIFH12 K4 O22 P8 Pt2P -4 b 213.335; 13.335; 7.989
90; 90; 90
1420.62Dos Remedios Pinto, M.A.F.; Sanderson, M.R.; Sadler, P.J.; Neidle, S.; Kuroda, R.; Subbiah, A.
A novel di-platinum(II) octaphosphite complex showing metal-metal bonding and intense luminescence, a potential probe for basic proteins. x-ray crystal and molecular structure
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 13-15
7117490 CIFC19 O19 Os5P -18.88; 10.244; 16.529
99.98; 93.44; 110.37
1376.39Farrar, D.H.; Rosales, M.J.; Lewis, J.; Nicholls, J.N.; Johnson, B.F.G.; Raithby, P.R.
Products of the reaction of carbon monoxide with Os6 (C O)18: X-ray crystal structure of Os5 (C O)19
Journal of the Chemical Society. Chemical Communications (1972-), 1981, 1981, 273-274
7117491 CIFC25 I2 O24 Os10P 21 21 2130.676; 12.323; 11.7
90; 90; 90
4422.84Farrar, D.H.; Jackson, P.G.; Johnson, B.F.G.; Lewis, J.; McPartlin, M.; Vargas, M.D.; Nelson, W.J.H.
Reversible Os-Os bond breaking in the high nuclearity carbido-dianion (Os10 C (C O)24)(2-) on reaction with halogens; X-Ray structure analysis of (Ph3 P)2 N Os10 C (C O)24 I and Os10 C (C O)24 I2
Journal of the Chemical Society. Chemical Communications (1972-), 1981, 1981, 1009-1011
7117492 CIFC44 I N2 O14 Rh5P n 21 a27.767; 18.652; 11.678
90; 90; 90
6048.15Martinengo, S.; Ciani, G.; Sironi, A.
Synthesis and X-Ray Crystal Structure of the (Rh5 (C O)8 (Mue-C O)6 I)(2-) Anion Containing A Trigonal Bipyramidal Rhodium Cluster
Journal of the Chemical Society. Chemical Communications (1972-), 1979, 1979, 1059-1061
7117493 CIFAs2 F12 O1.24 S4.62C 1 2/c 113.954; 7.653; 13.133
90; 100; 90
1381.17Passmore, J.; Sutherland, G.W.; White, P.S.
Preparation and Crystal Structures of (S7 I)4 S4 (As F6)6 and S4 (As F6)2*(S O2)0.6; A Convenient Synthesis of Hexafluoroarsenate Salts of Chalcogen Homoatomic Cations
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 330-331
7117494 CIFAs6 F36 I4 S32P 4/n :219.585; 19.585; 8.321
90; 90; 90
3191.7Passmore, J.; Sutherland, G.W.; White, P.S.
Preparation and crystal structures of (S7 I)4 S4 (As F6)6 and S4 (As F6)2*g(S O2)0.6; A convenient synthesis of hexafluoroarsenate salts of chalcogen homoatomic cations
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 330-331
7117495 CIFAs2 F12 I4 S2C 1 2/c 19.65; 12.874; 13.664
90; 93.79; 90
1693.82Passmore, J.; White, P.S.; Sutherland, G.W.; Whidden, T.K.
Preparation and crystal structure of S2 I4(2+) (As F6)2(-) containing the distorted right triangular prismatic disulphur tetraiodine (2+) cation and a disulphur unit of bond order greater than two
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 289-290
7117496 CIFCl5 O S8 SbP c m n10.52; 8.8; 16.21
90; 90; 90
1500.66Steudel, R.; Sandow, T.; Steidel, J.
Reversible Isomerization of Cyclo-octasulphur Monoxide; Preparation and X-Ray Crystal Structure of S8 O Sb Cl5
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 180-181
7117497 CIFLa3 Li5 O12 Ta2I a -3 d12.80654; 12.80654; 12.80654
90; 90; 90
2100.37Cussen, E.J.
The structure of lithium garnets: cation disorder and clustering in a new family of fast Li(+) conductors
Chemical Communications, 2006, 2006, 412-413
7117498 CIFLa3 Li5 Nb2 O12I a -3 d12.79432; 12.79432; 12.79432
90; 90; 90
2094.36Cussen, E.J.
The structure of lithium garnets: cation disorder and clustering in a new family of fast Li(+) conductors
Chemical Communications, 2006, 2006, 412-413
7117499 CIFC8 K5 N8 NbI -49.22; 9.22; 9.144
90; 90; 90
777.317Hursthouse, M.B.; Galas, A.M.R.
X-Ray Crystal Structure of K5 (Nb (C N)8) and a Change in the Structure of (Nb (C N)8)(5-) in Solution
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 1167-1168
7117500 CIFAl2.6 O24 Rb2.69 Si9.4P m m a9.9653; 7.5717; 9.3031
90; 90; 90
701.959Ikeda, T.; Itabashi, K.
RMA-3: Synthesis and structure of a novel Rb-C zeolite
Chemical Communications, 2005, 2005, 2753-2755
7117501 CIFC6 H6 Cu5 N8C 1 2/c 117.709; 6.762; 13.157
90; 126.4; 90
1268.13Kappenstein, C.; Schubert, U.
X-ray crystal structure of two new mixed-valence copper cyanide complexes: Unusual Bi-Co-ordinated copper(I) atoms in polymeric networks
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 1116-1118
7117502 CIFC5 H8 Cu4 N7 OP 1 21/n 16.733; 21.6; 9.339
90; 109.09; 90
1283.5Kappenstein, C.; Schubert, U.
X-Ray Crystal Structure of Two New Mixed-valence Copper Cyanide Complexes: Unusual Bi-Co-ordinated Copper(I) Atoms in Polymeric Networks
Journal of the Chemical Society. Chemical Communications (1972-), 1980, 1980, 1116-1118
7117503 CIFBa2 O6 Ta YF m -3 m8.42811; 8.42811; 8.42811
90; 90; 90
598.674Lufaso, M.W.; Macquart, R.B.; Lee, Y.; Vogt, T.; zur Loye, H.C.
Pressure induced octahedral tilting distortion in Ba2 Y Ta O6
Chemical Communications, 2006, 2006, 168-170
7117504 CIFBa2 O6 Ta YI 4/m5.8851; 5.8851; 8.3474
90; 90; 90
289.107Lufaso, M.W.; Vogt, T.; Lee, Y.; Macquart, R.B.; zur Loye, H.C.
Pressure induced octahedral tilting distortion in Ba2 Y Ta O6
Chemical Communications, 2006, 2006, 168-170
7117505 CIFH43 Mo12 N3 O57 Th UR -3 c :R13.513; 13.513; 13.513
87.56; 87.56; 87.56
2460.96Molchanov, V.N.; Torchenkova, E.A.; Tat'yanina, I.V.
A novel type of heteropolynuclear complex anion: X-ray crystal structure of the polymeric complex anion (Th (H2 O)3 U Mo12 O42)
Journal of the Chemical Society. Chemical Communications (1972-), 1981, 1981, 93-94
7117506 CIFCl Hf N Na0.125R -3 m :H3.581311; 3.581311; 57.75209
90; 90; 120
641.479Oro-Sole, J.; Martinez, B.; Frontera, C.; Beltran-Porter, D.; Palacin, M.R.; Fuertes, A.
A new intermediate intercalate in superconducting sodium-doped hafnium nitride chloride
Chemical Communications, 2005, 2005, 3352-3354
7117507 CIFCl Hf N Na0.25R -3 m :H3.587907; 3.587907; 29.67848
90; 90; 120
330.868Oro-Sole, J.; Frontera, C.; Martinez, B.; Beltran-Porter, D.; Fuertes, A.; Palacin, M.R.
A new intermediate intercalate in superconducting sodium-doped hafnium nitride chloride
Chemical Communications, 2005, 2005, 3352-3354
7117508 CIFC20 H17 N3 O0P 1 21/c 117.0546; 5.5978; 16.1901
90; 105.328; 90
1490.66R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117509 CIFC26 H21 N3P 1 21/c 113.1017; 20.7038; 7.3429
90; 105.921; 90
1915.4R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117510 CIFC30 H27 N3 O3P c a 2121.214; 8.2654; 27.017
90; 90; 90
4737.2R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117511 CIFC48 H39 N3 O3 S0C 1 2/c 114.8372; 26.503; 18.224
90; 96.42; 90
7121.3R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117512 CIFC12 H10 N2P 1 21/c 19.0822; 14.3844; 7.6234
90; 92.165; 90
995.2R. N. Prasad Tulichala; K. C. Kumara Swamy
Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
Chem.Commun., 2015, 51, 12008
7117513 CIFC32 H38 B20P -111.066; 13.248; 14.418
114.692; 103.244; 94.149
1835.3Jixi Guo; Danqing Liu; Jiahui Zhang; Jiji Zhang; Qian Miao; Zuowei Xie
o-Carborane functionalized pentacenes: synthesis, molecular packing and ambipolar organic thin-film transistors
Chem.Commun., 2015, 51, 12004
7117514 CIFC34 H42 B20C 1 2/c 120.184; 14.426; 14.526
90; 118.624; 90
3712.7Jixi Guo; Danqing Liu; Jiahui Zhang; Jiji Zhang; Qian Miao; Zuowei Xie
o-Carborane functionalized pentacenes: synthesis, molecular packing and ambipolar organic thin-film transistors
Chem.Commun., 2015, 51, 12004
7117515 CIFC38 H50 B20P 1 21/n 16.7399; 9.6832; 30.293
90; 93.691; 90
1972.9Jixi Guo; Danqing Liu; Jiahui Zhang; Jiji Zhang; Qian Miao; Zuowei Xie
o-Carborane functionalized pentacenes: synthesis, molecular packing and ambipolar organic thin-film transistors
Chem.Commun., 2015, 51, 12004
7117516 CIFC42 H21 O3 P SP 1 21 110.913; 16.97; 17.246
90; 100.936; 90
3135.8Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117517 CIFC42 H21 O3 PP 21 21 230.262; 51.48; 4.0818
90; 90; 90
6359Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117518 CIFC43 H22 Cl3 O3 P SP 1 21/n 114.036; 16.26; 16.551
90; 109.896; 90
3552Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117519 CIFC42 H23 O4 PP -320.785; 20.785; 4.1189
90; 90; 120
1541Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117520 CIFC144 H42 O6 P2R -3 :H19.058; 19.058; 20.787
90; 90; 120
6538Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117521 CIFC231 H87 Cl9 O12 P4 S4P 4131.8128; 31.8128; 16.4343
90; 90; 90
16632.4Masaki Yamamura; Kimiya Sukegawa; Tatsuya Nabeshima
Tuning the depth of bowl-shaped phosphine hosts: capsule and pseudo-cage architectures in host-guest complexes with C60 fullerene
Chem.Commun., 2015, 51, 12080
7117522 CIFC54 H56 N26 O16P -112.0755; 12.3189; 12.3197
106.538; 97.085; 107.693
1628.94Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117523 CIFC54 H52 N28 O22P -112.5869; 16.1378; 17.8631
87.78; 89.749; 67.888
3358.8Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117524 CIFC54 H56 N26 O22 S UP -115.4905; 15.7934; 16.7184
68.423; 89.602; 83.048
3772.4Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117525 CIFC108 H112 Br2 N52 O34 UP -112.6611; 15.3936; 17.0052
90.039; 97.817; 91.364
3282.6Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117526 CIFC108 H112 Br2 N52 O34 UP -112.6458; 15.6109; 17.1344
89.597; 82.238; 84.826
3337.85Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117527 CIFC120 H136 Br2 N60 O46 U2P -113.333; 26.409; 26.515
81.73; 84.73; 84.24
9164Lei Mei; Lin Wang; Li-yong Yuan; Shu-wen An; Yu-liang Zhao; Zhi-fang Chai; Peter C. Burns; Wei-qun Shi
Supramolecular inclusion-based molecular integral rigidity: a feasible strategy for controlling the structural connectivity of uranyl polyrotaxane networks
Chem.Commun., 2015, 51, 11990
7117528 CIFC56 H32 N6P -19; 19.58; 23.93
77.99; 83.67; 89.86
4098.6Shipan Wang; Yuewei Zhang; Weiping Chen; Jinbei Wei; Yu Liu; Yue Wang
Achieving high power efficiency and low roll-off OLEDs based on energy transfer from thermally activated delayed excitons to fluorescent dopants
Chem.Commun., 2015, 51, 11972
7117529 CIFC26 H24 Br N O4 SP 1 21 117.678; 9.856; 20.882
90; 103.673; 90
3535.3Zhong-Hua Gao; Xiang-Yu Chen; Han-Ming Zhang; Song Ye
N-Heterocyclic carbene-catalyzed [3+3] cyclocondensation of bromoenals with aldimines: highly enantioselective synthesis of dihydropyridinones
Chem.Commun., 2015, 51, 12040
7117530 CIFC23 H26 Cl N O5 Pt SP -19.583; 9.8654; 14.2517
104.643; 95.718; 114.866
1149.74Oliver J. Stacey; Angelo J. Amoroso; James A. Platts; Peter N. Horton; Simon J. Coles; David Lloyd; Catrin F. Williams; Anthony J. Hayes; Jay J. Dunsford; Simon J. A. Pope
Water soluble, cyclometalated Pt(II)-Ln(III) conjugates towards novel bimodal imaging agents
Chem.Commun., 2015, 51, 12305
7117531 CIFC6 H6 Cl N O2P 1 21/c 112.132; 6.7332; 8.752
90; 91.331; 90
714.7Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117532 CIFC7 H5 Cl N2 O2P -16.037; 8.101; 9.222
70.622; 74.48; 85.612
409.9Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117533 CIFC12 H10 Cl2 N2 O4P 1 21/n 14.4859; 20.457; 14.7
90; 97.6; 90
1337.1Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117534 CIFC24 H18 Cl4 N4 O4P 1 21/c 13.9469; 27.0301; 10.9065
90; 98.544; 90
1150.65Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117535 CIFC24 H18 Cl4 N4 O4P 1 21/c 14.1263; 23.8718; 11.9867
90; 98.803; 90
1166.81Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117536 CIFC29 H21 Cl4 N5 O4 ZnP 1 21/c 114.0391; 14.1663; 15.99
90; 113.95; 90
2906.3Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117537 CIFC29 H21 Cl4 N5 O4 ZnP 1 21/c 110.7037; 17.9473; 15.8353
90; 106.927; 90
2910.2Anup Rana; Pradeepta K. Panda
Beta-Tetrachlorotetramethoxyporphycenes: positional effect of substituents on structure and photophysical properties
Chem.Commun., 2015, 51, 12239
7117538 CIFC26 H18 Ba2 F8 N2 O11P 1 21/n 17.0904; 32.27; 7.2698
90; 117.997; 90
1468.72L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117539 CIFC16 H2 Ba2 F8 O9C 1 2/c 112.5647; 7.1406; 19.823
90; 101.663; 90
1741.8L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117540 CIFC13 H6 Ca F4 N2 O7P 1 21/n 14.4398; 23.038; 14.3878
90; 96.661; 90
1461.71L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117541 CIFC13 H8 Ca F4 N2 O8P n a 2114.2384; 16.3862; 6.845
90; 90; 90
1597.03L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117542 CIFC8 Cs F4 O4I 1 2/a 19.3605; 9.6918; 11.0752
90; 108.566; 90
952.45L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117543 CIFC8 F4 O4 RbI 1 2/a 19.2821; 9.7189; 10.9837
90; 110.34; 90
929.08L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117544 CIFC11 H10 F4 N O6 SrP -16.1469; 7.0452; 16.1438
94.495; 96.741; 101.639
676.26L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117545 CIFC42 H20 F16 N2 O20 Sr3C 1 2 132.076; 6.1638; 11.5618
90; 97.569; 90
2266L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117546 CIFC13 H8 F4 N2 O8 SrP n a 2114.2686; 16.7326; 7.0181
90; 90; 90
1675.6L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117547 CIFC11 H15 F4 N O9 SrP -18.8263; 8.9293; 10.863
92.612; 93.939; 100.991
836.95L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117548 CIFC13 H8 F4 N2 O8 SrP -17.3008; 9.1264; 13.1904
101.118; 93.83; 110.526
798.95L. H. Blair; A. Colakel; R. M. Vrcelj; I. Sinclair; S. J. Coles
Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials
Chem.Commun., 2015, 51, 12185
7117549 CIFC40 H20 O4 S8P 1 21/c 13.9761; 20.6573; 9.8948
90; 96.5712; 90
807.38Jie Liu; Jieshun Cui; Filipe Vilela; Jun He; Matthias Zeller; Allen D. Hunter; Zhengtao Xu
In situ production of silver nanoparticles on an aldehyde-equipped conjugated porous polymer and subsequent heterogeneous reduction of aromatic nitro groups at room temperature
Chem.Commun., 2015, 51, 12197
7117550 CIFC15 H25 N2 O3 P S2C 1 2/c 124.2051; 8.9799; 17.2946
90; 101.412; 90
3684.82Alexander, Benjamin E.; Coles, Simon J.; Fox, Bridget C.; Khan, Tahmina F.; Maliszewski, Joseph; Perry, Alexis; Pitak, Mateusz B.; Whiteman, Matthew; Wood, Mark E.
