Crystallography Open Database

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4516116 CIFC22 H18 Mn N4 O10P b c a7.5725; 11.9171; 24.932
90; 90; 90
2249.9Roy, Manasi; Adhikary, Amit; Mondal, Amit Kumar; Mondal, Raju
Multifunctional Properties of a 1D Helical Co(II) Coordination Polymer: Toward Single-Ion Magnetic Behavior and Efficient Dye Degradation.
ACS omega, 2018, 3, 15315-15324
4516117 CIFC22 H18 Co N4 O10P b c a7.4271; 11.953; 24.759
90; 90; 90
2198Roy, Manasi; Adhikary, Amit; Mondal, Amit Kumar; Mondal, Raju
Multifunctional Properties of a 1D Helical Co(II) Coordination Polymer: Toward Single-Ion Magnetic Behavior and Efficient Dye Degradation.
ACS omega, 2018, 3, 15315-15324
4516118 CIFC55 H47 Co2 N10 O10P 1 21/n 110.0616; 10.8559; 26.2066
90; 97.322; 90
2839.1Roy, Manasi; Adhikary, Amit; Mondal, Amit Kumar; Mondal, Raju
Multifunctional Properties of a 1D Helical Co(II) Coordination Polymer: Toward Single-Ion Magnetic Behavior and Efficient Dye Degradation.
ACS omega, 2018, 3, 15315-15324
4516119 CIFC30 H27 N OP -18.9867; 9.0117; 14.865
99.135; 106.863; 90.159
1136Chen, Jianfeng; Tian, Jiaxin; Liu, Feng; Liu, Yong; Zhao, Guoqing; Yuan, Weicheng; Zhao, Baoguo
Intramolecular Umpolung Synthesis of Exocyclic β-Amino Alcohols through Decarboxylative Amination.
ACS omega, 2018, 3, 14671-14679
4516120 CIFC16 H14 Cl N O2P 21 21 214.6994; 11.1712; 25.7495
90; 90; 90
1351.8Chen, Jianfeng; Tian, Jiaxin; Liu, Feng; Liu, Yong; Zhao, Guoqing; Yuan, Weicheng; Zhao, Baoguo
Intramolecular Umpolung Synthesis of Exocyclic β-Amino Alcohols through Decarboxylative Amination.
ACS omega, 2018, 3, 14671-14679
4516121 CIFC55 H54 B Br Cl9 F4 N5 O9 P2 PdP 114.1735; 14.6182; 17.4983
110.609; 92.046; 100.845
3312.32Leitão, Maria Inês P S; Herrera, Federico; Petronilho, Ana
N-Heterocyclic Carbenes Derived from Guanosine: Synthesis and Evidences of Their Antiproliferative Activity.
ACS omega, 2018, 3, 15653-15656
4516122 CIFC15 H12 N2C 1 2/c 116.9414; 17.1524; 17.6605
90; 109.597; 90
4834.6Mohamady, Samy; Kralt, Braden; Samwel, Shery K.; Taylor, Scott D.
Efficient One-Pot, Two-Component Modular Synthesis of 3,5-Disubstituted Pyrazoles.
ACS omega, 2018, 3, 15566-15574
4516123 CIFC22 H18 N2 O3P b c a15.6529; 9.5364; 23.3615
90; 90; 90
3487.2Cai, Panyuan; Zhang, Enshen; Wu, Yinsong; Fang, Taibei; Li, Qianqian; Yang, Chen; Wang, Jian; Shang, Yongjia
Ru(II)/Ir(III)-Catalyzed C-H Bond Activation/Annulation of Cyclic Amides with 1,3-Diketone-2-diazo Compounds: Facile Access to 8<i>H</i>-Isoquinolino[1,2-<i>b</i>]quinazolin-8-ones and Phthalazino[2,3-<i>a</i>]cinnoline-8,13-diones.
