Crystallography Open Database

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4515866 CIFC49 H60 Br2 Cl2 N8 O4 Pt2P b c n11.8035; 15.125; 28.887
90; 90; 90
5157.1McCready, Matthew S.; Puddephatt, Richard J.
Supramolecular Organoplatinum(IV) Chemistry: Dimers and Polymers Formed by Intermolecular Hydrogen Bonding.
ACS omega, 2018, 3, 13621-13629
4515867 CIFC30 H33 Br N4 O2 PtP 1 21/c 19.0266; 20.43; 14.744
90; 94.271; 90
2711.4McCready, Matthew S.; Puddephatt, Richard J.
Supramolecular Organoplatinum(IV) Chemistry: Dimers and Polymers Formed by Intermolecular Hydrogen Bonding.
ACS omega, 2018, 3, 13621-13629
4515868 CIFC32 H37 Br Cl2 N4 O2 PtP -110.258; 10.484; 16.122
80.57; 80.05; 72.63
1618.2McCready, Matthew S.; Puddephatt, Richard J.
Supramolecular Organoplatinum(IV) Chemistry: Dimers and Polymers Formed by Intermolecular Hydrogen Bonding.
ACS omega, 2018, 3, 13621-13629
4515869 CIFC21 H23 Br N4 PtP 1 21/c 118.083; 12.964; 8.3848
90; 92.263; 90
1964.1McCready, Matthew S.; Puddephatt, Richard J.
Supramolecular Organoplatinum(IV) Chemistry: Dimers and Polymers Formed by Intermolecular Hydrogen Bonding.
ACS omega, 2018, 3, 13621-13629
4515870 CIFC32 H37 Br Cl5 N4 O2 PtP 1 21/n 19.7737; 10.0964; 36.9181
90; 97.239; 90
3614McCready, Matthew S.; Puddephatt, Richard J.
Supramolecular Organoplatinum(IV) Chemistry: Dimers and Polymers Formed by Intermolecular Hydrogen Bonding.
ACS omega, 2018, 3, 13621-13629
4515871 CIFC32 H40 B Br N4 O3 PtP -18.8735; 10.971; 17.8017
94.577; 93.652; 113.547
1574.96McCready, Matthew S.; Puddephatt, Richard J.
Supramolecular Organoplatinum(IV) Chemistry: Dimers and Polymers Formed by Intermolecular Hydrogen Bonding.
ACS omega, 2018, 3, 13621-13629
4515872 CIFC37 H50 B Br N4 O4 PtP -19.8253; 9.9194; 19.4252
103.365; 95.89; 99.558
1796.64McCready, Matthew S.; Puddephatt, Richard J.
Supramolecular Organoplatinum(IV) Chemistry: Dimers and Polymers Formed by Intermolecular Hydrogen Bonding.
ACS omega, 2018, 3, 13621-13629
4515873 CIFC23 H17 N3 O4 S3P 1 21/n 112.59; 19.81; 18.88
90; 97.17; 90
4672Singsardar, Mukta; Mondal, Susmita; Sarkar, Rajib; Hajra, Alakananda
(Diacetoxy)iodobenzene-Mediated Regioselective Imidation of Imidazoheterocycles with <i>N</i>-Fluorobenzenesulfonimide.
ACS omega, 2018, 3, 12505-12512
4515874 CIFC27 H45 Cl Mo3 O10 S4P 63/m20.702; 20.702; 16.158
90; 90; 120
5997.1Fu, Dong; Fabre, Bruno; Loget, Gabriel; Mériadec, Cristelle; Ababou-Girard, Soraya; Cadot, Emmanuel; Leclerc-Laronze, Nathalie; Marrot, Jérôme; de Ponfilly, Quentin
Polyoxothiometalate-Derivatized Silicon Photocathodes for Sunlight-Driven Hydrogen Evolution Reaction.
ACS omega, 2018, 3, 13837-13849
4515875 CIFC7 H7 N OC 1 2/c 131.177; 6.1229; 14.3335
90; 113.771; 90
2504Pagliari, Anderson B.; Orlando, Tainára; Salbego, Paulo R. S.; Zimmer, Geórgia C; Hörner, Manfredo; Zanatta, Nilo; Bonacorso, Helio G.; Martins, Marcos A. P.
Supramolecular Packing of a Series of <i>N</i>-Phenylamides and the Role of NH···O=C Interactions.
ACS omega, 2018, 3, 13850-13861
4515876 CIFC8 H6 F3 N OP 1 21 15.1753; 19.084; 8.2765
90; 90.302; 90
817.4Pagliari, Anderson B.; Orlando, Tainára; Salbego, Paulo R. S.; Zimmer, Geórgia C; Hörner, Manfredo; Zanatta, Nilo; Bonacorso, Helio G.; Martins, Marcos A. P.
Supramolecular Packing of a Series of <i>N</i>-Phenylamides and the Role of NH···O=C Interactions.
ACS omega, 2018, 3, 13850-13861
4515877 CIFC11 H15 N OP c a 219.969; 10.642; 10.172
90; 90; 90
1079.1Pagliari, Anderson B.; Orlando, Tainára; Salbego, Paulo R. S.; Zimmer, Geórgia C; Hörner, Manfredo; Zanatta, Nilo; Bonacorso, Helio G.; Martins, Marcos A. P.
Supramolecular Packing of a Series of <i>N</i>-Phenylamides and the Role of NH···O=C Interactions.
ACS omega, 2018, 3, 13850-13861
4515878 CIFC8 H9 N OP b c a9.371; 7.7868; 19.5301
90; 90; 90
1425.1Pagliari, Anderson B.; Orlando, Tainára; Salbego, Paulo R. S.; Zimmer, Geórgia C; Hörner, Manfredo; Zanatta, Nilo; Bonacorso, Helio G.; Martins, Marcos A. P.
Supramolecular Packing of a Series of <i>N</i>-Phenylamides and the Role of NH···O=C Interactions.
ACS omega, 2018, 3, 13850-13861
4515879 CIFC13 H11 N OP -15.352; 7.971; 12.471
73.23; 79.202; 89.85
499.6Pagliari, Anderson B.; Orlando, Tainára; Salbego, Paulo R. S.; Zimmer, Geórgia C; Hörner, Manfredo; Zanatta, Nilo; Bonacorso, Helio G.; Martins, Marcos A. P.
Supramolecular Packing of a Series of <i>N</i>-Phenylamides and the Role of NH···O=C Interactions.
ACS omega, 2018, 3, 13850-13861
4515880 CIFC8 H6 Br3 N OP c a 2110.1863; 9.1483; 11.8856
90; 90; 90
1107.59Pagliari, Anderson B.; Orlando, Tainára; Salbego, Paulo R. S.; Zimmer, Geórgia C; Hörner, Manfredo; Zanatta, Nilo; Bonacorso, Helio G.; Martins, Marcos A. P.
Supramolecular Packing of a Series of <i>N</i>-Phenylamides and the Role of NH···O=C Interactions.
ACS omega, 2018, 3, 13850-13861
4515881 CIFC21 H22 N4 Ni O5 Pb S2P 1 21/n 112.3716; 9.6865; 20.7826
90; 105.941; 90
2394.8Roy, Sourav; Halder, Soumi; Drew, Michael G. B.; Ray, Partha Pratim; Chattopadhyay, Shouvik
Fabrication of an Active Electronic Device Using a Hetero-bimetallic Coordination Polymer.
ACS omega, 2018, 3, 12788-12796
4515882 CIFC24 H28 O8P -110.60195; 10.75301; 11.3032
59.987; 80.147; 88.894
1096.03Nomura, Eisaku; Noda, Takumi; Gomi, Daiki; Mori, Hajime
Substituent Effect on the Formation of Arylindanes by Dimerization of Ferulic Acid and its Related Compounds.
ACS omega, 2018, 3, 12746-12753
4515883 CIFC26 H32 O10P -18.7988; 10.50228; 13.8851
89.745; 76.69; 79.141
1225.25Nomura, Eisaku; Noda, Takumi; Gomi, Daiki; Mori, Hajime
Substituent Effect on the Formation of Arylindanes by Dimerization of Ferulic Acid and its Related Compounds.
ACS omega, 2018, 3, 12746-12753
4515884 CIFC62 H34 Cl2 Co15 N2 O38 Pd9P 1 21/n 113.5461; 25.518; 47.112
90; 94.719; 90
16230Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515885 CIFC63 H36 Cl4 Co15 N2 O38 Pd9P c a 2125.9095; 12.7628; 25.9267
90; 90; 90
8573.4Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515886 CIFC68 H46 Cl2 Co15 N2 O38 Pd9P 1 21/c 112.9658; 36.928; 18.5192
90; 98.141; 90
8777.7Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515887 CIFC68 H46 Cl2 Co15 N2 O38 Pd9P 1 21/c 113.0934; 37.1883; 18.6966
90; 97.344; 90
9029.1Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515888 CIFC81.5 H41 Cl5 Co15 O38 P2 Pd9P -112.6823; 12.8975; 30.7793
95.725; 98.686; 94.004
4933.5Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515889 CIFC81.5 H41 Cl5 Co15 O38 P2 Pd9P -113.0138; 13.0903; 31.023
96.767; 99.948; 93.099
5154.2Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515890 CIFC79 H36 Co15 O38 P2 Pd9R 3 :H18.8375; 18.8375; 22.4956
90; 90; 120
6913.1Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515891 CIFC79 H36 Co15 O38 P2 Pd9R 3 :H18.9827; 18.9827; 22.7666
90; 90; 120
7104.7Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515892 CIFC72 H50 Cl2 Co15 N3 O38 Pd9P -112.7371; 13.5459; 28.843
93.292; 93.675; 111.909
4589.7Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515893 CIFC72 H50 Cl2 Co15 N3 O38 Pd9P c a 2139.915; 12.8254; 17.5401
90; 90; 90
8979.2Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515894 CIFC99 H56 Cl2 Co15 O38 P3 Pd9P -112.7433; 16.7009; 28.227
90.39; 94.828; 112.141
5539.8Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515895 CIFC43 H18 Cl2 Co13 N O29 Pd3P -111.9099; 21.2639; 25.6686
114.096; 90.729; 100.805
5800Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515896 CIFC58 H72 Co8 N2 O24 Pd4P -111.3488; 13.6232; 14.1177
62.07; 79.979; 69.75
1809.07Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515897 CIFC58 H72 Co8 N2 O24 Pt4P -111.4009; 13.94; 14.213
62.21; 78.778; 69.642
1872.1Berti, Beatrice; Ciabatti, Iacopo; Femoni, Cristina; Iapalucci, Maria Carmela; Zacchini, Stefano
Cluster Core Isomerism Induced by Crystal Packing Effects in the [HCo<sub>15</sub>Pd<sub>9</sub>C<sub>3</sub>(CO)<sub>38</sub>]<sup>2-</sup> Molecular Nanocluster.
ACS omega, 2018, 3, 13239-13250
4515898 CIFC0 H0 Cl3 Cu KP 1 21/c 14.034; 13.7987; 8.7445
90; 97.123; 90
483Zhou, Huawei; Liu, Xuejing; He, Guohang; Fan, Lin; Shi, Shaozhen; Wei, Jiazhen; Xu, Wenli; Yuan, Cang; Chai, Ning; Chen, Baoli; Zhang, Yingtian; Zhang, Xianxi; Zhao, Jinsheng; Wei, Xinting; Yin, Jie; Tian, Dongxu
Synthesis, Crystal Structure, UV-Vis Adsorption Properties, Photoelectric Behavior, and DFT Computational Study of All-Inorganic and Lead-Free Copper Halide Salt K<sub>2</sub>Cu<sub>2</sub>Cl<sub>6</sub>.
ACS omega, 2018, 3, 14021-14026
4515899 CIFC38 H36 Cl4 Cu2 N8 O12 Zn2P 1 21/c 110.08; 17.9664; 12.4991
90; 96.773; 90
2247.81Majumder, Ishani; Chakraborty, Prateeti; Álvarez, Raquel; Gonzalez-Diaz, Myriam; Peláez, Rafael; Ellahioui, Younes; Bauza, Antonio; Frontera, Antonio; Zangrando, Ennio; Gómez-Ruiz, Santiago; Das, Debasis
Bioactive Heterometallic Cu<sup>II</sup>-Zn<sup>II</sup> Complexes with Potential Biomedical Applications.
ACS omega, 2018, 3, 13343-13353
4515900 CIFC42 H36 Cl4 Cu2 N10 O4 ZnP 1 21/c 110.3783; 20.893; 10.1906
90; 106.224; 90
2121.7Majumder, Ishani; Chakraborty, Prateeti; Álvarez, Raquel; Gonzalez-Diaz, Myriam; Peláez, Rafael; Ellahioui, Younes; Bauza, Antonio; Frontera, Antonio; Zangrando, Ennio; Gómez-Ruiz, Santiago; Das, Debasis
Bioactive Heterometallic Cu<sup>II</sup>-Zn<sup>II</sup> Complexes with Potential Biomedical Applications.
ACS omega, 2018, 3, 13343-13353
4515901 CIFC38 H36 Cl4 Cu2 N6 O11 ZnP 1 21/c 110.0431; 19.9558; 11.4121
90; 111.678; 90
2125.4Majumder, Ishani; Chakraborty, Prateeti; Álvarez, Raquel; Gonzalez-Diaz, Myriam; Peláez, Rafael; Ellahioui, Younes; Bauza, Antonio; Frontera, Antonio; Zangrando, Ennio; Gómez-Ruiz, Santiago; Das, Debasis
Bioactive Heterometallic Cu<sup>II</sup>-Zn<sup>II</sup> Complexes with Potential Biomedical Applications.
ACS omega, 2018, 3, 13343-13353
4515902 CIFC38 H36 Cl8 Cu2 N4 O4 Zn2P 1 21/c 19.7807; 16.605; 13.616
90; 90.203; 90
2211.3Majumder, Ishani; Chakraborty, Prateeti; Álvarez, Raquel; Gonzalez-Diaz, Myriam; Peláez, Rafael; Ellahioui, Younes; Bauza, Antonio; Frontera, Antonio; Zangrando, Ennio; Gómez-Ruiz, Santiago; Das, Debasis
Bioactive Heterometallic Cu<sup>II</sup>-Zn<sup>II</sup> Complexes with Potential Biomedical Applications.
ACS omega, 2018, 3, 13343-13353
4515903 CIFC19 H18 Cl2 Cu N2 O2P 1 21/n 16.9256; 23.3181; 11.7998
90; 103.829; 90
1850.34Majumder, Ishani; Chakraborty, Prateeti; Álvarez, Raquel; Gonzalez-Diaz, Myriam; Peláez, Rafael; Ellahioui, Younes; Bauza, Antonio; Frontera, Antonio; Zangrando, Ennio; Gómez-Ruiz, Santiago; Das, Debasis
Bioactive Heterometallic Cu<sup>II</sup>-Zn<sup>II</sup> Complexes with Potential Biomedical Applications.
ACS omega, 2018, 3, 13343-13353
4515904 CIFC41 H45 F6 N4 O4 PI 1 a 113.0575; 17.6855; 17.644
90; 103.694; 90
3958.7Greenlee, Andrew J.; Ofosu, Charles K.; Xiao, Qifan; Modan, Mohammed M.; Janzen, Daron E.; Cao, Dennis D.
Pyridinium-Functionalized Pyromellitic Diimides with Stabilized Radical Anion States.
ACS omega, 2018, 3, 240-245
4515905 CIFC19 H25 N3 O5C 1 2/c 121.969; 17.259; 20.669
90; 96.021; 90
7794Hu, Xing-Mei; Luo, Da-Yun; Zi, Quan-Xing; Lin, Jun; Yan, Sheng-Jiao
Diastereoselective Synthesis of Morphan Derivatives by Michael and Hetero-Michael Addition of 1,1-Enediamines to Quinone Monoketals.
ACS omega, 2018, 3, 8-21
4515906 CIFC18 H22 Cl N3 O5P 1 21/n 17.372; 19.312; 13.785
90; 105.509; 90
1891.1Hu, Xing-Mei; Luo, Da-Yun; Zi, Quan-Xing; Lin, Jun; Yan, Sheng-Jiao
Diastereoselective Synthesis of Morphan Derivatives by Michael and Hetero-Michael Addition of 1,1-Enediamines to Quinone Monoketals.
ACS omega, 2018, 3, 8-21
4515907 CIFC17 H21 N3 O5P 1 21/c 117.67; 8.064; 12.926
90; 102.53; 90
1798Hu, Xing-Mei; Luo, Da-Yun; Zi, Quan-Xing; Lin, Jun; Yan, Sheng-Jiao
Diastereoselective Synthesis of Morphan Derivatives by Michael and Hetero-Michael Addition of 1,1-Enediamines to Quinone Monoketals.
ACS omega, 2018, 3, 8-21
4515908 CIFC24 H25 F2 N3 O5P -18.3233; 8.3363; 17.223
102.674; 97.734; 98.563
1135.5Hu, Xing-Mei; Luo, Da-Yun; Zi, Quan-Xing; Lin, Jun; Yan, Sheng-Jiao
Diastereoselective Synthesis of Morphan Derivatives by Michael and Hetero-Michael Addition of 1,1-Enediamines to Quinone Monoketals.
ACS omega, 2018, 3, 8-21
4515909 CIFC21 H15 Br N2 O2P 1 21/c 110.92936; 12.8033; 13.37608
90; 112.081; 90
1734.45Leas, Derek A.; Wu, Jianbo; Ezell, Edward L.; Garrison, Jered C.; Vennerstrom, Jonathan L.; Dong, Yuxiang
Formation of 2-Imino Benzo[<i>e</i>]-1,3-oxazin-4-ones from Reactions of Salicylic Acids and Anilines with HATU: Mechanistic and Synthetic Studies.
ACS omega, 2018, 3, 781-787
4515910 CIFC14 H20 O4P 21 21 219.0317; 10.0478; 15.5635
90; 90; 90
1412.37Li, Yuelan; Zhu, Rongxiu; Zhang, Jiaozhen; Xie, Fei; Wang, Xiaoning; Xu, Ke; Qiao, Yanan; Zhao, Zuntian; Lou, Hongxiang
Ophiosphaerellins A-I, Polyketide-Derived Compounds from the Endolichenic Fungus <i>Ophiosphaerella korrae</i>.
ACS omega, 2018, 3, 176-180
4515911 CIFC14 H20 O3P 4113.4241; 13.4241; 7.2863
90; 90; 90
1313.04Li, Yuelan; Zhu, Rongxiu; Zhang, Jiaozhen; Xie, Fei; Wang, Xiaoning; Xu, Ke; Qiao, Yanan; Zhao, Zuntian; Lou, Hongxiang
Ophiosphaerellins A-I, Polyketide-Derived Compounds from the Endolichenic Fungus <i>Ophiosphaerella korrae</i>.
ACS omega, 2018, 3, 176-180
4515912 CIFC26 H22 OP 1 21/n 19.2774; 22.6668; 9.8223
90; 104.891; 90
1996.15Sahoo, Prakash Kumar; Gawali, Suhas Shahaji; Gunanathan, Chidambaram
Iron-Catalyzed Selective Etherification and Transetherification Reactions Using Alcohols.
ACS omega, 2018, 3, 124-136
4515913 CIFC54 H88 N2 O9C 1 2/c 122.2703; 15.8902; 15.2838
90; 93.297; 90
5399.7Rodríguez-Fortea, Antonio; Kaleta, Jiří; Mézière, Cécile; Allain, Magali; Canadell, Enric; Wzietek, Pawel; Michl, Josef; Batail, Patrick
Asymmetric Choreography in Pairs of Orthogonal Rotors.
ACS omega, 2018, 3, 1293-1297
4515914 CIFC54 H88 N2 O9C 1 2/c 122.3412; 15.9121; 15.4268
90; 93.24; 90
5475.4Rodríguez-Fortea, Antonio; Kaleta, Jiří; Mézière, Cécile; Allain, Magali; Canadell, Enric; Wzietek, Pawel; Michl, Josef; Batail, Patrick
Asymmetric Choreography in Pairs of Orthogonal Rotors.
ACS omega, 2018, 3, 1293-1297
4515915 CIFC13 H18 O3P 21 21 217.1234; 7.7506; 21.457
90; 90; 90
1184.7Yadav, Jhillu Singh; Singh, Shweta; Das, Saibal
Stereoselective Total Syntheses of Acutifolone A, Bisacutifolone A and B, Pinguisenol, and Isonaviculol.
ACS omega, 2018, 3, 636-647
4515916 CIFC16 H9 F5 OP -16.45; 7.2271; 15.5635
100.475; 94.555; 97.516
703.3Yamada, Shigeyuki; Mitsuda, Akira; Miyano, Kazuya; Tanaka, Tsuyoshi; Morita, Masato; Agou, Tomohiro; Kubota, Toshio; Konno, Tsutomu
Development of Novel Solid-State Light-Emitting Materials Based on Pentafluorinated Tolane Fluorophores.
ACS omega, 2018, 3, 9105-9113
4515917 CIFC20 H17 F5 OP -16.1612; 7.4665; 20.2688
89.766; 87.758; 83.16
925.07Yamada, Shigeyuki; Mitsuda, Akira; Miyano, Kazuya; Tanaka, Tsuyoshi; Morita, Masato; Agou, Tomohiro; Kubota, Toshio; Konno, Tsutomu
Development of Novel Solid-State Light-Emitting Materials Based on Pentafluorinated Tolane Fluorophores.
ACS omega, 2018, 3, 9105-9113
4515918 CIFC23 H21 Cl SP 1 21/n 112.4697; 8.9131; 17.456
90; 103.685; 90
1885Vu, Minh Duy; Foo, Ce Qing; Sadeer, Abdul; Shand, Sam S.; Li, Yongxin; Pullarkat, Sumod A.
Triflic-Acid-Catalyzed Tandem Allylic Substitution-Cyclization Reaction of Alcohols with Thiophenols-Facile Access to Polysubstituted Thiochromans.
ACS omega, 2018, 3, 8945-8951
4515919 CIFC18 H6 F8 N4 NiP 1 21/n 19.3936; 4.6798; 17.703
90; 100.44; 90
765.3Pilia, Luca; Shuku, Yoshiaki; Dalgleish, Simon; Awaga, Kunio; Robertson, Neil
Structural and Electronic Effects Due to Fluorine Atoms on Dibenzotetraaza-Annulenes Complexes.
ACS omega, 2018, 3, 10074-10083
4515920 CIFC18 H6 Cu F8 N4P 1 21/n 19.457; 4.715; 17.574
90; 100.787; 90
769.8Pilia, Luca; Shuku, Yoshiaki; Dalgleish, Simon; Awaga, Kunio; Robertson, Neil
Structural and Electronic Effects Due to Fluorine Atoms on Dibenzotetraaza-Annulenes Complexes.
ACS omega, 2018, 3, 10074-10083
4515921 CIFC37 H42 Hg4 N15 O13P -113.3372; 13.4107; 15.8542
66.936; 65.477; 73.256
2346.9Lemes, Maykon A.; Stein, Hilarie N.; Gabidullin, Bulat; Steinmann, Stephan N.; Murugesu, Muralee
Tetrazine-Based Ligand Transformation Driving Metal-Metal Bond and Mixed-Valence Hg<sup>I</sup>/Hg<sup>II</sup>.
ACS omega, 2018, 3, 10273-10277
4515922 CIFC42 H97 Cl N24 O36P -116.4068; 21.1877; 21.5464
94.827; 105.616; 110.717
6612Wang, Xin-Xin; Tian, Fei-Yang; Chen, Kai; Zhang, Yun-Qian; Tao, Zhu; Zhu, Qian-Jiang
Hexamethylcucurbit[3,3]uril-Based Porous Supramolecular Assemblies and Their Adsorption Properties.
ACS omega, 2018, 3, 9827-9833
4515923 CIFC40 H34 Cu2 N6 O18P 1 21/n 110.8505; 10.467; 18.8893
90; 105.253; 90
2069.73Hossain, Anowar; Dey, Arka; Seth, Saikat Kumar; Ray, Partha Pratim; Ballester, Pablo; Pritchard, Robin G.; Ortega-Castro, Joaquín; Frontera, Antonio; Mukhopadhyay, Subrata
Enhanced Photosensitive Schottky Diode Behavior of Pyrazine over 2-Aminopyrimidine Ligand in Copper(II)-Phthalate MOFs: Experimental and Theoretical Rationalization.
ACS omega, 2018, 3, 9160-9171
4515924 CIFC20 H18 Cu N2 O10C 1 2/c 116.9098; 11.4225; 10.4825
90; 95.3601; 90
2015.9Hossain, Anowar; Dey, Arka; Seth, Saikat Kumar; Ray, Partha Pratim; Ballester, Pablo; Pritchard, Robin G.; Ortega-Castro, Joaquín; Frontera, Antonio; Mukhopadhyay, Subrata
Enhanced Photosensitive Schottky Diode Behavior of Pyrazine over 2-Aminopyrimidine Ligand in Copper(II)-Phthalate MOFs: Experimental and Theoretical Rationalization.
ACS omega, 2018, 3, 9160-9171
4515925 CIFC7 H10 N4P 1 21/n 19.3247; 8.2469; 10.8377
90; 92.037; 90
832.89Tinson, Ryan A. J.; Hughes, David L.; Ward, Leanne; Stephenson, G. Richard
Unusual Nucleophilic Addition of Grignard Reagents in the Synthesis of 4-Amino-pyrimidines.
ACS omega, 2018, 3, 8937-8944
4515926 CIFC16 H9 N O2 SP 1 21/n 16.6437; 9.4377; 19.9115
90; 99.266; 90
1232.19Lohar, Somenath; Dhara, Koushik; Roy, Priya; Sinha Babu, Santi P.; Chattopadhyay, Pabitra
Highly Sensitive Ratiometric Chemosensor and Biomarker for Cyanide Ions in the Aqueous Medium.
ACS omega, 2018, 3, 10145-10153
4515927 CIFC34 H24 N2 O7 S2P -17.3648; 12.6013; 17.9669
71.88; 86.822; 86.863
1581.07Lohar, Somenath; Dhara, Koushik; Roy, Priya; Sinha Babu, Santi P.; Chattopadhyay, Pabitra
Highly Sensitive Ratiometric Chemosensor and Biomarker for Cyanide Ions in the Aqueous Medium.
ACS omega, 2018, 3, 10145-10153
4515928 CIFC46 H46 N2 O11P 1 21/n 110.8577; 14.2462; 13.918
90; 111.138; 90
2007.99Fang, Jing; Zhang, Qi; Li, Meiqi; Wang, Jian-Rong; Mei, Xuefeng
Isostructural Solvates of Naturally Occurring Allocryptopine Exhibit Both Mechanochromic and Hydrochromic Luminescent Properties.
ACS omega, 2018, 3, 9220-9226
4515929 CIFC45 H46 N3 O11P 1 21/n 110.6658; 14.335; 13.962
90; 110.1; 90
2004.7Fang, Jing; Zhang, Qi; Li, Meiqi; Wang, Jian-Rong; Mei, Xuefeng
Isostructural Solvates of Naturally Occurring Allocryptopine Exhibit Both Mechanochromic and Hydrochromic Luminescent Properties.
ACS omega, 2018, 3, 9220-9226
4515930 CIFC45 H46 N2 O11P 1 21/n 110.5721; 14.2791; 13.9602
90; 109.686; 90
1984.3Fang, Jing; Zhang, Qi; Li, Meiqi; Wang, Jian-Rong; Mei, Xuefeng
Isostructural Solvates of Naturally Occurring Allocryptopine Exhibit Both Mechanochromic and Hydrochromic Luminescent Properties.
ACS omega, 2018, 3, 9220-9226
4515931 CIFC52 H29 F9 N6 PtC 1 2/c 118.9584; 16.8577; 14.0096
90; 111.553; 90
4164.3Alemayehu, Abraham B.; McCormick, Laura J.; Gagnon, Kevin J.; Borisov, Sergey M.; Ghosh, Abhik
Stable Platinum(IV) Corroles: Synthesis, Molecular Structure, and Room-Temperature Near-IR Phosphorescence.
ACS omega, 2018, 3, 9360-9368
4515932 CIFC49 H32 N6 PtP -19.4792; 12.0922; 16.675
109.102; 95.415; 90.85
1795.9Alemayehu, Abraham B.; McCormick, Laura J.; Gagnon, Kevin J.; Borisov, Sergey M.; Ghosh, Abhik
Stable Platinum(IV) Corroles: Synthesis, Molecular Structure, and Room-Temperature Near-IR Phosphorescence.
ACS omega, 2018, 3, 9360-9368
4515933 CIFC24 H30 N2 O4P -18.0473; 11.4044; 13.7456
70.394; 75.041; 79.862
1142.53Reddy, Chatrala Ravikumar; Sridhar, Balasubramanian; V Subba Reddy, Basi
Ru(II)-Catalyzed Oxidative Functionalization of Arylhydrazine-1,2-dicarboxylates with Internal Alkynes for the Synthesis of Enecarbamates.
ACS omega, 2018, 3, 9746-9753
4515934 CIFC21 H24 N2 O5P -18.9744; 9.5414; 11.6948
95.027; 97.388; 96.992
980.27Reddy, Chatrala Ravikumar; Sridhar, Balasubramanian; V Subba Reddy, Basi
Ru(II)-Catalyzed Oxidative Functionalization of Arylhydrazine-1,2-dicarboxylates with Internal Alkynes for the Synthesis of Enecarbamates.
ACS omega, 2018, 3, 9746-9753
4515935 CIFC14 H18 I2 N2 O PtP b c a7.942; 19.31; 22.77
90; 90; 90
3492Fard, Mahmood A.; Behnia, Ava; Puddephatt, Richard J.
Supramolecular Polymer and Sheet and a Double Cubane Structure in Platinum(IV) Iodide Chemistry: Solution of a Longstanding Puzzle.
ACS omega, 2018, 3, 10267-10272
4515936 CIFC17 H24 I2 N2 O2 PtP 1 21/c 111.333; 13.086; 14.249
90; 94.272; 90
2107.3Fard, Mahmood A.; Behnia, Ava; Puddephatt, Richard J.
Supramolecular Polymer and Sheet and a Double Cubane Structure in Platinum(IV) Iodide Chemistry: Solution of a Longstanding Puzzle.
ACS omega, 2018, 3, 10267-10272
4515937 CIFC10 H30 I6 Pt4P -18.361; 8.63; 10.095
92.018; 113.755; 106.974
627.9Fard, Mahmood A.; Behnia, Ava; Puddephatt, Richard J.
Supramolecular Polymer and Sheet and a Double Cubane Structure in Platinum(IV) Iodide Chemistry: Solution of a Longstanding Puzzle.
ACS omega, 2018, 3, 10267-10272
4515938 CIFC11 H10 Cl2 O3C 1 2/c 117.4884; 7.707; 16.2535
90; 94.034; 90
2185.3Dethe, Dattatraya H.; Boda, Raghavender
Synthetic Studies toward the Natural Product Tripartin, the First Natural Histone Lysine Demethylase Inhibitor.
ACS omega, 2018, 3, 9303-9309
4515939 CIFC12 H34 B12 N4P 1 21/c 115.002; 8.676; 16.83
90; 91.384; 90
2189.9Kelley, Steven P.; Rachiero, Giovanni P.; Titi, Hatem M.; Rogers, Robin D.