Investigating the generation of hydrogen sulfide from the phosphonamidodithioate slow-release donor GYY4137
Med. Chem. Commun., 2015, 6, 1649
7117551 CIFC40 H132 Al18 Ga2 O110.5 S8P -110.0721; 16.7628; 17.7945
90.852; 99.861; 101.175
2900.3Fairley, M.; Corum, K. W.; Johns, A.; Unruh, D. K.; Basile, M.; de Groot, J.; Mason, S. E.; Forbes, T. Z.
Isolation and characterization of the [Ga2Al18O8(OH)36(H2O)12](8+) cluster: cationic variations on the Wells-Dawson topology.
Chemical communications (Cambridge, England), 2015, 51, 12467-12469
7117552 CIFC5 H8 B F3 N2P 1 21/m 17.169; 6.8769; 7.474
90; 105.675; 90
354.77Chansaenpak, Kantapat; Wang, Mengzhe; Wu, Zhanhong; Zaman, Rehmat; Li, Zibo; Gabbaï, François P
[^18^F]–NHC–BF~3~ adducts as water stable radio-prosthetic groups for PET imaging
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 12439-12442
7117553 CIFC5 H7 B F3 N3 O2P 1 21/c 17.4533; 9.5695; 11.8645
90; 105.049; 90
817.21Chansaenpak, Kantapat; Wang, Mengzhe; Wu, Zhanhong; Zaman, Rehmat; Li, Zibo; Gabbaï, François P
[^18^F]–NHC–BF~3~ adducts as water stable radio-prosthetic groups for PET imaging
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 12439-12442
7117554 CIFC9 H9 B F3 N3 O2P 21 21 217.5804; 7.9279; 18.431
90; 90; 90
1107.6Chansaenpak, Kantapat; Wang, Mengzhe; Wu, Zhanhong; Zaman, Rehmat; Li, Zibo; Gabbaï, François P
[^18^F]–NHC–BF~3~ adducts as water stable radio-prosthetic groups for PET imaging
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 12439-12442
7117555 CIFC64 H68 Cl2 N4 O P4P 1 21/c 16.515; 27.407; 16.8094
90; 97.149; 90
2978.1Iglesias, Manuel; Iturmendi, Amaia; Sanz Miguel, Pablo J.; Polo, Victor; Pérez-Torrente, Jesús J; Oro, Luis A.
Tuning PCP-Ir complexes: the impact of an N-heterocyclic olefin.
Chemical communications (Cambridge, England), 2015, 51, 12431-12434
7117556 CIFC41 H46 Cl2 F6 Ir N2 P3P 1 21/c 117.973; 11.5843; 19.988
90; 99.642; 90
4102.8Iglesias, Manuel; Iturmendi, Amaia; Sanz Miguel, Pablo J.; Polo, Victor; Pérez-Torrente, Jesús J; Oro, Luis A.
Tuning PCP-Ir complexes: the impact of an N-heterocyclic olefin.
Chemical communications (Cambridge, England), 2015, 51, 12431-12434
7117557 CIFC36 H40 Cl6 F6 Ir N2 O P3P 1 21/c 111.5979; 18.5435; 20.1876
90; 104; 90
4212.7Iglesias, Manuel; Iturmendi, Amaia; Sanz Miguel, Pablo J.; Polo, Victor; Pérez-Torrente, Jesús J; Oro, Luis A.
Tuning PCP-Ir complexes: the impact of an N-heterocyclic olefin.
Chemical communications (Cambridge, England), 2015, 51, 12431-12434
7117558 CIFC21 H14 Br F2 NC 1 c 111.1103; 19.8612; 8.6893
90; 119.104; 90
1675.31Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117559 CIFC22 H17 F2 NP -18.758; 9.0189; 12.1251
77.13; 80.995; 74.079
893.19Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117560 CIFC24 H16 Br3 NP -19.84; 13.6565; 15.873
102.909; 93.588; 95.664
2061.1Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117561 CIFC24 H16 F3 NP 111.219; 11.5; 14.861
72.7; 89.67; 77.32
1782.3Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117562 CIFC27 H22 F3 N O2P 1 21/n 117.8858; 5.3984; 24.0688
90; 107.814; 90
2212.5Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117563 CIFC43 H57 Au Cl3 NP 1 21/c 120.7969; 9.1006; 22.4423
90; 104.981; 90
4103.2Wang, Liliang; Kong, Lingbing; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei
Anti-Markovnikov hydroimination of terminal alkynes in gold-catalyzed pyridine construction from ammonia.
Chemical communications (Cambridge, England), 2015, 51, 12419-12422
7117564 CIFC19 H21 Cl N4 O6P 1 21 19.96; 8.9114; 12.427
90; 105.91; 90
1060.7Xie, Ming-Sheng; Wang, Yong; Li, Jian-Ping; Du, Cong; Zhang, Yan-Yan; Hao, Er-Jun; Zhang, Yi-Ming; Qu, Gui-Rong; Guo, Hai-Ming
A straightforward entry to chiral carbocyclic nucleoside analogues via the enantioselective [3+2] cycloaddition of α-nucleobase substituted acrylates.
Chemical communications (Cambridge, England), 2015, 51, 12451-12454
7117565 CIFC34 H29 F3 N4 O2P -110.748; 11.799; 12.2207
76.828; 73.111; 87.926
1443.17Nicholls-Allison, Emma C; Nawn, Graeme; Patrick, Brian O.; Hicks, Robin G.
Protoisomerization of indigo di- and monoimines.
Chemical communications (Cambridge, England), 2015, 51, 12482-12485
7117566 CIFC32 H29 B F4 N4P 1 21/c 112.7461; 9.883; 22.461
90; 106.476; 90
2713.2Nicholls-Allison, Emma C; Nawn, Graeme; Patrick, Brian O.; Hicks, Robin G.
Protoisomerization of indigo di- and monoimines.
Chemical communications (Cambridge, England), 2015, 51, 12482-12485
7117567 CIFC24 H20 Cl N3 OP -17.956; 9.421; 13.978
107.481; 96.743; 100.43
966.2Nicholls-Allison, Emma C; Nawn, Graeme; Patrick, Brian O.; Hicks, Robin G.
Protoisomerization of indigo di- and monoimines.
Chemical communications (Cambridge, England), 2015, 51, 12482-12485
7117568 CIFC24 H19 N3 OP 1 21/n 114.1344; 14.8496; 17.8584
90; 95.5371; 90
3730.8Nicholls-Allison, Emma C; Nawn, Graeme; Patrick, Brian O.; Hicks, Robin G.
Protoisomerization of indigo di- and monoimines.
Chemical communications (Cambridge, England), 2015, 51, 12482-12485
7117569 CIFC40 H40 Br4 Cl2 Dy F6 N4 O8 P Zn2C 1 2/c 117.1014; 18.2552; 15.9346
90; 97.4595; 90
4932.51Oyarzabal, I.; Ruiz, J.; Ruiz, E.; Aravena, D.; Seco, J. M.; Colacio, E.
Increasing the effective energy barrier promoted by the change of a counteranion in a Zn-Dy-Zn SMM: slow relaxation via the second excited state.
Chemical communications (Cambridge, England), 2015, 51, 12353-12356
7117570 CIFC73.5 H95 Au2 Cl3 F6 N5 O4 SbP 1 21/c 117.2829; 20.6778; 21.9456
90; 90.406; 90
7842.6Gimeno, Ana; Rodríguez-Gimeno, Alejandra; Cuenca, Ana B.; Ramírez de Arellano, Carmen; Medio-Simón, Mercedes; Asensio, Gregorio
Gold(i)-catalysed cascade reactions in the synthesis of 2,3-fused indole derivatives.
Chemical communications (Cambridge, England), 2015, 51, 12384-12387
7117571 CIFC30 H28 Cl2 N4 ZnP n n a14.7556; 22.5021; 10.5208
90; 90; 90
3493.2Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117572 CIFC31 H28 Cl5 N4 ZnP n n a14.6608; 22.7977; 9.9218
90; 90; 90
3316.2Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117573 CIFC62 H60 Cl8 N8 Zn2P n n a14.6639; 22.7525; 9.8535
90; 90; 90
3287.5Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117574 CIFC32 H28 Cl4 N4 ZnP n n a14.7255; 22.4827; 10.2852
90; 90; 90
3405.1Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117575 CIFC30 H28 N4P -15.599; 7.1074; 16.1003
92.646; 98.583; 112.049
583.53Martí-Rujas, Javier; Bonafede, Simone; Tushi, Dorearta; Cametti, Massimo
Multiple single-crystal-to-single-crystal guest exchange in a dynamic 1D coordination polymer.
Chemical communications (Cambridge, England), 2015, 51, 12357-12360
7117576 CIFC22 H22 OP 1 21/c 118.8889; 5.8024; 15.156
90; 95.856; 90
1652.44Vandavasi, Jaya Kishore; Hu, Wan-Ping; Boominathan, Siva Senthil Kumar; Guo, Bing-Chun; Hsiao, Cheng-Tien; Wang, Jeh-Jeng
Au(i)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
Chemical communications (Cambridge, England), 2015, 51, 12435-12438
7117577 CIFC25 H20 O3P -15.8013; 11.3046; 15.3699
110.966; 92.458; 102.961
908.83Vandavasi, Jaya Kishore; Hu, Wan-Ping; Boominathan, Siva Senthil Kumar; Guo, Bing-Chun; Hsiao, Cheng-Tien; Wang, Jeh-Jeng
Au(i)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
Chemical communications (Cambridge, England), 2015, 51, 12435-12438
7117578 CIFC20 H20 OP 1 21/n 16.2076; 15.3283; 16.201
90; 95.237; 90
1535.1Vandavasi, Jaya Kishore; Hu, Wan-Ping; Boominathan, Siva Senthil Kumar; Guo, Bing-Chun; Hsiao, Cheng-Tien; Wang, Jeh-Jeng
Au(i)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
Chemical communications (Cambridge, England), 2015, 51, 12435-12438
7117579 CIFC18 H16 OP 1 21/c 15.5946; 9.1084; 26.337
90; 90.82; 90
1341.94Vandavasi, Jaya Kishore; Hu, Wan-Ping; Boominathan, Siva Senthil Kumar; Guo, Bing-Chun; Hsiao, Cheng-Tien; Wang, Jeh-Jeng
Au(i)-catalyzed synthesis of 8-oxabicyclo[3.2.1]oct-2-enes and 9-oxabicyclo[3.3.1]nona-2,6-dienes from enynol via oxonium/Prins-type cyclization.
Chemical communications (Cambridge, England), 2015, 51, 12435-12438
7117580 CIFC9 H9 B F4 N2P 1 21/a 113.372; 6.2221; 13.8278
90; 112.232; 90
1065Leblanc, Nicolas; Sproules, Stephen; Pasquier, Claude; Auban-Senzier, Pascale; Raffy, Helene; Powell, Annie K.
Approaching the limit of Cu(II)/Cu(I) mixed valency in a Cu(I)Br2-N-methylquinoxalinium hybrid compound.
Chemical communications (Cambridge, England), 2015, 51, 12740-12743
7117581 CIFC9 H9 Br2 Cu N2C 1 2/m 115.373; 6.4099; 10.9646
90; 96.692; 90
1073.1Leblanc, Nicolas; Sproules, Stephen; Pasquier, Claude; Auban-Senzier, Pascale; Raffy, Helene; Powell, Annie K.
Approaching the limit of Cu(II)/Cu(I) mixed valency in a Cu(I)Br2-N-methylquinoxalinium hybrid compound.
Chemical communications (Cambridge, England), 2015, 51, 12740-12743
7117582 CIFC36 H108 N9 Nb9 O69.5 P5P 1 21/c 127.347; 15.4386; 24.5428
90; 91.742; 90
10357.2Son, Jung-Ho; Casey, William H.
A new Keggin-like niobium-phosphate cluster that reacts reversibly with hydrogen peroxide.
Chemical communications (Cambridge, England), 2015, 51, 12744-12747
7117583 CIFC24 H28 N2 O2P 1 21/n 111.8462; 7.6966; 22.1897
90; 94.024; 90
2018.2Rawling, M. J.; Storr, T. E.; Bawazir, W. A.; Cully, S. J.; Lewis, W.; Makki, M. S. I. T.; Strutt, I. R.; Jones, G.; Hamza, D.; Stockman, R. A.
Facile access to a heterocyclic, sp(3)-rich chemical scaffold via a tandem condensation/intramolecular nitrone-alkene [3+2] cycloaddition strategy.
Chemical communications (Cambridge, England), 2015, 51, 12867-12870
7117584 CIFC18 H24 N2 O2P -18.0233; 8.5269; 12.1531
107.964; 98.204; 97.133
770.22Rawling, M. J.; Storr, T. E.; Bawazir, W. A.; Cully, S. J.; Lewis, W.; Makki, M. S. I. T.; Strutt, I. R.; Jones, G.; Hamza, D.; Stockman, R. A.
Facile access to a heterocyclic, sp(3)-rich chemical scaffold via a tandem condensation/intramolecular nitrone-alkene [3+2] cycloaddition strategy.
Chemical communications (Cambridge, England), 2015, 51, 12867-12870
7117585 CIFC20 H21 N O3 SP 1 21/c 110.783; 12.0241; 14.0523
90; 93.965; 90
1817.6Liu, Bang; Song, Ren-Jie; Ouyang, Xuan-Hui; Li, Yang; Hu, Ming; Li, Jin-Heng
Palladium-catalyzed oxidative 6-exo-trig cyclization of 1,6-enynes: facile synthesis of bicyclo[4.1.0]heptan-5-ones.