ACS omega, 2018, 3, 14575-14584
4516124 CIFC21 H16 N2 O2P b c a16.3607; 8.454; 22.5078
90; 90; 90
3113.13Cai, Panyuan; Zhang, Enshen; Wu, Yinsong; Fang, Taibei; Li, Qianqian; Yang, Chen; Wang, Jian; Shang, Yongjia
Ru(II)/Ir(III)-Catalyzed C-H Bond Activation/Annulation of Cyclic Amides with 1,3-Diketone-2-diazo Compounds: Facile Access to 8<i>H</i>-Isoquinolino[1,2-<i>b</i>]quinazolin-8-ones and Phthalazino[2,3-<i>a</i>]cinnoline-8,13-diones.
ACS omega, 2018, 3, 14575-14584
4516125 CIFC39 H21 Fe N8 O2 SnP 1 21/c 113.9836; 20.8953; 11.0131
90; 103.717; 90
3126.16Konarev, Dmitri V.; Kuzmin, Alexey V.; Batov, Mikhail S.; Khasanov, Salavat S.; Otsuka, Akihiro; Yamochi, Hideki; Kitagawa, Hiroshi; Lyubovskaya, Rimma N.
{CpFe<sup>II</sup>(CO)<sub>2</sub>Sn<sup>II</sup>(Macrocycle<sup>•3-</sup>)} Radicals with Intrinsic Charge Transfer from CpFe(CO)<sub>2</sub> to Macrocycles (Cp: Cp or Cp*); Effective Magnetic Coupling between Radical Trianionic Macrocycles<sup>•3</sup>.
ACS omega, 2018, 3, 14875-14888
4516126 CIFC39 H21 Fe N8 O2 SnP -111.7126; 11.7544; 12.9014
108.604; 101.649; 105.849
1535.85Konarev, Dmitri V.; Kuzmin, Alexey V.; Batov, Mikhail S.; Khasanov, Salavat S.; Otsuka, Akihiro; Yamochi, Hideki; Kitagawa, Hiroshi; Lyubovskaya, Rimma N.
{CpFe<sup>II</sup>(CO)<sub>2</sub>Sn<sup>II</sup>(Macrocycle<sup>•3-</sup>)} Radicals with Intrinsic Charge Transfer from CpFe(CO)<sub>2</sub> to Macrocycles (Cp: Cp or Cp*); Effective Magnetic Coupling between Radical Trianionic Macrocycles<sup>•3</sup>.
ACS omega, 2018, 3, 14875-14888
4516127 CIFC47 H33 Cl Fe N8 O2 SnP -110.3737; 11.6856; 16.95
90.491; 91.962; 98.758
2029.38Konarev, Dmitri V.; Kuzmin, Alexey V.; Batov, Mikhail S.; Khasanov, Salavat S.; Otsuka, Akihiro; Yamochi, Hideki; Kitagawa, Hiroshi; Lyubovskaya, Rimma N.
{CpFe<sup>II</sup>(CO)<sub>2</sub>Sn<sup>II</sup>(Macrocycle<sup>•3-</sup>)} Radicals with Intrinsic Charge Transfer from CpFe(CO)<sub>2</sub> to Macrocycles (Cp: Cp or Cp*); Effective Magnetic Coupling between Radical Trianionic Macrocycles<sup>•3</sup>.
ACS omega, 2018, 3, 14875-14888
4516128 CIFC72 H47 Cl4 Fe N8 O2 SnP -111.6681; 16.5135; 16.9193
66.775; 86.024; 79.263
2943.4Konarev, Dmitri V.; Kuzmin, Alexey V.; Batov, Mikhail S.; Khasanov, Salavat S.; Otsuka, Akihiro; Yamochi, Hideki; Kitagawa, Hiroshi; Lyubovskaya, Rimma N.
{CpFe<sup>II</sup>(CO)<sub>2</sub>Sn<sup>II</sup>(Macrocycle<sup>•3-</sup>)} Radicals with Intrinsic Charge Transfer from CpFe(CO)<sub>2</sub> to Macrocycles (Cp: Cp or Cp*); Effective Magnetic Coupling between Radical Trianionic Macrocycles<sup>•3</sup>.