New Reactions for Old Ions: Cage Rearrangements, Hydrolysis, and Two-Electron Reduction of <i>nido</i>-Decaborane in Neat 1-Ethyl-3-Methylimidazolium Acetate.
ACS omega, 2018, 3, 8491-8496
4515940 CIFC12 H32 B10 N4C 1 2/c 114.0962; 10.5765; 14.3649
90; 91.92; 90
2140.4Kelley, Steven P.; Rachiero, Giovanni P.; Titi, Hatem M.; Rogers, Robin D.
New Reactions for Old Ions: Cage Rearrangements, Hydrolysis, and Two-Electron Reduction of <i>nido</i>-Decaborane in Neat 1-Ethyl-3-Methylimidazolium Acetate.
ACS omega, 2018, 3, 8491-8496
4515941 CIFC14 H38 B10 N4 O2P 1 21/c 19.553; 28.914; 9.7711
90; 116.859; 90
2407.8Kelley, Steven P.; Rachiero, Giovanni P.; Titi, Hatem M.; Rogers, Robin D.
New Reactions for Old Ions: Cage Rearrangements, Hydrolysis, and Two-Electron Reduction of <i>nido</i>-Decaborane in Neat 1-Ethyl-3-Methylimidazolium Acetate.
ACS omega, 2018, 3, 8491-8496
4515942 CIFC27 H21 B3 Cl6 F6 N4 O3P 1 21/n 114.8016; 12.2438; 18.4551
90; 99.793; 90
3295.84Zhang, Xiaohong; Shi, Jun; Song, Jintong; Wang, Man; Xu, Xuemei; Qu, Lang; Zhou, Xiangge; Xiang, Haifeng
Nonconjugated Fluorescent Molecular Cages of Trinuclear Fluoroborate Complexes with Salicylaldehyde-Based Schiff Base Ligands.
ACS omega, 2018, 3, 8992-9002
4515943 CIFC27 H27 B3 F6 N4 O3P 1 21/c 111.6042; 17.3471; 13.6414
90; 90.3913; 90
2745.94Zhang, Xiaohong; Shi, Jun; Song, Jintong; Wang, Man; Xu, Xuemei; Qu, Lang; Zhou, Xiangge; Xiang, Haifeng
Nonconjugated Fluorescent Molecular Cages of Trinuclear Fluoroborate Complexes with Salicylaldehyde-Based Schiff Base Ligands.
ACS omega, 2018, 3, 8992-9002
4515944 CIFC29 H21 N O2P -18.25787; 8.7682; 15.6385
96.208; 97.1322; 108.099
1054.98Baig, Moghal Zubair Khalid; Prusti, Banchhanidhi; Roy, Durba; Sahu, Prabhat Kumar; Sarkar, Moloy; Sharma, Aayushi; Chakravarty, Manab
Weak Donor-/Strong Acceptor-Linked Anthracenyl π-Conjugates as Solvato(fluoro)chromophore and AEEgens: Contrast between Nitro and Cyano Functionality.
ACS omega, 2018, 3, 9114-9125
4515945 CIFC31 H25 N O2P -18.0332; 8.569; 18.521
86.059; 79.08; 63.59
1121Baig, Moghal Zubair Khalid; Prusti, Banchhanidhi; Roy, Durba; Sahu, Prabhat Kumar; Sarkar, Moloy; Sharma, Aayushi; Chakravarty, Manab
Weak Donor-/Strong Acceptor-Linked Anthracenyl π-Conjugates as Solvato(fluoro)chromophore and AEEgens: Contrast between Nitro and Cyano Functionality.
ACS omega, 2018, 3, 9114-9125
4515946 CIFC32 H25 NP -18.5961; 11.2877; 12.684
110.581; 95.048; 95.743
1136.33Baig, Moghal Zubair Khalid; Prusti, Banchhanidhi; Roy, Durba; Sahu, Prabhat Kumar; Sarkar, Moloy; Sharma, Aayushi; Chakravarty, Manab
Weak Donor-/Strong Acceptor-Linked Anthracenyl π-Conjugates as Solvato(fluoro)chromophore and AEEgens: Contrast between Nitro and Cyano Functionality.
ACS omega, 2018, 3, 9114-9125
4515947 CIFC31 H25 N O2P 1 21/c 119.4514; 8.0224; 14.5787
90; 99.218; 90
2245.6Baig, Moghal Zubair Khalid; Prusti, Banchhanidhi; Roy, Durba; Sahu, Prabhat Kumar; Sarkar, Moloy; Sharma, Aayushi; Chakravarty, Manab
Weak Donor-/Strong Acceptor-Linked Anthracenyl π-Conjugates as Solvato(fluoro)chromophore and AEEgens: Contrast between Nitro and Cyano Functionality.
ACS omega, 2018, 3, 9114-9125
4515948 CIFC31 H26P -18.9806; 11.4991; 11.998
114.199; 96.923; 102.313
1073.66Baig, Moghal Zubair Khalid; Prusti, Banchhanidhi; Roy, Durba; Sahu, Prabhat Kumar; Sarkar, Moloy; Sharma, Aayushi; Chakravarty, Manab
Weak Donor-/Strong Acceptor-Linked Anthracenyl π-Conjugates as Solvato(fluoro)chromophore and AEEgens: Contrast between Nitro and Cyano Functionality.
ACS omega, 2018, 3, 9114-9125
4515949 CIFC27 H34 Cl N O3F d d 225.666; 46.332; 8.4689
90; 90; 90
10071Aghazadeh Meshgi, Mohammad; Zaitsev, Kirill V.; Vener, Mikhail V.; Churakov, Andrei V.; Baumgartner, Judith; Marschner, Christoph
Hypercoordinated Oligosilanes Based on Aminotrisphenols.
ACS omega, 2018, 3, 10317-10330
4515950 CIFC18 H12 Cl N O3 SiP 1 21/n 19.2802; 14.072; 11.6193
90; 90.084; 90
1517.4Aghazadeh Meshgi, Mohammad; Zaitsev, Kirill V.; Vener, Mikhail V.; Churakov, Andrei V.; Baumgartner, Judith; Marschner, Christoph
Hypercoordinated Oligosilanes Based on Aminotrisphenols.
ACS omega, 2018, 3, 10317-10330
4515951 CIFC54 H60 N2 O7 Si2R -3 :H14.414; 14.414; 24.558
90; 90; 120
4418.7Aghazadeh Meshgi, Mohammad; Zaitsev, Kirill V.; Vener, Mikhail V.; Churakov, Andrei V.; Baumgartner, Judith; Marschner, Christoph
Hypercoordinated Oligosilanes Based on Aminotrisphenols.
ACS omega, 2018, 3, 10317-10330
4515952 CIFC27 H39 N O3 Si5C 1 2/c 160.459; 12.913; 16.786
90; 100.08; 90
12903Aghazadeh Meshgi, Mohammad; Zaitsev, Kirill V.; Vener, Mikhail V.; Churakov, Andrei V.; Baumgartner, Judith; Marschner, Christoph
Hypercoordinated Oligosilanes Based on Aminotrisphenols.
ACS omega, 2018, 3, 10317-10330
4515953 CIFC37 H69 N O3 Si10P 1 21/c 119.675; 13.965; 18.335
90; 92.701; 90
5032.2Aghazadeh Meshgi, Mohammad; Zaitsev, Kirill V.; Vener, Mikhail V.; Churakov, Andrei V.; Baumgartner, Judith; Marschner, Christoph
Hypercoordinated Oligosilanes Based on Aminotrisphenols.
ACS omega, 2018, 3, 10317-10330
4515954 CIFC40 H65 N O4 Si5P -113.822; 17.584; 20.129
87.588; 75.904; 70.969
4482Aghazadeh Meshgi, Mohammad; Zaitsev, Kirill V.; Vener, Mikhail V.; Churakov, Andrei V.; Baumgartner, Judith; Marschner, Christoph
Hypercoordinated Oligosilanes Based on Aminotrisphenols.
ACS omega, 2018, 3, 10317-10330
4515955 CIFC36 H57 N O3 Si5P -3 c 114.3849; 14.3849; 22.169
90; 90; 120
3972.7Aghazadeh Meshgi, Mohammad; Zaitsev, Kirill V.; Vener, Mikhail V.; Churakov, Andrei V.; Baumgartner, Judith; Marschner, Christoph
Hypercoordinated Oligosilanes Based on Aminotrisphenols.
ACS omega, 2018, 3, 10317-10330
4515956 CIFC26 H17 N3 O5P b c a13.19; 16.96; 20.32
90; 90; 90
4546Mupparapu, Nagaraju; Khan, Shahnawaz; Bandhoria, Pankaj; Athimoolam, Shunmuganarayanan; Ahmed, Qazi Naveed
One-Pot Tandem Approach to Functionalized 3-Hydroxy-2-furanyl-acrylamides.
ACS omega, 2018, 3, 5445-5452
4515957 CIFC26 H16 Br2 N2 O3P 1 21/c 113.399; 10.904; 16.85
90; 112.68; 90
2271Mupparapu, Nagaraju; Khan, Shahnawaz; Bandhoria, Pankaj; Athimoolam, Shunmuganarayanan; Ahmed, Qazi Naveed
One-Pot Tandem Approach to Functionalized 3-Hydroxy-2-furanyl-acrylamides.
ACS omega, 2018, 3, 5445-5452
4515958 CIFC12 H16 N4 O2 SP 21 21 217.661; 7.8138; 23.4172
90; 90; 90
1401.79Yan, Xiao-Sheng; Luo, Huan; Zou, Kun-Shan; Cao, Jin-Lian; Li, Zhao; Jiang, Yun-Bao
Short Azapeptides of Folded Structures in Aqueous Solutions.
ACS omega, 2018, 3, 4786-4790
4515959 CIFC15 H24 N4 O3 SP 1 21 110.0167; 7.5935; 12.506
90; 107.618; 90
906.61Yan, Xiao-Sheng; Luo, Huan; Zou, Kun-Shan; Cao, Jin-Lian; Li, Zhao; Jiang, Yun-Bao
Short Azapeptides of Folded Structures in Aqueous Solutions.
ACS omega, 2018, 3, 4786-4790
4515960 CIFC19 H24 N4 O3 SP 21 21 219.453; 7.6077; 13.2277
90; 90; 90
1957.6Yan, Xiao-Sheng; Luo, Huan; Zou, Kun-Shan; Cao, Jin-Lian; Li, Zhao; Jiang, Yun-Bao
Short Azapeptides of Folded Structures in Aqueous Solutions.
ACS omega, 2018, 3, 4786-4790
4515961 CIFC46 H38 O2P -111.561; 20.663; 28.603
99.883; 90.591; 94.939
6704Liu, Rui; Ran, Huijuan; Zhao, Zhen; Yang, Xueli; Zhang, Jiali; Chen, Lijuan; Sun, Huaming; Hu, Jian-Yong
Synthesis and Optical Properties of Donor-Acceptor-Type 1,3,5,9-Tetraarylpyrenes: Controlling Intramolecular Charge-Transfer Pathways by the Change of π-Conjugation Directions for Emission Color Modulations.
ACS omega, 2018, 3, 5866-5875
4515962 CIFC46 H34 O2R -3 :H51.797; 51.797; 6.5592
90; 90; 120
15240.2Liu, Rui; Ran, Huijuan; Zhao, Zhen; Yang, Xueli; Zhang, Jiali; Chen, Lijuan; Sun, Huaming; Hu, Jian-Yong
Synthesis and Optical Properties of Donor-Acceptor-Type 1,3,5,9-Tetraarylpyrenes: Controlling Intramolecular Charge-Transfer Pathways by the Change of π-Conjugation Directions for Emission Color Modulations.
ACS omega, 2018, 3, 5866-5875
4515963 CIFC44 H65 B Cl7 Co N9 O3P 1 21 113.8545; 8.0296; 23.616
90; 99.037; 90
2594.6Pavlov, Alexander A.; Savkina, Svetlana A.; Belov, Alexander S.; Voloshin, Yan Z.; Nelyubina, Yulia V.; Novikov, Valentin V.
Very Large Magnetic Anisotropy of Cage Cobalt(II) Complexes with a Rigid Cholesteryl Substituent from Paramagnetic NMR Spectroscopy.
ACS omega, 2018, 3, 4941-4946
4515964 CIFC48 H66 B Cl Co N6 O7P 110.867; 10.9382; 22.644
90.95; 103.366; 116.98
2310.7Pavlov, Alexander A.; Savkina, Svetlana A.; Belov, Alexander S.; Voloshin, Yan Z.; Nelyubina, Yulia V.; Novikov, Valentin V.
Very Large Magnetic Anisotropy of Cage Cobalt(II) Complexes with a Rigid Cholesteryl Substituent from Paramagnetic NMR Spectroscopy.
ACS omega, 2018, 3, 4941-4946
4515965 CIFC20 H24 N O PP 1 21 19.384; 11.242; 9.451
90; 118.112; 90
879.4Soengas, Raquel; Belmonte Sánchez, Eva; Iglesias, María José; López Ortiz, Fernando
Synthesis of P-Stereogenic Benzoazaphosphole 1-Oxides via Alkynylation of P-Stereogenic ortho-Aurated and ortho-Iodo Phosphinic Amides.
ACS omega, 2018, 3, 5116-5124
4515966 CIFC20 H28 Cl N O P SnP 21 21 219.4402; 15.011; 15.5913
90; 90; 90
2209.4Soengas, Raquel; Belmonte Sánchez, Eva; Iglesias, María José; López Ortiz, Fernando
Synthesis of P-Stereogenic Benzoazaphosphole 1-Oxides via Alkynylation of P-Stereogenic ortho-Aurated and ortho-Iodo Phosphinic Amides.
ACS omega, 2018, 3, 5116-5124
4515967 CIFC25 H26 N2 O2P 1 21/n 17.8531; 7.4811; 34.767
90; 91.88; 90
2041.5Kim, Sonam; Lee, Hyuck Jin; Nam, Eunju; Jeong, Donghyun; Cho, Jaeheung; Lim, Mi Hee; You, Youngmin
Tailoring Hydrophobic Interactions between Probes and Amyloid-β Peptides for Fluorescent Monitoring of Amyloid-β Aggregation.
ACS omega, 2018, 3, 5141-5154
4515968 CIFC27 H18 F2 N2P -19.8032; 10.2942; 32.2199
84.987; 82.061; 79.035
3155.3Adak, Anirban; Panda, Tamas; Raveendran, Anju; Bejoymohandas, Kochan Sathyaseelan; Asha, K. S.; Prakasham, A. P.; Mukhopadhyay, Balaram; Panda, Manas K.
Distinct Mechanoresponsive Luminescence, Thermochromism, Vapochromism, and Chlorine Gas Sensing by a Solid-State Organic Emitter.
ACS omega, 2018, 3, 5291-5300
4515969 CIFC22 H28 N2 O3P 21 21 218.1549; 14.3911; 16.5026
90; 90; 90
1936.7Kalshetti, Manojkumar G.; Argade, Narshinha P.
Diastereoselective Synthesis of (±)-<i>epi</i>-Subincanadine C.
ACS omega, 2018, 3, 5308-5316
4515970 CIFC22 H26 N2 OP 1 21/c 16.8071; 23.863; 11.839
90; 106.646; 90
1842.5Kalshetti, Manojkumar G.; Argade, Narshinha P.
Diastereoselective Synthesis of (±)-<i>epi</i>-Subincanadine C.
ACS omega, 2018, 3, 5308-5316
4515971 CIFC64 H28.36 Cl8 Cu I7.64 N7P -113.9951; 14.273; 17.845
111.769; 91.652; 90.047
3308.7Thomassen, Ivar K.; McCormick, Laura J.; Ghosh, Abhik
Synthesis and Molecular Structure of a Copper Octaiodocorrole.
ACS omega, 2018, 3, 5106-5110
4515972 CIFC30 H29 N O2P -19.3213; 10.4713; 13.69
74.53; 72.545; 75.112
1205.56Yang, Ren-Yin; Sun, Jing; Yan, Chao-Guo
HOAc-Mediated Domino Diels-Alder Reaction for Synthesis of Spiro[cyclohexane-1,3'-indolines] in Ionic Liquid [Bmim]Br.
ACS omega, 2018, 3, 5406-5416
4515973 CIFC40 H33 N O2P -110.7035; 11.4095; 14.0481
73.172; 79.467; 69.183
1528.8Yang, Ren-Yin; Sun, Jing; Yan, Chao-Guo
HOAc-Mediated Domino Diels-Alder Reaction for Synthesis of Spiro[cyclohexane-1,3'-indolines] in Ionic Liquid [Bmim]Br.
ACS omega, 2018, 3, 5406-5416
4515974 CIFC40 H32 Cl N O2P -110.5416; 12.2467; 14.2079
68.214; 81.502; 69.115
1591.1Yang, Ren-Yin; Sun, Jing; Yan, Chao-Guo
HOAc-Mediated Domino Diels-Alder Reaction for Synthesis of Spiro[cyclohexane-1,3'-indolines] in Ionic Liquid [Bmim]Br.
ACS omega, 2018, 3, 5406-5416
4515975 CIFC34 H36 F N O3P 1 21/n 111.358; 17.3299; 14.9918
90; 104.821; 90
2852.7Yang, Ren-Yin; Sun, Jing; Yan, Chao-Guo
HOAc-Mediated Domino Diels-Alder Reaction for Synthesis of Spiro[cyclohexane-1,3'-indolines] in Ionic Liquid [Bmim]Br.
ACS omega, 2018, 3, 5406-5416
4515976 CIFC32 H23 N O4P -110.1699; 11.6903; 12.6092
96.819; 108.525; 113.464
1251Yang, Ren-Yin; Sun, Jing; Yan, Chao-Guo
HOAc-Mediated Domino Diels-Alder Reaction for Synthesis of Spiro[cyclohexane-1,3'-indolines] in Ionic Liquid [Bmim]Br.
ACS omega, 2018, 3, 5406-5416
4515977 CIFC16 H34 Br N Ni P2P 1 21 110.7169; 14.4134; 13.8384
90; 100.691; 90
2100.5Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515978 CIFC16 H37 Br2 N Ni P2P 1 c 18.6545; 10.983; 23.2849
90; 90.049; 90
2213.3Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515979 CIFC22 H41 N Ni P2P 1 21/n 110.0515; 12.4032; 18.8698
90; 96.8592; 90
2335.67Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515980 CIFC22 H39 N Ni P2P 1 21/n 110.1178; 12.3184; 18.8095
90; 96.5365; 90
2329.1Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515981 CIFC22 H42 Br N Ni P2P 1 21/n 18.0453; 26.962; 11.6488
90; 94.268; 90
2519.8Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515982 CIFC22 H42 F6 N Ni P3P 1 21/m 18.5129; 14.7798; 10.922
90; 98.3608; 90
1359.6Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515983 CIFC52 H74 B N Ni O1.5 P2C 1 2/c 123.872; 12.8733; 32.405
90; 102.298; 90
9729.9Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515984 CIFC68 H85 Cl4 D24 N2 Ni3 O0.5 P4C 1 2/c 132.1922; 15.3802; 17.2936
90; 119.352; 90
7463.2Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515985 CIFC17 H39 N Ni P2P -17.5986; 8.7665; 17.3743
76.1042; 85.058; 67.0003
1034.14Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515986 CIFC17 H40 Cl N Ni P2P 1 21/n 112.6037; 8.7388; 19.9677
90; 99.276; 90
2170.5Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515987 CIFC17 H40 Br N Ni P2P 1 21/n 112.7823; 8.7196; 20.1343
90; 99.226; 90
2215.1Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515988 CIFC41 H60 B N Ni P2P 1 21/n 117.6124; 12.9737; 18.4955
90; 112.686; 90
3899.2Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515989 CIFC16 H37 Cl2 N Ni P2P 1 c 18.7102; 10.8084; 22.818
90; 90.016; 90
2148.16Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515990 CIFC12 H21 I N2 NiP 42/n :218.8225; 18.8225; 8.3226
90; 90; 90
2948.58Wellala, Nadeesha P. N.; Luebking, John D.; Krause, Jeanette A.; Guan, Hairong
Roles of Hydrogen Bonding in Proton Transfer to κ<sup>P</sup>,κ<sup>N</sup>,κ<sup>P</sup>-N(CH<sub>2</sub>CH<sub>2</sub>P <i> <sup>i</sup> </i> Pr<sub>2</sub>)<sub>2</sub>-Ligated Nickel Pincer Complexes.
ACS omega, 2018, 3, 4986-5001
4515991 CIFC48 H30 Eu2 N12 O12P 1 21/c 129.3277; 21.7233; 15.2203
90; 103.351; 90
9434.7Yao, Jin; Zhao, Yan-Wu; Zhang, Xian-Ming
Breathing Europium-Terbium Co-doped Luminescent MOF as a Broad-Range Ratiometric Thermometer with a Contrasting Temperature-Intensity Relationship.
ACS omega, 2018, 3, 5754-5760
4515992 CIFC64 H100 N8 Ni4 O36 Y4P 1 21/n 112.9768; 15.5079; 23.549
90; 96.737; 90
4706.3Kalita, Pankaj; Goura, Joydeb; Herrera, Juan Manuel; Colacio, Enrique; Chandrasekhar, Vadapalli
Heterometallic Octanuclear Ni<sup>II</sup><sub>4</sub>Ln<sup>III</sup><sub>4</sub> (Ln = Y, Gd, Tb, Dy, Ho, Er) Complexes Containing Ni<sup>II</sup><sub>2</sub>Ln<sup>III</sup><sub>2</sub>O<sub>4</sub> Distorted Cubane Motifs: Synthesis, Structure, and Magnetic Properties.
ACS omega, 2018, 3, 5202-5211
4515993 CIFC64 H100 Gd4 N8 Ni4 O36P 1 21/n 112.8381; 15.4317; 23.4889
90; 96.593; 90
4622.7Kalita, Pankaj; Goura, Joydeb; Herrera, Juan Manuel; Colacio, Enrique; Chandrasekhar, Vadapalli
Heterometallic Octanuclear Ni<sup>II</sup><sub>4</sub>Ln<sup>III</sup><sub>4</sub> (Ln = Y, Gd, Tb, Dy, Ho, Er) Complexes Containing Ni<sup>II</sup><sub>2</sub>Ln<sup>III</sup><sub>2</sub>O<sub>4</sub> Distorted Cubane Motifs: Synthesis, Structure, and Magnetic Properties.
ACS omega, 2018, 3, 5202-5211
4515994 CIFC64 H100 N8 Ni4 O36 Tb4P 1 21/n 112.9219; 15.516; 23.5346
90; 96.576; 90
4687.6Kalita, Pankaj; Goura, Joydeb; Herrera, Juan Manuel; Colacio, Enrique; Chandrasekhar, Vadapalli
Heterometallic Octanuclear Ni<sup>II</sup><sub>4</sub>Ln<sup>III</sup><sub>4</sub> (Ln = Y, Gd, Tb, Dy, Ho, Er) Complexes Containing Ni<sup>II</sup><sub>2</sub>Ln<sup>III</sup><sub>2</sub>O<sub>4</sub> Distorted Cubane Motifs: Synthesis, Structure, and Magnetic Properties.
ACS omega, 2018, 3, 5202-5211
4515995 CIFC64 H100 Dy4 N8 Ni4 O36P 1 21/n 112.832; 15.413; 23.419
90; 96.765; 90
4599.6Kalita, Pankaj; Goura, Joydeb; Herrera, Juan Manuel; Colacio, Enrique; Chandrasekhar, Vadapalli
Heterometallic Octanuclear Ni<sup>II</sup><sub>4</sub>Ln<sup>III</sup><sub>4</sub> (Ln = Y, Gd, Tb, Dy, Ho, Er) Complexes Containing Ni<sup>II</sup><sub>2</sub>Ln<sup>III</sup><sub>2</sub>O<sub>4</sub> Distorted Cubane Motifs: Synthesis, Structure, and Magnetic Properties.
ACS omega, 2018, 3, 5202-5211
4515996 CIFC64 H100 Ho4 N8 Ni4 O36P 1 21/n 112.9771; 15.5019; 23.5655
90; 96.714; 90
4708.2Kalita, Pankaj; Goura, Joydeb; Herrera, Juan Manuel; Colacio, Enrique; Chandrasekhar, Vadapalli
Heterometallic Octanuclear Ni<sup>II</sup><sub>4</sub>Ln<sup>III</sup><sub>4</sub> (Ln = Y, Gd, Tb, Dy, Ho, Er) Complexes Containing Ni<sup>II</sup><sub>2</sub>Ln<sup>III</sup><sub>2</sub>O<sub>4</sub> Distorted Cubane Motifs: Synthesis, Structure, and Magnetic Properties.
ACS omega, 2018, 3, 5202-5211
4515997 CIFC64 H100 Er4 N8 Ni4 O36P 1 21/n 112.9222; 15.4758; 23.4658
90; 96.601; 90
4661.61Kalita, Pankaj; Goura, Joydeb; Herrera, Juan Manuel; Colacio, Enrique; Chandrasekhar, Vadapalli
Heterometallic Octanuclear Ni<sup>II</sup><sub>4</sub>Ln<sup>III</sup><sub>4</sub> (Ln = Y, Gd, Tb, Dy, Ho, Er) Complexes Containing Ni<sup>II</sup><sub>2</sub>Ln<sup>III</sup><sub>2</sub>O<sub>4</sub> Distorted Cubane Motifs: Synthesis, Structure, and Magnetic Properties.
ACS omega, 2018, 3, 5202-5211
4515998 CIFC13 H18 N4 SP -17.72; 8.727; 11.731
82.547; 79.592; 67.366
715.9Siddaraju, Yogesh; Prabhu, Kandikere Ramaiah
Iodine-Catalyzed Chemoselective Hydroamination Reaction Using 5-Mercaptotetrazoles Derivatives.
ACS omega, 2018, 3, 4908-4917
4515999 CIFC21 H30 Au B Cl PP 1 21/c 117.0948; 7.0396; 17.6526
90; 91.814; 90
2123.26Boom, Devin H. A.; Ehlers, Andreas W.; Nieger, Martin; Devillard, Marc; Bouhadir, Ghenwa; Bourissou, Didier; Slootweg, J. Chris
Gold(I) Complexes of the Geminal Phosphinoborane <i>t</i>Bu<sub>2</sub>PCH<sub>2</sub>BPh<sub>2</sub>.
ACS omega, 2018, 3, 3945-3951
4516000 CIFC42 H60 Au B2 Cl P2C 1 2/c 128.3351; 11.3935; 27.095
90; 112.237; 90
8096.7Boom, Devin H. A.; Ehlers, Andreas W.; Nieger, Martin; Devillard, Marc; Bouhadir, Ghenwa; Bourissou, Didier; Slootweg, J. Chris
Gold(I) Complexes of the Geminal Phosphinoborane <i>t</i>Bu<sub>2</sub>PCH<sub>2</sub>BPh<sub>2</sub>.
ACS omega, 2018, 3, 3945-3951
4516001 CIFC44 H57 Au B Cl P2P b c a19.0712; 18.7238; 23.2135
90; 90; 90
8289.2Boom, Devin H. A.; Ehlers, Andreas W.; Nieger, Martin; Devillard, Marc; Bouhadir, Ghenwa; Bourissou, Didier; Slootweg, J. Chris
Gold(I) Complexes of the Geminal Phosphinoborane <i>t</i>Bu<sub>2</sub>PCH<sub>2</sub>BPh<sub>2</sub>.
ACS omega, 2018, 3, 3945-3951
4516002 CIFC40 H40 Ag2 Br4 N4P -111.398; 13.023; 18.513
100.166; 103.867; 110.924
2385.6Liu, Qing-Xiang; Hu, Ze-Liang; Yu, Shao-Cong; Zhao, Zhi-Xiang; Wei, Deng-Che; Li, Hui-Long
NHC Pd(II) and Ag(I) Complexes: Synthesis, Structure, and Catalytic Activity in Three Types of C-C Coupling Reactions.
ACS omega, 2018, 3, 4035-4047
4516003 CIFC39 H38 Ag2 Br2 Cl2 N6P 1 21/c 18.4181; 29.944; 15.6855
90; 108.026; 90
3759.8Liu, Qing-Xiang; Hu, Ze-Liang; Yu, Shao-Cong; Zhao, Zhi-Xiang; Wei, Deng-Che; Li, Hui-Long
NHC Pd(II) and Ag(I) Complexes: Synthesis, Structure, and Catalytic Activity in Three Types of C-C Coupling Reactions.
ACS omega, 2018, 3, 4035-4047
4516004 CIFC32 H34 Ag2 Br2 N4P 1 21/c 113.0472; 12.5773; 18.2141
90; 90.564; 90
2988.8Liu, Qing-Xiang; Hu, Ze-Liang; Yu, Shao-Cong; Zhao, Zhi-Xiang; Wei, Deng-Che; Li, Hui-Long
NHC Pd(II) and Ag(I) Complexes: Synthesis, Structure, and Catalytic Activity in Three Types of C-C Coupling Reactions.
ACS omega, 2018, 3, 4035-4047
4516005 CIFC30 H34 Cl4 N4 Pd2P 1 21/c 120.0687; 8.9504; 18.1404
90; 106.464; 90
3124.8Liu, Qing-Xiang; Hu, Ze-Liang; Yu, Shao-Cong; Zhao, Zhi-Xiang; Wei, Deng-Che; Li, Hui-Long
NHC Pd(II) and Ag(I) Complexes: Synthesis, Structure, and Catalytic Activity in Three Types of C-C Coupling Reactions.
ACS omega, 2018, 3, 4035-4047
4516006 CIFC18 H26 N2 O5P 21 21 216.2327; 10.6629; 27.47
90; 90; 90
1825.62Nandi, Sujay Kumar; Maji, Krishnendu; Haldar, Debasish
Self-Healing Hydrogel from a Dipeptide and HCl Sensing.
ACS omega, 2018, 3, 3744-3751
4516007 CIFC32 H32 N10 O10P 1 21/n 120.8293; 7.7968; 22.183
90; 113.025; 90
3315.56Havel, Václav; Sadilová, Tereza; Šindelář, Vladimír
Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates.
ACS omega, 2018, 3, 4657-4663
4516008 CIFC10 H5 F3 N4 SP -17.2243; 8.0299; 9.8872
110.099; 90.348; 98.938
531Liu, Jin; Wang, Yu-Ling; Zhang, Ji-Hong; Yang, Jian-Shan; Mou, Han-Chuan; Lin, Jun; Yan, Sheng-Jiao
Phosphatase CDC25B Inhibitors Produced by Basic Alumina-Supported One-Pot Gram-Scale Synthesis of Fluorinated 2-Alkylthio-4-aminoquinazolines Using Microwave Irradiation.
ACS omega, 2018, 3, 4534-4544
4516009 CIFC23 H18 N4 O2P 1 21/n 16.07198; 26.2431; 11.6359
90; 96.071; 90
1843.75Sabat, Nazarii; Poštová Slavětínská, Lenka; Klepetářová, Blanka; Hocek, Michal
C-H Imidation of 7-Deazapurines.