Chemical communications (Cambridge, England), 2015, 51, 12819-12822
7117586 CIFC73 H67 N2 O PP n a 2118.9194; 14.8964; 20.0103
90; 90; 90
5639.5Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117587 CIFC88 H72 B F4 N2 PP -113.7202; 16.4329; 19.0854
74.147; 78.554; 81.404
4036.3Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117588 CIFC71 H58 F6 N2 O7 P S2P -114.4808; 14.6435; 15.4095
83.039; 84.164; 77.715
3159.5Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117589 CIFC73 H57 Fe N2 O4 PP 1 21/n 112.6626; 18.3247; 25.5405
90; 101.719; 90
5802.8Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117590 CIFC69 H57 Au2 Cl2 N2 PP 1 21/c 115.4817; 18.0766; 24.4404
90; 98.019; 90
6772.9Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117591 CIFC69 H63 B2 N2 PP 1 21/c 113.5874; 17.073; 24.447
90; 105.718; 90
5459.1Liu, Liu; Ruiz, David A.; Dahcheh, Fatme; Bertrand, Guy
Isolation of a Lewis base stabilized parent phosphenium (PH2(+)) and related species.
Chemical communications (Cambridge, England), 2015, 51, 12732-12735
7117592 CIFC22 H25 N OP 1 21/c 112.82457; 6.61539; 20.0798
90; 93.3829; 90
1700.59Paterson, Andrew J.; St John-Campbell, Sahra; Mahon, Mary F.; Press, Neil J.; Frost, Christopher G.
Catalytic meta-selective C-H functionalization to construct quaternary carbon centres.
Chemical communications (Cambridge, England), 2015, 51, 12807-12810
7117593 CIFC222 H218 Co12 N26 O50P -117.7558; 21.8506; 21.8517
60.483; 81.896; 68.78
6870Xu, Hong; Wang, Qian; Qin, Jian-Hua; Zang, Shuang-Quan; Langley, Stuart K.; Murray, Keith S.; Moubaraki, Boujemaa; Batten, Stuart R.; Mak, Thomas C. W.
A cyclic dodecanuclear cobalt cluster based on a derivative of the rhodamine 6G dye with unusual magnetization.
Chemical communications (Cambridge, England), 2015, 51, 12716-12719
7117594 CIFC50 H62 Cl4 Cu2 N8 O21 S5P b c a18.0973; 28.4369; 28.5016
90; 90; 90
14667.8Rancan, Marzio; Armelao, Lidia
Exploiting dimensional variability in coordination polymers: solvent promotes reversible conversion between 3D and chiral 1D architectures.
Chemical communications (Cambridge, England), 2015, 51, 12947-12949
7117595 CIFC9 H16 Cl Cu0.5 N O6 S2P 31 2 110.7197; 10.7197; 23.0839
90; 90; 120
2297.2Rancan, Marzio; Armelao, Lidia
Exploiting dimensional variability in coordination polymers: solvent promotes reversible conversion between 3D and chiral 1D architectures.
Chemical communications (Cambridge, England), 2015, 51, 12947-12949
7117596 CIFC9 H16 Cl Cu0.5 N O6 S2P 32 2 110.7314; 10.7314; 23.1419
90; 90; 120
2308.04Rancan, Marzio; Armelao, Lidia
Exploiting dimensional variability in coordination polymers: solvent promotes reversible conversion between 3D and chiral 1D architectures.
Chemical communications (Cambridge, England), 2015, 51, 12947-12949
7117597 CIFC16 H12 O3P 1 21/n 16.0914; 8.5177; 23.947
90; 90.598; 90
1242.4Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π+2π]-cycloadditions of tert-butyl propiolates with aldehydes and ketones to form 4H-1,3-dioxine derivatives.
Chemical communications (Cambridge, England), 2015, 51, 13004-13007
7117598 CIFC21 H18 F N O2C 1 2/c 140.945; 4.8118; 18.994
90; 114.23; 90
3412.5Zhou, Peng; Hao, Wen-Juan; Zhang, Jin-Peng; Jiang, Bo; Li, Guigen; Tu, Shu-Jiang
Cascade bicyclizations of o-alkynyl aldehydes with thiazolium salts: a new access toward poly-functionalized indeno[2,1-b]pyrroles.
Chemical communications (Cambridge, England), 2015, 51, 13012-13015
7117599 CIFC24 H18 Cu N6 O7I 1 2/a 116.6086; 7.1589; 19.141
90; 102.179; 90
2224.6Larragy, Ruth; Fitzgerald, Jenny; Prisecaru, Andreea; McKee, Vickie; Leonard, Paul; Kellett, Andrew
Protein engineering with artificial chemical nucleases.
Chemical communications (Cambridge, England), 2015, 51, 12908-12911
7117600 CIFC41 H56 B2 Cl4 Fe2 N2 O4P 1 21/c 19.156; 10.84; 22.94
90; 100.259; 90
2240Braunschweig, Holger; Ewing, William C.; Ferkinghoff, Katharina; Hermann, Alexander; Kramer, Thomas; Shang, Rong; Siedler, Eva; Werner, Christine
Activation of boryl-, borylene and metalloborylene complexes by isonitriles.
Chemical communications (Cambridge, England), 2015, 51, 13032-13035
7117601 CIFC21 H31 B Mn N3 O2P 1 21/c 19.5331; 12.839; 18.276
90; 97.456; 90
2217.99Braunschweig, Holger; Ewing, William C.; Ferkinghoff, Katharina; Hermann, Alexander; Kramer, Thomas; Shang, Rong; Siedler, Eva; Werner, Christine
Activation of boryl-, borylene and metalloborylene complexes by isonitriles.
Chemical communications (Cambridge, England), 2015, 51, 13032-13035
7117602 CIFC38 H48 B Cr Fe N3 O7P 1 21 110.8; 18.449; 19.691
90; 96.23; 90
3900Braunschweig, Holger; Ewing, William C.; Ferkinghoff, Katharina; Hermann, Alexander; Kramer, Thomas; Shang, Rong; Siedler, Eva; Werner, Christine
Activation of boryl-, borylene and metalloborylene complexes by isonitriles.
Chemical communications (Cambridge, England), 2015, 51, 13032-13035
7117603 CIFC14 H19 Cd N3 O2 SP b c a13.9096; 10.5234; 22.6923
90; 90; 90
3321.61Roy, Sumit; Dey, Arka; Ray, Partha Pratim; Ortega-Castro, Joaquín; Frontera, Antonio; Chattopadhyay, Shouvik
Application of a novel 2D cadmium(ii)-MOF in the formation of a photo-switch with a substantial on-off ratio.
Chemical communications (Cambridge, England), 2015, 51, 12974-12976
7117604 CIFC58 H44 F20 Ir2 N12 O P2P -19.382; 13.771; 14.966
63; 76.75; 82.82
1676.5Li, Guangfu; Ren, Xinyao; Shan, Guogang; Che, Weilong; Zhu, Dongxia; Yan, Likai; Su, Zhongmin; Bryce, Martin R.
New AIE-active dinuclear Ir(iii) complexes with reversible piezochromic phosphorescence behaviour.
Chemical communications (Cambridge, England), 2015, 51, 13036-13039
7117605 CIFC40 H49 Cu N3 O2P 1 21/c 114.9821; 27.9247; 18.0471
90; 107.42; 90
7204.1Doistau, Benjamin; Cantin, Jean-Louis; Chamoreau, Lise-Marie; Marvaud, Valérie; Hasenknopf, Bernold; Vives, Guillaume
Mechanical switching of magnetic interaction by tweezers-type complex.
Chemical communications (Cambridge, England), 2015, 51, 12916-12919
7117606 CIFC91 H99 Cu2 N7 O10P b c n11.3594; 40.7108; 19.0962
90; 90; 90
8831Doistau, Benjamin; Cantin, Jean-Louis; Chamoreau, Lise-Marie; Marvaud, Valérie; Hasenknopf, Bernold; Vives, Guillaume
Mechanical switching of magnetic interaction by tweezers-type complex.
Chemical communications (Cambridge, England), 2015, 51, 12916-12919
7117607 CIFC94 H101 Cl11 Cu2 N7 O4 ZnC 1 2/c 169.071; 14.7327; 19.7966
90; 98.123; 90
19943Doistau, Benjamin; Cantin, Jean-Louis; Chamoreau, Lise-Marie; Marvaud, Valérie; Hasenknopf, Bernold; Vives, Guillaume
Mechanical switching of magnetic interaction by tweezers-type complex.
Chemical communications (Cambridge, England), 2015, 51, 12916-12919
7117611 CIFC12 H9 F6 N O4P 1 21/c 113.0242; 13.3563; 8.2205
90; 100.66; 90
1405.32Sarkar, Satavisha; Khan, Abu T.
Beyond conventional routes, an unprecedented metal-free chemoselective synthesis of anthranilate esters via a multicomponent reaction (MCR) strategy.
Chemical communications (Cambridge, England), 2015, 51, 12673-12676
7117612 CIFC15 H20 N2 O3P 1 21/c 14.8164; 12.3382; 24.0676
90; 94.39; 90
1426.04Sarkar, Satavisha; Khan, Abu T.
Beyond conventional routes, an unprecedented metal-free chemoselective synthesis of anthranilate esters via a multicomponent reaction (MCR) strategy.
Chemical communications (Cambridge, England), 2015, 51, 12673-12676
7117613 CIFC8 H25 Ag6 Cl N16 O7I 41/a m d29.5862; 29.5862; 3.4563
90; 90; 90
3025.4Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117614 CIFC8 H13 Ag6 Cl N16 OP -4 n 219.3474; 19.3474; 3.5013
90; 90; 90
1310.61Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117615 CIFC12 H29 Ag6 Cl N12 O7I 41/a m d29.415; 29.415; 3.525
90; 90; 90
3050Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117616 CIFC12 H17 Ag6 Cl N12 OI -4 2 d28.708; 28.708; 3.5249
90; 90; 90
2905Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117617 CIFC8 H25 Ag6 Br N16 O7I 41/a m d29.6337; 29.6337; 3.4913
90; 90; 90
3065.9Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117618 CIFC8 H13 Ag6 Br N16 OP -4 n 219.455; 19.455; 3.5339
90; 90; 90
1337.6Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117619 CIFC12 H29 Ag6 Br N12 O7I 41/a m d29.419; 29.419; 3.5564
90; 90; 90
3078Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117620 CIFC12 H17 Ag6 Br N12 OI -4 2 d28.503; 28.503; 3.5383
90; 90; 90
2874.6Zhou, Dong-Dong; Liu, Zhi-Juan; He, Chun-Ting; Liao, Pei-Qin; Zhou, Hao-Long; Zhong, Zhen-Song; Lin, Rui-Biao; Zhang, Wei-Xiong; Zhang, Jie-Peng; Chen, Xiao-Ming
Controlling the flexibility and single-crystal to single-crystal interpenetration reconstitution of metal-organic frameworks.
Chemical communications (Cambridge, England), 2015, 51, 12665-12668
7117621 CIFC40 H36 F4 Ir N7 OP -111.9138; 12.3154; 14.3549
99.444; 98.544; 116.93
1791.9Feng, Yansong; Li, Ping; Zhuang, Xuming; Ye, Kaiqi; Peng, Tai; Liu, Yu; Wang, Yue
A novel bipolar phosphorescent host for highly efficient deep-red OLEDs at a wide luminance range of 1000-10 000 cd m(-2).
Chemical communications (Cambridge, England), 2015, 51, 12544-12547
7117622 CIFC29 H37 N3 O3P 113.8032; 14.0849; 14.8146
89.715; 77.329; 77.339
2738.9Wu, Xiaowei; Zhang, Dengyou; Zhou, Shengbin; Gao, Feng; Liu, Hong
Site-specific indolation of proline-based peptides via copper(ii)-catalyzed oxidative coupling of tertiary amine N-oxides.
Chemical communications (Cambridge, England), 2015, 51, 12571-12573
7117623 CIFC28 H27 N O5 SP 1 21/n 110.29; 16.124; 15.403
90; 106.6; 90
2449.1Gao, Zhenzhen; Wang, Chang; Yuan, Chunhao; Zhou, Leijie; Xiao, Yumei; Guo, Hongchao
Phosphine-catalyzed [4+1] annulation of 2-tosylaminochalcones with allenoates: synthesis of trans-2,3-disubstitued indolines.
Chemical communications (Cambridge, England), 2015, 51, 12653-12656
7117624 CIFC26 H20 N2 O4P -17.361; 8.3907; 16.3626
80.826; 89.447; 85.419
994.5Zou, Lin; Wang, Xiao-Ye; Zhang, Xiao-Xiao; Dai, Ya-Zhong; Wu, Yun-Dong; Wang, Jie-Yu; Pei, Jian
Toward electron-deficient pyrene derivatives: construction of pyrene tetracarboxylic diimide containing five-membered imide rings.
Chemical communications (Cambridge, England), 2015, 51, 12585-12588
7117625 CIFC20 H36 N4 P2P n m a9.2644; 14.3849; 17.7198
90; 90; 90
2361.5Su, Jing; Wang, Bingqiang; Liu, Dongling; Du, Libo; Liu, Yang; Su, Jihu; Zheng, Wenjun
A 1,2,4-diazaphospholyl radical and its nitrogen-phosphorus coupled dimer: synthesis, X-ray structural characterization, EPR analysis, and computational studies.
Chemical communications (Cambridge, England), 2015, 51, 12680-12683
7117626 CIFC27 H21 B0 Cl Co F0 N4 O2P b c m8.6043; 16.622; 21.331
90; 90; 90
3050.8Das, Biswanath; Orthaber, Andreas; Ott, Sascha; Thapper, Anders
Water oxidation catalysed by a mononuclear Co(II) polypyridine complex; possible reaction intermediates and the role of the chloride ligand.
Chemical communications (Cambridge, England), 2015, 51, 13074-13077
7117627 CIFC27 H29 Cl3 N2 O7P 21 21 2111.0927; 15.2908; 17.2201
90; 90; 90
2920.8Zhou, Rui; Wu, Qinjie; Guo, Mingrui; Huang, Wei; He, Xianghong; Yang, Lei; Peng, Fu; He, Gu; Han, Bo
Organocatalytic cascade reaction for the asymmetric synthesis of novel chroman-fused spirooxindoles that potently inhibit cancer cell proliferation.
Chemical communications (Cambridge, England), 2015, 51, 13113-13116
7117628 CIFC17 H13 F3 N2 O2 SC 1 2/c 117.549; 11.355; 18.82
90; 111.289; 90
3494.3Duan, Yaya; Zhou, Bin; Lin, Jin-Hong; Xiao, Ji-Chang
Diastereoselective Johnson-Corey-Chaykovsky trifluoroethylidenation.
Chemical communications (Cambridge, England), 2015, 51, 13127-13130
7117629 CIFC9 H6 F3 N O3P 21 21 214.8359; 6.4223; 30.645
90; 90; 90
951.8Duan, Yaya; Zhou, Bin; Lin, Jin-Hong; Xiao, Ji-Chang
Diastereoselective Johnson-Corey-Chaykovsky trifluoroethylidenation.