ACS omega, 2018, 3, 14875-14888
4516129 CIFC51 H33 Fe N4 O2 SnP -111.2634; 11.312; 14.9929
90.824; 91.078; 97.186
1894.66Konarev, Dmitri V.; Kuzmin, Alexey V.; Batov, Mikhail S.; Khasanov, Salavat S.; Otsuka, Akihiro; Yamochi, Hideki; Kitagawa, Hiroshi; Lyubovskaya, Rimma N.
{CpFe<sup>II</sup>(CO)<sub>2</sub>Sn<sup>II</sup>(Macrocycle<sup>•3-</sup>)} Radicals with Intrinsic Charge Transfer from CpFe(CO)<sub>2</sub> to Macrocycles (Cp: Cp or Cp*); Effective Magnetic Coupling between Radical Trianionic Macrocycles<sup>•3</sup>.
ACS omega, 2018, 3, 14875-14888
4516130 CIFC39 H21 Fe In N8 O2P 1 21/c 113.977; 21.1365; 11.0927
90; 105.033; 90
3164.91Konarev, Dmitri V.; Kuzmin, Alexey V.; Batov, Mikhail S.; Khasanov, Salavat S.; Otsuka, Akihiro; Yamochi, Hideki; Kitagawa, Hiroshi; Lyubovskaya, Rimma N.
{CpFe<sup>II</sup>(CO)<sub>2</sub>Sn<sup>II</sup>(Macrocycle<sup>•3-</sup>)} Radicals with Intrinsic Charge Transfer from CpFe(CO)<sub>2</sub> to Macrocycles (Cp: Cp or Cp*); Effective Magnetic Coupling between Radical Trianionic Macrocycles<sup>•3</sup>.
ACS omega, 2018, 3, 14875-14888
4516131 CIFC32 H63 Cl3 Cu2 N11 O12.5P b c n24.6695; 18.6531; 20.3858
90; 90; 90
9380.8Invernici, Michele; Ciarrocchi, Carlo; Dondi, Daniele; Fabbrizzi, Luigi; Lazzaroni, Simone; Licchelli, Maurizio; Boiocchi, Massimo; Bonizzoni, Marco
Bimacrocyclic Effect in Anion Recognition by a Copper(II) Bicyclam Complex.
ACS omega, 2018, 3, 15692-15701
4516132 CIFC23 H18 N6P n a 2112.7702; 28.911; 5.2268
90; 90; 90
1929.7Banerji, Biswadip; Chandrasekhar, Kadaiahgari; Sreenath, Kancham; Roy, Saheli; Nag, Sayoni; Saha, Krishna Das
Synthesis of Triazole-Substituted Quinazoline Hybrids for Anticancer Activity and a Lead Compound as the EGFR Blocker and ROS Inducer Agent.
ACS omega, 2018, 3, 16134-16142
4516133 CIFC24 H14 N2 OP 1 21/c 115.833; 6.44809; 15.5345
90; 90.5223; 90
1585.89Tabasi, Zahra A.; Younes, Eyad A.; Walsh, Joshua C.; Thompson, David W.; Bodwell, Graham J.; Zhao, Yuming
Pyrenoimidazolyl-Benzaldehyde Fluorophores: Synthesis, Properties, and Sensing Function for Fluoride Anions.
ACS omega, 2018, 3, 16387-16397
4516134 CIFC28 H26 N2 O3 S2P 1 21/n 113.7747; 8.1613; 22.0303
90; 102.249; 90
2420.25Tabasi, Zahra A.; Younes, Eyad A.; Walsh, Joshua C.; Thompson, David W.; Bodwell, Graham J.; Zhao, Yuming
Pyrenoimidazolyl-Benzaldehyde Fluorophores: Synthesis, Properties, and Sensing Function for Fluoride Anions.
ACS omega, 2018, 3, 16387-16397
4516135 CIFC34 H32 Cl2 Cu2 N6 P2P 1 21/n 113.4961; 7.3977; 17.2981
90; 108.456; 90
1638.22Kumar, Saurabh; Mondal, Dipanjan; Balakrishna, Maravanji S.