ACS omega, 2018, 3, 4674-4678
4516010 CIFC48 H54 Co1.5 N6P -15.2108; 17.0359; 21.6439
98.767; 92.401; 94.199
1891.05Koide, Taro; Aritome, Isao; Saeki, Tatsuya; Morita, Yoshitsugu; Shiota, Yoshihito; Yoshizawa, Kazunari; Shimakoshi, Hisashi; Hisaeda, Yoshio
Cobalt-Carbon Bond Formation Reaction via Ligand Reduction of Porphycene-Cobalt(II) Complex and Its Noninnocent Reactivity.
ACS omega, 2018, 3, 4027-4034
4516011 CIFC72 H68 Cu2 N8 O14P 1 21/c 123.6733; 18.9166; 17.611
90; 109.708; 90
7424.6Bhattacharyya, Sohini; Chakraborty, Anindita; Hazra, Arpan; Maji, Tapas Kumar
Tetracarboxylate Linker-Based Flexible Cu<sup>II</sup> Frameworks: Efficient Separation of CO<sub>2</sub> from CO<sub>2</sub>/N<sub>2</sub> and C<sub>2</sub>H<sub>2</sub> from C<sub>2</sub>H<sub>2</sub>/C<sub>2</sub>H<sub>4</sub> Mixtures.
ACS omega, 2018, 3, 2018-2026
4516012 CIFC112 H100 Cu4 N12 O37C 1 2/c 144.8511; 19.046; 14.7115
90; 102.38; 90
12274.8Bhattacharyya, Sohini; Chakraborty, Anindita; Hazra, Arpan; Maji, Tapas Kumar
Tetracarboxylate Linker-Based Flexible Cu<sup>II</sup> Frameworks: Efficient Separation of CO<sub>2</sub> from CO<sub>2</sub>/N<sub>2</sub> and C<sub>2</sub>H<sub>2</sub> from C<sub>2</sub>H<sub>2</sub>/C<sub>2</sub>H<sub>4</sub> Mixtures.
ACS omega, 2018, 3, 2018-2026
4516013 CIFH81.32 K12.87 O150.66 P5 W30P n n a32.6621; 21.5252; 19.0566
90; 90; 90
13397.9Hayashi, Akio; Wihadi, Muh Nur Khoiru; Ota, Hiromi; López, Xavier; Ichihashi, Katsuya; Nishihara, Sadafumi; Inoue, Katsuya; Tsunoji, Nao; Sano, Tsuneji; Sadakane, Masahiro
Preparation of Preyssler-type Phosphotungstate with One Central Potassium Cation and Potassium Cation Migration into the Preyssler Molecule to form Di-Potassium-Encapsulated Derivative.
ACS omega, 2018, 3, 2363-2373
4516014 CIFC27 H32 N0 O3 SP 1 21/c 112.43; 9.127; 21.477
90; 90.584; 90
2436.4Liu, Teng; Liu, Jianjun; Xia, Shubiao; Meng, Jie; Shen, Xianfu; Zhu, Xiufang; Chen, Wenchang; Sun, Chengke; Cheng, Feixiang
Catalyst-Free 1,6-Conjugate Addition/Aromatization/Sulfonylation of <i>para</i>-Quinone Methides: Facile Access to Diarylmethyl Sulfones.
ACS omega, 2018, 3, 1409-1415
4516015 CIFC29 H22 F3 N3 O3 SP 1 21/c 115.7722; 8.8439; 23.3357
90; 128.255; 90
2556.1Dutta, Champak; Ghorai, Debasish; Choudhury, Joyanta
To "Rollover" or Not? Stereoelectronically Guided C-H Functionalization Pathways from Rhodium-Abnormal NHC Intermediates.
ACS omega, 2018, 3, 1614-1620
4516016 CIFC20 H26 Cl F6 N3 P RhP 1 21/c 114.831; 8.5492; 18.749
90; 104.09; 90
2305.7Dutta, Champak; Ghorai, Debasish; Choudhury, Joyanta
To "Rollover" or Not? Stereoelectronically Guided C-H Functionalization Pathways from Rhodium-Abnormal NHC Intermediates.
ACS omega, 2018, 3, 1614-1620
4516017 CIFC24 H22 F6 N3 PC 1 2/c 124.1002; 15.1276; 13.5007
90; 116.068; 90
4421.4Dutta, Champak; Ghorai, Debasish; Choudhury, Joyanta
To "Rollover" or Not? Stereoelectronically Guided C-H Functionalization Pathways from Rhodium-Abnormal NHC Intermediates.
ACS omega, 2018, 3, 1614-1620
4516018 CIFC24 H28 Cl F6 N3 P RhP 1 21/n 19.1839; 27.796; 9.7373
90; 94.388; 90
2478.4Dutta, Champak; Ghorai, Debasish; Choudhury, Joyanta
To "Rollover" or Not? Stereoelectronically Guided C-H Functionalization Pathways from Rhodium-Abnormal NHC Intermediates.
ACS omega, 2018, 3, 1614-1620
4516019 CIFC36 H48 Cl2 N4 O RuP -111.612; 13.3307; 13.8927
62.692; 85.611; 70.196
1789.83Kumar, Dharmendra; Prakasham, A. P.; Das, Sharmistha; Datta, Anindya; Ghosh, Prasenjit
Cyanosilylation of Aromatic Aldehydes by Cationic Ruthenium(II) Complexes of Benzimidazole-Derived O-Functionalized N-Heterocyclic Carbenes at Ambient Temperature under Solvent-Free Conditions.
ACS omega, 2018, 3, 1922-1938
4516020 CIFC34 H44 Cl5 N3 O RuP -111.04197; 13.3361; 13.4517
69.6572; 83.3894; 82.6029
1836.57Kumar, Dharmendra; Prakasham, A. P.; Das, Sharmistha; Datta, Anindya; Ghosh, Prasenjit
Cyanosilylation of Aromatic Aldehydes by Cationic Ruthenium(II) Complexes of Benzimidazole-Derived O-Functionalized N-Heterocyclic Carbenes at Ambient Temperature under Solvent-Free Conditions.
ACS omega, 2018, 3, 1922-1938
4516021 CIFC30 H39 Cl2 N3 O2 RuP -19.9088; 11.7379; 14.6956
109.254; 99.6774; 107.508
1469.48Kumar, Dharmendra; Prakasham, A. P.; Das, Sharmistha; Datta, Anindya; Ghosh, Prasenjit
Cyanosilylation of Aromatic Aldehydes by Cationic Ruthenium(II) Complexes of Benzimidazole-Derived O-Functionalized N-Heterocyclic Carbenes at Ambient Temperature under Solvent-Free Conditions.
ACS omega, 2018, 3, 1922-1938
4516022 CIFC46 H56 Ag2 N6 O2P 1 21/n 19.8105; 15.9779; 14.0138
90; 106.163; 90
2109.85Kumar, Dharmendra; Prakasham, A. P.; Das, Sharmistha; Datta, Anindya; Ghosh, Prasenjit
Cyanosilylation of Aromatic Aldehydes by Cationic Ruthenium(II) Complexes of Benzimidazole-Derived O-Functionalized N-Heterocyclic Carbenes at Ambient Temperature under Solvent-Free Conditions.
ACS omega, 2018, 3, 1922-1938
4516023 CIFC33 H29 N2 O7 S2P -111.585; 11.6149; 13.2151
99.42; 113.923; 103.89
1508.1Wang, Ai-Fang; Hao, Wen-Juan; Zhu, Yi-Long; Li, Guigen; Zhou, Peng; Tu, Shu-Jiang; Jiang, Bo
Double SO<sub>2</sub> Insertion into 1,7-Diynes Leading to Functionalized Naphtho[1,2-<i>c</i>]thiophene 2,2-dioxides.
ACS omega, 2018, 3, 1482-1491
4516024 CIFC25 H33 Cl2 N3 PdP 1 21/n 18.6965; 13.393; 21.541
90; 95.392; 90
2497.8Singh, Chandan; Prakasham, A. P.; Gangwar, Manoj Kumar; Butcher, Raymond J.; Ghosh, Prasenjit
One-Pot Tandem Hiyama Alkynylation/Cyclizations by Palladium(II) Acyclic Diaminocarbene (ADC) Complexes Yielding Biologically Relevant Benzofuran Scaffolds.
ACS omega, 2018, 3, 1740-1756
4516025 CIFC24 H31 Cl2 N3 PdP n a 2114.7426; 8.5735; 19.6079
90; 90; 90
2478.35Singh, Chandan; Prakasham, A. P.; Gangwar, Manoj Kumar; Butcher, Raymond J.; Ghosh, Prasenjit
One-Pot Tandem Hiyama Alkynylation/Cyclizations by Palladium(II) Acyclic Diaminocarbene (ADC) Complexes Yielding Biologically Relevant Benzofuran Scaffolds.
ACS omega, 2018, 3, 1740-1756
4516026 CIFC24 H30 Cl2 N3 O PdP 1 21/n 18.6515; 13.5074; 21.4232
90; 98.636; 90
2475.12Singh, Chandan; Prakasham, A. P.; Gangwar, Manoj Kumar; Butcher, Raymond J.; Ghosh, Prasenjit
One-Pot Tandem Hiyama Alkynylation/Cyclizations by Palladium(II) Acyclic Diaminocarbene (ADC) Complexes Yielding Biologically Relevant Benzofuran Scaffolds.
ACS omega, 2018, 3, 1740-1756
4516027 CIFC22 H30 Cl N O4P 21 21 218.5727; 9.0053; 26.1687
90; 90; 90
2020.22Lan, Ping; Herlt, Anthony J.; Willis, Anthony C.; Taylor, Walter C.; Mander, Lewis N.
Structures of New Alkaloids from Rain Forest Trees <i>Galbulimima belgraveana</i> and <i>Galbulimima baccata</i> in Papua New Guinea, Indonesia, and Northern Australia.
ACS omega, 2018, 3, 1912-1921
4516028 CIFC21.488 H33.976 N O3P 21 21 217.8673; 9.5188; 26.3409
90; 90; 90
1972.6Lan, Ping; Herlt, Anthony J.; Willis, Anthony C.; Taylor, Walter C.; Mander, Lewis N.
Structures of New Alkaloids from Rain Forest Trees <i>Galbulimima belgraveana</i> and <i>Galbulimima baccata</i> in Papua New Guinea, Indonesia, and Northern Australia.
ACS omega, 2018, 3, 1912-1921
4516029 CIFC24 H33 N O5P 18.3874; 10.6644; 13.5952
69.268; 89.374; 71.779
1073.44Lan, Ping; Herlt, Anthony J.; Willis, Anthony C.; Taylor, Walter C.; Mander, Lewis N.
Structures of New Alkaloids from Rain Forest Trees <i>Galbulimima belgraveana</i> and <i>Galbulimima baccata</i> in Papua New Guinea, Indonesia, and Northern Australia.
ACS omega, 2018, 3, 1912-1921
4516030 CIFC21 H32 Cl N O2P 21 21 217.4614; 9.6133; 28.5458
90; 90; 90
2047.55Lan, Ping; Herlt, Anthony J.; Willis, Anthony C.; Taylor, Walter C.; Mander, Lewis N.
Structures of New Alkaloids from Rain Forest Trees <i>Galbulimima belgraveana</i> and <i>Galbulimima baccata</i> in Papua New Guinea, Indonesia, and Northern Australia.
ACS omega, 2018, 3, 1912-1921
4516031 CIFC22 H32 Cl N O4P 21 21 219.0105; 13.7999; 33.4435
90; 90; 90
4158.5Lan, Ping; Herlt, Anthony J.; Willis, Anthony C.; Taylor, Walter C.; Mander, Lewis N.
Structures of New Alkaloids from Rain Forest Trees <i>Galbulimima belgraveana</i> and <i>Galbulimima baccata</i> in Papua New Guinea, Indonesia, and Northern Australia.
ACS omega, 2018, 3, 1912-1921
4516032 CIFC46 H70 N2 O8P 21 21 2112.707; 18.741; 19.0369
90; 90; 90
4533.5Lan, Ping; Herlt, Anthony J.; Willis, Anthony C.; Taylor, Walter C.; Mander, Lewis N.
Structures of New Alkaloids from Rain Forest Trees <i>Galbulimima belgraveana</i> and <i>Galbulimima baccata</i> in Papua New Guinea, Indonesia, and Northern Australia.
ACS omega, 2018, 3, 1912-1921
4516033 CIFC21 H30 Cl N O2P 1 21 110.1135; 8.7052; 11.4139
90; 113.189; 90
923.7Lan, Ping; Herlt, Anthony J.; Willis, Anthony C.; Taylor, Walter C.; Mander, Lewis N.
Structures of New Alkaloids from Rain Forest Trees <i>Galbulimima belgraveana</i> and <i>Galbulimima baccata</i> in Papua New Guinea, Indonesia, and Northern Australia.
ACS omega, 2018, 3, 1912-1921
4516034 CIFC21 H20 Cl N3 O5P 1 21/c 120.5724; 9.8586; 9.7866
90; 97.143; 90
1969.47Joshi, Mayank; Roy Choudhury, Angshuman
Salts of Amoxapine with Improved Solubility for Enhanced Pharmaceutical Applicability.
ACS omega, 2018, 3, 2406-2416
4516035 CIFC37 H40 Cl2 N6 O8P 1 21/c 121.344; 9.9544; 17.4685
90; 102.041; 90
3629.8Joshi, Mayank; Roy Choudhury, Angshuman
Salts of Amoxapine with Improved Solubility for Enhanced Pharmaceutical Applicability.
ACS omega, 2018, 3, 2406-2416
4516036 CIFC40 H42 Cl2 N6 O10P -19.2238; 12.4815; 17.0725
86.285; 89.375; 82.224
1943.33Joshi, Mayank; Roy Choudhury, Angshuman
Salts of Amoxapine with Improved Solubility for Enhanced Pharmaceutical Applicability.
ACS omega, 2018, 3, 2406-2416
4516037 CIFC38 H48 Cl2 N6 O11P 1 21/c 115.721; 19.4546; 25.7568
90; 97.94; 90
7802.1Joshi, Mayank; Roy Choudhury, Angshuman
Salts of Amoxapine with Improved Solubility for Enhanced Pharmaceutical Applicability.
ACS omega, 2018, 3, 2406-2416
4516038 CIFC22.75 H23 Cl2 Fe N12 O12.75P -111.085; 16.394; 17.644
71.995; 83.901; 83.563
3021.4Kimura, Akifumi; Ishida, Takayuki
Spin-Crossover Temperature Predictable from DFT Calculation for Iron(II) Complexes with 4-Substituted Pybox and Related Heteroaromatic Ligands.
ACS omega, 2018, 3, 6737-6747
4516039 CIFC23 H24 Br2 Cl2 Fe N6 O13P -19.678; 9.79; 16.669
85.581; 80.683; 81.201
1538Kimura, Akifumi; Ishida, Takayuki
Spin-Crossover Temperature Predictable from DFT Calculation for Iron(II) Complexes with 4-Substituted Pybox and Related Heteroaromatic Ligands.
ACS omega, 2018, 3, 6737-6747
4516040 CIFC34 H36 Cl2 Fe N8 O14P 21 21 2114.284; 15.268; 17.484
90; 90; 90
3813.1Kimura, Akifumi; Ishida, Takayuki
Spin-Crossover Temperature Predictable from DFT Calculation for Iron(II) Complexes with 4-Substituted Pybox and Related Heteroaromatic Ligands.
ACS omega, 2018, 3, 6737-6747
4516041 CIFC8 H12 F6 O6 Pt S2P 1 21/c 110.4074; 8.6512; 18.1328
90; 101.926; 90
1597.37Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516042 CIFC24 H24 F3 N3 O5P 1 21/c 117.013; 8.5689; 16.9747
90; 105.959; 90
2379.24Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516043 CIFC47 H49 Cl N6 O2 PtP -112.0242; 13.0156; 14.2406
91.582; 102.85; 102.152
2117.7Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516044 CIFC46 H45 F3 N6 O2 PtP -112.8497; 13.011; 14.5696
113.345; 91.507; 100.935
2181.88Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516045 CIFC26 H28 F3 N3 O3 Pt SP 1 21/c 120.2522; 8.1634; 15.925
90; 94.862; 90
2623.36Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516046 CIFC26 H28 F3 N3 O6 Pt SP b c a20.8435; 7.8008; 34.8632
90; 90; 90
5668.6Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516047 CIFC44 H46 Cl2 N6 PtP -111.2411; 13.8079; 14.6138
90.265; 106.81; 109.349
2036Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516048 CIFC44 H44 Cl2 N6 Pt2P 1 21/n 19.7792; 18.2967; 11.3037
90; 98.915; 90
1998.1Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516049 CIFC57 H64 Cl2 N6 Pt2P -111.4693; 15.1911; 16.1768
99.025; 105.146; 106.101
2532.71Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516050 CIFC49 H46 Cl2 F6 N6 O4 Pt2P 1 21/n 112.3755; 18.4144; 22.6884
90; 94.834; 90
5152Mishra, Vishwesh; Thirupathi, Natesan
Critical Role of Anions in Platinum(II) Precursors upon the Structural Motifs of Six-Membered Cycloplatinated <i>N</i>,<i>N</i>',<i>N</i>″-Triarylguanidines.
ACS omega, 2018, 3, 6075-6090
4516051 CIFC25 H19 N11 O4C 1 2/c 120.463; 8.8637; 14.0198
90; 111.426; 90
2367.1De, Avik; Mondal, Raju
Toxic Metal Sequestration Exploiting a Unprecedented Low-Molecular-Weight Hydrogel-to-Metallogel Transformation.
ACS omega, 2018, 3, 6022-6030
4516052 CIFC19 H14 Ag Cl N4 O4P 1 21/n 17.1699; 20.7822; 12.9758
90; 102.72; 90
1886.02Santos, Ane F.; Ferreira, Isabella P.; Pinheiro, Carlos B.; Santos, Verlane G.; Lopes, Miriam T. P.; Teixeira, Letícia R; Rocha, Willian R.; Rodrigues, Gabriel L. S.; Beraldo, Heloisa
[Ag(L)NO<sub>3</sub>] Complexes with 2-Benzoylpyridine-Derived Hydrazones: Cytotoxic Activity and Interaction with Biomolecules.
ACS omega, 2018, 3, 7027-7035
4516053 CIFC20 H17 Ag N4 O4I 1 2/a 112.3045; 14.5456; 21.5645
90; 97.044; 90
3830.4Santos, Ane F.; Ferreira, Isabella P.; Pinheiro, Carlos B.; Santos, Verlane G.; Lopes, Miriam T. P.; Teixeira, Letícia R; Rocha, Willian R.; Rodrigues, Gabriel L. S.; Beraldo, Heloisa
[Ag(L)NO<sub>3</sub>] Complexes with 2-Benzoylpyridine-Derived Hydrazones: Cytotoxic Activity and Interaction with Biomolecules.
ACS omega, 2018, 3, 7027-7035
4516054 CIFC19 H15 Ag N4 O4P 1 21/c 19.0545; 9.0558; 21.896
90; 91.239; 90
1794.96Santos, Ane F.; Ferreira, Isabella P.; Pinheiro, Carlos B.; Santos, Verlane G.; Lopes, Miriam T. P.; Teixeira, Letícia R; Rocha, Willian R.; Rodrigues, Gabriel L. S.; Beraldo, Heloisa
[Ag(L)NO<sub>3</sub>] Complexes with 2-Benzoylpyridine-Derived Hydrazones: Cytotoxic Activity and Interaction with Biomolecules.
ACS omega, 2018, 3, 7027-7035
4516055 CIFC14 H21 N O5P 1 21/n 110.275; 9.5886; 14.718
90; 97.405; 90
1438Hu, Xing-Mei; Zhou, Bei; Yang, Chang-Long; Lin, Jun; Yan, Sheng-Jiao
Site-Selective Reaction of Enaminones and Enamine Esters for the Synthesis of Novel Diverse Morphan Derivatives.
ACS omega, 2018, 3, 5994-6005
4516056 CIFC29 H33 F N2 O6P -111.496; 12.24; 13.457
79.41; 67.16; 71.68
1652.5Hu, Xing-Mei; Zhou, Bei; Yang, Chang-Long; Lin, Jun; Yan, Sheng-Jiao
Site-Selective Reaction of Enaminones and Enamine Esters for the Synthesis of Novel Diverse Morphan Derivatives.
ACS omega, 2018, 3, 5994-6005
4516057 CIFC16 H22 F3 N O5P 1 21/c 18.7813; 8.4703; 24.136
90; 93.158; 90
1792.5Hu, Xing-Mei; Zhou, Bei; Yang, Chang-Long; Lin, Jun; Yan, Sheng-Jiao
Site-Selective Reaction of Enaminones and Enamine Esters for the Synthesis of Novel Diverse Morphan Derivatives.
ACS omega, 2018, 3, 5994-6005
4516058 CIFC25 H26 F N O4P 1 21/c 111.1233; 16.7726; 12.5093
90; 114.965; 90
2115.8Hu, Xing-Mei; Zhou, Bei; Yang, Chang-Long; Lin, Jun; Yan, Sheng-Jiao
Site-Selective Reaction of Enaminones and Enamine Esters for the Synthesis of Novel Diverse Morphan Derivatives.
ACS omega, 2018, 3, 5994-6005
4516059 CIFC63.5 H118 N12 O16.5P 110.612; 17.232; 21.162
88.192; 87.296; 79.182
3796Tsuji, Genichiro; Misawa, Takashi; Doi, Mitsunobu; Demizu, Yosuke
Extent of Helical Induction Caused by Introducing α-Aminoisobutyric Acid into an Oligovaline Sequence.
ACS omega, 2018, 3, 6395-6399
4516060 CIFC24 H36 Cl2 N Nb O3P 1 21/c 113.572; 9.116; 21.854
90; 103.824; 90
2625.5Srisupap, Natta; Wised, Kritdikul; Tsutsumi, Ken; Nomura, Kotohiro
Synthesis of (Arylmido)niobium(V) Complexes Containing Ketimide, Phenoxide Ligands, and Some Reactions with Phenols and Alcohols.
ACS omega, 2018, 3, 6166-6181
4516061 CIFC30 H32 Cl2 N Nb O3P -19.9108; 12.5655; 13.0149
95.967; 101.025; 106.341
1505.05Srisupap, Natta; Wised, Kritdikul; Tsutsumi, Ken; Nomura, Kotohiro
Synthesis of (Arylmido)niobium(V) Complexes Containing Ketimide, Phenoxide Ligands, and Some Reactions with Phenols and Alcohols.
ACS omega, 2018, 3, 6166-6181
4516062 CIFC39 H64 Cl2 N3 Nb OP 1 21/c 115.469; 10.6814; 24.897
90; 93.169; 90
4107.5Srisupap, Natta; Wised, Kritdikul; Tsutsumi, Ken; Nomura, Kotohiro
Synthesis of (Arylmido)niobium(V) Complexes Containing Ketimide, Phenoxide Ligands, and Some Reactions with Phenols and Alcohols.
ACS omega, 2018, 3, 6166-6181
4516063 CIFC40 H66 N3 Nb OP -112.5502; 14.0719; 23.5634
89.366; 88.443; 75.219
4022.2Srisupap, Natta; Wised, Kritdikul; Tsutsumi, Ken; Nomura, Kotohiro
Synthesis of (Arylmido)niobium(V) Complexes Containing Ketimide, Phenoxide Ligands, and Some Reactions with Phenols and Alcohols.
ACS omega, 2018, 3, 6166-6181
4516064 CIFC45 H55 F15 N3 Nb O3P -111.3778; 12.9307; 18.995
86.879; 81.525; 77.672
2699.58Srisupap, Natta; Wised, Kritdikul; Tsutsumi, Ken; Nomura, Kotohiro
Synthesis of (Arylmido)niobium(V) Complexes Containing Ketimide, Phenoxide Ligands, and Some Reactions with Phenols and Alcohols.
ACS omega, 2018, 3, 6166-6181
4516065 CIFC39 H64 F9 N4 Nb OP 1 21/n 111.7181; 18.3197; 20.1982
90; 91.823; 90
4333.79Srisupap, Natta; Wised, Kritdikul; Tsutsumi, Ken; Nomura, Kotohiro
Synthesis of (Arylmido)niobium(V) Complexes Containing Ketimide, Phenoxide Ligands, and Some Reactions with Phenols and Alcohols.
ACS omega, 2018, 3, 6166-6181
4516066 CIFC32 H48 F12 N3 Nb O2P 1 21/n 117.905; 12.0354; 19.691
90; 115.352; 90
3834.6Srisupap, Natta; Wised, Kritdikul; Tsutsumi, Ken; Nomura, Kotohiro
Synthesis of (Arylmido)niobium(V) Complexes Containing Ketimide, Phenoxide Ligands, and Some Reactions with Phenols and Alcohols.
ACS omega, 2018, 3, 6166-6181
4516067 CIFC41 H64 F5 N4 Nb OP 1 21/n 111.903; 18.13; 20.798
90; 104.299; 90
4349Srisupap, Natta; Wised, Kritdikul; Tsutsumi, Ken; Nomura, Kotohiro
Synthesis of (Arylmido)niobium(V) Complexes Containing Ketimide, Phenoxide Ligands, and Some Reactions with Phenols and Alcohols.
ACS omega, 2018, 3, 6166-6181
4516068 CIFC72 H78 Al2 Er2 N6 O18C 1 2/c 127.6738; 10.7124; 24.3659
90; 94.188; 90
7204.05Peng, Yan; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Butterfly M<sub>2</sub><sup>III</sup>Er<sub>2</sub> (M<sup>III</sup> = Fe and Al) SMMs: Synthesis, Characterization, and Magnetic Properties.
ACS omega, 2018, 3, 6360-6368
4516069 CIFC72 H78 Er2 Fe2 N6 O18C 1 2/c 128.6269; 10.5683; 24.3695
90; 94.926; 90
7345.5Peng, Yan; Mereacre, Valeriu; Anson, Christopher E.; Powell, Annie K.
Butterfly M<sub>2</sub><sup>III</sup>Er<sub>2</sub> (M<sup>III</sup> = Fe and Al) SMMs: Synthesis, Characterization, and Magnetic Properties.
ACS omega, 2018, 3, 6360-6368
4516070 CIFC14 H19 Br O TiP 1 21/c 115.0669; 12.2725; 15.5128
90; 90.079; 90
2868.45Boyde, Nicholas C.; Steelman, Grant W.; Hanusa, Timothy P.
Multicomponent Mechanochemical Synthesis of Cyclopentadienyl Titanium <i>tert</i>-Butoxy Halides, Cp <sub> <i>x</i> </sub> TiX <sub> <i>y</i> </sub> (O <sup> <i>t</i> </sup> Bu)<sub>4-(<i>x</i>+<i>y</i>)</sub> (<i>x</i>, <i>y</i> = 1, 2; X = Cl, Br).
ACS omega, 2018, 3, 8149-8159
4516071 CIFC14 H19 Cl O TiP b c a15.01162; 11.84446; 15.51368
90; 90; 90
2758.4Boyde, Nicholas C.; Steelman, Grant W.; Hanusa, Timothy P.
Multicomponent Mechanochemical Synthesis of Cyclopentadienyl Titanium <i>tert</i>-Butoxy Halides, Cp <sub> <i>x</i> </sub> TiX <sub> <i>y</i> </sub> (O <sup> <i>t</i> </sup> Bu)<sub>4-(<i>x</i>+<i>y</i>)</sub> (<i>x</i>, <i>y</i> = 1, 2; X = Cl, Br).
ACS omega, 2018, 3, 8149-8159
4516072 CIFC9 H14 Br2 O TiP 1 21/c 112.9173; 16.12491; 12.6854
90; 111.141; 90
2464.41Boyde, Nicholas C.; Steelman, Grant W.; Hanusa, Timothy P.
Multicomponent Mechanochemical Synthesis of Cyclopentadienyl Titanium <i>tert</i>-Butoxy Halides, Cp <sub> <i>x</i> </sub> TiX <sub> <i>y</i> </sub> (O <sup> <i>t</i> </sup> Bu)<sub>4-(<i>x</i>+<i>y</i>)</sub> (<i>x</i>, <i>y</i> = 1, 2; X = Cl, Br).
ACS omega, 2018, 3, 8149-8159
4516073 CIFC10.91 H12.73 Cl1.09 O0.91 TiP b c a12.489; 11.4556; 14.6289
90; 90; 90
2092.94Boyde, Nicholas C.; Steelman, Grant W.; Hanusa, Timothy P.
Multicomponent Mechanochemical Synthesis of Cyclopentadienyl Titanium <i>tert</i>-Butoxy Halides, Cp <sub> <i>x</i> </sub> TiX <sub> <i>y</i> </sub> (O <sup> <i>t</i> </sup> Bu)<sub>4-(<i>x</i>+<i>y</i>)</sub> (<i>x</i>, <i>y</i> = 1, 2; X = Cl, Br).
ACS omega, 2018, 3, 8149-8159
4516074 CIFC12 H15 Cl O TiP 1 21/n 17.9901; 17.6571; 7.9779
90; 90.444; 90
1125.5Boyde, Nicholas C.; Steelman, Grant W.; Hanusa, Timothy P.
Multicomponent Mechanochemical Synthesis of Cyclopentadienyl Titanium <i>tert</i>-Butoxy Halides, Cp <sub> <i>x</i> </sub> TiX <sub> <i>y</i> </sub> (O <sup> <i>t</i> </sup> Bu)<sub>4-(<i>x</i>+<i>y</i>)</sub> (<i>x</i>, <i>y</i> = 1, 2; X = Cl, Br).
ACS omega, 2018, 3, 8149-8159
4516075 CIFC13 H17 Cl O TiP n m a13.089; 10.6775; 9.3276
90; 90; 90
1303.6Boyde, Nicholas C.; Steelman, Grant W.; Hanusa, Timothy P.
Multicomponent Mechanochemical Synthesis of Cyclopentadienyl Titanium <i>tert</i>-Butoxy Halides, Cp <sub> <i>x</i> </sub> TiX <sub> <i>y</i> </sub> (O <sup> <i>t</i> </sup> Bu)<sub>4-(<i>x</i>+<i>y</i>)</sub> (<i>x</i>, <i>y</i> = 1, 2; X = Cl, Br).
ACS omega, 2018, 3, 8149-8159
4516076 CIFC16 H10 F N O2P -17.9674; 8.6081; 10.2555
87.587; 76.718; 67.665
632.4Saraiah, Bonagiri; Gautam, Vibha; Acharya, Anand; Pasha, Mohamed Afzal; Ila, Hiriyakkanavar
One-Pot Synthesis of 2-(Het)aryl/alkyl-3-cyanobenzofurans from 2-(2-Bromoaryl)-3-(het)aryl-3-(methylthio)acrylonitriles and Benzyl Carbamate.
ACS omega, 2018, 3, 8355-8364
4516077 CIFC10 H12 N4I 41/a :213.7647; 13.7647; 20.651
90; 90; 90
3912.7Yunusova, Sevilya N.; Bolotin, Dmitrii S.; Suslonov, Vitalii V.; Vovk, Mikhail A.; Tolstoy, Peter M.; Kukushkin, Vadim Yu
3-Dialkylamino-1,2,4-triazoles via Zn<sup>II</sup>-Catalyzed Acyl Hydrazide-Dialkylcyanamide Coupling.