Chemical communications (Cambridge, England), 2015, 51, 13127-13130
7117633 CIFC52 H54 S2 Si2P 1 21/c 117.7574; 14.7085; 17.0416
90; 90.251; 90
4451Xueliang Shi; Sangsu Lee; Minjung Son; Bin Zheng; Jingjing Chang; Linzhi Jing; Kuo-Wei Huang; Dongho Kim; Chunyan Chi
Pro-aromatic bisphenaleno-thieno[3,2-b]thiophene versus anti-aromatic bisindeno-thieno[3,2-b]thiophene: different ground-state properties and applications in field-effect transistors
Chem.Commun., 2015, 51, 13178
7117634 CIFC70 H68 N16 O8 ZnP -114.4171; 16.6908; 17.855
63.51; 76.303; 74.915
3676.5Lucas Kocher; Stephanie Durot; Valerie Heitz
Control of the cavity size of flexible covalent cages by silver coordination to the peripheral binding sites
Chem.Commun., 2015, 51, 13181
7117635 CIFC13 H15 F3 N4P 1 21/n 111.3589; 8.1467; 15.8924
90; 99.885; 90
1448.81Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117636 CIFC24 H22 F3 N O2C 1 2/c 133.4249; 6.2204; 20.9937
90; 96.885; 90
4333.5Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117637 CIFC21 H19 F3 N2P -19.987; 10.061; 10.168
71.21; 75.39; 79.84
930.9Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117638 CIFC14 H10 F3 N OP 1 21 19.2351; 5.3558; 12.9094
90; 104.113; 90
619.24Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117639 CIFC15 H10 F3 N OP 1 21/c 113.226; 13.605; 7.27
90; 92.84; 90
1306.6Yu-Tao He; Qiang Wang; Jiahui Zhao; Xue-Yuan Liu; Peng-Fei Xu; Yong-Min Liang
The copper-catalyzed synthesis of beta-trifluoromethylated acrylonitriles and trifluoromethyl-substituted 2H-azirines
Chem.Commun., 2015, 51, 13209
7117640 CIFC11 H17 N O5 PbR -3 :H14.4445; 14.4445; 34.0453
90; 90; 120
6151.7Saet Byeol Kim; Dong Woo Lee; Suk-Kyu Chang; Kang Min Ok
Pb3[C6(CH3)3(CO2)3H6]2[DMF]3: first layered Pb-Kemp's triacid complex
Chem.Commun., 2015, 51, 13166
7117641 CIFC36 H30 Ho N O11I m a 221.403; 34.255; 8.023
90; 90; 90
5882Gerard Tobin; Steve Comby; Nianyong Zhu; Rodolphe Clerac; Thorfinnur Gunnlaugsson; Wolfgang Schmitt
Towards multifunctional lanthanide-based metal-organic frameworks
Chem.Commun., 2015, 51, 13313
7117642 CIFC6 H14 O9C 1 2/c 17.3942; 9.2111; 14.029
90; 93.117; 90
954.1Nipuni-Dhanesh; H. Gamage; Benedikt Stiasny; Jorg Stierstorfer; Philip D. Martin; Thomas M. Klapotke; Charles H. Winter
Less sensitive oxygen-rich organic peroxides containing geminal hydroperoxy groups
Chem.Commun., 2015, 51, 13298
7117643 CIFC4 H5 O4P 1 21/c 19.776; 6.0458; 8.133
90; 100.964; 90
471.9Nipuni-Dhanesh; H. Gamage; Benedikt Stiasny; Jorg Stierstorfer; Philip D. Martin; Thomas M. Klapotke; Charles H. Winter
Less sensitive oxygen-rich organic peroxides containing geminal hydroperoxy groups
Chem.Commun., 2015, 51, 13298
7117644 CIFC16 H12 F3 N O2P -18.1909; 9.5693; 10.5301
75.88; 72.823; 67.507
720.5Haiqing Luo; Guojiao Wu; Shuai Xu; Kang Wang; Chaoqiang Wu; Yan Zhang; Jianbo Wang
Palladium-catalyzed cross-coupling of aryl fluorides with N-tosylhydrazones via C-F bond activation
Chem.Commun., 2015, 51, 13321
7117645 CIFC15 H10 F3 N O2P 21 21 215.8037; 15.049; 15.033
90; 90; 90
1313Haiqing Luo; Guojiao Wu; Shuai Xu; Kang Wang; Chaoqiang Wu; Yan Zhang; Jianbo Wang
Palladium-catalyzed cross-coupling of aryl fluorides with N-tosylhydrazones via C-F bond activation
Chem.Commun., 2015, 51, 13321
7117646 CIFC76 H180 K2 Mn2 O18 Si12P -112.5416; 16.0775; 27.2358
87.785; 85.0576; 79.8209
5383.7C.-Y. Lin; J. C. Fettinger; N. F. Chilton; A. Formanuik; F. Grandjean; G. J. Long; P. P. Power
Salts of the two-coordinate homoleptic manganese(I) dialkyl anion [Mn{C(SiMe3)3}2]^-^ with quenched orbital magnetism
Chem.Commun., 2015, 51, 13275
7117647 CIFC40 H94 K Mn O10 Si6I 1 2/a 118.4983; 14.4287; 21.2812
90; 90.821; 90
5679.5C.-Y. Lin; J. C. Fettinger; N. F. Chilton; A. Formanuik; F. Grandjean; G. J. Long; P. P. Power
Salts of the two-coordinate homoleptic manganese(I) dialkyl anion [Mn{C(SiMe3)3}2]^-^ with quenched orbital magnetism
Chem.Commun., 2015, 51, 13275
7117648 CIFC19 H21 B2 Cu F8 N4P 1 21/c 114.516; 9.366; 15.706
90; 97.731; 90
2115.9Hiroaki Kotani; Tomomi Yagi; Tomoya Ishizuka; Takahiko Kojima
Enhancement of 4-electron O2 reduction by a Cu(II)-pyridylamine complex via protonation of a pendant pyridine in the second coordination sphere in water
Chem.Commun., 2015, 51, 13385
7117650 CIFC51 H47 K2 N18 Ni2 O12P 1 21/n 112.536; 28.635; 15.794
90; 91.53; 90
5668Jesus Ferrando-Soria; Oscar Fabelo; Maria Castellano; Joan Cano; Stephen Fordham; Hong-Cai Zhou
Multielectron oxidation in a ferromagnetically coupled dinickel(II) triple mesocate
Chem.Commun., 2015, 51, 13381
7117651 CIFC32 H48 N5 PtP 1 21/c 122.614; 8.529; 17.808
90; 107.877; 90
3269Ogawa, Tomohiro; Yoshida, Masaki; Ohara, Hiroki; Kobayashi, Atsushi; Kato, Masako
A dual-emissive ionic liquid based on an anionic platinum(II) complex
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 13377-13380
7117652 CIFC31 H30 K2 N6 O3 Pt2P 1 21/c 119.743; 12.197; 14.509
90; 108.445; 90
3314.4Ogawa, Tomohiro; Yoshida, Masaki; Ohara, Hiroki; Kobayashi, Atsushi; Kato, Masako
A dual-emissive ionic liquid based on an anionic platinum(II) complex
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 13377-13380
7117653 CIFC39 H74 N6 O10P 19.7972; 10.4809; 12.3285
107.162; 102.474; 101.595
1132.47Mothukuri Ganesh Kumar; Sushil N. Benke; K. Muruga Poopathi Raja; Hosahudya N. Gopi
Engineering polypeptide folding through trans double bonds: transformation of miniature beta-meanders to hybrid helices
Chem.Commun., 2015, 51, 13397
7117654 CIFC49 H76 N6 O9P 1 21 19.286; 20.892; 27.661
90; 98.639; 90
5305Mothukuri Ganesh Kumar; Sushil N. Benke; K. Muruga Poopathi Raja; Hosahudya N. Gopi
Engineering polypeptide folding through trans double bonds: transformation of miniature beta-meanders to hybrid helices
Chem.Commun., 2015, 51, 13397
7117655 CIFC49 H72 N6 O9C 1 2 135.352; 10.43; 17.876
90; 107.549; 90
6285Mothukuri Ganesh Kumar; Sushil N. Benke; K. Muruga Poopathi Raja; Hosahudya N. Gopi
Engineering polypeptide folding through trans double bonds: transformation of miniature beta-meanders to hybrid helices
Chem.Commun., 2015, 51, 13397
7117656 CIFC27 H26 B Cl2 F2 N3P 1 21/c 119.318; 7.0637; 19.042
90; 101.007; 90
2550.6Sisi Wang; Hui Liu; John Mack; Jiangwei Tian; Bin Zou; Hua Lu; Zhifang Li; Jianxiong Jiang; Zhen Shen
A BODIPY-based 'turn-on' fluorescent probe for hypoxic cell imaging
Chem.Commun., 2015, 51, 13389
7117657 CIFC34 H11 B F20 SP 1 21/c 113.4674; 13.8265; 17.2405
90; 94.8693; 90
3198.72Yoshiaki Shoji; Naoki Tanaka; Daisuke Hashizume; Takanori Fukushima
The molecular and electronic structures of a thioaroyl cation formed by borinium ion-mediated C[double bond, length as m-dash]S double bond cleavage of CS2
Chem.Commun., 2015, 51, 13342
7117658 CIFC34 H11 B F20 SP 1 21/c 113.4674; 13.8265; 17.2405
90; 94.8693; 90
3198.72Yoshiaki Shoji; Naoki Tanaka; Daisuke Hashizume; Takanori Fukushima
The molecular and electronic structures of a thioaroyl cation formed by borinium ion-mediated C[double bond, length as m-dash]S double bond cleavage of CS2
Chem.Commun., 2015, 51, 13342
7117659 CIFC162 H162 Au13 F18 N4 O2 P13C 1 2/c 125.72; 21.2708; 31.007
90; 96.865; 90
16842Mizuho Sugiuchi; Yukatsu Shichibu; Takayuki Nakanishi; Yasuchika Hasegawa; Katsuaki Konishi
Cluster-pi electronic interaction in a superatomic Au13 cluster bearing sigma-bonded acetylide ligands
Chem.Commun., 2015, 51, 13519
7117660 CIFC21 H22 Cl2 Mn4 P4C 1 2/c 140.9164; 9.3302; 27.2353
90; 116.922; 90
9270.5Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117661 CIFC20 H20 Br Cu Mn4 P4C 1 c 114.1032; 12.6047; 12.7139
90; 101.172; 90
2217.28Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117662 CIFC22 H24 Cl5 Cu Mn4 P4C 1 2/c 123.8316; 12.8659; 18.4127
90; 93.404; 90
5635.6Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117663 CIFC28 H27 Cl2 Mn5 O2 P4P 1 21/n 111.9099; 14.821; 17.9552
90; 106.097; 90
3045.13Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117664 CIFC36 H34 Cl4 Mn6 O4 P4P -110.5319; 10.8158; 18.0191
77.832; 80.265; 85.858
1976.14Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117665 CIFC85 H76 Cl6 Mn14 O12 P8P -110.3548; 10.5563; 20.4728
79.072; 82.668; 83.529
2170.28Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117666 CIFC50 H44 Cl4 Mn8 O8 P4C 1 2/c 129.4777; 11.0635; 21.2608
90; 132.06; 90
5147.9Sebastian Heinl; Konrad Kiefer; Gabor Balazs; Claudia Wickleder; Manfred Scheer
The synthesis of the heterocubane cluster [{CpMn}4(mu3-P)4] as a tetrahedral shaped starting material for the formation of polymeric coordination compounds
Chem.Commun., 2015, 51, 13474
7117667 CIFC20 H16 Br N O6 SP 21 21 218.30101; 10.28989; 23.4389
90; 90; 90
2002.07Lewis S. Aitken; Lisa E. Hammond; Rajkumar Sundaram; Kenneth Shankland; Geoffrey D. Brown; Alexander J. A. Cobb
Asymmetric cyclopropanation of conjugated cyanosulfones using a novel cupreine organocatalyst: rapid access to delta^3^-amino acids
Chem.Commun., 2015, 51, 13558
7117668 CIFC18 H26 B F4 N RuP n a 2116.1385; 14.1014; 8.2801
90; 90; 90
1884.35Andrey I. Konovalov; Evgeniya O. Gorbacheva; Fedor M. Miloserdov; Vladimir V. Grushin
Ruthenium-catalyzed nucleophilic fluorination of halobenzenes
Chem.Commun., 2015, 51, 13527
7117669 CIFC12 H11 N O2P 1 21 17.7718; 5.5207; 11.7443
90; 91.969; 90
503.6Dipak Kumar Tiwari; Jaya Pogula; B. Sridhar; Dharmendra Kumar Tiwari; Pravin R. Likhar
Nano-copper catalysed highly regioselective synthesis of 2,4-disubstituted pyrroles from terminal alkynes and isocyanides
Chem.Commun., 2015, 51, 13646
7117670 CIFC20 H20 Br N O3P 1 21 15.3126; 9.6321; 18.149
90; 92.117; 90
928.1Francesco Berti; Federico Malossi; Fabio Marchetti; Mauro Pineschi
A highly enantioselective Mannich reaction of aldehydes with cyclic N-acyliminium ions by synergistic catalysis
Chem.Commun., 2015, 51, 13694
7117671 CIFC8 H8 F6 N4 Ni O2 SiP 4/m m m7.0148; 7.0148; 7.5655
90; 90; 90
372.28Osama Shekhah; Youssef Belmabkhout; Karim Adil; Prashant M. Bhatt; Amy J. Cairns; Mohamed Eddaoudi
A facile solvent-free synthesis route for the assembly of a highly CO2 selective and H2S tolerant NiSIFSIX metal-organic framework
Chem.Commun., 2015, 51, 13595
7117672 CIFC18 H16 Cl2 Hg N2 S2C 1 2/c 126.6229; 10.0005; 13.9461
90; 93.414; 90
3706.45Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117673 CIFC19 H19 Ag F3 N2 O3 S3C 1 2/c 123.7546; 9.6388; 18.5295
90; 93.688; 90
4233.84Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117674 CIFC20 H19 Cl2 N3 S2 ZnP 1 21/c 18.5494; 18.8079; 13.9638
90; 99.017; 90
2217.58Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117675 CIFC18 H12 Hg I2 N2 S2C 1 2/c 126.4973; 10.4756; 14.4782
90; 94.642; 90
4005.6Hui Xue; Feilong Jiang; Qihui Chen; Daqiang Yuan; Jiandong Pang; Guangxun Lv; Xiuyan Wan; Linfeng Liang; Maochun Hong
Conformation driven in situ interlock: from discrete metallocycles to infinite polycatenanes
Chem.Commun., 2015, 51, 13706
7117676 CIFC28 H22 Br F3 O4P 1 21 110.6758; 9.3185; 25.405
90; 99.557; 90
2492.3Bjarke S. Donslund; Alicia Monleon; Jesper Larsen; Lise Ibsen; Karl Anker Jorgensen
The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks
Chem.Commun., 2015, 51, 13666
7117677 CIFC24 H22 Br F3 O3P 21 21 219.671; 10.892; 21.822
90; 90; 90
2298.7Bjarke S. Donslund; Alicia Monleon; Jesper Larsen; Lise Ibsen; Karl Anker Jorgensen
The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks
Chem.Commun., 2015, 51, 13666
7117678 CIFC27 H27 N O5 SP -19.687; 10.731; 12.624
99.142; 109.67; 102.46
1168Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117679 CIFC28 H26 F3 N O7 S2P 1 21/n 110.689; 16.049; 16.697
90; 103.962; 90
2780Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117680 CIFC23 H27 N O5 SP 21 21 217.466; 13.997; 20.362
90; 90; 90
2128Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117681 CIFC17 H21 N O5 SP 1 21/n 113.648; 8.763; 14.28
90; 91.288; 90
1707.4Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117682 CIFC23 H27 N O6 SP 1 21/c 18.2174; 25.204; 10.5671
90; 95.161; 90
2179.7Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117683 CIFC27 H29 N O4 SP -18.05; 16.385; 18.274
94.603; 93.801; 94.487
2388.8Santosh J. Gharpure; V. Prasath; Vinod Kumar
Stereoselective synthesis of 2,3-disubstituted indoline, pyrrolidine and cyclic ether-fused 1,2-dihydroquinoline derivatives using alkyne iminium ion cyclization of vinylogous carbamates: switch of regioselectivity using an internal hydroxy group as a nucleophile
Chem.Commun., 2015, 51, 13623
7117684 CIFC42 H46 N2 O2P 1 21/n 111.2948; 16.3779; 19.5856
90; 103.789; 90