Diverse Architectures and Luminescence Properties of Group 11 Complexes Containing Pyrimidine-Based Phosphine, <i>N</i>-((Diphenylphosphine)methyl)pyrimidin-2-amine.
ACS omega, 2018, 3, 16601-16614
4516136 CIFC17 H16 Br Cu N3 PP 1 21/n 113.4532; 7.4445; 17.5935
90; 106.285; 90
1691.34Kumar, Saurabh; Mondal, Dipanjan; Balakrishna, Maravanji S.
Diverse Architectures and Luminescence Properties of Group 11 Complexes Containing Pyrimidine-Based Phosphine, <i>N</i>-((Diphenylphosphine)methyl)pyrimidin-2-amine.
ACS omega, 2018, 3, 16601-16614
4516137 CIFC38 H38 Cu4 I4 N8 P2P -19.636; 10.2333; 12.8232
69.01; 81.979; 71.386
1118.36Kumar, Saurabh; Mondal, Dipanjan; Balakrishna, Maravanji S.
Diverse Architectures and Luminescence Properties of Group 11 Complexes Containing Pyrimidine-Based Phosphine, <i>N</i>-((Diphenylphosphine)methyl)pyrimidin-2-amine.
ACS omega, 2018, 3, 16601-16614
4516138 CIFC36 H32 Ag2 F6 N6 O6 P2 S2P 21 21 219.3162; 18.1124; 23.9326
90; 90; 90
4038.4Kumar, Saurabh; Mondal, Dipanjan; Balakrishna, Maravanji S.
Diverse Architectures and Luminescence Properties of Group 11 Complexes Containing Pyrimidine-Based Phosphine, <i>N</i>-((Diphenylphosphine)methyl)pyrimidin-2-amine.
ACS omega, 2018, 3, 16601-16614
4516139 CIFC34 H32 Ag2 B2 F8 N6 P2P -19.3737; 10.3726; 11.0196
108.252; 102.115; 110.351
890.77Kumar, Saurabh; Mondal, Dipanjan; Balakrishna, Maravanji S.
Diverse Architectures and Luminescence Properties of Group 11 Complexes Containing Pyrimidine-Based Phosphine, <i>N</i>-((Diphenylphosphine)methyl)pyrimidin-2-amine.
ACS omega, 2018, 3, 16601-16614
4516140 CIFC17 H16 Au Cl N3 PP 1 21/c 119.4767; 8.5915; 20.9829
90; 96.19; 90
3490.7Kumar, Saurabh; Mondal, Dipanjan; Balakrishna, Maravanji S.
Diverse Architectures and Luminescence Properties of Group 11 Complexes Containing Pyrimidine-Based Phosphine, <i>N</i>-((Diphenylphosphine)methyl)pyrimidin-2-amine.
ACS omega, 2018, 3, 16601-16614
4516141 CIFC32 H48 Bi2 Br10 N4P 1 21 111.9962; 14.6765; 13.8899
90; 93.394; 90
2441.2Moon, Tae Hwan; Oh, Seung-Jin; Ok, Kang Min
[((<i>R</i>)-C<sub>8</sub>H<sub>12</sub>N)<sub>4</sub>][Bi<sub>2</sub>Br<sub>10</sub>] and [((<i>S</i>)-C<sub>8</sub>H<sub>12</sub>N)<sub>4</sub>][Bi<sub>2</sub>Br<sub>10</sub>]: Chiral Hybrid Bismuth Bromides Templated by Chiral Organic Cations.
ACS omega, 2018, 3, 17895-17903
4516142 CIFC32 H48 Bi2 Br10 N4P 1 21 111.997; 14.728; 13.94
90; 93.44; 90
2458.6Moon, Tae Hwan; Oh, Seung-Jin; Ok, Kang Min
[((<i>R</i>)-C<sub>8</sub>H<sub>12</sub>N)<sub>4</sub>][Bi<sub>2</sub>Br<sub>10</sub>] and [((<i>S</i>)-C<sub>8</sub>H<sub>12</sub>N)<sub>4</sub>][Bi<sub>2</sub>Br<sub>10</sub>]: Chiral Hybrid Bismuth Bromides Templated by Chiral Organic Cations.