ACS omega, 2018, 3, 7224-7234
4516078 CIFC10 H12 N4P -18.4665; 10.312; 11.9037
100.24; 103.121; 103.246
955.83Yunusova, Sevilya N.; Bolotin, Dmitrii S.; Suslonov, Vitalii V.; Vovk, Mikhail A.; Tolstoy, Peter M.; Kukushkin, Vadim Yu
3-Dialkylamino-1,2,4-triazoles via Zn<sup>II</sup>-Catalyzed Acyl Hydrazide-Dialkylcyanamide Coupling.
ACS omega, 2018, 3, 7224-7234
4516079 CIFC10 H13 Cl N4 OI 1 2/c 113.8204; 7.1084; 24.264
90; 105.34; 90
2298.8Yunusova, Sevilya N.; Bolotin, Dmitrii S.; Suslonov, Vitalii V.; Vovk, Mikhail A.; Tolstoy, Peter M.; Kukushkin, Vadim Yu
3-Dialkylamino-1,2,4-triazoles via Zn<sup>II</sup>-Catalyzed Acyl Hydrazide-Dialkylcyanamide Coupling.
ACS omega, 2018, 3, 7224-7234
4516080 CIFC11 H14 N4 OI 41/a :214.9349; 14.9349; 20.242
90; 90; 90
4515Yunusova, Sevilya N.; Bolotin, Dmitrii S.; Suslonov, Vitalii V.; Vovk, Mikhail A.; Tolstoy, Peter M.; Kukushkin, Vadim Yu
3-Dialkylamino-1,2,4-triazoles via Zn<sup>II</sup>-Catalyzed Acyl Hydrazide-Dialkylcyanamide Coupling.
ACS omega, 2018, 3, 7224-7234
4516081 CIFC12 H16 N4P -18.6523; 11.7604; 12.8395
75.686; 82.561; 71.602
1199.33Yunusova, Sevilya N.; Bolotin, Dmitrii S.; Suslonov, Vitalii V.; Vovk, Mikhail A.; Tolstoy, Peter M.; Kukushkin, Vadim Yu
3-Dialkylamino-1,2,4-triazoles via Zn<sup>II</sup>-Catalyzed Acyl Hydrazide-Dialkylcyanamide Coupling.
ACS omega, 2018, 3, 7224-7234
4516082 CIFC12 H14 N4I 41/a :214.81904; 14.81904; 20.4674
90; 90; 90
4494.72Yunusova, Sevilya N.; Bolotin, Dmitrii S.; Suslonov, Vitalii V.; Vovk, Mikhail A.; Tolstoy, Peter M.; Kukushkin, Vadim Yu
3-Dialkylamino-1,2,4-triazoles via Zn<sup>II</sup>-Catalyzed Acyl Hydrazide-Dialkylcyanamide Coupling.
ACS omega, 2018, 3, 7224-7234
4516083 CIFC22 H18 N2P 1 21/n 19.7088; 11.3662; 14.8567
90; 97.069; 90
1627Salfeena, Chettiyan Thodi F.; Jalaja, Renjitha; Davis, Rincy; Suresh, Eringathodi; Somappa, Sasidhar B.
Synthesis of 1,2,4-Trisubstituted-(1<i>H</i>)-imidazoles through Cu(OTf)<sub>2</sub>-/I<sub>2</sub>-Catalyzed C-C Bond Cleavage of Chalcones and Benzylamines.
ACS omega, 2018, 3, 8074-8082
4516084 CIFC17 H16 O13P c a 2119.3428; 6.4501; 28.2467
90; 90; 90
3524.14Tokutomi, Hisashi; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Molecular Structure of the Photo-Oxidation Product of Ellagic Acid in Solution.
ACS omega, 2018, 3, 11179-11183
4516085 CIFC26.67 H27 F6 N5.33 O P RuR 3 :H28.322; 28.322; 9.9011
90; 90; 120
6878Nakagawa, Yoko; Imokawa, Yusuke; Fujisawa, Ikuhide; Nakayama, Naofumi; Goto, Hitoshi; Chanthamath, Soda; Shibatomi, Kazutaka; Iwasa, Seiji
Ligand Exchange Reaction on a Ru(II)-Pheox Complex as a Mechanistic Study of Catalytic Reactions.
ACS omega, 2018, 3, 11286-11289
4516086 CIFC38 H26 N2 O6 ZnP 1 c 115.9559; 20.5495; 9.8687
90; 105.489; 90
3118.3Dutta, Basudeb; Dey, Arka; Maity, Suvendu; Sinha, Chittaranjan; Ray, Partha Pratim; Mir, Mohammad Hedayetullah
Supramolecular Assembly of a Zn(II)-Based 1D Coordination Polymer through Hydrogen Bonding and π···π Interactions: Crystal Structure and Device Applications.
ACS omega, 2018, 3, 12060-12067
4516087 CIFC20 H19 N3 O3P 1 21 16.79795; 9.9618; 12.8161
90; 98.897; 90
857.46Chennapuram, Madhu; Owolabi, Isiaka Alade; Seki, Chigusa; Okuyama, Yuko; Kwon, Eunsang; Uwai, Koji; Tokiwa, Michio; Takeshita, Mitsuhiro; Nakano, Hiroto
New Hybrid-type Squaramide-Fused Amino Alcohol Organocatalyst for Enantioselective Domino Michael Addition/Cyclization Reaction of Oxoindolines with Cyclic 1,3-Diketones.
ACS omega, 2018, 3, 11718-11726
4516088 CIFC14 H15 N O2P 1 21/n 112.6496; 9.9333; 19.755
90; 100.395; 90
2441.5Bai, Hairui; Liu, Fujun; Wang, Xiaojing; Wang, Ping; Huang, Chao
Three-Component One-Pot Approach to Highly Efficient and Sustainable Synthesis of the Functionalized Quinolones via Linear/Branched Domino Protocols, Key Synthetic Methods for the Floxacin of Quinolone Drugs.
ACS omega, 2018, 3, 11233-11251
4516089 CIFC32 H56 N6 Ni2 O20C 1 2 120.1803; 6.2496; 17.1447
90; 100.701; 90
2124.67Kumar, Navnita; Khullar, Sadhika; Mandal, Sanjay K.
Encapsulation of a Water Octamer Chain in a Chiral 2D Sheetlike Supramolecular Coordination Network Composed of Dinickel-Dicarboxylate Subunits.
ACS omega, 2018, 3, 11062-11070
4516090 CIFC36 H48 Cl2 O2 S2 TiP 1 21/c 114.2494; 15.1062; 17.1323
90; 101.223; 90
3617.3Lapenta, Rosita; Buonerba, Antonio; Luciano, Ermanno; Della Monica, Francesco; De Nisi, Assunta; Monari, Magda; Grassi, Alfonso; Capacchione, Carmine; Milione, Stefano
Phenylene-Bridged OSSO-Type Titanium Complexes in the Polymerization of Ethylene and Propylene.
ACS omega, 2018, 3, 11608-11616
4516091 CIFC64 H40 Cl2 O12 P2 Re2 S4P 1 21/n 119.755; 13.633; 24.145
90; 103.603; 90
6320Procopio, Elsa Quartapelle; Dova, Davide; Cauteruccio, Silvia; Forni, Alessandra; Licandro, Emanuela; Panigati, Monica
Dirhenium Coordination Complex Endowed with an Intrinsically Chiral Helical-Shaped Diphosphine Oxide.
ACS omega, 2018, 3, 11649-11654
4516092 CIFC21 H23 N3 OP b c n25.524; 13.835; 9.914
90; 90; 90
3500.9Fanna, Daniel J.; Lima, Luís M P; Craze, Alexander R.; Trinchi, Adrian; Wuhrer, Richard; Lindoy, Leonard F.; Wei, Gang; Reynolds, Jason K.; Li, Feng
Ultrasensitive Colorimetric and Ratiometric Detection of Cu<sup>2+</sup>: Acid-Base Properties, Complexation, and Binding Studies.
ACS omega, 2018, 3, 10471-10480
4516093 CIFC22 H30 N4 O2P -16.898; 8.2874; 9.6802
79.149; 69.618; 83.152
508.6Ghosh, Milan; Ta, Sabyasachi; Banerjee, Mahuya; Das, Debasis
Metal-Ion Displacement Approach for Optical Recognition of Thorium: Application of a Molybdenum(VI) Complex for Nanomolar Determination and Enrichment of Th(IV).
ACS omega, 2018, 3, 16089-16098
4516094 CIFC35 H51 Mo2 N6 O10P -112.6435; 12.8892; 13.5633
65.757; 76.834; 81.409
1958.5Ghosh, Milan; Ta, Sabyasachi; Banerjee, Mahuya; Das, Debasis
Metal-Ion Displacement Approach for Optical Recognition of Thorium: Application of a Molybdenum(VI) Complex for Nanomolar Determination and Enrichment of Th(IV).
ACS omega, 2018, 3, 16089-16098
4516095 CIFC34 H29 I N O4I 1 2/a 114.6664; 10.081; 40.221
90; 97.759; 90
5892.3Yaragorla, Srinivasarao; Bag, Debojyoti; Dada, Ravikrishna; Jose, K. V. Jovan
Iodo-Cycloisomerization of Aryl(indol-3-yl)methane-Tethered Propargyl Alcohols to 3-Iodocarbazoles via Selective 1,2-Alkyl Migration.
ACS omega, 2018, 3, 15024-15034
4516096 CIFC36 H27 I N2 OP 1 21/c 115.8788; 9.357; 21.2905
90; 92.12; 90
3161.1Yaragorla, Srinivasarao; Bag, Debojyoti; Dada, Ravikrishna; Jose, K. V. Jovan
Iodo-Cycloisomerization of Aryl(indol-3-yl)methane-Tethered Propargyl Alcohols to 3-Iodocarbazoles via Selective 1,2-Alkyl Migration.
ACS omega, 2018, 3, 15024-15034
4516097 CIFC48 H37 I N2 O2P 1 21/c 111.5071; 38.741; 9.4077
90; 113.662; 90
3841.3Yaragorla, Srinivasarao; Bag, Debojyoti; Dada, Ravikrishna; Jose, K. V. Jovan
Iodo-Cycloisomerization of Aryl(indol-3-yl)methane-Tethered Propargyl Alcohols to 3-Iodocarbazoles via Selective 1,2-Alkyl Migration.
ACS omega, 2018, 3, 15024-15034
4516098 CIFC67 H82 B2 Cl4 F8 N4 O4 Ru2P 1 21/n 110.653; 19.224; 17.802
90; 93.951; 90
3637.1César, Vincent; Mallardo, Valentina; Nano, Adela; DePeter, Sadie F.; Bastin, Stéphanie; Sournia-Saquet, Alix; Maisse-François, Aline; Lugan, Noël; Bellemin-Laponnaz, Stéphane
Homo- and Heteropolymetallic Complexes of the Hybrid, Ambidentate N-Heterocyclic Carbene Ligand IMes-acac.
ACS omega, 2018, 3, 15582-15591
4516099 CIFCs2 Hg2 Sb2 Se6P -18.029; 8.869; 12.091
68.492; 84.217; 74.128
770.5Du, Cui-Xia; Qi, Fei-Yan; Chen, Juan; Baiyin, Menghe
Two Mercury Antimony Chalcogenides Cs<sub>2</sub>HgSb<sub>4</sub>S<sub>8</sub> and Cs<sub>2</sub>Hg<sub>2</sub>Sb<sub>2</sub>Se<sub>6</sub> with Cesium Cations as Counterions.
ACS omega, 2018, 3, 15168-15173
4516100 CIFCs2 Hg S8 Sb4P -17.3196; 10.6224; 11.7739
99.51; 92.06; 92.1
901.4Du, Cui-Xia; Qi, Fei-Yan; Chen, Juan; Baiyin, Menghe
Two Mercury Antimony Chalcogenides Cs<sub>2</sub>HgSb<sub>4</sub>S<sub>8</sub> and Cs<sub>2</sub>Hg<sub>2</sub>Sb<sub>2</sub>Se<sub>6</sub> with Cesium Cations as Counterions.
ACS omega, 2018, 3, 15168-15173
4516101 CIFC0 H0 Cs2 Hg N0 O0 S8 Sb4P -17.3196; 10.6224; 11.7739
99.51; 92.06; 92.1
901.4Du, Cui-Xia; Qi, Fei-Yan; Chen, Juan; Baiyin, Menghe
Two Mercury Antimony Chalcogenides Cs<sub>2</sub>HgSb<sub>4</sub>S<sub>8</sub> and Cs<sub>2</sub>Hg<sub>2</sub>Sb<sub>2</sub>Se<sub>6</sub> with Cesium Cations as Counterions.
ACS omega, 2018, 3, 15168-15173
4516102 CIFCs2 Hg2 Sb2 Se6P -18.029; 8.869; 12.091
68.492; 84.217; 74.128
770.5Du, Cui-Xia; Qi, Fei-Yan; Chen, Juan; Baiyin, Menghe
Two Mercury Antimony Chalcogenides Cs<sub>2</sub>HgSb<sub>4</sub>S<sub>8</sub> and Cs<sub>2</sub>Hg<sub>2</sub>Sb<sub>2</sub>Se<sub>6</sub> with Cesium Cations as Counterions.
ACS omega, 2018, 3, 15168-15173
4516103 CIFC46 H46 Cl6 S8 Si4P -111.9267; 15.095; 17.872
108.373; 105.652; 101.258
2798.6Li, Bingbing; Zhang, Sheng; Li, Lu; Ma, Zhiying; Li, Chunli; Xu, Li; Wang, Hua
All-Thiophene-Based Double Helix: Synthesis, Crystal Structure, Chiroptical Property and Arylation.
ACS omega, 2018, 3, 16014-16020
4516104 CIFC15 H18 Cu3 I6 N3P 1 21/m 18.804; 14.0866; 11.5559
90; 111.296; 90
1335.28Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516105 CIFC18 H27 Cu6 I8 N3P 1 21/n 113.9901; 10.819; 24.0532
90; 99.243; 90
3593.4Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516106 CIFC36 H56 Cu10 I14 N4P 1 21/c 110.455; 26.2454; 23.854
90; 97.093; 90
6495.3Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516107 CIFC46 H75 Cu10 I14 N5C 1 2/c 133.6214; 10.7706; 25.1921
90; 124.618; 90
7507.5Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516108 CIFC20 H29 Cl2 Cu5 I7 N3P 1 21/c 114.4604; 10.8225; 25.1937
90; 106.194; 90
3786.3Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516109 CIFC20 H29 Br2 Cu5 I7 N3P 1 21/c 128.346; 11.4404; 24.058
90; 106.029; 90
7498.4Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516110 CIFC18 H26 Cu3 I7 N2P -19.1888; 11.3217; 16.2778
73.591; 77.461; 87.998
1585.08Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516111 CIFC22 H29 Cu5 I7 N5P 1 21/c 114.1523; 10.6793; 25.264
90; 104.984; 90
3688.5Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516112 CIFC21 H33.5 Cu5 I7 N2.5 O2C 1 2/c 136.7069; 10.6697; 24.9824
90; 129.192; 90
7583.2Wheaton, Amelia M.; Streep, Michaela E.; Ohlhaver, Christopher M.; Nicholas, Aaron D.; Barnes, Francis H.; Patterson, Howard H.; Pike, Robert D.
Alkyl Pyridinium Iodocuprate(I) Clusters: Structural Types and Charge Transfer Behavior.
ACS omega, 2018, 3, 15281-15292
4516113 CIFC34 H28 Br2 Cl N3 PdP -19.14864; 11.5032; 15.6073
72.6495; 81.6726; 72.6336
1493.48Mollar-Cuni, Andrés; Ventura-Espinosa, David; Martín, Santiago; Mayoral, Álvaro; Borja, Pilar; Mata, Jose A.
Stabilization of Nanoparticles Produced by Hydrogenation of Palladium-N-Heterocyclic Carbene Complexes on the Surface of Graphene and Implications in Catalysis.
ACS omega, 2018, 3, 15217-15228
4516114 CIFC48 H40 Co F12 N8 O8 P2I 41/a :212.8106; 12.8106; 30.5131
90; 90; 90
5007.5Emhoff, Kylin A.; Balaraman, Lakshmi; Simpson, Sydney R.; Stromyer, Michael L.; Kalil, Haitham F.; Beemiller, James R.; Sikatzki, Philipp; Eshelman, Teya S.; Salem, Ahmed M. H.; DeBord, Michael A.; Panzner, Matthew J.; Youngs, Wiley J.; Boyd, W. Christopher
Synthesis and Characterization of Cobalt(II) <i>N</i>,<i>N</i>'-Diphenylazodioxide Complexes.
ACS omega, 2018, 3, 16021-16027
4516115 CIFC35 H30 Cl2 Co F12 N6 O4 P2C 1 2/c 128.0797; 13.4393; 25.3112
90; 103.746; 90
9278.2Emhoff, Kylin A.; Balaraman, Lakshmi; Simpson, Sydney R.; Stromyer, Michael L.; Kalil, Haitham F.; Beemiller, James R.; Sikatzki, Philipp; Eshelman, Teya S.; Salem, Ahmed M. H.; DeBord, Michael A.; Panzner, Matthew J.; Youngs, Wiley J.; Boyd, W. Christopher
Synthesis and Characterization of Cobalt(II) <i>N</i>,<i>N</i>'-Diphenylazodioxide Complexes.
ACS omega, 2018, 3, 16021-16027
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
4516166 CIFC32 H30 N2C 1 2/c 134.0363; 7.9956; 18.5251
90; 97.374; 90
4999.7Dong, Chao; Dickie, Diane A.; Maio, William A.; Manz, Thomas A.
Synthesis and Characterization of <i>N</i>,<i>N</i>'-Bismesityl Phenanthrene-9,10-diimine and Imine-Nitrone.
ACS omega, 2018, 3, 16858-16865
4516167 CIFC8 H4 F3 N3 S2P -17.62509; 8.44847; 15.92585
104.231; 94.45; 103.15
958.65Boeré, René T
Experimental and Computational Evidence for "Double Pancake Bonds": The Role of Dispersion-Corrected DFT Methods in Strongly Dimerized 5-Aryl-1λ<sup>2</sup>,3λ<sup>2</sup>-dithia-2,4,6-triazines.
ACS omega, 2018, 3, 18170-18180
4516168 CIFC8 H4 F3 N5 S3C 1 2/c 122.90772; 4.66989; 22.2724
90; 106.678; 90
2282.39Boeré, René T
Experimental and Computational Evidence for "Double Pancake Bonds": The Role of Dispersion-Corrected DFT Methods in Strongly Dimerized 5-Aryl-1λ<sup>2</sup>,3λ<sup>2</sup>-dithia-2,4,6-triazines.
ACS omega, 2018, 3, 18170-18180
4516169 CIFC33 H29 N O5 SP 1 21 110.4125; 7.9214; 17.1706
90; 100.71; 90
1391.59Chen, Ying-Han; Li, De-Hai; Liu, Yan-Kai
Diversified Synthesis of Chiral Chromane-Containing Polyheterocyclic Compounds via Asymmetric Organocatalytic Cascade Reactions.
ACS omega, 2018, 3, 16615-16625
4516170 CIFC48 H38 N2 O6 S2P 6111.977; 11.977; 47.127
90; 90; 120
5854.6Chen, Ying-Han; Li, De-Hai; Liu, Yan-Kai
Diversified Synthesis of Chiral Chromane-Containing Polyheterocyclic Compounds via Asymmetric Organocatalytic Cascade Reactions.
ACS omega, 2018, 3, 16615-16625
4516171 CIFC23 H13 N O3P 21 21 216.2228; 16.253; 17.111
90; 90; 90
1730.6Grolleau, Jérémie; Petrov, Ravil; Allain, Magali; Skene, William G.; Frère, Pierre
Solid-State Emission Enhancement via Molecular Engineering of Benzofuran Derivatives.
ACS omega, 2018, 3, 18542-18552
4516172 CIFC16 H12 OP 1 21/c 113.4246; 5.6336; 7.7042
90; 90.883; 90
582.59Grolleau, Jérémie; Petrov, Ravil; Allain, Magali; Skene, William G.; Frère, Pierre
Solid-State Emission Enhancement via Molecular Engineering of Benzofuran Derivatives.
ACS omega, 2018, 3, 18542-18552
4516173 CIFC21 H13 N O2P b c a7.353; 13.0226; 32.757
90; 90; 90
3136.7Grolleau, Jérémie; Petrov, Ravil; Allain, Magali; Skene, William G.; Frère, Pierre
Solid-State Emission Enhancement via Molecular Engineering of Benzofuran Derivatives.
ACS omega, 2018, 3, 18542-18552
4516174 CIFC19 H11 N O2P 1 c 15.843; 3.9026; 30.318
90; 94.535; 90
689.17Grolleau, Jérémie; Petrov, Ravil; Allain, Magali; Skene, William G.; Frère, Pierre
Solid-State Emission Enhancement via Molecular Engineering of Benzofuran Derivatives.
ACS omega, 2018, 3, 18542-18552
4516175 CIFC20 H14 O2P n a 2111.0189; 5.6659; 46.0573
90; 90; 90
2875.45Grolleau, Jérémie; Petrov, Ravil; Allain, Magali; Skene, William G.; Frère, Pierre
Solid-State Emission Enhancement via Molecular Engineering of Benzofuran Derivatives.
ACS omega, 2018, 3, 18542-18552
4516176 CIFC17 H11 N OP 1 n 13.8218; 5.7496; 27.25
90; 93.862; 90
597.43Grolleau, Jérémie; Petrov, Ravil; Allain, Magali; Skene, William G.; Frère, Pierre
Solid-State Emission Enhancement via Molecular Engineering of Benzofuran Derivatives.
ACS omega, 2018, 3, 18542-18552
4516177 CIFC18 H12 O2P 1 21 16.4009; 7.3211; 13.9114
90; 100.161; 90
641.69Grolleau, Jérémie; Petrov, Ravil; Allain, Magali; Skene, William G.; Frère, Pierre
Solid-State Emission Enhancement via Molecular Engineering of Benzofuran Derivatives.
ACS omega, 2018, 3, 18542-18552
4516178 CIFC13 H24 N O23 P Tb2P 1 21/n 111.4973; 14.4173; 15.8364
90; 109.373; 90
2476.4Jiao, Cheng-Qi; Sun, Meng; Liu, Fang; Zhou, Ya-Nan; Zhu, Yan-Yu; Sun, Zhen-Gang; Dong, Da-Peng; Li, Jing
Terbium Oxalatophosphonate as Efficient Multiresponsive Luminescent Sensors for Chromate Anions and Tryptophan Molecules.
ACS omega, 2018, 3, 16735-16742
4516179 CIFC23 H22 N6P 1 21/c 124.483; 4.4738; 19.705
90; 113.73; 90
1975.8Naik, Indravath K.; Bodapati, Ramakrishna; Sarkar, Rudraditya; Mondal, Navendu; Das, Samar K.
Functional Molecular System of Bis(pyrazolyl)pyridine Derivatives: Photophysics, Spectroscopy, Computation, and Ion Sensing.
ACS omega, 2018, 3, 3022-3035
4516180 CIFC16 H20 N5 O3 PP -17.4514; 10.2478; 12.0251
74.076; 89.764; 85.604
880.27Naik, Indravath K.; Bodapati, Ramakrishna; Sarkar, Rudraditya; Mondal, Navendu; Das, Samar K.
Functional Molecular System of Bis(pyrazolyl)pyridine Derivatives: Photophysics, Spectroscopy, Computation, and Ion Sensing.
ACS omega, 2018, 3, 3022-3035
4516181 CIFC68 H92 N12 O20 Re4 S4P -113.5644; 14.7817; 23.8992
103.053; 95.08; 108.299
4365.7Karthikeyan, Muthuraman; Ramakrishna, Buthanapalli; Vellaiyadevan, Sivalingam; Divya, Dhanaraj; Manimaran, Bala
Amide-Functionalized Chalcogen-Bridged Flexible Tetranuclear Rhenacycles: Synthesis, Characterization, Solvent Effect on the Structure, and Guest Binding.
ACS omega, 2018, 3, 3257-3266
4516182 CIFC68 H56 N8 O16 Re4 S4P 1 21/n 120.384; 17.0684; 21.821
90; 94.39; 90
7570Karthikeyan, Muthuraman; Ramakrishna, Buthanapalli; Vellaiyadevan, Sivalingam; Divya, Dhanaraj; Manimaran, Bala
Amide-Functionalized Chalcogen-Bridged Flexible Tetranuclear Rhenacycles: Synthesis, Characterization, Solvent Effect on the Structure, and Guest Binding.
ACS omega, 2018, 3, 3257-3266
4516183 CIFC74 H70 N10 O18 Re4 S4P -114.247; 14.3139; 25.3456
79.388; 82.079; 84.365
5017.8Karthikeyan, Muthuraman; Ramakrishna, Buthanapalli; Vellaiyadevan, Sivalingam; Divya, Dhanaraj; Manimaran, Bala
Amide-Functionalized Chalcogen-Bridged Flexible Tetranuclear Rhenacycles: Synthesis, Characterization, Solvent Effect on the Structure, and Guest Binding.
ACS omega, 2018, 3, 3257-3266
4516184 CIFC92 H92 Fe4 N12 O20 Re4 S4P -113.8133; 13.9339; 14.4964
71.743; 78.559; 80.466
2580.96Karthikeyan, Muthuraman; Ramakrishna, Buthanapalli; Vellaiyadevan, Sivalingam; Divya, Dhanaraj; Manimaran, Bala
Amide-Functionalized Chalcogen-Bridged Flexible Tetranuclear Rhenacycles: Synthesis, Characterization, Solvent Effect on the Structure, and Guest Binding.
ACS omega, 2018, 3, 3257-3266
4516185 CIFC102 H96 N12 O20 Re4 S4P -114.9664; 17.7611; 22.4582
92.133; 101.334; 106.648
5580.2Karthikeyan, Muthuraman; Ramakrishna, Buthanapalli; Vellaiyadevan, Sivalingam; Divya, Dhanaraj; Manimaran, Bala
Amide-Functionalized Chalcogen-Bridged Flexible Tetranuclear Rhenacycles: Synthesis, Characterization, Solvent Effect on the Structure, and Guest Binding.
ACS omega, 2018, 3, 3257-3266
4516186 CIFC40 H29 Ir N6 O2P 1 21/c 113.305; 21.832; 12.476
90; 101.87; 90
3546.5Chandrasekhar, Vadapalli; Mahanti, Bani; Pandey, Mrituanjay D.; Narayanan, R. Suriya
Cyclometalated Ir(III) Complex as a Metalloligand and a Selective Cu(II) Sensor: Synthesis and Structural Characterization of a Heterometallic Tetranuclear Ir(III)/Cu(II) Complex.
ACS omega, 2018, 3, 2786-2792
4516187 CIFC80 H56 Cl2 Cu2 Ir2 N12 O4P -112.147; 12.958; 14.044
75.832; 67.388; 74.135
1938.5Chandrasekhar, Vadapalli; Mahanti, Bani; Pandey, Mrituanjay D.; Narayanan, R. Suriya
Cyclometalated Ir(III) Complex as a Metalloligand and a Selective Cu(II) Sensor: Synthesis and Structural Characterization of a Heterometallic Tetranuclear Ir(III)/Cu(II) Complex.
ACS omega, 2018, 3, 2786-2792
4516188 CIFC112 H124 Ir2 N10 O4P 1 21 19.0272; 29.178; 18.4176
90; 99.641; 90
4782.6Huckaba, Aron J.; Senes, Alessia; Aghazada, Sadig; Babaei, Azin; Meskers, Stefan C. J.; Zimmermann, Iwan; Schouwink, Pascal; Gasilova, Natalia; Janssen, René A J; Bolink, Henk J.; Nazeeruddin, Mohammad Khaja
Bis(arylimidazole) Iridium Picolinate Emitters and Preferential Dipole Orientation in Films.
ACS omega, 2018, 3, 2673-2682
4516189 CIFC49 H52 Ir N5 O2P 1 21/c 118.644; 8.9321; 25.915
90; 96.994; 90
4283.5Huckaba, Aron J.; Senes, Alessia; Aghazada, Sadig; Babaei, Azin; Meskers, Stefan C. J.; Zimmermann, Iwan; Schouwink, Pascal; Gasilova, Natalia; Janssen, René A J; Bolink, Henk J.; Nazeeruddin, Mohammad Khaja
Bis(arylimidazole) Iridium Picolinate Emitters and Preferential Dipole Orientation in Films.
ACS omega, 2018, 3, 2673-2682
4516190 CIFC98 H104 Ir2 N10 O7P 1 21/c 119.025; 9.09; 25.534
90; 96.237; 90
4390Huckaba, Aron J.; Senes, Alessia; Aghazada, Sadig; Babaei, Azin; Meskers, Stefan C. J.; Zimmermann, Iwan; Schouwink, Pascal; Gasilova, Natalia; Janssen, René A J; Bolink, Henk J.; Nazeeruddin, Mohammad Khaja
Bis(arylimidazole) Iridium Picolinate Emitters and Preferential Dipole Orientation in Films.
ACS omega, 2018, 3, 2673-2682
4516191 CIFC14 H11 Cl N2P 1 21/c 110.914; 11.6724; 9.8263
90; 106.975; 90
1197.3Dey, Amrita; Singsardar, Mukta; Sarkar, Rajib; Hajra, Alakananda
Environment-Friendly Protocol for the Chlorination of Imidazoheterocycles by Chloramine-T.
ACS omega, 2018, 3, 3513-3521
4516192 CIFCo2.44 Na9 O54 W9.56P 1 21/n 113.101; 17.775; 21.174
90; 93.628; 90
4920.9Thakur, Neha; Das Adhikary, Subhasis; Kumar, Mukesh; Mehta, Daisy; Padhan, Anil K.; Mandal, Debaprasad; Nagaiah, Tharamani C.
Ultrasensitive and Highly Selective Electrochemical Detection of Dopamine Using Poly(ionic liquids)-Cobalt Polyoxometalate/CNT Composite.
ACS omega, 2018, 3, 2966-2973
4516193 CIFC22 H26 N2 OP 1 21/c 19.163; 8.368; 24.984
90; 97.39; 90
1900Sheng, Lan; Chen, Qiaonan; Wang, Chunyu; Chen, Hongwei; Zhang, Ting; Qin, Tianyou; Li, Minjie; Zhang, Jinyan; Ma, Jing; Zhang, Sean Xiao-An
Oxazolidine Transient Bases as Molecular Platforms for Testing Dynamic CO<sub>2</sub> Capture in Biochemical Systems.
ACS omega, 2018, 3, 2883-2894
4516194 CIFC22 H25 N3 O3P 1 21/c 121.333; 7.865; 11.834
90; 100.552; 90
1952Sheng, Lan; Chen, Qiaonan; Wang, Chunyu; Chen, Hongwei; Zhang, Ting; Qin, Tianyou; Li, Minjie; Zhang, Jinyan; Ma, Jing; Zhang, Sean Xiao-An
Oxazolidine Transient Bases as Molecular Platforms for Testing Dynamic CO<sub>2</sub> Capture in Biochemical Systems.