3518.6Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117685 CIFC36 H34 N2 O2P b c a15.3406; 16.1078; 22.8598
90; 90; 90
5648.7Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117686 CIFC36 H36 N2 O2C 1 c 122.1106; 8.5517; 15.1278
90; 93.349; 90
2855.5Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117687 CIFC43 H51 B Cl2 F4 N2 OP 21 21 2112.1048; 16.0393; 21.3761
90; 90; 90
4150.22Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117688 CIFC43 H48 Cl0.5 N3.5 O2.5P -113.2188; 16.6509; 19.82
68.92; 86.793; 67.534
3744.8Anup Bhunia; Shridhar Thorat; Rajesh G. Gonnade; Akkattu T. Biju
Reaction of N-heterocyclic carbenes with chalcones leading to the synthesis of deoxy-Breslow intermediates in their oxidized form
Chem.Commun., 2015, 51, 13690
7117689 CIFC32 H23 N3 O2C 1 2/c 133.04; 21.838; 7.2037
90; 95.946; 90
5169.7Rui Chen; Ru-Qiang Lu; Ke Shi; Fan Wu; Hong-Xun Fang; Zhe-Xuan Niu; Xiao-Yun Yan; Ming Luo; Xin-Chang Wang; Chi-Yuan Yang; Xiao-Ye Wang; Binbin Xu; Haiping Xia; Jian Pei; Xiao-Yu Cao
Corannulene derivatives with low LUMO levels and dense convex-concave packing for n-channel organic field-effect transistors
Chem.Commun., 2015, 51, 13768
7117690 CIFC30 H19 N3 O2I 1 2/a 17.2119; 21.7175; 31.966
90; 95.488; 90
4983.7Rui Chen; Ru-Qiang Lu; Ke Shi; Fan Wu; Hong-Xun Fang; Zhe-Xuan Niu; Xiao-Yun Yan; Ming Luo; Xin-Chang Wang; Chi-Yuan Yang; Xiao-Ye Wang; Binbin Xu; Haiping Xia; Jian Pei; Xiao-Yu Cao
Corannulene derivatives with low LUMO levels and dense convex-concave packing for n-channel organic field-effect transistors
Chem.Commun., 2015, 51, 13768
7117691 CIFC96 H86 F4 N2 Sn2P -110.1387; 14.5652; 15.407
109.721; 103.913; 101.78
1974.97C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117692 CIFC94 H86 N2 Sn2P -110.3114; 12.6833; 14.8438
101.757; 90.344; 99.28
1874.19C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117693 CIFC72 H66 Cl2 N2 Sb2P -110.5945; 12.3644; 12.5871
98.608; 105.285; 100.205
1531.5C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117694 CIFC48 H43 Cl4 F2 N Sb2P 1 21/n 116.2248; 10.8555; 26.4376
90; 106.24; 90
4470.6C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117695 CIFC74 H70 Bi Cl7 N2 SnP -110.519; 14.7566; 22.9059
75.62; 86.231; 80.569
3396.4C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117696 CIFC84 H76 Bi Cl3 F2 N2 SnP n a 2121.3654; 31.1166; 10.7124
90; 90; 90
7121.8C. Hering-Junghans; A. Schulz; A. Villinger
A neutral low-coordinate heterocyclic bismuth-in species
Chem.Commun., 2015, 51, 13834
7117697 CIFC26 H36 N2 S4P -14.5302; 10.3934; 14.1186
81.405; 86.591; 82.721
651.44Te-Fang Yang; Sheng-Han Huang; Yi-Pang Chiu; Bo-Hsiang Chen; Yu-Wei Shih; Yu-Chang Chang; Jie-Yi Yao; Yao-Jen Lee; Ming-Yu Kuo
Pyromellitic dithioimides: thionation improves air-stability and electron mobility of N-type organic field-effect transistors
Chem.Commun., 2015, 51, 13772
7117698 CIFC19 H19 N O4 S2P -18.0274; 8.1297; 14.6961
76.433; 74.709; 85.528
899.17Sridhar Undeela; Srinivas Thadkapally; Jagadeesh Babu Nanubolu; Kiran Kumar Singarapu; Rajeev S. Menon
Catalyst-controlled divergence in cycloisomerisation reactions of N-propargyl-N-vinyl sulfonamides: gold-catalysed synthesis of 2-sulfonylmethyl pyrroles and dihydropyridines
Chem.Commun., 2015, 51, 13748
7117699 CIFC22 H14 N2P -15.8666; 11.4535; 12.2113
83.981; 81.526; 76.578
787.26Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117700 CIFC22 H15 N O2P 1 21/c 110.0557; 10.3647; 15.6302
90; 97.658; 90
1614.5Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117701 CIFC16 H10 N2P 1 21/n 111.476; 6.7685; 15.8831
90; 106.572; 90
1182.5Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117702 CIFC24 H16 N2 OP 1 21/c 113.1944; 9.7945; 14.6162
90; 100.206; 90
1859Gopal Chandru Senadi; Wan-Ping Hu; Amol Milind Garkhedkar; Siva Senthil Kumar Boominathan; Jeh-Jeng Wang
Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity
Chem.Commun., 2015, 51, 13795
7117703 CIFC94 H116 N8 O17P 1 21 118.7521; 23.0271; 25.3314
90; 89.8645; 90
10938.2Hanna Jedrzejewska; Marcin Kwit; Agnieszka Szumna
Switching of inherent chirality driven by self-assembly
Chem.Commun., 2015, 51, 13799
7117704 CIFFe11 H78 Na27 O258 Sb6 W60P -117.5189; 24.8676; 25.0737
60.828; 74.889; 72.982
9028.7Xiaoqiang Du; Yong Ding; Fangyuan Song; Baochun Ma; Junwei Zhao; Jie Song
Efficient photocatalytic water oxidation catalyzed by polyoxometalate [Fe11(H2O)14(OH)2(W3O10)2(alpha-SbW9O33)6]^27-^ based on abundant metals
Chem.Commun., 2015, 51, 13925
7117705 CIFC50 H70 F12 N4 O2.93 P2P 1 21/c 115.137; 14.675; 13.735
90; 114.58; 90
2774.6Saioa Cobo; Frederic Lafolet; Eric Saint-Aman; Christian Philouze; Christophe Bucher; Serena Silvi; Alberto Credi; Guy Royal
Reactivity of a pyridinium-substituted dimethyldihydropyrene switch under aerobic conditions: self-sensitized photo-oxygenation and thermal release of singlet oxygen
Chem.Commun., 2015, 51, 13886
7117706 CIFC39 H32 Br2 Fe N2P 1 21/n 113.1652; 12.2178; 20.8109
90; 107.514; 90
3192.3C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117707 CIFC47 H55 Fe N2 Na O3P 1 21/n 121.2714; 16.1257; 24.0679
90; 99.18; 90
8149.9C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117708 CIFC67.63 H55.63 Fe3 N4 O0.63P 21 21 225.8932; 14.78371; 13.25563
90; 90; 90
5074.22C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117709 CIFC274 H230 Fe4 N16 O3P n a 2126.9704; 17.93806; 21.5915
90; 90; 90
10445.9C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117710 CIFC44 H44P -110.4488; 12.4887; 13.5525
71.996; 79.884; 82.754
1650.87C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117711 CIFC58 H47 Fe N2P -110.1232; 14.1732; 15.1866
103.795; 93.762; 92.887
2106.63C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117712 CIFC36 H34 N2 O2P 1 21/c 18.9045; 8.871; 17.5783
90; 96.259; 90
1380.3C. Lichtenberg; L. Viciu; M. Vogt; R. E. Rodriguez-Lugo; M. Adelhardt; J. Sutter; M. M. Khusniyarov; K. Meyer; B. de Bruin; E. Billd; H. Grutzmacher
Low-valent iron: an Fe(I) ate compound as a building block for a linear trinuclear Fe cluster
Chem.Commun., 2015, 51, 13890
7117713 CIFC17 H17 N O3P -16.0589; 8.071; 15.6647
100.41; 96.485; 93.141
746.38Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117714 CIFC12 H12 Cl3 N O3P -18.6581; 11.8588; 14.7395
101.56; 104.761; 90.004
1431.65Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117715 CIFC15 H16 Cl3 N O3P -16.0347; 11.3911; 13.0283
67.611; 89.839; 85.877
825.64Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117716 CIFC15 H19 N O4P c a 2111.5083; 13.3657; 9.5834
90; 90; 90
1474.08Isai Ramakrishna; Gowri Sankar Grandhi; Harekrishna Sahoo; Mahiuddin Baidya
The Mukaiyama aldol reaction of in situ generated nitrosocarbonyl compounds: selective C-N bond formation and N-O bond cleavage in one-pot for alpha-amination of ketones
Chem.Commun., 2015, 51, 13976
7117717 CIFC14 H20 O2 S2P 21 21 2110.1194; 11.6313; 12.1672
90; 90; 90
1432.1Amol P. Jadhav; V. U. Bhaskara Rao; Pradeep Singh; R. G. Gonnade; Ravi P. Singh
Asymmetric vinylogous Michael reaction of cyclic enones with silyloxy furans
Chem.Commun., 2015, 51, 13941
7117718 CIFC13 H18 O2 S2P 21 21 216.6349; 8.9609; 21.6859
90; 90; 90
1289.33Amol P. Jadhav; V. U. Bhaskara Rao; Pradeep Singh; R. G. Gonnade; Ravi P. Singh
Asymmetric vinylogous Michael reaction of cyclic enones with silyloxy furans
Chem.Commun., 2015, 51, 13941
7117719 CIFC105 H113 F27 N4 O18 P4.5P -114.1777; 20.5414; 24.643
71.116; 78.71; 76.663
6549.9Wei-Bo Hu; Wen-Jing Hu; Xiao-Li Zhao; Yahu A. Liu; Jiu-Sheng Li; Biao Jiang; Ke Wen
A [2]rota[2]catenane, constructed from a pillar[5]arene-crown ether fused double-cavity macrocycle: synthesis and structural characterization
Chem.Commun., 2015, 51, 13882
7117720 CIFC166 H205 F30 N8 O26 P5P -120.5486; 21.3959; 24.984
65.622; 74.313; 66.014
9071.3Wei-Bo Hu; Wen-Jing Hu; Xiao-Li Zhao; Yahu A. Liu; Jiu-Sheng Li; Biao Jiang; Ke Wen
A [2]rota[2]catenane, constructed from a pillar[5]arene-crown ether fused double-cavity macrocycle: synthesis and structural characterization
Chem.Commun., 2015, 51, 13882
7117721 CIFC199 H189 N23 O53 Zn11P 1 2/c 122.018; 20.783; 37.062
90; 94.845; 90
16899S. A. Sapchenko; D. N. Dybtsev; D. G. Samsonenko; R. V. Belosludov; V. R. Belosludov; Y. Kawazoe; M. Schroder; V. P. Fedin
Selective gas adsorption in microporous metal-organic frameworks incorporating urotropine basic sites: an experimental and theoretical study
Chem.Commun., 2015, 51, 13918
7117722 CIFC17 H15 N O2 SP 21 21 216.2454; 7.9709; 30.185
90; 90; 90
1502.7Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117723 CIFC30 H27.5 N O5.25 SC 1 2/c 141.536; 9.8916; 25.763
90; 93.59; 90
10564Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117724 CIFC24 H23 N O5 SP -111.0389; 13.5784; 24.5769
87.24; 84.094; 69.682
3436Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117725 CIFC25 H25 N O5 SC 1 c 18.4273; 18.696; 14.628
90; 96.208; 90
2291.2Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117726 CIFC24 H23 N O5 SP b c a12.5654; 18.5476; 18.7414
90; 90; 90
4367.8Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117727 CIFC25 H26 N2 O4 SP 1 21/n 112.5847; 17.5982; 20.1268
90; 92.772; 90
4452.2Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117728 CIFC31 H29 N2 O6 S2P 1 21/c 118.1593; 10.1358; 15.6691
90; 91.647; 90
2882.8Yin-Wei Sun; Xiang-Ying Tang; Min Shi
A gold-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade: syntheses of medium-sized heterocycles
Chem.Commun., 2015, 51, 13937
7117729 CIFC94.5 H81.75 Eu F9 N23.25 O27 S3P -115.608; 15.7058; 22.744
88.97; 80.503; 77.211
5361.5Eoin P. McCarney; Joseph P. Byrne; Brendan Twamley; Miguel Martinez-Calvo; Gavin Ryan; Matthias E. Mobius; Thorfinnur Gunnlaugsson
Self-assembly formation of a healable lanthanide luminescent supramolecular metallogel from 2,6-bis(1,2,3-triazol-4-yl)pyridine (btp) ligands
Chem.Commun., 2015, 51, 14123
7117730 CIFC34 H33 Cl2 F6 Ir N7 PP b c a10.918; 16.0878; 39.16
90; 90; 90
6878.3Kamrul Hasan; Amlan K. Pal; Thomas Auvray; Eli Zysman-Colman; Garry S. Hanan
Blue-green emissive cationic iridium(III) complexes using partially saturated strongly-donating guanidyl-pyridine/-pyrazine ancillary ligands
Chem.Commun., 2015, 51, 14060
7117731 CIFC96 H122.5 Cl10.5 Mg2 N13 O2.5P 1 21/c 113.281; 26.435; 28.814
90; 94.579; 90
10084Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath
Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers
Chem.Commun., 2015, 51, 14107
7117732 CIFC177 H219 Cl3 Mg4 N26P -113.848; 16.029; 19.255
96.237; 97.714; 105.938
4025Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath
Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers
Chem.Commun., 2015, 51, 14107
7117733 CIFC96 H121 Cl6 Mg2 N14 O2P 1 21/n 114.137; 26.982; 25.473
90; 105.387; 90
9368Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath
Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers
Chem.Commun., 2015, 51, 14107
7117734 CIFC92 H121 Cl4 Mg2 N9 O4P -113.267; 18.521; 20.98
86.112; 73.433; 69.33
4620Sk Asif Ikbal; Avinash Dhamija; Sankar Prasad Rath
Metal-coordination-driven mixed ligand binding in supramolecular bisporphyrin tweezers
Chem.Commun., 2015, 51, 14107
7117735 CIFC4 H9 B11 Cs F9 O9 S3P 1 21/c 112.5292; 18.424; 10.6894
90; 106.109; 90
2370.6Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117736 CIFC2 H5.94 B11 Br5.06 Cs F3 O3 SP b c n11.355; 27.735; 13.353
90; 90; 90
4205.3Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117737 CIFC8 H16 B11 Cl10 F3 O3 S SiP 1 21/n 116.213; 21.072; 17.832
90; 102.362; 90
5951Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117738 CIFC38 H61 B11 Cl11 F5 O7 P4 Pd2 SP 1 21/n 114.477; 35.02; 26.24
90; 92.565; 90
13290Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117739 CIFC17 H27 B11 Cl10 F4 O3 S SiP 1 21/c 19.327; 20.08; 20.281
90; 94.518; 90
3786.5Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117740 CIFC27 H21 B11 Cl10 F4 O3 SP b c a12.5691; 22.529; 27.755
90; 90; 90
7859.4Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117741 CIFC26 H36 B11 Br Cl10 F4 O5 P2 Pd SP 1 21/n 114.099; 12.676; 28.345
90; 102.072; 90
4954Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117742 CIFC20 H31 B11 Cl10 F4 O5 P2 Pd SP -112.224; 13.31; 14.337
72.268; 74.431; 78.566
2123Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117743 CIFC19 H31 B11 Cl11 F O2 P2 PdP -19.1582; 12.0726; 20.864
76.534; 88.597; 78.715
2199.5Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117744 CIFC3 H B11 Cl9 Cs F6 O6 S2P b c a17.7687; 15.7898; 18.9559
90; 90; 90
5318.3Loren P. Press; Billy J. McCulloch; Weixing Gu; Chun-Hsing Chen; Bruce M. Foxman; Oleg V. Ozerov