ACS omega, 2018, 3, 17895-17903
4516143 CIFC22 H13 F2 I O2 SP 1 21/n 115.127; 9.2725; 15.5544
90; 109.256; 90
2059.7Zhang, Jitan; Liang, Zhenda; Wang, Jun; Guo, Ziyi; Liu, Changqing; Xie, Meihua
Metal-Free Synthesis of Functionalized Tetrasubstituted Alkenes by Three-Component Reaction of Alkynes, Iodine, and Sodium Sulfinates.
ACS omega, 2018, 3, 18002-18015
4516144 CIFC22 H17 I O3 SP n a 2117.286; 8.3835; 14.2909
90; 90; 90
2071Zhang, Jitan; Liang, Zhenda; Wang, Jun; Guo, Ziyi; Liu, Changqing; Xie, Meihua
Metal-Free Synthesis of Functionalized Tetrasubstituted Alkenes by Three-Component Reaction of Alkynes, Iodine, and Sodium Sulfinates.
ACS omega, 2018, 3, 18002-18015
4516145 CIFC17 H16 Br I O3 SP -18.3914; 10.1833; 11.436
66.578; 82.676; 85.465
888.96Zhang, Jitan; Liang, Zhenda; Wang, Jun; Guo, Ziyi; Liu, Changqing; Xie, Meihua
Metal-Free Synthesis of Functionalized Tetrasubstituted Alkenes by Three-Component Reaction of Alkynes, Iodine, and Sodium Sulfinates.
ACS omega, 2018, 3, 18002-18015
4516146 CIFC11 H16 N O13 P Pb2 SP -18.9059; 10.388; 11.1079
64.715; 88.475; 80.124
914.16Cai, Xiao-Ou; Sun, Meng; Shao, Yu-Jing; Liu, Fang; Liu, Qun-Li; Zhu, Yan-Yu; Sun, Zhen-Gang; Dong, Da-Peng; Li, Jing
Two Highly Stable Luminescent Lead Phosphonates Based on Mixed Ligands: Highly Selective and Sensitive Sensing for Thymine Molecule and VO<sub>3</sub><sup>-</sup> Anion.
ACS omega, 2018, 3, 16443-16452
4516147 CIFC17 H28 N2 O16 P2 Pb3 SP -19.4266; 12.5779; 13.2779
100.972; 90.825; 104.333
1494.3Cai, Xiao-Ou; Sun, Meng; Shao, Yu-Jing; Liu, Fang; Liu, Qun-Li; Zhu, Yan-Yu; Sun, Zhen-Gang; Dong, Da-Peng; Li, Jing
Two Highly Stable Luminescent Lead Phosphonates Based on Mixed Ligands: Highly Selective and Sensitive Sensing for Thymine Molecule and VO<sub>3</sub><sup>-</sup> Anion.
ACS omega, 2018, 3, 16443-16452
4516148 CIFC28 H32 F N O2 SP 1 21 110.19; 6.636; 18.242
90; 104.79; 90
1192.7Okolo, ChrisTina; Ali, Mohamad Akbar; Newman, Matthew; Chambers, Steven A.; Whitt, Jedidiah; Alsharif, Zakeyah A.; Day, Victor W.; Alam, Mohammad A.
Hexafluoroisopropanol-Mediated Domino Reaction for the Synthesis of Thiazolo-androstenones: Potent Anticancer Agents.
ACS omega, 2018, 3, 17991-18001
4516149 CIFC26 H28 F N O SP 21 21 217.212; 8.116; 36.696
90; 90; 90
2147.9Okolo, ChrisTina; Ali, Mohamad Akbar; Newman, Matthew; Chambers, Steven A.; Whitt, Jedidiah; Alsharif, Zakeyah A.; Day, Victor W.; Alam, Mohammad A.