ACS omega, 2018, 3, 2883-2894
4516195 CIFC23 H28 N2 O3 SP 1 21/c 123.398; 7.4277; 12.2111
90; 92.075; 90
2120.8Sheng, Lan; Chen, Qiaonan; Wang, Chunyu; Chen, Hongwei; Zhang, Ting; Qin, Tianyou; Li, Minjie; Zhang, Jinyan; Ma, Jing; Zhang, Sean Xiao-An
Oxazolidine Transient Bases as Molecular Platforms for Testing Dynamic CO<sub>2</sub> Capture in Biochemical Systems.
ACS omega, 2018, 3, 2883-2894
4516196 CIFC4 H14 Cl4 N2 PbI m m a14.1404; 5.79829; 14.2252
90; 90; 90
1166.33Wu, Guanhong; Zhou, Chenkun; Ming, Wenmei; Han, Dan; Chen, Shiyou; Yang, Dong; Besara, Tiglet; Neu, Jennifer; Siegrist, Theo; Du, Mao-Hua; Ma, Biwu; Dong, Angang
A One-Dimensional Organic Lead Chloride Hybrid with Excitation-Dependent Broadband Emissions
ACS Energy Letters, 2018, 3, 1443
4516197 CIFC5.4 H22.2 I7 N3.6 O2.4 Sn2P 4/m14.62; 14.62; 6.392
90; 90; 90
1366.3Tsai, Cheng-Min; Lin, Yu-Pei; Pola, Murali Krishna; Narra, Sudhakar; Jokar, Efat; Yang, Yaw-Wen; Diau, Eric Wei-Guang
Control of Crystal Structures and Optical Properties with Hybrid Formamidinium and 2-Hydroxyethylammonium Cations for Mesoscopic Carbon-Electrode Tin-Based Perovskite Solar Cells
ACS Energy Letters, 2018, 3, 2077
4516198 CIFC4 H16 I4 N2 O2 SnP n m a13.0062; 19.617; 6.3852
90; 90; 90
1629.1Tsai, Cheng-Min; Lin, Yu-Pei; Pola, Murali Krishna; Narra, Sudhakar; Jokar, Efat; Yang, Yaw-Wen; Diau, Eric Wei-Guang
Control of Crystal Structures and Optical Properties with Hybrid Formamidinium and 2-Hydroxyethylammonium Cations for Mesoscopic Carbon-Electrode Tin-Based Perovskite Solar Cells
ACS Energy Letters, 2018, 3, 2077
4516199 CIFC4 H16 I4 N2 O2 SnP 1 21/c 110.1959; 9.0234; 8.9297
90; 100.36; 90
808.15Tsai, Cheng-Min; Lin, Yu-Pei; Pola, Murali Krishna; Narra, Sudhakar; Jokar, Efat; Yang, Yaw-Wen; Diau, Eric Wei-Guang
Control of Crystal Structures and Optical Properties with Hybrid Formamidinium and 2-Hydroxyethylammonium Cations for Mesoscopic Carbon-Electrode Tin-Based Perovskite Solar Cells
ACS Energy Letters, 2018, 3, 2077
4516200 CIFC1.4 H6.2 I3 N1.6 O0.4 SnR 3 :H8.92; 8.92; 10.934
90; 90; 120
753.4Tsai, Cheng-Min; Lin, Yu-Pei; Pola, Murali Krishna; Narra, Sudhakar; Jokar, Efat; Yang, Yaw-Wen; Diau, Eric Wei-Guang
Control of Crystal Structures and Optical Properties with Hybrid Formamidinium and 2-Hydroxyethylammonium Cations for Mesoscopic Carbon-Electrode Tin-Based Perovskite Solar Cells
ACS Energy Letters, 2018, 3, 2077
4516781 CIFC38 H33 Cl4 N3 O13P 18.2491; 10.4883; 11.6077
82.052; 77.374; 88.501
970.58Chu, Hang; Smith, Joel M.; Felding, Jakob; Baran, Phil S.
Scalable Synthesis of (-)-Thapsigargin.
ACS central science, 2017, 3, 47-51
4516782 CIFC25 H33 N O8P 21 21 218.9642; 11.2161; 13.5628
90; 90; 90
2884.87Xu, Chen; Han, Arthur; Virgil, Scott C.; Reisman, Sarah E.
Chemical Synthesis of (+)-Ryanodine and (+)-20-Deoxyspiganthine.
ACS central science, 2017, 3, 278-282
4516783 CIFC42 H48 B N O10P 1 21 18.7826; 22.1496; 10.3099
90; 109.928; 90
1885.5Xu, Chen; Han, Arthur; Virgil, Scott C.; Reisman, Sarah E.
Chemical Synthesis of (+)-Ryanodine and (+)-20-Deoxyspiganthine.
ACS central science, 2017, 3, 278-282
4516784 CIFC33 H57 N O12P 21 21 2110.9374; 11.9604; 27.4814
90; 90; 90
3595Xu, Chen; Han, Arthur; Virgil, Scott C.; Reisman, Sarah E.
Chemical Synthesis of (+)-Ryanodine and (+)-20-Deoxyspiganthine.
ACS central science, 2017, 3, 278-282
4516785 CIFC58 H90.76 N2 O18.38P 3220.8804; 20.8804; 11.5639
90; 90; 120
4366.3Xu, Chen; Han, Arthur; Virgil, Scott C.; Reisman, Sarah E.
Chemical Synthesis of (+)-Ryanodine and (+)-20-Deoxyspiganthine.
ACS central science, 2017, 3, 278-282
4516786 CIFC27 H15 N3 O3P c c n3.8199; 19.117; 25.488
90; 90; 90
1861.3Mamada, Masashi; Inada, Ko; Komino, Takeshi; Potscavage, Jr, William J; Nakanotani, Hajime; Adachi, Chihaya
Highly Efficient Thermally Activated Delayed Fluorescence from an Excited-State Intramolecular Proton Transfer System.
ACS central science, 2017, 3, 769-777
4516787 CIFC102 H100 B2 N6 Ni O2P -112.6909; 16.3914; 20.9924
81.335; 76.622; 80.613
4162.4Bunescu, Ala; Lee, Sunwoo; Li, Qian; Hartwig, John F.
Catalytic Hydroxylation of Polyethylenes.
ACS central science, 2017, 3, 895-903
4516788 CIFC22 H26 O8C 1 2/c 125.102; 6.0323; 28.707
90; 111.423; 90
4046.6Roach, Jeremy J.; Sasano, Yusuke; Schmid, Cullen L.; Zaidi, Saheem; Katritch, Vsevolod; Stevens, Raymond C.; Bohn, Laura M.; Shenvi, Ryan A.
Dynamic Strategic Bond Analysis Yields a Ten-Step Synthesis of 20-nor-Salvinorin A, a Potent κ-OR Agonist.
ACS central science, 2017, 3, 1329-1336
4516789 CIFC16 H22 O5P 1 21/n 115.183; 6.01; 36.8552
90; 95.228; 90
3349Roach, Jeremy J.; Sasano, Yusuke; Schmid, Cullen L.; Zaidi, Saheem; Katritch, Vsevolod; Stevens, Raymond C.; Bohn, Laura M.; Shenvi, Ryan A.
Dynamic Strategic Bond Analysis Yields a Ten-Step Synthesis of 20-nor-Salvinorin A, a Potent κ-OR Agonist.
ACS central science, 2017, 3, 1329-1336
4516951 CIFC29 H30 Cl N O RuP 21 21 219.044; 13.524; 20.436
90; 90; 90
2499.5Brunner, Henri; Balázs, Gábor; Tsuno, Takashi; Iwabe, Haruka
PPh<sub>3</sub> Propeller Diastereomers: Bonding Motif Ph<sub>PPh<sub>3</sub></sub> Face-On π-Ar in Half-Sandwich Compounds [(π-Ar)LL'MPPh<sub>3</sub>].
ACS omega, 2018, 3, 982-990
4516952 CIFC47 H45 F6 N O P2 RuP 1 21 110.5006; 17.8634; 34.4468
90; 98.1; 90
6396.95Brunner, Henri; Balázs, Gábor; Tsuno, Takashi; Iwabe, Haruka
PPh<sub>3</sub> Propeller Diastereomers: Bonding Motif Ph<sub>PPh<sub>3</sub></sub> Face-On π-Ar in Half-Sandwich Compounds [(π-Ar)LL'MPPh<sub>3</sub>].
ACS omega, 2018, 3, 982-990
4516953 CIFC49 H49 Cl4 F6 N O P2 RuP 1 21 110.429; 16.431; 14.06
90; 98.59; 90
2382.3Brunner, Henri; Balázs, Gábor; Tsuno, Takashi; Iwabe, Haruka
PPh<sub>3</sub> Propeller Diastereomers: Bonding Motif Ph<sub>PPh<sub>3</sub></sub> Face-On π-Ar in Half-Sandwich Compounds [(π-Ar)LL'MPPh<sub>3</sub>].
ACS omega, 2018, 3, 982-990
4517034 CIFC9.5 H13 N O2 Zn0.5C 1 2/c 110.994; 12.322; 15.365
90; 104.93; 90
2011Anthony, S. Philip; Raghavaiah, P.; Radhakrishnan, T. P.
Extreme Molecular Orientations in a Dimorphic System: Polar/Centric and Polar/Polar Cogrowth Crystal Architectures
Crystal Growth & Design, 2003, 3, 631
4517138 CIFC31 H33 Fe O2 PP -19.2693; 9.4061; 15.4687
88.6025; 87.6725; 80.3371
1328.24Lanigan, Nicholas; Assoud, Abdeljalil; Wang, Xiaosong
Intermolecular Interactions of CpFePPh3(CO)CO(CH2)5CH3: From a Crystalline Solid to a Supramolecular “Iron-Truss” Polymer
ACS Macro Letters, 2014, 3, 1281
4517139 CIFC30 H31 Fe O2 PF d d 241.3534; 64.6397; 8.1309
90; 90; 90
21734.5Lanigan, Nicholas; Assoud, Abdeljalil; Wang, Xiaosong
Intermolecular Interactions of CpFePPh3(CO)CO(CH2)5CH3: From a Crystalline Solid to a Supramolecular “Iron-Truss” Polymer
ACS Macro Letters, 2014, 3, 1281
4517357 CIFC9.5 H13 N O2 Zn0.5F d d 211.181; 28.583; 12.309
90; 90; 90
3933.8Anthony, S. Philip; Raghavaiah, P.; Radhakrishnan, T. P.
Extreme Molecular Orientations in a Dimorphic System: Polar/Centric and Polar/Polar Cogrowth Crystal Architectures
Crystal Growth & Design, 2003, 3, 631
4518396 CIFC110 H172 N4 O6 Si2 ZnC 1 2/c 138.361; 15.8528; 17.6645
90; 100.831; 90
10550.9Choi, Sunghan; Kim, Chul Hoon; Baeg, Jin-Ook; Son, Ho-Jin; Pac, Chyongjin; Kang, Sang Ook
Collisional Electron Transfer Route between Homogeneous Porphyrin Dye and Catalytic TiO2/Re(I) Particles for CO2 Reduction
ACS Applied Energy Materials, 2020, 3, 11581-11596
5000155 CIFC6 H5 N O2P 1 21/c 13.8014; 11.6153; 12.9843
90; 94.984; 90
571.15Boese, Roland; Bläser, Dieter; Nussbaumer, Michael; Krygowski, Tadeusz Marek
Low temperature crystal and molecular structure of nitrobenzene
Structural Chemistry, 1992, 3, 363-368
5900002 CIFC H4 N2 OP -4 21 m5.67; 5.67; 4.726
90; 90; 90
151.94Strukturbericht, 3, 660
5900004 CIFC2 H6 N2 OP 21 21 216.89; 6.96; 8.45
90; 90; 90
405.21Strukturbericht, 3, 660
5900006 CIFC H5 B F3 NP 1 21/m 15.06; 7.28; 5.81
90; 101.52; 90
209.71Geller, S.; Hoard, J. L.
Structures of molecular addition compounds. I. Monomethyl amine–boron trifluoride, H~3~CH~2~N–BF~3~
Acta Crystallographica, 1950, 3, 121-129
5900007 CIFC2 H3 B F3 NP n m a7.76; 7.2; 8.34
90; 90; 90
465.97Hoard, J. L.; Owen, T. B.; Buzzell, A.; Salmon, O. N.
Structures of molecular addition compounds. II. Methyl cyanide‒boron trifluoride, H~3~CCN‒BF~3~
Acta Crystallographica, 1950, 3, 130-137
5900011 CIFC2 H2 I2P 1 21/c 14.58; 13.31; 4.58
90; 105.33; 90
269.26Strukturbericht, 3, 666
5900012 CIFC2 H4 I2P 1 21/c 14.768; 12.897; 4.784
90; 105.08; 90
284.05Strukturbericht, 3, 665
5900026 CIFC3 H10 Cl NC 1 2/m 19.06; 8.58; 7.34
90; 98; 90
565.02King, M. V.; Lipscomb, W. N.
The low-temperature modification of n-propyl-ammonium chloride
Acta Crystallographica, 1950, 3, 227-230
5900027 CIFC3 H10 Cl NP 4/n m m6.22; 6.22; 7.377
90; 90; 90
285.4King, M. V.; Lipscomb, W. N.
The structures of the n-propylammonium halides at room temperature
Acta Crystallographica, 1950, 3, 222-227
5900028 CIFC6 H16 N2P b c a6.94; 5.77; 19.22
90; 90; 90
769.64Binnie, W. P.; Robertson, J. M.
The crystal structure of hexamethylenediamine
Acta Crystallographica, 1950, 3, 424-429
5900032 CIFC2 H2 O4P c a b6.546; 7.847; 6.086
90; 90; 90
312.62Strukturbericht, 3, 671
5900033 CIFC2 H2 O4P 1 21/c 15.3; 6.09; 5.51
90; 115.5; 90
160.52Strukturbericht, 3, 672
5910156 CIFF10 Ho3 NaP m -3 n5.81; 5.81; 5.81
90; 90; 90
196.123Wyckoff, R. W. G.
Page 484-486 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 484-484
5910158 CIFO4 W ZnP 1 2/c 14.691; 5.72; 4.925
90; 90.38; 90
132.147Wyckoff, R. W. G.
Page 41-43 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 41-41
5910159 CIFF8 N4 P4P 1 21/a 17.4; 13.83; 5.16
90; 109.3; 90
498.407Wyckoff, R. W. G.
Page 467 & 468 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 467-468
5910160 CIFO7 P2 SiP a -37.46; 7.46; 7.46
90; 90; 90
415.161Wyckoff, R. W. G.
Pages 429 & 431 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 429-431
5910161 CIFMn2 Ni O4F d -3 m :28.4028; 8.4028; 8.4028
90; 90; 90
593.297Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910163 CIFNa O4 ReI 41/a :25.362; 5.362; 11.718
90; 90; 90
336.905Wyckoff, R. W. G.
Pages 19-21 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-19
5910164 CIFO7 P2 SnP a -37.89; 7.89; 7.89
90; 90; 90
491.169Wyckoff, R. W. G.
Pages 429 & 431 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 429-431
5910166 CIFF14 Fe3 Na5P 4/m n c7.34; 7.34; 10.38
90; 90; 90
559.229Wyckoff, R. W. G.
Page 492 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 492-492
5910167 CIFMn O4 Ti2F d -3 m :28.6; 8.6; 8.6
90; 90; 90
636.056Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910168 CIFCu O4 SP n m a8.3956; 6.6982; 4.8291
90; 90; 90
271.566Wyckoff, R. W. G.
Page 40 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 40-40
5910169 CIFCu S4 Ti2F d -3 m :29.88; 9.88; 9.88
90; 90; 90
964.43Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910170 CIFCd2 Mo3 O8P 63 m c5.835; 5.835; 10.815
90; 90; 120
318.889Wyckoff, R. W. G.
Page 467 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 467-467
5910171 CIFHo O4 VI 41/a m d :27.1214; 7.1214; 6.2926
90; 90; 90
319.125Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910172 CIFCu2 S4 SnF d -3 m :210.87; 10.87; 10.87
90; 90; 90
1284.37Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910173 CIFCd O4 Rh2F d -3 m :28.781; 8.781; 8.781
90; 90; 90
677.067Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910174 CIFCd In2 S4F d -3 m :210.818; 10.818; 10.818
90; 90; 90
1266.02Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910175 CIFCl9 Cs3 V2P 63/m m c7.24; 7.24; 17.94
90; 90; 120
814.386Wyckoff, R. W. G.
Page 475 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 475-475
5910176 CIFCr K3 O8I -4 2 m6.7; 6.7; 7.6
90; 90; 90
341.164Wyckoff, R. W. G.
Page 455 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 455-455
5910177 CIFAl2 Hg Se4I -45.708; 5.708; 10.74
90; 90; 90
349.923Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910178 CIFBa Cr O4P n m a9.103; 5.526; 7.337
90; 90; 90
369.074Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910180 CIFCl9 Cs3 Ti2P 63/m m c7.32; 7.32; 17.97
90; 90; 120
833.875Wyckoff, R. W. G.
Page 475 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 475-475
5910181 CIFO4 Rb2 SeP n m a8.01; 6.18; 10.85
90; 90; 90
537.095Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910182 CIFAs Bi O4I 41/a :25.08; 5.08; 11.7
90; 90; 90
301.935Wyckoff, R. W. G.
Pages 19-21 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-19
5910184 CIFBi O4 SbC 1 2/c 15.464; 4.887; 11.81
90; 101; 90
309.563Wyckoff, R. W. G.
Page 44 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 44-44
5910185 CIFMg O4 Rh2F d -3 m :28.53; 8.53; 8.53
90; 90; 90
620.65Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910186 CIFIn2 Mg S4F d -3 m :210.708; 10.708; 10.708
90; 90; 90
1227.79Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910187 CIFK O4 TcI 41/a :25.654; 5.654; 13.03
90; 90; 90
416.539Wyckoff, R. W. G.
Pages 19-21 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-19
5910189 CIFCs F13 Sb4I 4/m9.639; 9.639; 6.785
90; 90; 90
630.397Wyckoff, R. W. G.
Page 489 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 489-489
5910190 CIFNb O4 YI 41/a :25.16; 5.16; 10.91
90; 90; 90
290.485Wyckoff, R. W. G.
Pages 19, 20 & 21 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-21
5910191 CIFO4 Pb SeP n m a8.592; 5.63; 7.129
90; 90; 90
344.851Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910193 CIFMo3 O8 Zn2P 63 m c5.775; 5.775; 9.915
90; 90; 120
286.37Wyckoff, R. W. G.
Page 467 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 467-467
5910194 CIFAg I O4I 41/a :25.374; 5.374; 12.094
90; 90; 90
349.273Wyckoff, R. W. G.
Pages 19 & 21 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-21
5910195 CIFCu Ga2 O4F d -3 m :28.39; 8.39; 8.39
90; 90; 90
590.59Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910196 CIFF8 Na3 TaC 1 2/c 17.05; 7.05; 8.05
90; 120.55; 90
344.565Wyckoff, R. W. G.
Page 456 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 456-456
5910197 CIFK2 O4 TeP n m a7.9; 6.25; 10.5
90; 90; 90
518.438Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910198 CIFK3 O8 TaI -4 2 m6.78; 6.78; 7.88
90; 90; 90
362.231Wyckoff, R. W. G.
Page 455 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 455-455
5910199 CIFGa O4 PC 2 2 216.967; 6.967; 6.866
90; 90; 90
333.269Wyckoff, R. W. G.
Pages 19, 20 & 22 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-22
5910200 CIFCo2 Mg O4F d -3 m :28.107; 8.107; 8.107
90; 90; 90
532.82Wyckoff, R. W. G.
Page 76 & 78 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-78
5910202 CIFMo Na2 O4F d -3 m :29.108; 9.108; 9.108
90; 90; 90
755.56Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910203 CIFCr O4 ZnC m c m5.505; 8.383; 6.219
90; 90; 90
286.997Wyckoff, R. W. G.
Page 37 & 38 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 37-38
5910204 CIFCe O4 VI 41/a m d :27.399; 7.399; 6.496
90; 90; 90
355.625Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910206 CIFMn2 Mo3 O8P 63 m c5.795; 5.795; 10.267
90; 90; 120
298.594Wyckoff, R. W. G.
Page 467 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 467-467
5910207 CIFCu S4 V2F d -3 m :29.824; 9.824; 9.824
90; 90; 90
948.124Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910208 CIFAl2 Cd O4F d -3 m :28.078; 8.078; 8.078
90; 90; 90
527.122Wyckoff, R. W. G.
Page 76 & 78 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-78
5910211 CIFAs O4 ScI 41/a m d :26.7101; 6.7101; 6.1126
90; 90; 90
275.223Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910212 CIFCl9 Cs3 Fe2P -3 m 17.28; 7.28; 8.9
90; 90; 120
408.492Wyckoff, R. W. G.
Page 478 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 478-478
5910215 CIFCr Cu O4C m c m5.426; 8.925; 5.878
90; 90; 90
284.654Wyckoff, R. W. G.
Page 37 & 38 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 37-38
5910219 CIFK2 O4 SeP n m a7.66; 6; 10.47
90; 90; 90
481.201Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910221 CIFO4 Sm VI 41/a m d :27.266; 7.266; 6.394
90; 90; 90
337.57Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910222 CIFLu O4 VI 41/a m d :27.026; 7.026; 6.231
90; 90; 90
307.591Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910223 CIFO4 Tm VI 41/a m d :27.071; 7.071; 6.263
90; 90; 90
313.144Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910224 CIFNa2 O4 WF d -3 m :29.1297; 9.1297; 9.1297
90; 90; 90
760.973Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910225 CIFAl2 Cr S4F d -3 m :29.914; 9.914; 9.914
90; 90; 90
974.421Wyckoff, R. W. G.
Page 76 & 78 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-78
5910226 CIFMo3 Ni2 O8P 63 m c5.752; 5.752; 9.865
90; 90; 120
282.661Wyckoff, R. W. G.
Page 467 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 467-467
5910228 CIFBi4 O12 Ti3F m m m5.51; 5.448; 32.84
90; 90; 90
985.807Wyckoff, R. W. G.
Page 488-489 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 488-488
5910230 CIFCo O4 Rh2F d -3 m :28.495; 8.495; 8.495
90; 90; 90
613.042Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910231 CIFCo In2 S4F d -3 m :210.58; 10.58; 10.58
90; 90; 90
1184.29Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910233 CIFGd O4 VI 41/a m d :27.211; 7.211; 6.35
90; 90; 90
330.191Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910234 CIFAl P S4P 2 2 25.61; 5.67; 9.05
90; 90; 90
287.869Wyckoff, R. W. G.
Page 36 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 36-36
5910235 CIFBa2 Ge O4P n m a10.33; 7.74; 5.88
90; 90; 90
470.131Wyckoff, R. W. G.
Pages 91 & 94 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 91-94
5910236 CIFCd Ga2 O4F d -3 m :28.57; 8.57; 8.57
90; 90; 90
629.423Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910237 CIFHg In2 Te4I -46.186; 6.186; 12.37
90; 90; 90
473.358Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910238 CIFCs3 O8 TaI -4 2 m7.37; 7.37; 8.34
90; 90; 90
453.003Wyckoff, R. W. G.
Page 455 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 455-455
5910239 CIFCl8 I SbP 416.98; 6.98; 24.2
90; 90; 90
1179.03Wyckoff, R. W. G.
Pages 452-455 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 452-452
5910241 CIFCu Mn2 O4F d -3 m :28.33; 8.33; 8.33
90; 90; 90
578.01Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910242 CIFCr2 Mn S4F d -3 m :210.045; 10.045; 10.045
90; 90; 90
1013.56Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910244 CIFMn O4 Rh2F d -3 m :28.613; 8.613; 8.613
90; 90; 90
638.945Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910245 CIFIn2 Mn S4F d -3 m :210.715; 10.715; 10.715
90; 90; 90
1230.2Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910246 CIFNd O4 VI 41/a m d :27.329; 7.329; 6.4356
90; 90; 90
345.683Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910247 CIFCr2 Cu Te4F d -3 m :211.051; 11.051; 11.051
90; 90; 90
1349.6Wyckoff, R. W. G.
Page 76 & 78 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-78
5910248 CIFAs O4 TbI 41/a m d :27.1025; 7.1025; 6.3536
90; 90; 90
320.511Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910249 CIFO4 Sc TaP 1 2/c 14.8; 5.65; 5.1
90; 91.3; 90
138.276Wyckoff, R. W. G.
Page 41-43 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 41-41
5910250 CIFBe Cr2 O4P n m a9.792; 5.663; 4.555
90; 90; 90
252.584Wyckoff, R. W. G.
Pages 91 & 94 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 91-94
5910251 CIFAl2 Cd Se4I -45.746; 5.746; 10.68
90; 90; 90
352.616Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910252 CIFCo2 Ge O4F d -3 m :28.318; 8.318; 8.318
90; 90; 90
575.515Wyckoff, R. W. G.
Page 76 & 78 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-78
5910253 CIFGe O7 P2P a -37.52; 7.52; 7.52
90; 90; 90
425.259Wyckoff, R. W. G.
Pages 429 & 431 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 429-431
5910254 CIFAl2 Hg S4I -45.488; 5.488; 10.26
90; 90; 90
309.012Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910255 CIFCr Ga2 S4F d -3 m :29.95; 9.95; 9.95
90; 90; 90
985.075Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910256 CIFAs O4 TlI 41/a m d :26.9939; 6.9939; 6.2595
90; 90; 90
306.181Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910257 CIFAs Lu O4I 41/a m d :26.952; 6.952; 6.23
90; 90; 90
301.098Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910258 CIFGe Ni2 O4F d -3 m :28.221; 8.221; 8.221
90; 90; 90
555.615Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910259 CIFAs O4 TmI 41/a m d :27; 7; 6.256
90; 90; 90
306.544Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910261 CIFFe In2 S4F d -3 m :210.619; 10.619; 10.619
90; 90; 90
1197.43Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910262 CIFBa O4 WI 41/a :25.64; 5.64; 12.7
90; 90; 90
403.982Wyckoff, R. W. G.
Pages 19-21 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-19
5910263 CIFO4 Sr WI 41/a :25.4; 5.4; 11.9
90; 90; 90
347.004Wyckoff, R. W. G.
Pages 19, 20 & 22 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-22
5910264 CIFCs2 O4 SeP n m a8.36; 6.42; 11.26
90; 90; 90
604.338Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910266 CIFBe F4 Rb2P n m a7.66; 5.85; 10.13
90; 90; 90
453.935Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910267 CIFF13 Rb Sb4I 4/m9.635; 9.635; 6.563
90; 90; 90
609.264Wyckoff, R. W. G.
Page 489 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 489-489
5910268 CIFF10 Na Tm3P m -3 n5.74; 5.74; 5.74
90; 90; 90
189.119Wyckoff, R. W. G.
Page 484-486 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 484-484
5910269 CIFO7 P2 ThP a -38.721; 8.721; 8.721
90; 90; 90
663.283Wyckoff, R. W. G.
Pages 429 & 431 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 429-431
5910272 CIFAl2 S4 ZnF d -3 m :29.968; 9.968; 9.968
90; 90; 90
990.431Wyckoff, R. W. G.
Page 76 & 78 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-78
5910273 CIFCr O4 VC m c m5.568; 8.208; 5.977
90; 90; 90
273.162Wyckoff, R. W. G.
Page 37 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 37-37
5910274 CIFGa2 Te4 ZnI -45.937; 5.937; 11.87
90; 90; 90
418.393Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910275 CIFGa2 Hg S4I -45.507; 5.507; 10.23
90; 90; 90
310.246Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910276 CIFAs Eu O4I 41/a m d :27.1541; 7.1541; 6.3953
90; 90; 90
327.319Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910277 CIFNi O4 WP 1 2/c 14.6; 5.665; 4.912
90; 90.5; 90
127.997Wyckoff, R. W. G.
Page 41 & 42 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 41-42
5910278 CIFFe2 O4 PbF d -3 m :27.81; 7.81; 7.81
90; 90; 90
476.38Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910280 CIFBe F4 PbP n m a8.435; 5.341; 6.875
90; 90; 90
309.728Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910282 CIFGa2 Hg Se4I -45.714; 5.714; 10.78
90; 90; 90
351.965Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910283 CIFHf O7 P2P a -38.18; 8.18; 8.18
90; 90; 90
547.343Wyckoff, R. W. G.
Pages 429 & 431 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 429-431
5910284 CIFK3 O14 V5P 3 1 m8.6796; 8.6796; 4.9914
90; 90; 120
325.651Wyckoff, R. W. G.
Page 493 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 493-493
5910285 CIFF13 K Sb4I 4/m9.636; 9.636; 6.365
90; 90; 90
591.006Wyckoff, R. W. G.
Page 489 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 489-489
5910286 CIFIn2 Te4 ZnI -46.122; 6.122; 12.24
90; 90; 90
458.742Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910287 CIFEr3 F10 NaP m -3 n5.78; 5.78; 5.78
90; 90; 90
193.101Wyckoff, R. W. G.
Page 484-486 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 484-484
5910288 CIFHg In2 Se4I -45.763; 5.763; 11.8
90; 90; 90
391.904Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910289 CIFCr In2 S4F d -3 m :210.59; 10.59; 10.59
90; 90; 90
1187.65Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910290 CIFCl O4 RbP n m a9.269; 5.814; 7.49
90; 90; 90
403.636Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910291 CIFB5 K O8P b c a7.42; 11.69; 14.72
90; 90; 90
1276.81Wyckoff, R. W. G.
Pages 469-471 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 469-469
5910292 CIFGa2 S4 ZnI -45.273; 5.273; 10.44
90; 90; 90
290.279Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910293 CIFCr O4 Tl2P n m a7.908; 5.913; 10.73
90; 90; 90
501.735Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910294 CIFO7 P2 PuP a -38.56; 8.56; 8.56
90; 90; 90
627.222Wyckoff, R. W. G.
Pages 429 & 431 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 429-431
5910295 CIFCd Ga2 Te4I -46.093; 6.093; 11.81
90; 90; 90
438.442Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910296 CIFCo Ga2 O4F d -3 m :28.325; 8.325; 8.325
90; 90; 90
576.969Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910297 CIFO4 Tb VI 41/a m d :27.179; 7.179; 6.324
90; 90; 90
325.927Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910299 CIFEr O4 VI 41/a m d :27.1; 7.1; 6.279
90; 90; 90
316.524Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910300 CIFO4 V YbI 41/a m d :27.043; 7.043; 6.248
90; 90; 90
309.925Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910301 CIFK3 Nb O8I -4 2 m6.78; 6.78; 7.86
90; 90; 90
361.312Wyckoff, R. W. G.
Page 455 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 455-455
5910302 CIFAs2 Cl9 Cs3P 3 2 17.39; 7.39; 8.93
90; 90; 120
422.349Wyckoff, R. W. G.