Triflyloxy-substituted carboranes as useful weakly coordinating anions
Chem.Commun., 2015, 51, 14034
7117745 CIFC34 H45 B2 F N12 O UP -110.4532; 11.0258; 18.1147
102.153; 98.067; 96.74
1997.41Christopher L. Clark; Jill J. Lockhart; Phillip E. Fanwick; Suzanne C. Bart
Synthesis of low-valent uranium fluorides by C-F bond activation
Chem.Commun., 2015, 51, 14084
7117746 CIFC30 H43 B2 F2 N12 UP 1 21/n 111.784; 22.3831; 17.0603
90; 93.165; 90
4493Christopher L. Clark; Jill J. Lockhart; Phillip E. Fanwick; Suzanne C. Bart
Synthesis of low-valent uranium fluorides by C-F bond activation
Chem.Commun., 2015, 51, 14084
7117747 CIFC7 H14 Cl3 N O4P 1 21/n 112.6911; 12.471; 14.9357
90; 91.68; 90
2362.87A. J. K. Roth; M. Tretbar; C. B. W. Stark
Mimicking the active site of aldehyde dehydrogenases: stabilization of carbonyl hydrates through hydrogen bonds
Chem.Commun., 2015, 51, 14175
7117748 CIFC7 H8 Cl3 N O3P 1 21/c 16.1594; 12.8396; 13.3985
90; 101.56; 90
1038.12A. J. K. Roth; M. Tretbar; C. B. W. Stark
Mimicking the active site of aldehyde dehydrogenases: stabilization of carbonyl hydrates through hydrogen bonds
Chem.Commun., 2015, 51, 14175
7117749 CIFC6 H6 S0.95 Se0.05P b c n13.8535; 11.4448; 7.1913
90; 90; 90
1140.2Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117750 CIFC6 H6 S0.91 Se0.09P b c n13.856; 11.425; 7.1934
90; 90; 90
1138.7Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117751 CIFC6 H6 S0.75 Se0.25P n a b7.2109; 11.3897; 13.9705
90; 90; 90
1147.4Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117752 CIFC6 H6 SeP n a b7.329; 11.226; 14.422
90; 90; 90
1186.6Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117753 CIFC6 H6 SP n a b7.1905; 11.4643; 13.815
90; 90; 90
1138.8Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117754 CIFC6 H6 S0.57 Se0.43P n a b7.2621; 11.371; 14.155
90; 90; 90
1168.9Sajesh P. Thomas; R. Sathishkumar; T. N. Guru Row
Organic alloys of room temperature liquids thiophenol and selenophenol
Chem.Commun., 2015, 51, 14255
7117755 CIFC25 H28 N2 O3 SC 1 2/c 110.9399; 21.02; 20.547
90; 98.769; 90
4669.7Dongari Yadagiri; Pazhamalai Anbarasan
An iodine(III) mediated oxidative rearrangement of enamines: efficient synthesis of alpha-amino ketones
Chem.Commun., 2015, 51, 14203
7117756 CIFC54 H18 N0 O41 Zn9I 2 323.503; 23.503; 23.503
90; 90; 90
12983Yun-Wu Li; Jian Xu; Da-Cheng Li; Jian-Min Dou; Hui Yan; Tong-Liang Hu; Xian-He Bu
Two microporous MOFs constructed from different metal cluster SBUs for selective gas adsorption
Chem.Commun., 2015, 51, 14211
7117757 CIFC15 H20 Cd N2 O7P 1 21/n 110.099; 14.363; 12.975
90; 105.69; 90
1811.9Yun-Wu Li; Jian Xu; Da-Cheng Li; Jian-Min Dou; Hui Yan; Tong-Liang Hu; Xian-He Bu
Two microporous MOFs constructed from different metal cluster SBUs for selective gas adsorption
Chem.Commun., 2015, 51, 14211
7117758 CIFC30 H26 N2 SC 1 2/c 119.059; 5.647; 42.733
90; 93.669; 90
4590Alok Ranjan; Anupam Mandal; Swapnil G. Yerande; Dattatraya H. Dethe
An asymmetric alkynylation/hydrothiolation cascade: an enantioselective synthesis of thiazolidine-2-imines from imines, acetylenes and isothiocyanates
Chem.Commun., 2015, 51, 14215
7117759 CIFC30 H23 Br N2 O SP 19.724; 11.581; 11.774
75.443; 87.986; 89.04
1282.5Alok Ranjan; Anupam Mandal; Swapnil G. Yerande; Dattatraya H. Dethe
An asymmetric alkynylation/hydrothiolation cascade: an enantioselective synthesis of thiazolidine-2-imines from imines, acetylenes and isothiocyanates
Chem.Commun., 2015, 51, 14215
7117760 CIFC88 H88 Cl2 F36 N13 O2 S6C 1 2/c 120.3759; 35.024; 16.9047
90; 98.951; 90
11917Hennie Valkenier; Christopher M. Dias; Kathryn L. Porter Goff; Ondrej Jurcek; Rakesh Puttreddy; Kari Rissanen; Anthony P. Davis
Sterically geared tris-thioureas; transmembrane chloride transporters with unusual activity and accessibility
Chem.Commun., 2015, 51, 14235
7117761 CIFC25 H19 N O3P 21 21 214.11501; 10.0552; 45.8911
90; 90; 90
1898.85Zhong-Jian Cai; Chao Yang; Shun-Yi Wang; Shun-Jun Ji
Palladium-catalyzed highly regioselective 6-exo-dig cyclization and alkenylation of ortho-ethynylanilides: the synthesis of polyene-substituted benzo[d][1,3]oxazines
Chem.Commun., 2015, 51, 14267
7117762 CIFC110 H56 Br2I 41/a c d39.709; 39.709; 39.724
90; 90; 90
62637Melanie Kitchin; Kristina Konstas; Christopher J. Sumby; Milena L. Czyz; Peter Valente; Matthew R. Hill; Anastasios Polyzos; Christian J. Doonan
Continuous flow synthesis of a carbon-based molecular cage macrocycle via a three-fold homocoupling reaction
Chem.Commun., 2015, 51, 14231
7117763 CIFC21 H20 Br2 O4 SP 1 21 110.927; 19.507; 19.81
90; 105.742; 90
4064.2Nagamoto, Midori; Nishimura, Takahiro
Stereoselective hydroacylation of bicyclic alkenes with 2-hydroxybenzaldehydes catalyzed by hydroxoiridium/diene complexes.
Chemical communications (Cambridge, England), 2015, 51, 13791-13794
7117766 CIFC168 H162 Ag3 F18 N18 P3R -335.4661; 35.4661; 26.194
90; 90; 120
28534Mejuto, Carmen; Guisado-Barrios, Gregorio; Gusev, Dmitry; Peris, Eduardo
First homoleptic MIC and heteroleptic NHC-MIC coordination cages from 1,3,5-triphenylbenzene-bridged tris-MIC and tris-NHC ligands.
Chemical communications (Cambridge, England), 2015, 51, 13914-13917
7117767 CIFC31 H25 N O2 SP 1 21/c 113.1; 16.35; 13.048
90; 117.404; 90
2481.1Pi, Rui; Zhou, Ming-Bo; Yang, Yuan; Gao, Cai; Song, Ren-Jie; Li, Jin-Heng
Rhodium(iii)-catalyzed oxidative bicyclization of 4-arylbut-3-yn-1-amines with internal alkynes through C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 13550-13553
7117768 CIFC26 H23 N O2 SP 21 21 219.311; 10.003; 23.556
90; 90; 90
2194Pi, Rui; Zhou, Ming-Bo; Yang, Yuan; Gao, Cai; Song, Ren-Jie; Li, Jin-Heng
Rhodium(iii)-catalyzed oxidative bicyclization of 4-arylbut-3-yn-1-amines with internal alkynes through C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 13550-13553
7117769 CIFC34 H30 Br2 N2 O4 S2P b c a9.5442; 15.093; 45.323
90; 90; 90
6528.8Pi, Rui; Zhou, Ming-Bo; Yang, Yuan; Gao, Cai; Song, Ren-Jie; Li, Jin-Heng
Rhodium(iii)-catalyzed oxidative bicyclization of 4-arylbut-3-yn-1-amines with internal alkynes through C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 13550-13553
7117770 CIFC22 H16 Cl N2 OP 1 21/c 113.5275; 7.5746; 18.3908
90; 111.098; 90
1758.1Kalalbandi, Veerendra Kumar A.; Seetharamappa, J.
1-[(2E)-3-Phenylprop-2-enoyl]-1H-benzimidazoles as anticancer agents: synthesis, crystal structure analysis and binding studies of the most potent anticancer molecule with serum albumin
Med. Chem. Commun., 2015, 6, 1942
7117771 CIFCo2 O4 SiP n m a10.328; 6.019; 4.782
90; 90; 90
297.269Kratochvil, B.; Podlahova, J.; Hasek, J.
Determination of the crystal structure of cobalt(II) orthosilicate
Collection of Czechoslovak Chemical Communication, 1979, 44, 3350-3356
7117772 CIFC16 H21 Br Co N O4C 1 m 18.2934; 13.814; 7.8377
90; 92.388; 90
897.1Jeremy Demarteau; Anthony Kermagoret; Ian German; Daniela Cordella; Koen Robeyns; Julien De Winter; Pascal Gerbaux; Christine Jerome; Antoine Debuigne; Christophe Detrembleur
Halomethyl-cobalt(bis-acetylacetonate) for the controlled synthesis of functional polymers
Chem.Commun., 2015, 51, 14334
7117773 CIFC16 H21 Cl Co N O4C 1 m 18.1891; 13.7998; 7.73787
90; 91.89; 90
873.97Jeremy Demarteau; Anthony Kermagoret; Ian German; Daniela Cordella; Koen Robeyns; Julien De Winter; Pascal Gerbaux; Christine Jerome; Antoine Debuigne; Christophe Detrembleur
Halomethyl-cobalt(bis-acetylacetonate) for the controlled synthesis of functional polymers
Chem.Commun., 2015, 51, 14334
7117774 CIFC10 H10 Cu2 I2 N6 O4P 1 n 14.1982; 14.3433; 13.6017
90; 94.707; 90
816.28P. Amo-Ochoa; K. Hassanein; C. J. Gomez-Garcia; S. Benmansour; J. Perles; O. Castillo; J. I. Martinez; P. Oconf; F. Zamora
Reversible stimulus-responsive Cu(I) iodide pyridine coordination polymer
Chem.Commun., 2015, 51, 14306
7117775 CIFC5 H5 Cu I N3 O2P 1 21/n 14.2284; 14.3638; 13.684
90; 95.241; 90
827.64P. Amo-Ochoa; K. Hassanein; C. J. Gomez-Garcia; S. Benmansour; J. Perles; O. Castillo; J. I. Martinez; P. Oconf; F. Zamora
Reversible stimulus-responsive Cu(I) iodide pyridine coordination polymer
Chem.Commun., 2015, 51, 14306
7117776 CIFC5 H5 Cu I N3 O2P 1 21/c 14.0708; 7.5386; 28.2779
90; 90.88; 90
867.69P. Amo-Ochoa; K. Hassanein; C. J. Gomez-Garcia; S. Benmansour; J. Perles; O. Castillo; J. I. Martinez; P. Oconf; F. Zamora
Reversible stimulus-responsive Cu(I) iodide pyridine coordination polymer
Chem.Commun., 2015, 51, 14306
7117777 CIFC18 H15 N OP 1 21/c 112.7421; 7.5139; 14.7733
90; 106.877; 90
1353.52Bole Yu; Ying Chen; Mei Hong; Pingping Duan; Shifeng Gan; Hui Chao; Zujin Zhao; Jing Zhao
Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chem.Commun., 2015, 51, 14365
7117778 CIFC30 H21 N OP b c a11.1528; 12.1629; 32.522
90; 90; 90
4411.6Bole Yu; Ying Chen; Mei Hong; Pingping Duan; Shifeng Gan; Hui Chao; Zujin Zhao; Jing Zhao
Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chem.Commun., 2015, 51, 14365
7117779 CIFC32 H25 N OP 1 21/c 117.0755; 11.3454; 12.5168
90; 103.806; 90
2354.8Bole Yu; Ying Chen; Mei Hong; Pingping Duan; Shifeng Gan; Hui Chao; Zujin Zhao; Jing Zhao
Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chem.Commun., 2015, 51, 14365
7117780 CIFC32 H23 N OP -19.948; 10.1669; 12.7171
88.203; 70.071; 73.961
1159.31Bole Yu; Ying Chen; Mei Hong; Pingping Duan; Shifeng Gan; Hui Chao; Zujin Zhao; Jing Zhao
Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chem.Commun., 2015, 51, 14365
7117781 CIFC18 H18 Au2 N8 S4C 1 2/c 117.112; 12.896; 11.447
90; 90.276; 90
2526.1Ryan J. Roberts; Debbie Le; Daniel B. Leznoff
Controlling intermolecular aurophilicity in emissive dinuclear Au(I) materials and their luminescent response to ammonia vapour
Chem.Commun., 2015, 51, 14299
7117782 CIFC18 H24 Au2 N6 S4P 1 21/c 19.6338; 22.019; 11.351
90; 91.513; 90
2407Ryan J. Roberts; Debbie Le; Daniel B. Leznoff
Controlling intermolecular aurophilicity in emissive dinuclear Au(I) materials and their luminescent response to ammonia vapour
Chem.Commun., 2015, 51, 14299
7117783 CIFC18 H32 Au2 N8 O S4P 1 21/c 110.5756; 23.18; 11.6908
90; 99.794; 90
2824.1Ryan J. Roberts; Debbie Le; Daniel B. Leznoff
Controlling intermolecular aurophilicity in emissive dinuclear Au(I) materials and their luminescent response to ammonia vapour
Chem.Commun., 2015, 51, 14299
7117784 CIFC22 H20 N2P 1 21 110.8234; 6.6783; 12.8182
90; 108.899; 90
876.58Tsuneomi Kawasaki; Naoya Takamatsu; Shohei Aiba; Yuji Tokunaga
Spontaneous formation and amplification of an enantioenriched alpha-amino nitrile: a chiral precursor for Strecker amino acid synthesis
Chem.Commun., 2015, 51, 14377
7117785 CIFC32 H30 F N O5P 1 21 111.665; 18.047; 13.71
90; 106.488; 90
2767.5Junjun Feng; Xin Li; Jin-Pei Cheng
An asymmetric allylic alkylation reaction of 3-alkylidene oxindoles
Chem.Commun., 2015, 51, 14342
7117786 CIFC20 H34 B2 N2P 1 21/n 110.4675; 14.4066; 13.3847
90; 112.212; 90
1868.64Jeffrey M. Farrell; Douglas W. Stephan
Synthesis of a diboryl-N-heterocycle and its conversion to a bidentate cationic Lewis acid
Chem.Commun., 2015, 51, 14322
7117787 CIFC20 H33 B2 I N2P 1 21/n 114.5093; 7.7961; 18.6255
90; 106.364; 90
2021.5Jeffrey M. Farrell; Douglas W. Stephan
Synthesis of a diboryl-N-heterocycle and its conversion to a bidentate cationic Lewis acid
Chem.Commun., 2015, 51, 14322
7117788 CIFC44 H32 B3 F20 N2P b c a17.2516; 17.706; 27.4233
90; 90; 90
8376.6Jeffrey M. Farrell; Douglas W. Stephan
Synthesis of a diboryl-N-heterocycle and its conversion to a bidentate cationic Lewis acid
Chem.Commun., 2015, 51, 14322
7117789 CIFC40 H30 B2 F8 N2 O2P b c a12.1706; 19.581; 27.574
90; 90; 90
6571.2Yuto Sakano; Ryo Katoono; Kenshu Fujiwara; Takanori Suzuki
Two-way chromic interconversion of the 2,2'-biphenol-6,6'-diyl dication with 5H,10H-dioxapyrene or 9H,10H-4,5-dihydroxyphenanthrene
Chem.Commun., 2015, 51, 14303
7117790 CIFC40 H28 N2 O2P 1 21/c 19.176; 8.514; 18.197
90; 104.035; 90
1379.2Yuto Sakano; Ryo Katoono; Kenshu Fujiwara; Takanori Suzuki
Two-way chromic interconversion of the 2,2'-biphenol-6,6'-diyl dication with 5H,10H-dioxapyrene or 9H,10H-4,5-dihydroxyphenanthrene
Chem.Commun., 2015, 51, 14303
7117791 CIFC44 H38 B2 F8 N2 O4P 1 21/c 120.444; 13.566; 28.627
90; 90.776; 90
7939Yuto Sakano; Ryo Katoono; Kenshu Fujiwara; Takanori Suzuki
Two-way chromic interconversion of the 2,2'-biphenol-6,6'-diyl dication with 5H,10H-dioxapyrene or 9H,10H-4,5-dihydroxyphenanthrene
Chem.Commun., 2015, 51, 14303
7117792 CIFBi2 Cu2 O4 Se2 YI 4/m m m3.86463; 3.86463; 24.428
90; 90; 90
364.841Evans, J.S.O.; Brogden, E.R.; Cordiner, R.L.; Thompson, A.L.