Hexafluoroisopropanol-Mediated Domino Reaction for the Synthesis of Thiazolo-androstenones: Potent Anticancer Agents.
ACS omega, 2018, 3, 17991-18001
4516150 CIFC26 H28 Br N O SP 21 21 219.5976; 37.906; 55.277
90; 90; 90
20110Okolo, ChrisTina; Ali, Mohamad Akbar; Newman, Matthew; Chambers, Steven A.; Whitt, Jedidiah; Alsharif, Zakeyah A.; Day, Victor W.; Alam, Mohammad A.
Hexafluoroisopropanol-Mediated Domino Reaction for the Synthesis of Thiazolo-androstenones: Potent Anticancer Agents.
ACS omega, 2018, 3, 17991-18001
4516151 CIFC26 H28 F N O SP 1 21 19.603; 7.0203; 15.771
90; 93.616; 90
1061.1Okolo, ChrisTina; Ali, Mohamad Akbar; Newman, Matthew; Chambers, Steven A.; Whitt, Jedidiah; Alsharif, Zakeyah A.; Day, Victor W.; Alam, Mohammad A.
Hexafluoroisopropanol-Mediated Domino Reaction for the Synthesis of Thiazolo-androstenones: Potent Anticancer Agents.
ACS omega, 2018, 3, 17991-18001
4516152 CIFC22 H21 N O2 SP 1 21/n 111.8883; 7.4114; 20.6224
90; 95.281; 90
1809.31Mane, Vaijinath; Baiju, Thekke V.; Namboothiri, Irishi N. N.
Synthesis of Functionalized Thieno[2,3-<i>b</i>]indoles via One-Pot Reaction of Indoline-2-thiones with Morita-Baylis-Hillman and Rauhut-Currier Adducts of Nitroalkenes.
ACS omega, 2018, 3, 17617-17628
4516153 CIFC28 H33 N3 O4 SP 1 21/c 115.959; 8.47; 21.482
90; 108.034; 90
2761.1Mane, Vaijinath; Baiju, Thekke V.; Namboothiri, Irishi N. N.
Synthesis of Functionalized Thieno[2,3-<i>b</i>]indoles via One-Pot Reaction of Indoline-2-thiones with Morita-Baylis-Hillman and Rauhut-Currier Adducts of Nitroalkenes.
ACS omega, 2018, 3, 17617-17628
4516154 CIFC26 H32 N3 O4 SP -111.08; 11.755; 11.961
63.18; 66.29; 71.29
1254Mane, Vaijinath; Baiju, Thekke V.; Namboothiri, Irishi N. N.
Synthesis of Functionalized Thieno[2,3-<i>b</i>]indoles via One-Pot Reaction of Indoline-2-thiones with Morita-Baylis-Hillman and Rauhut-Currier Adducts of Nitroalkenes.
ACS omega, 2018, 3, 17617-17628
4516155 CIFC21 H17 Cl2 N O2P 1 21/c 116.4194; 10.6606; 11.1508
90; 107.03; 90
1866.26Zhang, Mingming; Prior, Allan M.; Maddox, Marcus M.; Shen, Wan-Jou; Hevener, Kirk E.; Bruhn, David F.; Lee, Robin B.; Singh, Aman P.; Reinicke, Justin; Simmons, Charles J.; Hurdle, Julian G.; Lee, Richard E.; Sun, Dianqing
Pharmacophore Modeling, Synthesis, and Antibacterial Evaluation of Chalcones and Derivatives.
ACS omega, 2018, 3, 18343-18360
4516156 CIFC12 H28 I3 P PbP 1 21 116.077; 16.3313; 16.9952
90; 107.066; 90
4265.7Omahen, Emily H.; Binder, Justin F.; Jacobs, Brad F.; Swidan, Ala'aeddeen; Macdonald, Charles L. B.
Phosphonium-Templated Iodoplumbates.