Page 475-477 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 475-475
5910303 CIFB O4 TaI 41/a m d :26.213; 6.213; 5.486
90; 90; 90
211.767Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910304 CIFO4 Pr VI 41/a m d :27.367; 7.367; 6.468
90; 90; 90
351.036Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910305 CIFFe2 Mo O4F d -3 m :28.501; 8.501; 8.501
90; 90; 90
614.342Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910306 CIFB F4 TlP n m a9.47; 5.81; 7.4
90; 90; 90
407.153Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910307 CIFCd In2 Te4I -46.204; 6.204; 12.4
90; 90; 90
477.271Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910308 CIFBe F4 K2P n m a7.29; 5.63; 9.83
90; 90; 90
403.45Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910309 CIFHg In2 S4F d -3 m :210.833; 10.833; 10.833
90; 90; 90
1271.3Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910310 CIFF10 Na Y3P m -3 n5.675; 5.675; 5.675
90; 90; 90
182.767Wyckoff, R. W. G.
Page 484-486 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 484-484
5910311 CIFBi O4 VI 41/a m d :27.2999; 7.2999; 6.4573
90; 90; 90
344.1Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910312 CIFBa Be F4P n m a8.73; 5.65; 6.613
90; 90; 90
326.183Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910314 CIFCo O4 SP n m a8.624; 6.715; 4.744
90; 90; 90
274.726Wyckoff, R. W. G.
Pages 40 & 41 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 40-41
5910315 CIFNa O4 TeI 41/a :25.339; 5.339; 11.869
90; 90; 90
338.325Wyckoff, R. W. G.
Pages 19-21 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-19
5910316 CIFCo O4 WP 1 2/c 14.66; 5.69; 4.98
90; 90; 90
132.047Wyckoff, R. W. G.
Page 41-43 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 41-41
5910317 CIFAl2 Cd S4I -45.564; 5.564; 10.32
90; 90; 90
319.488Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910318 CIFGa2 Se4 ZnI -45.496; 5.496; 10.99
90; 90; 90
331.964Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910319 CIFF13 Sb4 TlI 4/m9.637; 9.637; 6.584
90; 90; 90
611.468Wyckoff, R. W. G.
Page 489 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 489-489
5910320 CIFGa2 Ni O4F d -3 m :28.262; 8.262; 8.262
90; 90; 90
563.969Wyckoff, R. W. G.
Page 76 & 80 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-80
5910321 CIFCr2 Se4 ZnF d -3 m :210.443; 10.443; 10.443
90; 90; 90
1138.87Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910322 CIFDy O4 VI 41/a m d :27.1434; 7.1434; 6.313
90; 90; 90
322.141Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910323 CIFO4 Rh2 ZnF d -3 m :28.54; 8.54; 8.54
90; 90; 90
622.836Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910324 CIFCo2 Mo3 O8P 63 m c5.767; 5.767; 9.915
90; 90; 120
285.577Wyckoff, R. W. G.
Page 467 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 467-467
5910325 CIFK2 Mn O4P n m a7.66; 5.89; 10.33
90; 90; 90
466.063Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910326 CIFIn2 Se4 ZnI -45.71; 5.71; 11.42
90; 90; 90
372.339Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910327 CIFCr O4 Rb2P n m a8.001; 6.074; 10.722
90; 90; 90
521.069Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910328 CIFI O4 RbI 41/a :25.921; 5.921; 13.052
90; 90; 90
457.58Wyckoff, R. W. G.
Pages 19, 20 & 22 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-22
5910329 CIFBa Mn O4P n m a9.065; 5.472; 7.304
90; 90; 90
362.305Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910330 CIFAl2 O4 SnF d -3 m :28.12; 8.12; 8.12
90; 90; 90
535.387Wyckoff, R. W. G.
Page 76 & 78 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-78
5910331 CIFMo O4 SrI 41/a :25.36; 5.36; 11.94
90; 90; 90
343.031Wyckoff, R. W. G.
Pages 19, 20 & 22 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-22
5910332 CIFBe F4 Na2P n m a6.56; 4.892; 10.9
90; 90; 90
349.798Wyckoff, R. W. G.
Pages 95 & 102 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 95-102
5910333 CIFCr2 Cu S4F d -3 m :29.629; 9.629; 9.629
90; 90; 90
892.778Wyckoff, R. W. G.
Page 76 & 78 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-78
5910334 CIFGe O4 Sr2P n m a9.85; 7.42; 5.73
90; 90; 90
418.789Wyckoff, R. W. G.
Pages 91 & 94 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 91-94
5910336 CIFCd Ga2 S4I -45.577; 5.577; 10.08
90; 90; 90
313.518Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910337 CIFBe Cs2 F4P n m a10; 5.8; 4.5
90; 90; 90
261Wyckoff, R. W. G.
Pages 91 & 94 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 91-94
5910338 CIFNb O4 ScP 1 2/c 14.8; 5.65; 5.09
90; 91.42; 90
137.998Wyckoff, R. W. G.
Page 41-43 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 41-41
5910339 CIFFe2 Ge O4F d -3 m :28.411; 8.411; 8.411
90; 90; 90
595.036Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910340 CIFCd Ga2 Se4I -45.742; 5.742; 10.73
90; 90; 90
353.774Wyckoff, R. W. G.
Page 72 & 74 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 72-74
5910341 CIFAs Ho O4I 41/a m d :27.0548; 7.0548; 6.3159
90; 90; 90
314.344Wyckoff, R. W. G.
Pages 15 & 17 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 15-17
5910342 CIFCe O7 P2P a -38.338; 8.338; 8.338
90; 90; 90
579.676Wyckoff, R. W. G.
Pages 429 & 431 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 429-431
5910343 CIFBa Fe O4P n m a9.103; 5.446; 7.301
90; 90; 90
361.947Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910345 CIFCl O4 TlP n m a9.304; 5.845; 7.51
90; 90; 90
408.408Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910346 CIFCd O4 V2F d -3 m :28.68; 8.68; 8.68
90; 90; 90
653.972Wyckoff, R. W. G.
Page 76 & 81 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-81
5910347 CIFMn O4 WP 1 2/c 14.829; 5.759; 4.998
90; 91.1; 90
138.97Wyckoff, R. W. G.
Page 41-43 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 41-41
5910348 CIFGe Mg2 O4P n m a10.304; 6.032; 4.913
90; 90; 90
305.361Wyckoff, R. W. G.
Pages 91 & 94 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 91-94
5910349 CIFCr2 Fe O4F d -3 m :28.376; 8.376; 8.376
90; 90; 90
587.638Wyckoff, R. W. G.
Page 76 & 79 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 76-79
5910350 CIFCl9 Cr2 Cs3P 63/m m c7.22; 7.22; 17.93
90; 90; 120
809.441Wyckoff, R. W. G.
Page 475 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 475-475
5910351 CIFCl9 Cs3 Sb2P -3 m 17.61; 7.61; 9.32
90; 90; 120
467.429Wyckoff, R. W. G.
Page 478 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 478-478
5910352 CIFCr3 K O8C 1 2/m 18.593; 5.466; 7.641
90; 96.39; 90
356.663Wyckoff, R. W. G.
Page 464 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 464-464
5910353 CIFBa O4 SeP n m a9.034; 5.645; 7.364
90; 90; 90
375.541Wyckoff, R. W. G.
Pages 46 & 47 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 46-47
5910354 CIFGe O4 ZrI 41/a :24.871; 4.871; 10.57
90; 90; 90
250.791Wyckoff, R. W. G.
Pages 19, 20 & 21 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 19-21
5910355 CIFBa O9 Ti4P m m n :214.53; 3.79; 6.29
90; 90; 90
346.382Wyckoff, R. W. G.
Page 479 & 480 from the Structure of Crystals, vol. 3 by Wyckoff R W G. published by Interscience Publishers, Inc. in 1951
The Structure of Crystals, 1951, 3, 479-480
6000464 CIFC H2 Ag3 O9 P2 VP 1 21/n 18.9404; 8.0226; 11.7395
90; 100.72; 90
827.32Barthelet, K.; Riou, D.; Ferey, G.
Hydrothermal synthesis and structure determination of Ag-3((VO2)-O-V){O3P-CH2-PO3} or MIL-42: a new vanadium(V) methylendiphosphonate inserting silver cations
Solid State Sciences, 2001, 3, 203-209
6000473 CIFC3 H16 Be3 N2 O16 P4P 1 21/n 17.4219; 31.5289; 13.6682
90; 91.807; 90
3196.83Harrison, W. T. A.
[H3N(CH2)(3)NH3].Be3(HPO4)(4), a three-dimensional framework beryllophosphate containing tetrahedral 10-rings and 12-rings
International Journal of Inorganic Materials, 2001, 3, 17-22
6000545 CIFD6 K O9 P UP 21 c n6.9931; 6.9733; 17.6113
90; 90; 90
858.81Cole, M.; Fitch, A. N.; Prince, E.
Low-temperature structure of KUO2PO4.3D2O determined from combined synchrotron radiation and neutron powder diffraction measurements
Journal of Materials Chemistry, 1993, 3, 519-522
6000750 CIFO3P b c a7.7888; 6.6973; 6.8413
90; 90; 90
356.87Marx, R.; Ibberson, R. M.
Powder diffraction study on solid ozone
Solid State Sciences, 2001, 3, 195-202
6000756 CIFH O31 P6 Rb6 V6Pmn213.5505; 7.1407; 14.704
90; 90; 90
1422.76Le, Fur E; De, Villars B; Tortelier, J.; Pivan, J. Y.
New data on rubidium vanadium phosphate Structure determination of the disordered (V-V-P-V) compound Rb-6(V2O3)(2)(VO)(2)(PO4)(4)(HP2-xVxO7) with x similar to 0.6
International Journal of Inorganic Materials, 2001, 3, 9-15
7101000 CIFC19 H18 O4P 1 21/c 113.0132; 8.6004; 14.162
90; 91.558; 90
1584.4Clarke, Paul A.; Martin, William H. C.; Hargreaves, Jason M.; Wilson, Claire; Blake, Alexander J.
The one-pot, multi-component construction of highly substituted tetrahydropyran-4-ones using the Maitland–Japp reaction
Organic & Biomolecular Chemistry, 2005, 3, 3551
7101001 CIFC19 H18 O4P -15.5429; 9.5351; 15.1955
82.937; 85.273; 77.19
775.9Clarke, Paul A.; Martin, William H. C.; Hargreaves, Jason M.; Wilson, Claire; Blake, Alexander J.
The one-pot, multi-component construction of highly substituted tetrahydropyran-4-ones using the Maitland–Japp reaction
Organic & Biomolecular Chemistry, 2005, 3, 3551
7112563 CIFC19 H17 N3 O3P 1 21/c 116.266; 11.114; 9.8401
90; 101.629; 90
1742.4Ongarora, Benson G.; Hu, Xiaoke; Li, Hairong; Fronczek, Frank R.; Vicente, M Graça H
Syntheses and properties of trimethylaminophenoxy-substituted Zn((II))-phthalocyanines.
MedChemComm, 2012, 3, 179-194
7112564 CIFC19 H17 N3 O3P c a 2110.139; 8.597; 20.157
90; 90; 90
1757Ongarora, Benson G.; Hu, Xiaoke; Li, Hairong; Fronczek, Frank R.; Vicente, M Graça H
Syntheses and properties of trimethylaminophenoxy-substituted Zn((II))-phthalocyanines.
MedChemComm, 2012, 3, 179-194
7112565 CIFC30 H30 N4 O6P -110.0348; 12.0728; 13.3158
110.46; 102.622; 101.132
1409.38Ongarora, Benson G.; Hu, Xiaoke; Li, Hairong; Fronczek, Frank R.; Vicente, M Graça H
Syntheses and properties of trimethylaminophenoxy-substituted Zn((II))-phthalocyanines.
MedChemComm, 2012, 3, 179-194
7112566 CIFC30.4 H18.8 Cl4.8 N4 O2P -18.9371; 10.3208; 16.1899
77.863; 81.983; 78.622
1423.75Ongarora, Benson G.; Hu, Xiaoke; Li, Hairong; Fronczek, Frank R.; Vicente, M Graça H
Syntheses and properties of trimethylaminophenoxy-substituted Zn((II))-phthalocyanines.
MedChemComm, 2012, 3, 179-194
7112567 CIFC49 H63 Cl N2 O6 ZnP -19.608; 14.966; 17.648
112.645; 98.126; 90.686
2312.4Pucci, Daniela; Bellini, Tommaso; Crispini, Alessandra; D'Agnano, Igea; Liguori, Paola F.; Garcia-Orduña, Pilar; Pirillo, Sante; Valentini, Alessandra; Zanchetta, Giuliano
DNA binding and cytotoxicity of fluorescent curcumin-based Zn(ii) complexes
MedChemComm, 2012, 3, 462
7112568 CIFC13 H21 B F3 PP n a 2111.372; 11.428; 11.129
90; 90; 90
1446.3Li, Zibo; Chansaenpak, Kantapat; Liu, Shuanglong; Wade, Casey R.; Conti, Peter S.; Gabbaï, François P.
Harvesting 18F-fluoride ions in water via direct 18F–19F isotopic exchange: radiofluorination of zwitterionic aryltrifluoroborates and in vivo stability studies
MedChemComm, 2012, 3, 1305
7112569 CIFC21 H19 B F3 O2 PP 1 21/c 19.163; 12.426; 17.335
90; 100.483; 90
1941Li, Zibo; Chansaenpak, Kantapat; Liu, Shuanglong; Wade, Casey R.; Conti, Peter S.; Gabbaï, François P.
Harvesting 18F-fluoride ions in water via direct 18F–19F isotopic exchange: radiofluorination of zwitterionic aryltrifluoroborates and in vivo stability studies
MedChemComm, 2012, 3, 1305
7112570 CIFC25 H28 O5P 1 21/c 111.7974; 13.942; 13.4238
90; 101.254; 90
2165.5Venkatesham, A.; Rao, R. Srinivasa; Nagaiah, K.; Yadav, J. S.; RoopaJones, G.; Basha, S. J.; Sridhar, B.; Addlagatta, A.
Synthesis of new chromeno-annulated cis-fused pyrano[3,4-c]pyran derivatives via domino Knoevenagel–hetero-Diels–Alder reactions and their biological evaluation towards antiproliferative activity
MedChemComm, 2012, 3, 652
7112571 CIFC22 H22 O5P 1 21/n 115.4539; 7.4613; 16.2148
90; 106.214; 90
1795.3Venkatesham, A.; Rao, R. Srinivasa; Nagaiah, K.; Yadav, J. S.; RoopaJones, G.; Basha, S. J.; Sridhar, B.; Addlagatta, A.
Synthesis of new chromeno-annulated cis-fused pyrano[3,4-c]pyran derivatives via domino Knoevenagel–hetero-Diels–Alder reactions and their biological evaluation towards antiproliferative activity
MedChemComm, 2012, 3, 652
7112572 CIFC28 H28 N2 O2P 1 21/c 115.248; 12.5719; 14.0243
90; 115.645; 90
2423.6Mahesh Kumar, P.; Siva Kumar, K.; Meda, Chandana L. T.; Rajeshwar Reddy, G.; Mohakhud, Pradeep K.; Mukkanti, K.; Rama Krishna, G.; Malla Reddy, C.; Rambabu, D.; Shiva Kumar, K.; Krishna Priya, K.; Chennubhotla, Keerthana Sarma; Banote, Rakesh Kumar; Kulkarni, Pushkar; Parsa, Kishore V. L.; Pal, Manojit
(Pd/C-mediated)coupling‒iodocyclization‒coupling strategy in discovery of novel PDE4 inhibitors: a new synthesis of pyrazolopyrimidines
MedChemComm, 2012, 3, 667
7112573 CIFC22 H19 I N2 O2P 1 21/c 17.3912; 12.3586; 20.4375
90; 94.331; 90
1861.53Mahesh Kumar, P.; Siva Kumar, K.; Meda, Chandana L. T.; Rajeshwar Reddy, G.; Mohakhud, Pradeep K.; Mukkanti, K.; Rama Krishna, G.; Malla Reddy, C.; Rambabu, D.; Shiva Kumar, K.; Krishna Priya, K.; Chennubhotla, Keerthana Sarma; Banote, Rakesh Kumar; Kulkarni, Pushkar; Parsa, Kishore V. L.; Pal, Manojit
(Pd/C-mediated)coupling‒iodocyclization‒coupling strategy in discovery of novel PDE4 inhibitors: a new synthesis of pyrazolopyrimidines
MedChemComm, 2012, 3, 667
7112574 CIFC21 H23 N8 O2P -19.1873; 10.2806; 11.8644
94.876; 103.767; 102.245
1052.76Goldberg, Kristin; Groombridge, Sam; Hudson, Julian; Leach, Andrew G.; MacFaul, Philip A.; Pickup, Adrian; Poultney, Ruth; Scott, James S.; Svensson, Per H.; Sweeney, Joseph
Oxadiazole isomers: all bioisosteres are not created equal
MedChemComm, 2012, 3, 600
7112575 CIFC19 H18 F2 N8 O2P 21 21 216.8535; 11.759; 24.167
90; 90; 90
1947.6Goldberg, Kristin; Groombridge, Sam; Hudson, Julian; Leach, Andrew G.; MacFaul, Philip A.; Pickup, Adrian; Poultney, Ruth; Scott, James S.; Svensson, Per H.; Sweeney, Joseph
Oxadiazole isomers: all bioisosteres are not created equal
MedChemComm, 2012, 3, 600
7112576 CIFC23 H25 N3 O2 SP 1 21/c 118.4455; 5.8641; 20.5004
90; 114.067; 90
2024.69Lecoutey, Cédric; Rochais, Christophe; Genest, David; Butt-Gueulle, Sabrina; Ballandonne, Céline; Corvaisier, Sophie; Dulin, Fabienne; Lepailleur, Alban; Sopkova-de Oliveira Santos, Jana; Dallemagne, Patrick
Synthesis of dual AChE/5-HT4 receptor multi-target directed ligands
MedChemComm, 2012, 3, 627
7112577 CIFC16 H9 Cl F3 N3 O2P 1 c 111.115; 5.008; 14.112
90; 92.28; 90
784.9Masciocchi, Daniela; Villa, Stefania; Meneghetti, Fiorella; Pedretti, Alessandro; Barlocco, Daniela; Legnani, Laura; Toma, Lucio; Kwon, Byoung-Mog; Nakano, Shintaro; Asai, Akira; Gelain, Arianna
Biological and computational evaluation of an oxadiazole derivative (MD77) as a new lead for direct STAT3 inhibitors
MedChemComm, 2012, 3, 592
7112578 CIFC29 H32 Cr O5P 1 21/c 19.8549; 15.641; 16.5024
90; 100.507; 90
2501Saiai, Aroonchai; Bielig, Harald; Velder, Janna; Neudörfl, Jörg-Martin; Menning, Maureen; Kufer, Thomas A.; Schmalz, Hans-Günther
Hydrophenalene‒Cr(CO)3 complexes as anti-inflammatory agents based on specific inhibition of NOD2 signalling: a SAR study
MedChemComm, 2012, 3, 1377
7112579 CIFC29 H31 Cr F O5P -17.9722; 12.8619; 13.5661
68.848; 81.683; 81.459
1276.66Saiai, Aroonchai; Bielig, Harald; Velder, Janna; Neudörfl, Jörg-Martin; Menning, Maureen; Kufer, Thomas A.; Schmalz, Hans-Günther
Hydrophenalene‒Cr(CO)3 complexes as anti-inflammatory agents based on specific inhibition of NOD2 signalling: a SAR study
MedChemComm, 2012, 3, 1377
7112580 CIFC30 H34 Cr O5P -18.9498; 11.2208; 13.8926
90.023; 106.008; 104.171
1296.78Saiai, Aroonchai; Bielig, Harald; Velder, Janna; Neudörfl, Jörg-Martin; Menning, Maureen; Kufer, Thomas A.; Schmalz, Hans-Günther
Hydrophenalene‒Cr(CO)3 complexes as anti-inflammatory agents based on specific inhibition of NOD2 signalling: a SAR study
MedChemComm, 2012, 3, 1377
7112581 CIFC30 H31 Cr F3 O5F d d 232.4358; 34.6; 9.8268
90; 90; 90
11028.4Saiai, Aroonchai; Bielig, Harald; Velder, Janna; Neudörfl, Jörg-Martin; Menning, Maureen; Kufer, Thomas A.; Schmalz, Hans-Günther
Hydrophenalene‒Cr(CO)3 complexes as anti-inflammatory agents based on specific inhibition of NOD2 signalling: a SAR study
MedChemComm, 2012, 3, 1377
7112582 CIFC19 H11 Br Cl2 N2 O4 SP -19.2497; 10.8904; 11.0733
84.708; 73.497; 69.745
1003.34Ali, Sher; Saeed, Aamer; Abbas, Naeem; Shahid, Mohammad; Bolte, Michael; Iqbal, Jamshed
Design, synthesis and molecular modelling of novel methyl[4-oxo-2-(aroylimino)-3-(substituted phenyl)thiazolidin-5-ylidene]acetates as potent and selective aldose reductase inhibitors
MedChemComm, 2012, 3, 1428
7112583 CIFC12 H10 O2 S2P 1 21/n 15.6345; 6.2244; 16.3779
90; 92.902; 90
573.66Luo, Yi; Li, Xiaoling; Chen, Tianfeng; Wang, Yi; Zheng, Wenjie
Synthesis of a novel thiophene derivative that induces cancer cell apoptosis through modulation of AKT and MAPK pathways
MedChemComm, 2012, 3, 1143
7112584 CIFC21 H27 Fe N3 O2C 1 2/c 151.309; 7.2426; 10.7246
90; 94.098; 90
3975.2Spencer, John; Amin, Jahangir; Boddiboyena, Ramesh; Packham, Graham; Cavell, Breeze E.; Syed Alwi, Sharifah S.; Paranal, Ronald M.; Heightman, Tom D.; Wang, Minghua; Marsden, Brian; Coxhead, Peter; Guille, Matthew; Tizzard, Graham J.; Coles, Simon J.; Bradner., James E.
Click JAHAs: conformationally restricted ferrocene-based histone deacetylase inhibitors
MedChemComm, 2012, 3, 61
7150000 CIFC22 H31 N O15P 1 21 15.773; 22.641; 10.86
90; 105.38; 90
1369Pritchard, Robin G.; Stoodley, Richard J.; Yuen, Wai-Hung
Studies related to carba-pyranoses: synthesis of acetylated derivatives of 4-amino-2,4-dideoxy-3-O-(beta-D-glucopyranosyl)-beta-L-(and beta-D-) altrocarba-pyranose from a D-glucose template.
Organic & biomolecular chemistry, 2005, 3, 162-171
7150001 CIFC4 H5 N O4P 1 21/n 15.356; 6.688; 16.787
90; 96.99; 90
596.9Pritchard, Robin G.; Stoodley, Richard J.; Yuen, Wai-Hung
Studies related to carba-pyranoses: synthesis of acetylated derivatives of 4-amino-2,4-dideoxy-3-O-(beta-D-glucopyranosyl)-beta-L-(and beta-D-) altrocarba-pyranose from a D-glucose template.
Organic & biomolecular chemistry, 2005, 3, 162-171
7150002 CIFC26 H35 N3 O7P 1 21 110.131; 20.904; 12.459
90; 92.53; 90
2636Kazmaier, Uli; Hebach, Christina; Watzke, Anja; Maier, Sabine; Mues, Heike; Huch, Volker
A straightforward approach towards cyclic peptides via ring-closing metathesis‒scope and limitations.
Organic & biomolecular chemistry, 2005, 3, 136-145
7150003 CIFC24 H33 N3 O7P 21 21 2110.967; 14.024; 16.422
90; 90; 90
2525.7Kazmaier, Uli; Hebach, Christina; Watzke, Anja; Maier, Sabine; Mues, Heike; Huch, Volker
A straightforward approach towards cyclic peptides via ring-closing metathesis‒scope and limitations.
Organic & biomolecular chemistry, 2005, 3, 136-145
7150004 CIFC26 H37 N3 O7P 21 21 219.491; 9.73; 28.504
90; 90; 90
2632.3Kazmaier, Uli; Hebach, Christina; Watzke, Anja; Maier, Sabine; Mues, Heike; Huch, Volker
A straightforward approach towards cyclic peptides via ring-closing metathesis–scope and limitations.
Organic & biomolecular chemistry, 2005, 3, 136-145
7150005 CIFC20 H10 Ag Cl O4P b a m20.362; 7.2285; 10.2891
90; 90; 90
1514.4Elliott, Eric L.; Hernández, Gerardo A; Linden, Anthony; Siegel, Jay S.
Anion mediated structural motifs in silver(I) complexes with corannulene.
Organic & biomolecular chemistry, 2005, 3, 407-413
7150006 CIFC42 H20 Ag2 F6 O6 S2P 1 21/n 112.6903; 22.206; 12.8975
90; 107.637; 90
3463.7Elliott, Eric L.; Hernández, Gerardo A; Linden, Anthony; Siegel, Jay S.
Anion mediated structural motifs in silver(I) complexes with corannulene.
Organic & biomolecular chemistry, 2005, 3, 407-413
7150007 CIFC20 H10 Ag2 B2 F8P -19.5741; 9.6621; 10.6735
98.3042; 110.394; 101.488
882.01Elliott, Eric L.; Hernández, Gerardo A; Linden, Anthony; Siegel, Jay S.
Anion mediated structural motifs in silver(I) complexes with corannulene.
Organic & biomolecular chemistry, 2005, 3, 407-413
7150008 CIFC14 H14 O4P 1 21/c 13.9763; 11.8245; 24.323
90; 94.353; 90
1140.31Pittelkow, Michael; Boas, Ulrik; Jessing, Mikkel; Jensen, Knud J.; Christensen, Jørn B
Role of the peri-effect in synthesis and reactivity of highly substituted naphthaldehydes: a novel backbone amide linker for solid-phase synthesis.
Organic & biomolecular chemistry, 2005, 3, 508-514
7150009 CIFC13 H12 O4P 1 21/c 118.985; 3.9181; 14.504
90; 103.443; 90
1049.3Pittelkow, Michael; Boas, Ulrik; Jessing, Mikkel; Jensen, Knud J.; Christensen, Jørn B
Role of the peri-effect in synthesis and reactivity of highly substituted naphthaldehydes: a novel backbone amide linker for solid-phase synthesis.
Organic & biomolecular chemistry, 2005, 3, 508-514
7150010 CIFC13 H23 N OP 1 21/c 19.766; 9.337; 13.7672
90; 102.381; 90
1226.2Rejzek, Martin; Stockman, Robert A.; Hughes, David L.
Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (+/-)-hippodamine and (+/-)-epi-hippodamine.
Organic & biomolecular chemistry, 2005, 3, 73-83
7150011 CIFC13 H23 N OP 1 21/n 17.66; 14.61; 10.367
90; 91.13; 90
1160Rejzek, Martin; Stockman, Robert A.; Hughes, David L.
Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (+/-)-hippodamine and (+/-)-epi-hippodamine.
Organic & biomolecular chemistry, 2005, 3, 73-83
7150012 CIFC149 H116 N4 ZnP -110.263; 16.066; 16.779
82.544; 85.022; 80.666
2700.8Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150013 CIFC162 H107 Br9 N4P 42/n :222.627; 22.627; 12.7634
90; 90; 90
6534.6Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150014 CIFC168 H110 Cl10 N4 ZnP 42/n :222.4739; 22.4739; 12.8564
90; 90; 90
6493.5Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150015 CIFC180 H134 N4I 41/a :219.39; 19.39; 36.077
90; 90; 90
13563.9Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150016 CIFC180 H134 N4I 41/a :219.3904; 19.3904; 36.077
90; 90; 90
13564.5Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150017 CIFC168 H134 Cl8 N4 O4I 41/a :219.72; 19.72; 35.239
90; 90; 90
13703.7Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150018 CIFC180 H132 N4 ZnI 41/a :219.612; 19.612; 36.445
90; 90; 90
14018Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150019 CIFC180 H132 N4 NiI 41/a :219.2176; 19.2176; 36.142
90; 90; 90
13347.8Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150020 CIFC168 H132 Cl8 N4 Ni O4I 41/a :219.6502; 19.6502; 35.387
90; 90; 90
13664Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150021 CIFC180 H132 N4 NiI 41/a :219.2176; 19.2176; 36.142
90; 90; 90
13347.8Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150022 CIFC127 H88 Cl14 N4P -116.2354; 18.758; 19.2789
78.364; 63.381; 88.391
5128Uno, Hidemitsu; Watanabe, Hikaru; Yamashita, Yuko; Ono, Noboru
Extremely large cavity assembled by self-interlocking of distorted biconcave porphyrins.
Organic & biomolecular chemistry, 2005, 3, 448-453
7150023 CIFC7 H6 N4 O6P 1 21/c 18.0407; 11.7673; 11.2852
90; 108.476; 90
1012.74Katritzky, Alan R.; Scriven, Eric F. V.; Majumder, Suman; Akhmedova, Rena G.; Vakulenko, Anatoliy V.; Akhmedov, Novruz G.; Murugan, Ramiah; Abboud, Khalil A.
Preparation of nitropyridines by nitration of pyridines with nitric acid.
Organic & biomolecular chemistry, 2005, 3, 538-541
7150024 CIFC64 H64 N4 O12C 1 2/c 116.7651; 29.395; 24.507
90; 95.993; 90
12011.3Danila, Crenguta; Bolte, Michael; Böhmer, Volker
1,3-Alternate calix[4]arenes, selectively functionalized by amino groups.
Organic & biomolecular chemistry, 2005, 3, 172-184
7150025 CIFC64 H64 N4 O12P -114.1953; 14.6587; 15.3671
111.121; 92.666; 99.425
2923.2Danila, Crenguta; Bolte, Michael; Böhmer, Volker
1,3-Alternate calix[4]arenes, selectively functionalized by amino groups.
Organic & biomolecular chemistry, 2005, 3, 172-184
7150026 CIFC67 H70 Cl2 N4 O12P -113.4904; 14.1373; 17.7409
83.459; 69.464; 76.454
3078.5Danila, Crenguta; Bolte, Michael; Böhmer, Volker
1,3-Alternate calix[4]arenes, selectively functionalized by amino groups.
Organic & biomolecular chemistry, 2005, 3, 172-184
7150027 CIFC48 H58 N2 O8P -110.3423; 13.161; 16.5605
101.868; 96.988; 91.968
2185.5Danila, Crenguta; Bolte, Michael; Böhmer, Volker
1,3-Alternate calix[4]arenes, selectively functionalized by amino groups.
Organic & biomolecular chemistry, 2005, 3, 172-184
7150028 CIFC14 H17 N O3P 21 21 215.5369; 8.5297; 27.769
90; 90; 90
1311.5Cobb, Alexander J. A.; Shaw, David M.; Longbottom, Deborah A.; Gold, Johan B.; Ley, Steven V.
Organocatalysis with proline derivatives: improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions.
Organic & biomolecular chemistry, 2005, 3, 84-96
7150029 CIFC27 H20 O SP 21 21 216.4273; 15.6636; 18.992
90; 90; 90
1912.01ter Wiel, Matthijs K. J.; Vicario, Javier; Davey, Stephen G.; Meetsma, Auke; Feringa, Ben L.
New procedure for the preparation of highly sterically hindered alkenes using a hypervalent iodine reagent.