Synthesis and characterisation of the new oxyselenide Bi2 Y O4 Cu2 Se2
Chemical Communications, 2002, 2002, 912-913
7117793 CIFC2 H6 Cu N4 S2P n a 2113.94; 6.01; 8.81
90; 90; 90
738.097Kabesova, M.; Garaj, J.; Gazo, J.
The nature of the structural differences between the modifications of the dithiocyanate-diamine cupric complex
Collection of Czechoslovak Chemical Communication, 1972, 37, 942-950
7117794 CIFGe La2 Mg O6R 3 :H5.5125; 5.5125; 13.3295
90; 90; 120
350.786Swaffer, M.; Slater, P.R.; Matsumura, T.; Kamiyama, T.; Gover, R.K.B.; Kanno, R.
La2 Mg Ge O6 : a novel Ge based perovskite synthesised under ambient pressure
Chemical Communications, 2002, 2002, 1776-1777
7117795 CIFC13 H17 Br O5P n a 2114.3578; 11.7005; 8.2619
90; 90; 90
1387.9Jola Pospech; Alastair J. J. Lennox; Matthias Beller
Rhodium-catalysed alkoxylation/acetalization of diazo compounds: one-step synthesis of highly functionalised quaternary carbon centres
Chem.Commun., 2015, 51, 14505
7117796 CIFC20 H22 O7P 1 21/n 19.7096; 7.1009; 26.6401
90; 100.031; 90
1808.68Jola Pospech; Alastair J. J. Lennox; Matthias Beller
Rhodium-catalysed alkoxylation/acetalization of diazo compounds: one-step synthesis of highly functionalised quaternary carbon centres
Chem.Commun., 2015, 51, 14505
7117797 CIFC12 H15 Br O5P 1 21/c 112.7047; 8.5755; 13.6576
90; 115.546; 90
1342.52Jola Pospech; Alastair J. J. Lennox; Matthias Beller
Rhodium-catalysed alkoxylation/acetalization of diazo compounds: one-step synthesis of highly functionalised quaternary carbon centres
Chem.Commun., 2015, 51, 14505
7117798 CIFC25 H18 OP 1 21 18.2582; 6.2091; 17.8371
90; 103.148; 90
890.64Beom Shin Cho; Young Keun Chung
Palladium-catalyzed bisarylation of 3-alkylbenzofurans to 3-arylalkyl-2-arylbenzofurans on water: tandem C(sp3)-H and C(sp2)-H activation reactions of 3-alkylbenzofurans
Chem.Commun., 2015, 51, 14543
7117799 CIFC19 H25 N O4P 21 21 215.8467; 17.0069; 17.374
90; 90; 90
1727.57Jorge M. M. Verkade; Peter J. L. M. Quaedflieg; Gerard K. M. Verzijl; Laurent Lefort; Floris L. van Delft; Johannes G. de Vries; Floris P. J. T. Rutjes
Enantio- and diastereoselective synthesis of upsilon-amino alcohol
Chem.Commun., 2015, 51, 14462
7117800 CIFC75 H84 F12 Fe2 N17 O16 S4P 1 21/n 116.179; 15.362; 17.899
90; 90.91; 90
4448Sujoy Rana; Aniruddha Dey; Debabrata Maiti
Mechanistic elucidation of C-H oxidation by electron rich non-heme iron(IV)-oxo at room temperature
Chem.Commun., 2015, 51, 14469
7117801 CIFC149 H135 Cl3 N12 O Zn2P -112.1388; 21.415; 25.499
83.635; 80.874; 83.613
6474.6Tuan Anh Pham; Fei Song; Mariza N. Alberti; Manh-Thuong Nguyen; Nils Trapp; Carlo Thilgen; Francois Diederich; Meike Stohr
Heat-induced formation of one-dimensional coordination polymers on Au(111): an STM study
Chem.Commun., 2015, 51, 14473
7117802 CIFC23 H18 N4 O SP 1 21/c 17.387; 32.39; 8.251
90; 92.434; 90
1972Masood Ayoub Kaloo; Jeyaraman Sankar
Reusable and specific proton transfer signalling by inorganic cyanide in solution and solid phase
Chem.Commun., 2015, 51, 14528
7117803 CIFC47 H36 B N OC 1 2/c 119.192; 10.293; 35.255
90; 96.3; 90
6922Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Florian Rauch
O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones
Chem.Commun., 2015, 51, 14513
7117804 CIFC50 H42 B N OP -112.592; 15.365; 20.175
103.7; 92.293; 94.425
3774Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Florian Rauch
O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones
Chem.Commun., 2015, 51, 14513
7117805 CIFC51 H46 B N OP 1 21/n 113.873; 17.556; 16.244
90; 102.03; 90
3869Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Florian Rauch
O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones
Chem.Commun., 2015, 51, 14513
7117806 CIFC48 H46 B N OP 1 21/c 110.604; 32.49; 11.704
90; 114.4; 90
3672Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Florian Rauch
O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones
Chem.Commun., 2015, 51, 14513
7117807 CIFC152 H120 Cd8 N4 O54P 1 21 117.656; 16.2741; 26.219
90; 90.609; 90
7533.2Yun-Hu Han; Yue-Cheng Liu; Xiu-Shuang Xing; Chong-Bin Tian; Ping Lin; Shao-Wu Du
Chiral template induced homochiral MOFs built from achiral components: SHG enhancement and enantioselective sensing of chiral alkamines by ion-exchange
Chem.Commun., 2015, 51, 14481
7117808 CIFC152 H120 Cd8 N4 O54P 1 21 117.745; 16.263; 26.25
90; 90.775; 90
7575Yun-Hu Han; Yue-Cheng Liu; Xiu-Shuang Xing; Chong-Bin Tian; Ping Lin; Shao-Wu Du
Chiral template induced homochiral MOFs built from achiral components: SHG enhancement and enantioselective sensing of chiral alkamines by ion-exchange
Chem.Commun., 2015, 51, 14481
7117809 CIFC74.1 H109.2 Mg2 N6P 1 21/c 118.9579; 19.7413; 18.7107
90; 99.765; 90
6901.1Catherine Weetman; Michael S. Hill; Mary F. Mahon
Magnesium-catalysed hydroboration of isonitriles
Chem.Commun., 2015, 51, 14477
7117810 CIFC24 H15 Co6 N13 O12P 21 317.4611; 17.4611; 17.4611
90; 90; 90
5323.72Ya-Dong Yu; Chan Luo; Bao-Yu Liu; Xiao-Chun Huang; Dan Li
Spontaneous symmetry breaking of Co(II) metal-organic frameworks from achiral precursors via asymmetrical crystallization
Chem.Commun., 2015, 51, 14489
7117811 CIFC24 H15 Co6 N13 O12P 21 317.4882; 17.4882; 17.4882
90; 90; 90
5348.54Ya-Dong Yu; Chan Luo; Bao-Yu Liu; Xiao-Chun Huang; Dan Li
Spontaneous symmetry breaking of Co(II) metal-organic frameworks from achiral precursors via asymmetrical crystallization
Chem.Commun., 2015, 51, 14489
7117812 CIFC24 H14 Co6 N12 O13P 21 317.5279; 17.5279; 17.5279
90; 90; 90
5385Ya-Dong Yu; Chan Luo; Bao-Yu Liu; Xiao-Chun Huang; Dan Li
Spontaneous symmetry breaking of Co(II) metal-organic frameworks from achiral precursors via asymmetrical crystallization
Chem.Commun., 2015, 51, 14489
7117813 CIFC33 H25 N O3P 1 21/n 115.116; 11.464; 15.484
90; 105.324; 90
2587.8Rong Zhou; Kai Zhang; Yusong Chen; Qiang Meng; Yiyi Liu; Ruifeng Li; Zhengjie He
P(NMe2)3-mediated reductive [1+4] annulation of isatins with enones: a facile synthesis of spirooxindole-dihydrofurans
Chem.Commun., 2015, 51, 14663
7117814 CIFC31 H22 Br N O3P 1 21/n 115.016; 11.906; 15.221
90; 100.25; 90
2677.8Rong Zhou; Kai Zhang; Yusong Chen; Qiang Meng; Yiyi Liu; Ruifeng Li; Zhengjie He
P(NMe2)3-mediated reductive [1+4] annulation of isatins with enones: a facile synthesis of spirooxindole-dihydrofurans
Chem.Commun., 2015, 51, 14663
7117815 CIFC27 H19 N3 O3C 1 2/c 121.917; 9.529; 23.123
90; 115.112; 90
4373Rong Zhou; Kai Zhang; Yusong Chen; Qiang Meng; Yiyi Liu; Ruifeng Li; Zhengjie He
P(NMe2)3-mediated reductive [1+4] annulation of isatins with enones: a facile synthesis of spirooxindole-dihydrofurans
Chem.Commun., 2015, 51, 14663
7117816 CIFC25 H55 B2 O7 P2 RhP 1 21/n 110.9348; 25.1626; 12.1658
90; 93.209; 90
3342.1Sabrina I. Kallane; Thomas Braun; Michael Teltewskoi; Beatrice Braun; Roy Herrmann; Reik Laubenstein
Remarkable reactivity of a rhodium(I) boryl complex towards CO2 and CS2: isolation of a carbido complex
Chem.Commun., 2015, 51, 14613
7117817 CIFC24 H57 B O3 P3 RhP 1 21 110.8214; 13.3028; 11.7681
90; 113.017; 90
1559.21Sabrina I. Kallane; Thomas Braun; Michael Teltewskoi; Beatrice Braun; Roy Herrmann; Reik Laubenstein
Remarkable reactivity of a rhodium(I) boryl complex towards CO2 and CS2: isolation of a carbido complex
Chem.Commun., 2015, 51, 14613
7117818 CIFC25 H47 B N O3 P2 RhP 19.0037; 11.2268; 15.1421
83.982; 80.95; 82.455
1492.9Sabrina I. Kallane; Thomas Braun; Michael Teltewskoi; Beatrice Braun; Roy Herrmann; Reik Laubenstein
Remarkable reactivity of a rhodium(I) boryl complex towards CO2 and CS2: isolation of a carbido complex
Chem.Commun., 2015, 51, 14613
7117819 CIFC81 H181 B4 O8 P8 Rh4 S4C 1 2/c 140.16; 15.9681; 20.1668
90; 118.333; 90
11383.3Sabrina I. Kallane; Thomas Braun; Michael Teltewskoi; Beatrice Braun; Roy Herrmann; Reik Laubenstein
Remarkable reactivity of a rhodium(I) boryl complex towards CO2 and CS2: isolation of a carbido complex
Chem.Commun., 2015, 51, 14613
7117820 CIFC17 H20 O5P b c a14.3785; 10.3694; 19.867
90; 90; 90
2962.1Dong Chen; Hao-Miao Liu; Ming-Ming Li; Yong-Min Yan; Wen-Dan Xu; Xiao-Nian Li; Yong-Xian Cheng; Hong-Bo Qin
Concise synthesis of (+/-)-Lingzhiol via epoxy-arene cyclization
Chem.Commun., 2015, 51, 14594
7117821 CIFC20 H17 Cl O4P 1 21 19.7149; 5.7291; 15.133
90; 91.157; 90
842.1Qijian Ni; Jiawen Xiong; Xiaoxiao Song; Gerhard Raabe; Dieter Enders
NHC-catalyzed activation of alpha,beta-unsaturated N-acyltriazoles: an easy access to dihydropyranones
Chem.Commun., 2015, 51, 14628
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
7117863 CIFCu2 S4 WI -4 2 m5.44427; 5.44427; 10.0687
90; 90; 90
298.437Crossland, C.J.; Evans, J.S.O.