ACS omega, 2018, 3, 17077-17082
4516157 CIFC40 H39 I6 N P2 Pb2C 1 2/c 124.56; 13.0686; 16.1499
90; 110.037; 90
4869.8Omahen, Emily H.; Binder, Justin F.; Jacobs, Brad F.; Swidan, Ala'aeddeen; Macdonald, Charles L. B.
Phosphonium-Templated Iodoplumbates.
ACS omega, 2018, 3, 17077-17082
4516158 CIFC8 H22 I6 P2 Pb2C 1 2/m 115.3593; 11.1506; 7.9441
90; 100.889; 90
1336.05Omahen, Emily H.; Binder, Justin F.; Jacobs, Brad F.; Swidan, Ala'aeddeen; Macdonald, Charles L. B.
Phosphonium-Templated Iodoplumbates.
ACS omega, 2018, 3, 17077-17082
4516159 CIFC4 H12 I PP 4/n m m :28.1978; 8.1978; 6.0037
90; 90; 90
403.47Omahen, Emily H.; Binder, Justin F.; Jacobs, Brad F.; Swidan, Ala'aeddeen; Macdonald, Charles L. B.
Phosphonium-Templated Iodoplumbates.
ACS omega, 2018, 3, 17077-17082
4516160 CIFC4 H12 I3 P PbP 6510.0382; 10.0382; 23.738
90; 90; 120
2071.5Omahen, Emily H.; Binder, Justin F.; Jacobs, Brad F.; Swidan, Ala'aeddeen; Macdonald, Charles L. B.
Phosphonium-Templated Iodoplumbates.
ACS omega, 2018, 3, 17077-17082
4516161 CIFC27 H20 Br N3 O3P 1 21/n 116.097; 9.1111; 17.2334
90; 114.177; 90
2305.8Maity, Pampa; Naskar, Barnali; Goswami, Sanchita; Prodhan, Chandraday; Chaudhuri, Tandrima; Chaudhuri, Keya; Mukhopadhyay, Chhanda
Pyrrolo[3,4-c]pyridine-Based Fluorescent Chemosensor for Fe3+/Fe2+ Sensitivity and Their Application in Living HepG2 Cells
ACS Omega, 2018, 3, 18646
4516162 CIFC24 H18 B2 F8 N18 NiI a -3 d18.4872; 18.4872; 18.4872
90; 90; 90
6318.5Berdiell, Izar Capel; Kulak, Alexander N.; Warriner, Stuart L.; Halcrow, Malcolm A.
Heterometallic Coordination Polymer Gels Supported by 2,4,6-Tris(pyrazol-1-yl)-1,3,5-triazine.
ACS omega, 2018, 3, 18466-18474
4516163 CIFC54.25 H55.75 B3 Cu2 F12 N42.25 O13.5P -112.3764; 16.8545; 21.0272
107.562; 91.665; 106.956
3966.9Berdiell, Izar Capel; Kulak, Alexander N.; Warriner, Stuart L.; Halcrow, Malcolm A.
Heterometallic Coordination Polymer Gels Supported by 2,4,6-Tris(pyrazol-1-yl)-1,3,5-triazine.
ACS omega, 2018, 3, 18466-18474
4516164 CIFC26 H20 B2 F8 Fe N16F d d d :217.8353; 25.3177; 27.4906
90; 90; 90
12413.3Berdiell, Izar Capel; Kulak, Alexander N.; Warriner, Stuart L.; Halcrow, Malcolm A.
Heterometallic Coordination Polymer Gels Supported by 2,4,6-Tris(pyrazol-1-yl)-1,3,5-triazine.
ACS omega, 2018, 3, 18466-18474
4516165 CIFC26.9 H23.2 Cl2 Fe N16.9 O9.93P 1 21/n 115.2393; 31.6772; 15.9371
90; 111.945; 90
7136.01Berdiell, Izar Capel; Kulak, Alexander N.; Warriner, Stuart L.; Halcrow, Malcolm A.
Heterometallic Coordination Polymer Gels Supported by 2,4,6-Tris(pyrazol-1-yl)-1,3,5-triazine.
ACS omega, 2018, 3, 18466-18474

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