Organic & biomolecular chemistry, 2005, 3, 28-30
7150030 CIFC11 H14 O2 SP 1 21/n 110.5744; 9.1217; 11.7111
90; 115.825; 90
1016.8Bedford, Simon T.; Grainger, Richard S.; Steed, Jonathan W.; Tisselli, Patrizia
Stereoselective synthesis of 2,5-disubstituted-1,4-oxathiane S-oxides.
Organic & biomolecular chemistry, 2005, 3, 404-406
7150031 CIFC11 H14 O2 SP 1 21 17.5387; 6; 11.4544
90; 91.308; 90
517.97Bedford, Simon T.; Grainger, Richard S.; Steed, Jonathan W.; Tisselli, Patrizia
Stereoselective synthesis of 2,5-disubstituted-1,4-oxathiane S-oxides.
Organic & biomolecular chemistry, 2005, 3, 404-406
7150032 CIFC12 H19 N O2 SI 41/a :220.9699; 20.9699; 11.2756
90; 90; 90
4958.3Bedford, Simon T.; Grainger, Richard S.; Steed, Jonathan W.; Tisselli, Patrizia
Stereoselective synthesis of 2,5-disubstituted-1,4-oxathiane S-oxides.
Organic & biomolecular chemistry, 2005, 3, 404-406
7150033 CIFC8 H12 N2 O5P -17.4377; 8.3035; 9.2515
73.265; 67.994; 71.219
492.34Hibbs, David E.; Overgaard, Jacob; Howard, Siân T; Nguyen, Thanh Ha
Experimental charge density of a potential DHO synthetase inhibitor: dimethyl-trans-2-oxohexahydro-pyrimidine-4,6-dicarboxylate.
Organic & biomolecular chemistry, 2005, 3, 441-447
7150034 CIFC12 H13 I O2P 21 21 216.6491; 6.8227; 25.8973
90; 90; 90
1174.83Allin, Steven M.; Essat, Munira; Pita, Catarina Horro; Baird, Robert D.; McKee, Vickie; Elsegood, Mark; Edgar, Mark; Andrews, David M.; Shah, Pritom; Aspinall, Ian
Applications of the amino-Cope rearrangement: synthesis of tetrahydropyran, delta-lactone and piperidine targets.
Organic & biomolecular chemistry, 2005, 3, 809-815
7150035 CIFC21 H25 N OP 21 21 214.9818; 9.4157; 37.792
90; 90; 90
1772.7Allin, Steven M.; Essat, Munira; Pita, Catarina Horro; Baird, Robert D.; McKee, Vickie; Elsegood, Mark; Edgar, Mark; Andrews, David M.; Shah, Pritom; Aspinall, Ian
Applications of the amino-Cope rearrangement: synthesis of tetrahydropyran, delta-lactone and piperidine targets.
Organic & biomolecular chemistry, 2005, 3, 809-815
7150036 CIFC19 H30 N O8 P SP 1 21 17.997; 12.221; 11.812
90; 100.647; 90
1134.5Kjaersgaard, Anne; Jørgensen, Karl Anker
Catalytic asymmetric addition of beta-keto phosphonates to an activated imine‒formation of optically active functionalized phosphonate alpha-amino acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 804-808
7150037 CIFC24 H21 O3P -18.3773; 9.1657; 12.7261
94.81; 96.374; 108.948
910.99Jacobs, Ayesha; Nassimbeni, Luigi R.; Su, Hong; Taljaard, Benjamin
Xanthenol clathrates: structure, thermal stability, guest exchange and kinetics of desolvation.
Organic & biomolecular chemistry, 2005, 3, 1319-1322
7150038 CIFC24 H21 O3P -18.3762; 9.1588; 12.7193
94.893; 96.401; 108.872
909.89Jacobs, Ayesha; Nassimbeni, Luigi R.; Su, Hong; Taljaard, Benjamin
Xanthenol clathrates: structure, thermal stability, guest exchange and kinetics of desolvation.
Organic & biomolecular chemistry, 2005, 3, 1319-1322
7150039 CIFC23 H19 O3P -18.3719; 9.1093; 12.6935
97.482; 103.946; 109.425
862.3Jacobs, Ayesha; Nassimbeni, Luigi R.; Su, Hong; Taljaard, Benjamin
Xanthenol clathrates: structure, thermal stability, guest exchange and kinetics of desolvation.
Organic & biomolecular chemistry, 2005, 3, 1319-1322
7150040 CIFC23 H19 O3P -18.3763; 9.0965; 12.6943
97.485; 104.164; 109.388
860.68Jacobs, Ayesha; Nassimbeni, Luigi R.; Su, Hong; Taljaard, Benjamin
Xanthenol clathrates: structure, thermal stability, guest exchange and kinetics of desolvation.
Organic & biomolecular chemistry, 2005, 3, 1319-1322
7150041 CIFC23 H19 O3P -18.3757; 9.1004; 12.6928
97.541; 104.053; 109.405
861.14Jacobs, Ayesha; Nassimbeni, Luigi R.; Su, Hong; Taljaard, Benjamin
Xanthenol clathrates: structure, thermal stability, guest exchange and kinetics of desolvation.
Organic & biomolecular chemistry, 2005, 3, 1319-1322
7150042 CIFC24 H21 O3P -18.3654; 9.0652; 12.873
96.696; 94.048; 109.717
906.38Jacobs, Ayesha; Nassimbeni, Luigi R.; Su, Hong; Taljaard, Benjamin
Xanthenol clathrates: structure, thermal stability, guest exchange and kinetics of desolvation.
Organic & biomolecular chemistry, 2005, 3, 1319-1322
7150043 CIFC24 H21 O3P -18.4902; 9.1923; 12.9946
95.62; 94.84; 109.66
942.97Jacobs, Ayesha; Nassimbeni, Luigi R.; Su, Hong; Taljaard, Benjamin
Xanthenol clathrates: structure, thermal stability, guest exchange and kinetics of desolvation.
Organic & biomolecular chemistry, 2005, 3, 1319-1322
7150044 CIFC48 H42 O6P -18.415; 18.2852; 12.7741
95.637; 94.919; 109.717
1826.48Jacobs, Ayesha; Nassimbeni, Luigi R.; Su, Hong; Taljaard, Benjamin
Xanthenol clathrates: structure, thermal stability, guest exchange and kinetics of desolvation.
Organic & biomolecular chemistry, 2005, 3, 1319-1322
7150045 CIFC35 H36 N2 O4P 1 21 110.197; 16.139; 10.043
90; 114.16; 90
1508Kawabata, Takeo; Majumdar, Swapan; Tsubaki, Kazunori; Monguchi, Daiki
Memory of chirality in intramolecular conjugate addition of enolates: a novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters.
Organic & biomolecular chemistry, 2005, 3, 1609-1611
7150046 CIFC18 H12 N2P 1 21/n 18.964; 6.265; 11.241
90; 107.109; 90
603.4Fitchett, Christopher M.; Richardson, Chris; Steel, Peter J.
Solid state conformations of symmetrical aromatic biheterocycles: an X-ray crystallographic investigation.
Organic & biomolecular chemistry, 2005, 3, 498-502
7150047 CIFC16 H10 N4P 1 21/n 18.557; 6.33; 11.841
90; 106.689; 90
614.4Fitchett, Christopher M.; Richardson, Chris; Steel, Peter J.
Solid state conformations of symmetrical aromatic biheterocycles: an X-ray crystallographic investigation.
Organic & biomolecular chemistry, 2005, 3, 498-502
7150048 CIFC16 H10 N4P 1 21/n 15.779; 5.35; 18.906
90; 91.466; 90
584.3Fitchett, Christopher M.; Richardson, Chris; Steel, Peter J.
Solid state conformations of symmetrical aromatic biheterocycles: an X-ray crystallographic investigation.
Organic & biomolecular chemistry, 2005, 3, 498-502
7150049 CIFC16 H10 N4C 1 2 122.523; 3.912; 6.979
90; 106.14; 90
590.7Fitchett, Christopher M.; Richardson, Chris; Steel, Peter J.
Solid state conformations of symmetrical aromatic biheterocycles: an X-ray crystallographic investigation.
Organic & biomolecular chemistry, 2005, 3, 498-502
7150050 CIFC14 H8 N2 O2P 1 21/n 14.627; 16.48; 7.004
90; 94.34; 90
532.54Fitchett, Christopher M.; Richardson, Chris; Steel, Peter J.
Solid state conformations of symmetrical aromatic biheterocycles: an X-ray crystallographic investigation.
Organic & biomolecular chemistry, 2005, 3, 498-502
7150051 CIFC14 H8 N2 S2P 1 21/c 18.993; 5.988; 11.445
90; 110.87; 90
575.88Fitchett, Christopher M.; Richardson, Chris; Steel, Peter J.
Solid state conformations of symmetrical aromatic biheterocycles: an X-ray crystallographic investigation.
Organic & biomolecular chemistry, 2005, 3, 498-502
7150052 CIFC12 H8 N6P 21 21 217.277; 7.639; 19.94
90; 90; 90
1108.4Fitchett, Christopher M.; Richardson, Chris; Steel, Peter J.
Solid state conformations of symmetrical aromatic biheterocycles: an X-ray crystallographic investigation.
Organic & biomolecular chemistry, 2005, 3, 498-502
7150053 CIFC29 H50 O11P 1 21 113.3374; 7.6406; 15.5158
90; 98.311; 90
1564.5Okuzumi, Keiko; Hara, Noriyuki; Uekusa, Hidehiro; Fujimoto, Yoshinori
Structure elucidation of cyasterone stereoisomers isolated from Cyathula officinalis.
Organic & biomolecular chemistry, 2005, 3, 1227-1232
7150054 CIFC32 H56 O11P 1 21 113.6542; 7.7755; 15.7636
90; 100.215; 90
1647.1Okuzumi, Keiko; Hara, Noriyuki; Uekusa, Hidehiro; Fujimoto, Yoshinori
Structure elucidation of cyasterone stereoisomers isolated from Cyathula officinalis.
Organic & biomolecular chemistry, 2005, 3, 1227-1232
7150055 CIFC23 H19 N3 O2 SP c a 2122.845; 11.858; 7.188
90; 90; 90
1947.2Bogza, Sergei L.; Kobrakov, Konstantin I.; Malienko, Anna A.; Perepichka, Igor F.; Sujkov, Sergei Yu; Bryce, Martin R.; Lyubchik, Svetlana B.; Batsanov, Andrei S.; Bogdan, Natalya M.
A versatile synthesis of pyrazolo[3,4-c]isoquinoline derivatives by reaction of 4-aryl-5-aminopyrazoles with aryl/heteroaryl aldehydes: the effect of the heterocycle on the reaction pathways.
Organic & biomolecular chemistry, 2005, 3, 932-940
7150056 CIFC21 H20 N4 O2P -17.086; 10.791; 12.85
104.16; 105.87; 95.86
901.2Bogza, Sergei L.; Kobrakov, Konstantin I.; Malienko, Anna A.; Perepichka, Igor F.; Sujkov, Sergei Yu; Bryce, Martin R.; Lyubchik, Svetlana B.; Batsanov, Andrei S.; Bogdan, Natalya M.
A versatile synthesis of pyrazolo[3,4-c]isoquinoline derivatives by reaction of 4-aryl-5-aminopyrazoles with aryl/heteroaryl aldehydes: the effect of the heterocycle on the reaction pathways.
Organic & biomolecular chemistry, 2005, 3, 932-940
7150057 CIFC35 H34 N4 O2P -18.944; 12.945; 13.918
64.13; 73.04; 81
1386.1Bogza, Sergei L.; Kobrakov, Konstantin I.; Malienko, Anna A.; Perepichka, Igor F.; Sujkov, Sergei Yu; Bryce, Martin R.; Lyubchik, Svetlana B.; Batsanov, Andrei S.; Bogdan, Natalya M.
A versatile synthesis of pyrazolo[3,4-c]isoquinoline derivatives by reaction of 4-aryl-5-aminopyrazoles with aryl/heteroaryl aldehydes: the effect of the heterocycle on the reaction pathways.
Organic & biomolecular chemistry, 2005, 3, 932-940
7150058 CIFC40 H36 O2P 21 21 2110.113; 10.206; 29.277
90; 90; 90
3021.8Huang, Jin-Wen; Shi, Min
Carbolithiation of gem-aryl disubstituted methylenecyclopropanes.
Organic & biomolecular chemistry, 2005, 3, 399-400
7150059 CIFC17 H16 O2C 1 2/c 119.3595; 8.8441; 16.7833
90; 115.701; 90
2589.3Foot, Jonathan S.; Giblin, Gerard M. P.; Whitwood, A. C.; Taylor, R. J. K.
Unexpected Z-stereoselectivity in the Ramberg-Bäcklund reaction of diarylsulfones leading to cis-stilbenes: the effect of aryl substituents and application in the synthesis of the integrastatin nucleus.
Organic & biomolecular chemistry, 2005, 3, 756-763
7150060 CIFC17 H14 O3P -19.2508; 9.313; 15.5363
100.325; 90.36; 99.592
1297.5Foot, Jonathan S.; Giblin, Gerard M. P.; Whitwood, A. C.; Taylor, R. J. K.
Unexpected Z-stereoselectivity in the Ramberg-Bäcklund reaction of diarylsulfones leading to cis-stilbenes: the effect of aryl substituents and application in the synthesis of the integrastatin nucleus.
Organic & biomolecular chemistry, 2005, 3, 756-763
7150061 CIFC9 H12 N6 O4P 32 2 19.7754; 9.7754; 20.3627
90; 90; 120
1685.1Lin, Wenqing; Li, Hong; Ming, Xin; Seela, Frank
1,N6-Etheno-7-deaza-2,8-diazaadenosine: syntheses, properties and conversion to 7-deaza-2,8-diazaadenosine.
Organic & biomolecular chemistry, 2005, 3, 1714-1718
7150062 CIFC18 H22 O4P 1 21 110.0036; 27.0011; 12.1811
90; 95.159; 90
3276.9Lemiègre, Loïc; Stevens, Richard L.; Combret, Jean-Claude; Maddaluno, Jacques
Ring fission of chiral cyclic acetals plus intramolecular [4 + 2] cycloaddition: a sequential access to medium-size lactones. Application to the synthesis of carbasugars.
Organic & biomolecular chemistry, 2005, 3, 1308-1318
7150063 CIFC22 H18 Br N3 OP -19.3969; 10.5034; 10.5516
71.075; 88.902; 81.541
973.97Sim°unek, Petr; Bertolasi, Valerio; Pesková, Markéta; Machácek, Vladimír; Lycka, Antonín
Solution and solid state structure and tautomerism of azo coupled enaminone derivatives of benzoylacetone.
Organic & biomolecular chemistry, 2005, 3, 1217-1226
7150064 CIFC21.5 H24 N4 OC 1 2/c 125.8225; 10.7493; 15.627
90; 117.694; 90
3840.74Simůnek, Petr; Bertolasi, Valerio; Pesková, Markéta; Machácek, Vladimír; Lycka, Antonín
Solution and solid state structure and tautomerism of azo coupled enaminone derivatives of benzoylacetone.
Organic & biomolecular chemistry, 2005, 3, 1217-1226
7150065 CIFC17 H17 N3 OP 1 21/n 15.7502; 29.873; 9.1184
90; 101.11; 90
1536.97Simůnek, Petr; Bertolasi, Valerio; Pesková, Markéta; Machácek, Vladimír; Lycka, Antonín
Solution and solid state structure and tautomerism of azo coupled enaminone derivatives of benzoylacetone.
Organic & biomolecular chemistry, 2005, 3, 1217-1226
7150066 CIFC41 H56 Cu N4 O6P 21 21 2111.48; 12.8012; 28.1994
90; 90; 90
4144.1Gottschaldt, Michael; Koth, Daniel; Görls, Helmar
Synthesis and crystal structure of a salen-type copper(II) complex derived from 3,5'-O-dimethyl-2',3'-diamino-2',3'-dideoxy-beta-D-xylo-uridine.
Organic & biomolecular chemistry, 2005, 3, 1170-1171
7150067 CIFC19 H33 N O6P 21 21 215.7388; 9.4909; 38.243
90; 90; 90
2082.96Woodhall, Thomas; Williams, Gavin; Berry, Alan; Nelson, Adam
Synthesis of screening substrates for the directed evolution of sialic acid aldolase: towards tailored enzymes for the preparation of influenza A sialidase inhibitor analogues.
Organic & biomolecular chemistry, 2005, 3, 1795-1800
7150068 CIFC17 H31 N O7P 1 21 18.7774; 8.3066; 13.4961
90; 96.211; 90
978.23Woodhall, Thomas; Williams, Gavin; Berry, Alan; Nelson, Adam
Synthesis of screening substrates for the directed evolution of sialic acid aldolase: towards tailored enzymes for the preparation of influenza A sialidase inhibitor analogues.
Organic & biomolecular chemistry, 2005, 3, 1795-1800
7150069 CIFC13 H16 S5P 1 21 16.3217; 13.4551; 17.512
90; 93.06; 90
1487.43Griffiths, Jon-Paul; Nie, Hui; Brown, R. James; Day, Peter; Wallis, John D.
Synthetic strategies to chiral organosulfur donors related to bis(ethylenedithio)tetrathiafulvalene.
Organic & biomolecular chemistry, 2005, 3, 2155-2166
7150070 CIFC13 H16 S5P 1 21 17.2322; 9.3635; 11.3961
90; 106.405; 90
740.31Griffiths, Jon-Paul; Nie, Hui; Brown, R. James; Day, Peter; Wallis, John D.
Synthetic strategies to chiral organosulfur donors related to bis(ethylenedithio)tetrathiafulvalene.
Organic & biomolecular chemistry, 2005, 3, 2155-2166
7150071 CIFC13 H16 S5P 21 21 217.609; 9.789; 20.1711
90; 90; 90
1502.43Griffiths, Jon-Paul; Nie, Hui; Brown, R. James; Day, Peter; Wallis, John D.
Synthetic strategies to chiral organosulfur donors related to bis(ethylenedithio)tetrathiafulvalene.
Organic & biomolecular chemistry, 2005, 3, 2155-2166
7150072 CIFC42.26 H53.06 F6 N O12.27 PC 1 2/c 114.324; 22.806; 26.47
90; 97.2; 90
8579Gibson, Harry W.; Wang, Hong; Bonrad, Klaus; Jones, Jason W.; Slebodnick, Carla; Zackharov, Lev N.; Rheingold, Arnold L.; Habenicht, Bradley; Lobue, Peter; Ratliff, Amy E.
Regioselective routes to disubstituted dibenzo crown ethers and their complexations.
Organic & biomolecular chemistry, 2005, 3, 2114-2121
7150073 CIFC28 H36 F6 K O12 PP -110.3429; 12.6823; 13.1381
83.774; 72.711; 77.938
1607.17Gibson, Harry W.; Wang, Hong; Bonrad, Klaus; Jones, Jason W.; Slebodnick, Carla; Zackharov, Lev N.; Rheingold, Arnold L.; Habenicht, Bradley; Lobue, Peter; Ratliff, Amy E.
Regioselective routes to disubstituted dibenzo crown ethers and their complexations.
Organic & biomolecular chemistry, 2005, 3, 2114-2121
7150074 CIFC28 H36 O12P 1 21/c 113.8926; 12.4235; 8.2043
90; 105.243; 90
1366.2Gibson, Harry W.; Wang, Hong; Bonrad, Klaus; Jones, Jason W.; Slebodnick, Carla; Zackharov, Lev N.; Rheingold, Arnold L.; Habenicht, Bradley; Lobue, Peter; Ratliff, Amy E.
Regioselective routes to disubstituted dibenzo crown ethers and their complexations.
Organic & biomolecular chemistry, 2005, 3, 2114-2121
7150075 CIFC28 H36 F6 K O12 PC 1 2/c 116.84; 19.447; 19.41
90; 91.429; 90
6354.6Gibson, Harry W.; Wang, Hong; Bonrad, Klaus; Jones, Jason W.; Slebodnick, Carla; Zackharov, Lev N.; Rheingold, Arnold L.; Habenicht, Bradley; Lobue, Peter; Ratliff, Amy E.
Regioselective routes to disubstituted dibenzo crown ethers and their complexations.
Organic & biomolecular chemistry, 2005, 3, 2114-2121
7150076 CIFC18 H17 Br O TiP -17.7237; 9.8885; 11.0929
81.444; 70.937; 89.529
791.12Han, Zhenfu; Fujioka, Takuma; Usugi, Shin-Ichi; Yorimitsu, Hideki; Shinokubo, Hiroshi; Oshima, Koichiro
A new method for the synthesis of acyltitanium complexes and their application to copper-mediated acylmetallation of carbon-carbon multiple bonds in aqueous media.
Organic & biomolecular chemistry, 2005, 3, 1622-1623
7150077 CIFC14 H15 N O4P 1 21/n 16.9505; 28.848; 7.3706
90; 116.961; 90
1317.2Fifer, Nathan L.; White, Jonathan M.
Determining the sigma-donor ability of the cyclopropane C-C bond.
Organic & biomolecular chemistry, 2005, 3, 1776-1780
7150078 CIFC10 H10 N2 O5 SP 1 21/c 15.1517; 11.726; 18.705
90; 94.289; 90
1126.8Fifer, Nathan L.; White, Jonathan M.
Determining the sigma-donor ability of the cyclopropane C-C bond.
Organic & biomolecular chemistry, 2005, 3, 1776-1780
7150079 CIFC11 H10 N2 O6P n a 2110.162; 21.4665; 5.435
90; 90; 90
1185.6Fifer, Nathan L.; White, Jonathan M.
Determining the sigma-donor ability of the cyclopropane C-C bond.
Organic & biomolecular chemistry, 2005, 3, 1776-1780
7150080 CIFC11 H11 N O4P 1 21/c 111.503; 7.7574; 12.737
90; 111.04; 90
1060.8Fifer, Nathan L.; White, Jonathan M.
Determining the sigma-donor ability of the cyclopropane C-C bond.
Organic & biomolecular chemistry, 2005, 3, 1776-1780
7150081 CIFC10 H11 N O3P 1 21/c 111.1796; 7.2234; 12.745
90; 115.033; 90
932.5Fifer, Nathan L.; White, Jonathan M.
Determining the sigma-donor ability of the cyclopropane C-C bond.
Organic & biomolecular chemistry, 2005, 3, 1776-1780
7150082 CIFC14 H14 N2 O6P 1 21/n 114.0459; 7.8502; 14.279
90; 115.424; 90
1422Fifer, Nathan L.; White, Jonathan M.
Determining the sigma-donor ability of the cyclopropane C-C bond.
Organic & biomolecular chemistry, 2005, 3, 1776-1780
7150083 CIFC13 H14 N2 O5 SP 1 21/c 110.3778; 12.0317; 11.3503
90; 104.395; 90
1372.73Fifer, Nathan L.; White, Jonathan M.
Determining the sigma-donor ability of the cyclopropane C-C bond.
Organic & biomolecular chemistry, 2005, 3, 1776-1780
7150084 CIFC10 H9 N3 O7P 21 21 216.1596; 7.902; 24.235
90; 90; 90
1179.59Fifer, Nathan L.; White, Jonathan M.
Determining the sigma-donor ability of the cyclopropane C-C bond.
Organic & biomolecular chemistry, 2005, 3, 1776-1780
7150085 CIFC41 H43 N O5P 21 21 215.225; 15.283; 43.03
90; 90; 90
3436Masson, Géraldine; Philouze, Christian; Py, Sandrine
Cis-stereoselective SmI2-promoted reductive coupling of keto-nitrones: first synthesis of 1-epitrehazolamine.
Organic & biomolecular chemistry, 2005, 3, 2067-2069
7150086 CIFC20 H32 O8P 1 21 111.2674; 19.6076; 12.0348
90; 117.463; 90
2359.2Zammit, Steven C.; White, Jonathan M.; Rizzacasa, Mark A.
Enantiospecific synthesis of (-)-trachyspic acid.
Organic & biomolecular chemistry, 2005, 3, 2073-2074
7150087 CIFC50 H82 N30 O31 PtP 21 21 2123.6543; 30.2367; 31.2827
90; 90; 90
22374.3Jeon, Young Jin; Kim, Soo-Young; Ko, Young Ho; Sakamoto, Shigeru; Yamaguchi, Kentaro; Kim, Kimoon
Novel molecular drug carrier: encapsulation of oxaliplatin in cucurbit[7]uril and its effects on stability and reactivity of the drug.
Organic & biomolecular chemistry, 2005, 3, 2122-2125
7150088 CIFC22 H31 N3 O6 SP 1 21 112.723; 5.3119; 17.908
90; 100.305; 90
1190.76Sakai, Kenichi; Sakurai, Rumiko; Akimoto, Toshio; Hirayama, Noriaki
Molecular mechanism of dielectrically controlled optical resolution (DCR).
Organic & biomolecular chemistry, 2005, 3, 360-365
7150089 CIFC22 H29 N3 O5 SP 1 21 111.2302; 5.539; 17.85
90; 95.444; 90
1105.33Sakai, Kenichi; Sakurai, Rumiko; Akimoto, Toshio; Hirayama, Noriaki
Molecular mechanism of dielectrically controlled optical resolution (DCR).
Organic & biomolecular chemistry, 2005, 3, 360-365
7150090 CIFC6 H13 Cl N2 OP 21 21 215.0426; 7.6092; 21.615
90; 90; 90
829.37Sakai, Kenichi; Sakurai, Rumiko; Akimoto, Toshio; Hirayama, Noriaki
Molecular mechanism of dielectrically controlled optical resolution (DCR).
Organic & biomolecular chemistry, 2005, 3, 360-365
7150091 CIFC16 H17 N O4 SP 21 21 215.212; 13.5426; 22.162
90; 90; 90
1564.3Sakai, Kenichi; Sakurai, Rumiko; Akimoto, Toshio; Hirayama, Noriaki
Molecular mechanism of dielectrically controlled optical resolution (DCR).
Organic & biomolecular chemistry, 2005, 3, 360-365
7150092 CIFC20 H31 Br K N5 O4P 21 21 2110.7; 13.81; 15.55
90; 90; 90
2298Tönshoff, Christina; Merz, Klaus; Bucher, Götz
Azidocryptands-synthesis, structure, and complexation properties.
Organic & biomolecular chemistry, 2005, 3, 303-308
7150093 CIFC18 H26 N5 O S2P -18.321; 9.079; 14.321
101.75; 101.706; 103.15
995.6Tönshoff, Christina; Merz, Klaus; Bucher, Götz
Azidocryptands-synthesis, structure, and complexation properties.
Organic & biomolecular chemistry, 2005, 3, 303-308
7150094 CIFC20 H31 N5 O4P 1 21/n 19.572; 23.209; 10.117
90; 112.214; 90
2080.7Tönshoff, Christina; Merz, Klaus; Bucher, Götz
Azidocryptands-synthesis, structure, and complexation properties.
Organic & biomolecular chemistry, 2005, 3, 303-308
7150095 CIFC18 H27 N5 O3P 1 21/n 18.324; 17.781; 13.033
90; 103.797; 90
1873.3Tönshoff, Christina; Merz, Klaus; Bucher, Götz
Azidocryptands-synthesis, structure, and complexation properties.
Organic & biomolecular chemistry, 2005, 3, 303-308
7150096 CIFC36 H56 N10 S6P 1 21/n 112.683; 14.165; 23.626
90; 98.43; 90
4199Tönshoff, Christina; Merz, Klaus; Bucher, Götz
Azidocryptands-synthesis, structure, and complexation properties.
Organic & biomolecular chemistry, 2005, 3, 303-308
7150097 CIFC29 H27 O4 PP 21 21 2110.7399; 12.8444; 17.6182
90; 90; 90
2430.4Boesen, Thomas; Fox, David J.; Galloway, Warren; Pedersen, Daniel Sejer; Tyzack, Charles R.; Warren, Stuart
Asymmetric cyclopropane synthesis via phosphine oxide mediated cascade reactions.
Organic & biomolecular chemistry, 2005, 3, 630-637
7150098 CIFC17 H16 O2P c c n13.165; 28.102; 7.2735
90; 90; 90
2690.9Boesen, Thomas; Fox, David J.; Galloway, Warren; Pedersen, Daniel Sejer; Tyzack, Charles R.; Warren, Stuart
Asymmetric cyclopropane synthesis via phosphine oxide mediated cascade reactions.
Organic & biomolecular chemistry, 2005, 3, 630-637
7150099 CIFC9 H14 O2P 1 21/n 17.32; 8.396; 13.236
90; 90.07; 90
813.5Hayes, Christopher J.; Herbert, Nicola M. A.; Harrington-Frost, Nicole M; Pattenden, Gerald
alpha,beta-Unsaturated and cyclopropyl acyl radicals, and their ketene alkyl radical equivalents. Ring synthesis and tandem cyclisation reactions.
Organic & biomolecular chemistry, 2005, 3, 316-327
7150100 CIFC13 H10 N2 O2P 1 21/c 110.245; 7.16; 15.02
90; 107.943; 90
1048.2Broussy, Sylvain; Bernardes-Génisson, Vania; Gornitzka, Heinz; Bernadou, Jean; Meunier, Bernard
Studies on the 4-benzoylpyridine-3-carboxamide entity as a fragment model of the Isoniazid-NAD adduct.
Organic & biomolecular chemistry, 2005, 3, 666-669
7150101 CIFC25 H39 N3 O6P 1 21 18.889; 11.196; 13.856
90; 92.09; 90
1378Dutt, Anita; Fröhlich, Roland; Pramanik, Animesh
Beta-turn mimic in tripeptide with Phe(1)-Aib(2) as corner residues and beta-strand structure in an isomeric tripeptide: an X-ray diffraction study.
Organic & biomolecular chemistry, 2005, 3, 661-665
7150102 CIFC76 H123 N9 O20C 1 2 147.011; 13.325; 14.106
90; 95.26; 90
8799.1Dutt, Anita; Fröhlich, Roland; Pramanik, Animesh
Beta-turn mimic in tripeptide with Phe(1)-Aib(2) as corner residues and beta-strand structure in an isomeric tripeptide: an X-ray diffraction study.
Organic & biomolecular chemistry, 2005, 3, 661-665
7150103 CIFC136 H191 N2 Na7 O69 S8P 1 21 125.9377; 31.857; 26.5255
90; 106.746; 90
20988Cooper, Alan; Nutley, Margaret; MacLean, Elizabeth J.; Cameron, Ken; Fielding, Lee; Mestres, Jordi; Palin, Ronald
Mutual induced fit in cyclodextrin-rocuronium complexes.
Organic & biomolecular chemistry, 2005, 3, 1863-1871
7150104 CIFC104 H83 Na8 O63 S8I 4 2 223.135; 23.135; 31.904
90; 90; 90
17076Cooper, Alan; Nutley, Margaret; MacLean, Elizabeth J.; Cameron, Ken; Fielding, Lee; Mestres, Jordi; Palin, Ronald
Mutual induced fit in cyclodextrin-rocuronium complexes.
Organic & biomolecular chemistry, 2005, 3, 1863-1871
7150105 CIFC108 H192 N4 O88P 115.44; 15.483; 17.971
112.852; 99.09; 103.334
3702.5Liu, Yu; Zhao, Yan-Li; Chen, Yong; Guo, Dong-Sheng
Assembly behavior of inclusion complexes of beta-cyclodextrin with 4-hydroxyazobenzene and 4-aminoazobenzene.