Synthesis and characterisation of a new high pressure polymorph of Cu2 W S4
Chemical Communications, 2003, 2003, 2292-2293
7117864 CIFC23 H23 F N4 O5P 1 21/c 17.8954; 24.3573; 12.7445
90; 94.249; 90
2444.2Sha, Shao; Han, Hong-Wei; Gao, Fei; Liu, Tian-Bao; Li, Zhen; Xu, Chi; Zhong, Wei-Qing; Zhu, Hai-Liang
Discovery of fluoroquinolone derivatives as potent, selective inhibitors of PI3Kγ
Med. Chem. Commun., 2015, 6, 2029
7117865 CIFBa2 F2 O2 PdI 4/m m m4.1398; 4.1398; 14.0459
90; 90; 90
240.718Baikie, T.; Rooms, J.F.; Dixon, E.L.; Young, N.A.; Francesconi, M.G.
Ba2-x Srx Pd O2 F2 (0 <= x <= 1.5): the first palladium - oxide - fluorides
Chemical Communications, 2003, 2003, 1580-1581
7117866 CIFBa0.5 F2 O2 Pd Sr1.5I 4/m m m4.0701; 4.0701; 13.1072
90; 90; 90
217.13Baikie, T.; Dixon, E.L.; Rooms, J.F.; Francesconi, M.G.; Young, N.A.
Ba2-x Srx Pd O2 F2 (0 <= x <= 1.5): the first palladium - oxide - fluorides
Chemical Communications, 2003, 2003, 1580-1581
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
7117898 CIFAl3 Na7 O8P -17.972; 5.851; 11.272
89.71; 110.57; 108.99
461.902Barker, M.G.; Gadd, P.G.; Begley, M.J.
Preparation and crystal structures of the first alkali-rich sodium aluminates Na7 Al3 O8 and Na5 Al O4
Journal of the Chemical Society. Chemical Communications (1972-), 1981, 1981, 379-381
7117899 CIFAl Na5 O4P b c a5.894; 17.87; 10.095
90; 90; 90
1063.26Barker, M.G.; Gadd, P.G.; Begley, M.J.
Preparation and crystal structures of the first alkali-rich sodium aluminates Na7 Al3 O8 and Na5 Al O4
Journal of the Chemical Society. Chemical Communications (1972-), 1981, 1981, 379-381
7117900 CIFAs2 F12 I4A 1 2/m 15.907; 9.815; 12.514
90; 103.71; 90
704.855Gillespie, R.J.; Kapoor, R.; Faggiani, R.; Murchie, M.; Lock, C.J.L.; Passmore, J.
The I4(2+) cation. X-Ray Crystal structures of (I4(2+)) (As F6(-))2 and (I4(2+)) (Sb3 F14(-)) (Sb F6(-))
Journal of the Chemical Society. Chemical Communications (1972-), 1983, 1983, 8-9
7117901 CIFF20 I4 Sb4P 1 21/c 18.425; 15.98; 16.804
90; 100.53; 90
2224.25Gillespie, R.J.; Faggiani, R.; Kapoor, R.; Lock, C.J.L.; Passmore, J.; Murchie, M.
The I4(2+) cation. X-Ray Crystal structures of (I4(2+)) (As F6(-))2 and (I4(2+)) (Sb3 F14(-)) (Sb F6(-))
Journal of the Chemical Society. Chemical Communications (1972-), 1983, 1983, 8-9
7117902 CIFCl2 Co H18 N6F m -3 m10.122; 10.122; 10.122
90; 90; 90
1037.05Barnet, M. T.; Craven, B. M.; Freeman, H. C.; Kime, N. E.; Ibers, J. A.
The Co-N bond length in Co(II) and Co(III) hexammines
Chemical Communications (London), 1966, 307-308
7117903 CIFCo H18 I3 N6F m -3 m10.82; 10.82; 10.82
90; 90; 90
1266.72Barnet, M. T.; Craven, B. M.; Freeman, H. C.; Kime, N. E.; Ibers, J. A.
The Co-N bond length in Co(II) and Co(III) hexammines
Chemical Communications (London), 1966, 307-308
7117904 CIFF4 S WP c a 2116.934; 5.514; 9.46
90; 90; 90
883.319Holloway, J.H.; Kaucic, V.; Russell, D.R.
Synthesis, Chemistry, and Crystal Structures of High-valent Transition-metal Chalcogenide Fluorides and Their Derivatives
Journal of the Chemical Society. Chemical Communications (1972-), 1983, 1983, 1079-1081
7117905 CIFF4 Re SP c a 2110.893; 8.278; 27.663
90; 90; 90
2494.44Holloway, J.H.; Kaucic, V.; Russell, D.R.
Synthesis, Chemistry, and Crystal Structures of High-valent Transition-metal Chalcogenide Fluorides and Their Derivatives
Journal of the Chemical Society. Chemical Communications (1972-), 1983, 1983, 1079-1081
7117906 CIFAs2 Co F28 N8 O6 S9P 1 21/c 117.126; 11.424; 18.441
90; 116.54; 90
3227.74Hoppenheit, R.; Lork, E.; Petersen, J.; Mews, R.
A sulfur nitrogen triple, double and single bond in one ligand: synthesis and structure of (Co (N S F2 N S (O) F2)4) (As F6)2 S O2
Chemical Communications, 1997, 1997, 1659-1660
7117907 CIFC11 H3 N O11 Ru4P -19.554; 12.743; 16.012
91.39; 96.23; 90.59
1937.16Collins, M.A.; McPartlin, M.; Johnson, B.F.G.; Lewis, J.; Raithby, P.R.; Morris, J.; Mace, J.M.; Nelson, W.J.H.; Puga, J.
Formation of Nitride Clusters by the Action of N O(+) on (M4 H3 (C O)12)(-) (M= Ru, Os): the Synthesis and Structural Characterization of (Ru4(mue-H)3(C O)11 (mue 4-N)) and (N(P Ph3)2)(Os4(C O)12(mue 4-N))
Journal of the Chemical Society. Chemical Communications (1972-), 1983, 1983, 689-691
7117908 CIFC16 O15 Ru5P 1 21/c 116.448; 14.274; 20.834
90; 91.358; 90
4890.01Farrar, D.H.; McPartlin, M.; Johnson, B.F.G.; Lewis, J.; Nicholls, J.N.; Jackson, P.F.
A high-yield synthesis of Ru5 C (C O)15 by the carbonylation of Ru6 C (C O)17; the x-ray structure analyses of Ru5 C (C O)15 and Ru5 C (C O)14 P Ph3
Journal of the Chemical Society. Chemical Communications (1972-), 1981, 1981, 415-416
7117909 CIFC8 Cl4 Ge O8 Os2P 1 n 110.038; 21.042; 13.385
90; 106.81; 90
2706.37Einstein, F.W.B.; Rushman, P.; Pomeroy, R.K.; Willis, A.C.
Preparation and Crystal Structure of (O C)5 Os Os(C O)3 (Ge Cl3)(Cl): A Compound With an Unsupported, Donor-Acceptor Metal-Metal Bond
Journal of the Chemical Society. Chemical Communications (1972-), 1983, 1983, 854-855
7117910 CIFAs Cs F4P 1 21 16.5966; 4.8723; 8.4922
90; 111.92; 90
253.212Klampfer, P.; Benkic, P.; Lesar, A.; Volavsek, B.; Ponikvar, M.; Jesih, A.
New alkalimetal and tetramethylammonium tetrafluoroarsenates(III), their vibrational spectra and crystal structure of cesium tetrafluoroarsenate(III)
Collection of Czechoslovak Chemical Communication, 2004, 69, 339-350
7117911 CIFH3 K O6 SC 1 2/c 118.392; 7.701; 7.498
90; 90.89; 90
1061.86Flanagan, J.; Griffith, W.P.; Skapski, A.C.
The active principle of Caro's acid, (HS O5)(-): X-ray crystal structure of K H S O4 (H2 O)
Journal of the Chemical Society. Chemical Communications (1972-), 1984, 1984, 1574-1575
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
7117935 CIFC10 H2 O10 Os3P -18.604; 11.887; 9.225
80.19; 118.53; 98.98
813.755Orpen, A.G.; Rivera, A.V.; Bryan, E.G.; Pippard, D.; Sheldrick, G.M.; Rouse, K.D.
Bridging Hydrides in (H2 Os3 (C O)10) and ((C2 H3) H Os3 (C O)10): A Combined X-Ray - Neutron Diffraction Study
Journal of the Chemical Society. Chemical Communications (1972-), 1978, 1978, 723-724
7117936 CIFC8 Cl4 Fe2 N3 O8 P3P 1 21 18.15; 16.723; 15.556
90; 97.22; 90
2103.35Suszko, P.R.; Allcock, H.R.; Whittle, R.R.
Synthesis of a Di-iron-spirocyclotriphosphazene and a Tri-iron-cluster-cyclotriphosphazene
Journal of the Chemical Society. Chemical Communications (1972-), 1982, 1982, 1344-1344
7117937 CIFC10 Cl4 Fe3 N3 O10 P3P 42/n :224.153; 24.153; 8.468
90; 90; 90
4939.96Suszko, P.R.; Whittle, R.R.; Allcock, H.R.
Synthesis of a Di-iron-spirocyclotriphosphazene and a Tri-iron-cluster-cyclotriphosphazene
Journal of the Chemical Society. Chemical Communications (1972-), 1982, 1982, 1344-1344
7117938 CIFH44 K2 Na6 O58 Pd2 W10P -19.229; 11.277; 15.102
108.33; 96.15; 109.74
1363.7Angus-Dunne, S.J.; Burns, R.C.; Craig, D.C.; Lawrance, G.A.
A novel hetropolymetalate containing palladsium(II): Synthesis and crystal structure of K2 Na6 (Pd2 W10 O36) . 22(H2 O)
Journal of the Chemical Society. Chemical Communications (1972-), 1994, 1994, 523-524
7117939 CIFCl Cs N O4 TcP 21 21 216.376; 8.552; 11.406
90; 90; 90
621.941Baldas, J.; Colmanet, S.F.; MacKay, M.F.
Preparation and structure of Cs (Tc N (O2)2 Cl); the first example of a nitridoperoxo complex
Journal of the Chemical Society. Chemical Communications (1972-), 1989, 1989, 1890-1891
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
7117971 CIFC18 H Bi O18 Ru5P -111.378; 16.286; 17.391
73.52; 89.71; 80.22
3042.12Johnson, B.F.G.; Lewis, J.; Raithby, P.R.; Whitton, A.J.
Synthesis and characterisation of the hexanuclear bimetallic Cluster, (Ru2 (C O)8) (mue4-Bi) ((mue-H) Ru3 (C O)10)
Journal of the Chemical Society. Chemical Communications (1972-), 1988, 1988, 401-402
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
7117995 CIFC26 H15 B F2 I2C 1 2/c 120.082; 9.3614; 14.777
90; 126.854; 90
2222.9Schickedanz, Kai; Trageser, Timo; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A boron-doped helicene as a highly soluble, benchtop-stable green emitter
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 15808-15810
7117996 CIFC26 H15 B Br4P 1 21/c 112.6333; 14.6789; 12.1639
90; 94.908; 90
2247.4Schickedanz, Kai; Trageser, Timo; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A boron-doped helicene as a highly soluble, benchtop-stable green emitter
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 15808-15810
7117997 CIFC26 H15 BP 21 21 213.9791; 19.948; 20.208
90; 90; 90
1604Schickedanz, Kai; Trageser, Timo; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A boron-doped helicene as a highly soluble, benchtop-stable green emitter
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 15808-15810
7117998 CIFC31 H20 B NF -4 3 c48.2907; 48.2907; 48.2907
90; 90; 90
112614Schickedanz, Kai; Trageser, Timo; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A boron-doped helicene as a highly soluble, benchtop-stable green emitter
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 15808-15810
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
7118020 CIFC116 H128 Cl4 N12 O12P 1 21 19.2218; 27.5508; 24.8963
90; 92.701; 90
6318.3Zhao, Xiaohu; Liu, Xiaohua; Xiong, Qian; Mei, Hongjiang; Ma, Baiwei; Lin, Lili; Feng, Xiaoming
The asymmetric synthesis of polycyclic 3-spirooxindole alkaloids via the cascade reaction of 2-isocyanoethylindoles
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 16076-16079
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
7118033 CIFC25 H23.8 F3 N5 O3.4P 1 21/c 113.8619; 10.1495; 17.3464
90; 104.941; 90
2357.98Bernard-Gauthier, Vadim; Bailey, Justin J.; Aliaga, Arturo; Kostikov, Alexey; Rosa-Neto, Pedro; Wuest, Melinda; Brodeur, Garrett M.; Bedell, Barry J.; Wuest, Frank; Schirrmacher, Ralf
Development of subnanomolar radiofluorinated (2-pyrrolidin-1-yl)imidazo[1,2-b]pyridazine pan-Trk inhibitors as candidate PET imaging probes
Med. Chem. Commun., 2015, 6, 2184
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
7118048 CIFC69 H66 Cd4 N12 O29R 3 2 :H26.9207; 26.9207; 20.9044
90; 90; 120
13120.2Wu, Xin; Zhang, Hua-Bin; Xu, Zhong-Xuan; Zhang, Jian
Asymmetric induction in homochiral MOFs: from interweaving double helices to single helices
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 16331-16333
7118049 CIFC69 H66 Cd4 N12 O29R 3 2 :H26.8706; 26.8706; 20.9
90; 90; 120
13068.7Wu, Xin; Zhang, Hua-Bin; Xu, Zhong-Xuan; Zhang, Jian
Asymmetric induction in homochiral MOFs: from interweaving double helices to single helices
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 16331-16333
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
7118058 CIFC20 H18 Br2 N2 O4 ZnP 1 21/c 15.06412; 18.1609; 11.4569
90; 97.646; 90
1044.31Zhang, Hai-Rong; Liu, Yan-Cheng; Meng, Ting; Qin, Qi-Pin; Tang, Shang-Feng; Chen, Zhen-Feng; Zou, Bi-Qun; Liu, You-Nian; Liang, Hong
Cytotoxicity, DNA binding and cell apoptosis induction of a zinc(ii) complex of HBrQ
Med. Chem. Commun., 2015, 6, 2224
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
7118071 CIFC8 H6 Ag N3 O3P n a 2113.678; 10.566; 12.076
90; 90; 90
1745.2Savić, Nada D.; Glišić, Biljana Đ.; Wadepohl, Hubert; Pavic, Aleksandar; Senerovic, Lidija; Nikodinovic-Runic, Jasmina; Djuran, Miloš I.
Silver(i) complexes with quinazoline and phthalazine: synthesis, structural characterization and evaluation of biological activities
Med. Chem. Commun., 2016, 7, 282
7118072 CIFC20 H18 Ag2 B2 F8 N6P -17.544; 8.109; 11.175
110.495; 99.22; 98.036
617.7Savić, Nada D.; Glišić, Biljana Đ.; Wadepohl, Hubert; Pavic, Aleksandar; Senerovic, Lidija; Nikodinovic-Runic, Jasmina; Djuran, Miloš I.
Silver(i) complexes with quinazoline and phthalazine: synthesis, structural characterization and evaluation of biological activities
Med. Chem. Commun., 2016, 7, 282
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

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