Organic & biomolecular chemistry, 2005, 3, 584-591
7150106 CIFC108 H205 N6 O91.5P 1 21 115.46; 32.209; 15.512
90; 103.096; 90
7523Liu, Yu; Zhao, Yan-Li; Chen, Yong; Guo, Dong-Sheng
Assembly behavior of inclusion complexes of beta-cyclodextrin with 4-hydroxyazobenzene and 4-aminoazobenzene.
Organic & biomolecular chemistry, 2005, 3, 584-591
7150107 CIFC12 H14 N2 OP b c a9.6984; 16.5958; 25.445
90; 90; 90
4095.44Nitta, Makoto; Sakakida, Tsuyoshi; Miyabara, Hideo; Yamamoto, Hiroyuki; Naya, Shin-ichi
Novel synthesis, static and dynamic properties, and structural characteristics of 5-cyano[n](2,4)pyridinophane-6-ones (n= 9-6) and their chemical transformations.
Organic & biomolecular chemistry, 2005, 3, 638-644
7150108 CIFC5 H11 N O5 SP 1 21/n 17.4175; 8.7683; 12.4464
90; 90.586; 90
809.46Kenworthy, Martin N.; Taylor, Richard J. K.
Tethered aminohydroxylation using acyclic homo-allylic sulfamate esters and sulfonamides as substrates.
Organic & biomolecular chemistry, 2005, 3, 603-611
7150109 CIFC5 H11 N O5 SP -17.3712; 7.4301; 9.0586
66.362; 87.942; 64.538
404.73Kenworthy, Martin N.; Taylor, Richard J. K.
Tethered aminohydroxylation using acyclic homo-allylic sulfamate esters and sulfonamides as substrates.
Organic & biomolecular chemistry, 2005, 3, 603-611
7150110 CIFC52 H40C 1 2/c 117.705; 21.289; 19.354
90; 96.336; 90
7250.4Elliott, Eric L.; Orita, Akihiro; Hasegawa, Daiki; Gantzel, Peter; Otera, Junzo; Siegel, Jay S.
Synthesis and properties of 1,6,7,12,13,18,19,24-octamethylacenaphthyleno[b,l]tetraphenylene.
Organic & biomolecular chemistry, 2005, 3, 581-583
7150111 CIFC12 H18 Br6P 1 21/n 115.676; 6.4009; 18.702
90; 112.578; 90
1732.7Smith, Keith; Liu, Chia-Hui; El-Hiti, Gamal A; Kang, Gurvinder S.; Jones, Elfyn; Clement, Simon G.; Checquer, Alex D.; Howarth, Oliver W.; Hursthouse, Michael B.; Coles, Simon J.
An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.
Organic & biomolecular chemistry, 2005, 3, 1880-1892
7150112 CIFC12 H18 Br4C 1 c 16.574; 31.53; 7.667
90; 108.03; 90
1511.16Smith, Keith; Liu, Chia-Hui; El-Hiti, Gamal A; Kang, Gurvinder S.; Jones, Elfyn; Clement, Simon G.; Checquer, Alex D.; Howarth, Oliver W.; Hursthouse, Michael B.; Coles, Simon J.
An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.
Organic & biomolecular chemistry, 2005, 3, 1880-1892
7150113 CIFC12 H18 Br4P 1 21/a 19.9321; 13.1468; 11.9463
90; 109.373; 90
1471.57Smith, Keith; Liu, Chia-Hui; El-Hiti, Gamal A; Kang, Gurvinder S.; Jones, Elfyn; Clement, Simon G.; Checquer, Alex D.; Howarth, Oliver W.; Hursthouse, Michael B.; Coles, Simon J.
An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.
Organic & biomolecular chemistry, 2005, 3, 1880-1892
7150114 CIFC12 H18 Br4P 1 21/n 111.4559; 7.4771; 17.7504
90; 91.342; 90
1520Smith, Keith; Liu, Chia-Hui; El-Hiti, Gamal A; Kang, Gurvinder S.; Jones, Elfyn; Clement, Simon G.; Checquer, Alex D.; Howarth, Oliver W.; Hursthouse, Michael B.; Coles, Simon J.
An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.
Organic & biomolecular chemistry, 2005, 3, 1880-1892
7150115 CIFC12 H18 Br2P 1 21/a 17.733; 15.842; 10.62
90; 102.83; 90
1268.53Smith, Keith; Liu, Chia-Hui; El-Hiti, Gamal A; Kang, Gurvinder S.; Jones, Elfyn; Clement, Simon G.; Checquer, Alex D.; Howarth, Oliver W.; Hursthouse, Michael B.; Coles, Simon J.
An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.
Organic & biomolecular chemistry, 2005, 3, 1880-1892
7150116 CIFC14 H21 Br6 NP -110.2529; 13.9866; 14.4984
75.851; 79.144; 83.639
1975.4Smith, Keith; Liu, Chia-Hui; El-Hiti, Gamal A; Kang, Gurvinder S.; Jones, Elfyn; Clement, Simon G.; Checquer, Alex D.; Howarth, Oliver W.; Hursthouse, Michael B.; Coles, Simon J.
An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.
Organic & biomolecular chemistry, 2005, 3, 1880-1892
7150117 CIFC12 H18 Br4P b c a17.163; 12.517; 14.25
90; 90; 90
3061.3Smith, Keith; Liu, Chia-Hui; El-Hiti, Gamal A; Kang, Gurvinder S.; Jones, Elfyn; Clement, Simon G.; Checquer, Alex D.; Howarth, Oliver W.; Hursthouse, Michael B.; Coles, Simon J.
An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.
Organic & biomolecular chemistry, 2005, 3, 1880-1892
7150118 CIFC12 H18 Br6P b c a11.67; 28.998; 10.483
90; 90; 90
3547.5Smith, Keith; Liu, Chia-Hui; El-Hiti, Gamal A; Kang, Gurvinder S.; Jones, Elfyn; Clement, Simon G.; Checquer, Alex D.; Howarth, Oliver W.; Hursthouse, Michael B.; Coles, Simon J.
An extensive study of bromination of cis,trans,trans-1,5,9-cyclododecatriene: product structures and conformations.
Organic & biomolecular chemistry, 2005, 3, 1880-1892
7150119 CIFC13 H9.43 N3 OP -110.057; 13.722; 15.423
72.17; 80.39; 86.9
1997.7Jónsson, Stefán; Arribas, Carlos Solano; Wendt, Ola F.; Siegel, Jay S.; Wärnmark, Kenneth
Synthesis of 2-pyridone-fused 2,2'-bipyridine derivatives. An unexpectedly complex solid state structure of 3,6-dimethyl-9H-4,5,9-triazaphenanthren-10-one.
Organic & biomolecular chemistry, 2005, 3, 996-1001
7150120 CIFC39 H24 O3P 63/m15.358; 15.358; 20.1237
90; 90; 120
4110.6Wooi, Goh Yit; White, Jonathan M.
Structural manifestations of the cheletropic reaction.
Organic & biomolecular chemistry, 2005, 3, 972-974
7150121 CIFC38 H26.5 N1.5 OC 1 2/c 120.7668; 10.7728; 25.164
90; 104.376; 90
5453.3Wooi, Goh Yit; White, Jonathan M.
Structural manifestations of the cheletropic reaction.
Organic & biomolecular chemistry, 2005, 3, 972-974
7150122 CIFC35 H22 O3P -110.0236; 10.4368; 12.1152
109.755; 103.475; 90.167
1155.4Wooi, Goh Yit; White, Jonathan M.
Structural manifestations of the cheletropic reaction.
Organic & biomolecular chemistry, 2005, 3, 972-974
7150123 CIFC18 H30 O6P 21 21 217.0435; 16.1734; 16.3288
90; 90; 90
1860.13Austin, Kerrie A. B.; Banwell, Martin G.; Loong, David T. J.; Rae, A. David; Willis, Anthony C.
A chemoenzymatic total synthesis of the undecenolide (-)-cladospolide B via a mid-stage ring-closing metathesis and a late-stage photo-rearrangement of the E-isomer.
Organic & biomolecular chemistry, 2005, 3, 1081-1088
7150124 CIFC16 H26 O6P 3118.685; 18.685; 12.2539
90; 90; 120
3705.03Austin, Kerrie A. B.; Banwell, Martin G.; Loong, David T. J.; Rae, A. David; Willis, Anthony C.
A chemoenzymatic total synthesis of the undecenolide (-)-cladospolide B via a mid-stage ring-closing metathesis and a late-stage photo-rearrangement of the E-isomer.
Organic & biomolecular chemistry, 2005, 3, 1081-1088
7150125 CIFC46 H38 O6P n m a17.357; 13.487; 14.83
90; 90; 90
3472Tellenbröker, Jörg; Barth, Dieter; Neumann, Beate; Stammler, Hans-Georg; Kuck, Dietmar
Methoxy-substituted centrohexaindanes through the fenestrane route.
Organic & biomolecular chemistry, 2005, 3, 570-571
7150126 CIFC14 H10 O3P 1 21/n 112.543; 7.122; 12.956
90; 102.4; 90
1130.4Kuhnert, Nikolai; Burzlaff, Nicolai; Patel, Chirag; Lopez-Periago, Ana
Tuning the size of macrocyclic cavities in trianglimine macrocycles.
Organic & biomolecular chemistry, 2005, 3, 1911-1921
7150127 CIFC17 H25 B F4 O3 SP 21 21 216.7991; 14.3737; 18.467
90; 90; 90
1804.75Aggarwal, Varinder K.; Hebach, Christina
Carboxylate-stabilised sulfur ylides (thetin salts) in asymmetric epoxidation for the synthesis of glycidic acids. Mechanism and implications.
Organic & biomolecular chemistry, 2005, 3, 1419-1427
7150128 CIFC31 H38 O9P 18.5216; 8.6643; 10.4987
92.857; 96.328; 113.673
701.82Loeb, Stephen J.; Tramontozzi, David A.
Branched [n]rotaxanes (n = 2-4) from multiple dibenzo-24-crown-8 ether wheels and 1,2-bis(4,4'-dipyridinium)ethane axles.
Organic & biomolecular chemistry, 2005, 3, 1393-1401
7150129 CIFC10 H10 N2 O5P 1 21 15.6; 24.29; 7.74
90; 96.24; 90
1046.6Cwik, Agnieszka; Fuchs, Aliz; Hell, Zoltán; Böjtös, Ildikó; Halmai, Dóra; Bombicz, Petra
Modified Mg : Al hydrotalcite in the synthesis of oxazolidin-2-ones.
Organic & biomolecular chemistry, 2005, 3, 967-969
7150130 CIFC13 H13 N3 O2P 1 21/c 19.891; 10.066; 11.732
90; 96.743; 90
1160Coogan, Michael P.; Ooi, Li-ling; Pertusati, Fabrizio
Synthesis of unsymmetrical 3,3'-biquinazoline-2,2'-diones by condensation of 3-aminoquinazolinones with benzoxazinones; fortuitous discovery, and further syntheses of 4-H-3-oxo-1,9a,10-triazaanthracen-9-ones.
Organic & biomolecular chemistry, 2005, 3, 1134-1139
7150131 CIFC19 H31 N O2P -110.6747; 12.0073; 15.319
101.634; 99.209; 90.717
1896.34Kanamori, Daisuke; Furukawa, Atsushi; Okamura, Taka-aki; Yamamoto, Hitoshi; Ueyama, Norikazu
Contribution of the intramolecular hydrogen bond to the shift of the pKa value and the oxidation potential of phenols and phenolate anions.
Organic & biomolecular chemistry, 2005, 3, 1453-1459
7150132 CIFC11 H15 N O2P 1 21/c 114.266; 12.599; 19.587
90; 100.86; 90
3457Kanamori, Daisuke; Furukawa, Atsushi; Okamura, Taka-aki; Yamamoto, Hitoshi; Ueyama, Norikazu
Contribution of the intramolecular hydrogen bond to the shift of the pKa value and the oxidation potential of phenols and phenolate anions.
Organic & biomolecular chemistry, 2005, 3, 1453-1459
7150133 CIFC19 H36 N2 O3P -110.0678; 12.211; 9.0829
97.147; 92.285; 109.753
1038.7Kanamori, Daisuke; Furukawa, Atsushi; Okamura, Taka-aki; Yamamoto, Hitoshi; Ueyama, Norikazu
Contribution of the intramolecular hydrogen bond to the shift of the pKa value and the oxidation potential of phenols and phenolate anions.
Organic & biomolecular chemistry, 2005, 3, 1453-1459
7150134 CIFC16 H24 N2 O3P -112.233; 13.207; 11.841
105.46; 109.07; 90.81
1731.8Kanamori, Daisuke; Furukawa, Atsushi; Okamura, Taka-aki; Yamamoto, Hitoshi; Ueyama, Norikazu
Contribution of the intramolecular hydrogen bond to the shift of the pKa value and the oxidation potential of phenols and phenolate anions.
Organic & biomolecular chemistry, 2005, 3, 1453-1459
7150135 CIFC20 H35 N3 O3C m c 2113.2912; 13.0775; 12.1094
90; 90; 90
2104.8Kanamori, Daisuke; Furukawa, Atsushi; Okamura, Taka-aki; Yamamoto, Hitoshi; Ueyama, Norikazu
Contribution of the intramolecular hydrogen bond to the shift of the pKa value and the oxidation potential of phenols and phenolate anions.
Organic & biomolecular chemistry, 2005, 3, 1453-1459
7150136 CIFC16 H15 F2 N3 O3 SP 1 21/c 110.5772; 17.2951; 9.394
90; 109.781; 90
1617.08Norris, Timothy; Colon-Cruz, Roberto; Ripin, David H. B.
New hydroxy-pyrazoline intermediates, subtle regio-selectivity and relative reaction rate variations observed during acid catalyzed and neutral pyrazole cyclization.
Organic & biomolecular chemistry, 2005, 3, 1844-1849
7150137 CIFC16 H12 F3 N3 O2 SC 1 2/c 131.208; 5.051; 21.756
90; 110.08; 90
3221Norris, Timothy; Colon-Cruz, Roberto; Ripin, David H. B.
New hydroxy-pyrazoline intermediates, subtle regio-selectivity and relative reaction rate variations observed during acid catalyzed and neutral pyrazole cyclization.
Organic & biomolecular chemistry, 2005, 3, 1844-1849
7150138 CIFC16 H13 F2 N3 O2 SP 1 21/c 110.614; 7.484; 20.523
90; 96.25; 90
1620.6Norris, Timothy; Colon-Cruz, Roberto; Ripin, David H. B.
New hydroxy-pyrazoline intermediates, subtle regio-selectivity and relative reaction rate variations observed during acid catalyzed and neutral pyrazole cyclization.
Organic & biomolecular chemistry, 2005, 3, 1844-1849
7150139 CIFC16 H17 N3 O3 SP 1 21/c 115.9809; 9.4557; 10.5313
90; 90.471; 90
1591.34Norris, Timothy; Colon-Cruz, Roberto; Ripin, David H. B.
New hydroxy-pyrazoline intermediates, subtle regio-selectivity and relative reaction rate variations observed during acid catalyzed and neutral pyrazole cyclization.
Organic & biomolecular chemistry, 2005, 3, 1844-1849
7150140 CIFC16 H14 F3 N3 O3 SP 1 21/n 18.3741; 19.8459; 10.4665
90; 108.845; 90
1646.2Norris, Timothy; Colon-Cruz, Roberto; Ripin, David H. B.
New hydroxy-pyrazoline intermediates, subtle regio-selectivity and relative reaction rate variations observed during acid catalyzed and neutral pyrazole cyclization.
Organic & biomolecular chemistry, 2005, 3, 1844-1849
7150141 CIFC16 H11 F3 N2P 1 21/n 18.46; 16.282; 10.706
90; 107.52; 90
1406.3Norris, Timothy; Colon-Cruz, Roberto; Ripin, David H. B.
New hydroxy-pyrazoline intermediates, subtle regio-selectivity and relative reaction rate variations observed during acid catalyzed and neutral pyrazole cyclization.
Organic & biomolecular chemistry, 2005, 3, 1844-1849
7150142 CIFC25 H37 N2 O4 S2P -15.0885; 15.5224; 16.5379
102.839; 95.947; 94.025
1260.9Marsman, Albert W.; van Poecke, Bart L. A.; Jenneskens, Leonardus W.; Spek, Anthony L.; Lutz, Egbertus T. G.; van der Maas, Joop H.
4-(Tetrahydro-4H-thiopyran-1-oxide-4-ylidene)-cyclohexanone oxime in the solid-state. A two-dimensional network of enantiomorphous chains interconnected by weak hydrogen bonds.
Organic & biomolecular chemistry, 2005, 3, 1402-1409
7150143 CIFC27 H34 N2 O4P 1 21 113.383; 7.0716; 13.9236
90; 110.93; 90
1230.77Davies, Stephen G.; Rodriguez-Solla, Humberto; Tamayo, Juan A.; Cowley, Andrew R.; Concellon, Carmen; Garner, A. Christopher; Parkes, Alastair L.; Smith, Andrew D.
Asymmetric conjugate reductions with samarium diiodide: asymmetric synthesis of (2S,3R)- and (2S,3S)-[2-2H,3-2H]-leucine-(S)-phenylalanine dipeptides and (2S,3R)-[2-(2)H,3-2H]-phenylalanine methyl ester.
Organic & biomolecular chemistry, 2005, 3, 1435-1447
7150144 CIFC12 H18 N2 O6P 1 21/n 16.2236; 9.575; 10.455
90; 92.63; 90
622.4Giovenzana, Giovanni B.; Palmisano, Giovanni; Del Grosso, Erika; Giovannelli, Lorella; Penoni, Andrea; Pilati, Tullio
Polycyclic compounds from aminopolyols and alpha-dicarbonyls: structure and application in the synthesis of exoditopic ligands.
Organic & biomolecular chemistry, 2005, 3, 1489-1494
7150145 CIFC18 H19 N O4C 1 c 115.63; 12.6665; 7.9832
90; 93.946; 90
1576.7Giovenzana, Giovanni B.; Palmisano, Giovanni; Del Grosso, Erika; Giovannelli, Lorella; Penoni, Andrea; Pilati, Tullio
Polycyclic compounds from aminopolyols and alpha-dicarbonyls: structure and application in the synthesis of exoditopic ligands.
Organic & biomolecular chemistry, 2005, 3, 1489-1494
7150146 CIFC37 H41 N3 O7P 1 21/n 112.47; 15.549; 16.864
90; 98.63; 90
3233Banthia, Sandip; Samanta, Anunay
Calix[4]azacrown and 4-aminophthalimide-appended calix[4]azacrown: synthesis, structure, complexation and fluorescence signaling behaviour.
Organic & biomolecular chemistry, 2005, 3, 1428-1434
7150147 CIFC72 H86 Cl2 N6 O25P -112.7722; 15.865; 20.138
78.132; 71.638; 69.81
3613.3Banthia, Sandip; Samanta, Anunay
Calix[4]azacrown and 4-aminophthalimide-appended calix[4]azacrown: synthesis, structure, complexation and fluorescence signaling behaviour.
Organic & biomolecular chemistry, 2005, 3, 1428-1434
7150148 CIFC25 H26 O8P 21 21 216.622; 8.534; 39.364
90; 90; 90
2224.5Boyd, Derek R.; Sharma, Narain D.; Llamas, Nuria M.; Malone, John F.; O'Dowd, Colin R; Allen, Christopher C. R.
Chemoenzymatic synthesis of carbasugars from iodobenzene.
Organic & biomolecular chemistry, 2005, 3, 1953-1963
7150149 CIFC16 H22 O10P 15.871; 9.395; 16.257
87.588; 86.434; 81.819
885.4Boyd, Derek R.; Sharma, Narain D.; Llamas, Nuria M.; Malone, John F.; O'Dowd, Colin R; Allen, Christopher C. R.
Chemoenzymatic synthesis of carbasugars from iodobenzene.
Organic & biomolecular chemistry, 2005, 3, 1953-1963
7150150 CIFC17 H12 O2 TeP 1 21/n 111.8427; 6.0131; 20.0259
90; 90.914; 90
1425.89Fry, Fiona H.; Holme, Andrea L.; Giles, Niroshini M.; Giles, Gregory I.; Collins, Catriona; Holt, Kim; Pariagh, Sandra; Gelbrich, Thomas; Hursthouse, Michael B.; Gutowski, Nick J.; Jacob, Claus
Multifunctional redox catalysts as selective enhancers of oxidative stress.
Organic & biomolecular chemistry, 2005, 3, 2579-2587
7150151 CIFC16 H21 Br O4P 1 21/n 19.3004; 14.8301; 11.6244
90; 108.528; 90
1520.2Buttler, Thomas; Fleming, Ian; Gonsior, Sabine; Kim, Bo-Hye; Sung, A-Young; Woo, Hee-Gweon
A synthesis of (+/-)-sparteine.
Organic & biomolecular chemistry, 2005, 3, 1557-1567
7150152 CIFC17 H24 O4P -19.6393; 9.6637; 17.7208
78.728; 79.019; 76.781
1557.5Buttler, Thomas; Fleming, Ian; Gonsior, Sabine; Kim, Bo-Hye; Sung, A-Young; Woo, Hee-Gweon
A synthesis of (+/-)-sparteine.
Organic & biomolecular chemistry, 2005, 3, 1557-1567
7150153 CIFC10 H15 Cl N2 O3P 21 21 216.4839; 12.5501; 13.7734
90; 90; 90
1120.79Duggan, Heather M. E.; Hitchcock, Peter B.; Young, Douglas W.
Synthesis of 5/7-, 5/8- and 5/9-bicyclic lactam templates as constraints for external beta-turns.
Organic & biomolecular chemistry, 2005, 3, 2287-2295
7150154 CIFC20 H21 N3 O5 SP 21 21 216.0476; 10.1799; 32.0263
90; 90; 90
1971.67Fox, David J.; Morley, Thomas J.; Taylor, Sarah; Warren, Stuart
Selective five- and six-membered cyclic amine syntheses via capture of episulfonium ions.
Organic & biomolecular chemistry, 2005, 3, 1369-1371
7150155 CIFC20 H25 N O2 S2P c a 2115.717; 6.1884; 39.42
90; 90; 90
3834.1Fox, David J.; Morley, Thomas J.; Taylor, Sarah; Warren, Stuart
Selective five- and six-membered cyclic amine syntheses via capture of episulfonium ions.
Organic & biomolecular chemistry, 2005, 3, 1369-1371
7150156 CIFC13 H20 Cl N SP b c a8.5638; 14.0302; 23.1201
90; 90; 90
2777.92Fox, David J.; Morley, Thomas J.; Taylor, Sarah; Warren, Stuart
Selective five- and six-membered cyclic amine syntheses via capture of episulfonium ions.
Organic & biomolecular chemistry, 2005, 3, 1369-1371
7150157 CIFC25 H30 N2 O2C 1 2 124.525; 8.188; 26.609
90; 116.853; 90
4767.2Koepler, Oliver; Mazzini, Stefania; Bellucci, Maria Cristina; Mondelli, Rosanna; Baro, Angelika; Laschat, Sabine; Hotfilder, Marc; Viseur, Christophle; Frey, Wolfgang
Synthesis and DNA binding properties of novel benzo[b]isoquino[2,3-h]-naphthyridines.
Organic & biomolecular chemistry, 2005, 3, 2848-2858
7150158 CIFC3 F9 K N2 O5 S3P b c n22.385; 16.653; 7.093
90; 90; 90
2644.1Garlyauskayte, Romute Yu; Chernega, Alexander N.; Michot, Christophe; Armand, Michel; Yagupolskii, Yurii L.; Yagupolskii, Lev M.
Synthesis of new organic super acids-N-(trifluoromethylsulfonyl)imino derivatives of trifluoromethanesulfonic acid and bis(trifluoromethylsulfonyl)imide.
Organic & biomolecular chemistry, 2005, 3, 2239-2243
7150159 CIFC4 F12 K N3 O6 S4P b c a13.479; 11.203; 24.545
90; 90; 90
3706Garlyauskayte, Romute Yu; Chernega, Alexander N.; Michot, Christophe; Armand, Michel; Yagupolskii, Yurii L.; Yagupolskii, Lev M.
Synthesis of new organic super acids-N-(trifluoromethylsulfonyl)imino derivatives of trifluoromethanesulfonic acid and bis(trifluoromethylsulfonyl)imide.
Organic & biomolecular chemistry, 2005, 3, 2239-2243
7150160 CIFC14 H25 N O2P 1 21/c 117.354; 9.797; 17.737
90; 104.153; 90
2924.06Feuillet, Fred J. P.; Cheeseman, Matt; Mahon, Mary F.; Bull, Steven D.
Stereoselective synthesis of (E)-trisubstituted alpha,beta-unsaturated amides and acids.
Organic & biomolecular chemistry, 2005, 3, 2976-2989
7150161 CIFC12 H14 Cl3 N3 O5P b c a11.4775; 11.1987; 24.918
90; 90; 90
3202.8Aburel, Pompiliu S.; Zhuang, Wei; Hazell, Rita G.; Jørgensen, Karl Anker
Catalytic and enantioselective aza-ene and hetero-Diels-Alder reactions of alkenes and dienes with azodicarboxylates.
Organic & biomolecular chemistry, 2005, 3, 2344-2349
7150162 CIFC11 H22 N6 O4P 21 21 212.9893; 22.218; 5.2165
90; 90; 90
1505.5Hysell, Michelle; Siegel, Jay S.; Tor, Yitzhak
Synthesis and stability of exocyclic triazine nucleosides.
Organic & biomolecular chemistry, 2005, 3, 2946-2952
7150163 CIFC16 H27 N O6 SP 1 21/c 115.095; 10.338; 11.718
90; 97.582; 90
1812.6Spivey, Alan C.; Colley, Jacqueline; Sprigens, Lindsey; Hancock, Susan M.; Cameron, D. Stuart; Chigboh, Kordi I.; Veitch, Gemma; Frampton, Christopher S.; Adams, Harry
The synthesis of water soluble decalin-based thiols and S-nitrosothiols–model systems for studying the reactions of nitric oxide with protein thiols.
Organic & biomolecular chemistry, 2005, 3, 1942-1952
7150164 CIFC14 H22 O5 SP -16.8076; 9.3008; 12.201
96.4; 105.284; 92.286
738.62Spivey, Alan C.; Colley, Jacqueline; Sprigens, Lindsey; Hancock, Susan M.; Cameron, D. Stuart; Chigboh, Kordi I.; Veitch, Gemma; Frampton, Christopher S.; Adams, Harry
The synthesis of water soluble decalin-based thiols and S-nitrosothiols–model systems for studying the reactions of nitric oxide with protein thiols.
Organic & biomolecular chemistry, 2005, 3, 1942-1952
7150165 CIFC12 H18 N O4 SP 1 21 110.927; 8.372; 14.62
90; 96.444; 90
1329Spivey, Alan C.; Colley, Jacqueline; Sprigens, Lindsey; Hancock, Susan M.; Cameron, D. Stuart; Chigboh, Kordi I.; Veitch, Gemma; Frampton, Christopher S.; Adams, Harry
The synthesis of water soluble decalin-based thiols and S-nitrosothiols‒model systems for studying the reactions of nitric oxide with protein thiols.
Organic & biomolecular chemistry, 2005, 3, 1942-1952
7150166 CIFC24 H34 N2 O10 P2P -16.9456; 8.5692; 12.8364
95.764; 92.302; 113.556
694.09Siu, Jason; Baxendale, Ian R.; Lewthwaite, Russell A.; Ley, Steven V.
A phase-switch purification approach for the expedient removal of tagged reagents and scavengers following their application in organic synthesis.
Organic & biomolecular chemistry, 2005, 3, 3140-3160
7150167 CIFC21 H20 O4P b c a22.3809; 17.2516; 9.034
90; 90; 90
3488.1Yamashita, Masayuki; Inaba, Tomoki; Nagahama, Masaki; Shimizu, Takashi; Kosaka, Sachiko; Kawasaki, Ikuo; Ohta, Shunsaku
Novel stereoconvergent transformation of 1,2a-disubstituted 1,2,2a,8b-tetrahydro-3H-benzo[b]cyclobuta[d]pyran-3-ones to 1,3-disubstituted 1,2,4a,9b-tetrahydrodibenzofuran-4-ols and its application to the second-generation synthesis of (+/-)-linderol A.
Organic & biomolecular chemistry, 2005, 3, 2296-2304
7150168 CIFC20 H18 O4P n a 218.471; 11.811; 16.531
90; 90; 90
1653.9Yamashita, Masayuki; Inaba, Tomoki; Nagahama, Masaki; Shimizu, Takashi; Kosaka, Sachiko; Kawasaki, Ikuo; Ohta, Shunsaku
Novel stereoconvergent transformation of 1,2a-disubstituted 1,2,2a,8b-tetrahydro-3H-benzo[b]cyclobuta[d]pyran-3-ones to 1,3-disubstituted 1,2,4a,9b-tetrahydrodibenzofuran-4-ols and its application to the second-generation synthesis of (+/-)-linderol A.
Organic & biomolecular chemistry, 2005, 3, 2296-2304
7150169 CIFC18 H20 O6P -19.275; 13.425; 7.83
106.14; 114.52; 71.4
828.6Yamashita, Masayuki; Inaba, Tomoki; Nagahama, Masaki; Shimizu, Takashi; Kosaka, Sachiko; Kawasaki, Ikuo; Ohta, Shunsaku
Novel stereoconvergent transformation of 1,2a-disubstituted 1,2,2a,8b-tetrahydro-3H-benzo[b]cyclobuta[d]pyran-3-ones to 1,3-disubstituted 1,2,4a,9b-tetrahydrodibenzofuran-4-ols and its application to the second-generation synthesis of (+/-)-linderol A.
Organic & biomolecular chemistry, 2005, 3, 2296-2304
7150170 CIFC20 H18 O4P 1 21/n 111.759; 9.091; 15.774
90; 103.766; 90
1637.8Yamashita, Masayuki; Inaba, Tomoki; Nagahama, Masaki; Shimizu, Takashi; Kosaka, Sachiko; Kawasaki, Ikuo; Ohta, Shunsaku
Novel stereoconvergent transformation of 1,2a-disubstituted 1,2,2a,8b-tetrahydro-3H-benzo[b]cyclobuta[d]pyran-3-ones to 1,3-disubstituted 1,2,4a,9b-tetrahydrodibenzofuran-4-ols and its application to the second-generation synthesis of (+/-)-linderol A.
Organic & biomolecular chemistry, 2005, 3, 2296-2304
7150171 CIFC123 H193.5 O35.5P 21 21 2116.378; 27.7666; 30.3256
90; 90; 90
13790.9Armspach, Dominique; Poorters, Laurent; Matt, Dominique; Benmerad, Belkacem; Balegroune, Fadila; Toupet, Loic
A new approach to A,B-difunctionalisation of cyclodextrins using bulky 1,3-bis[bis(aryl)chloromethyl]benzenes as capping reagents.
Organic & biomolecular chemistry, 2005, 3, 2588-2592
7150172 CIFC16 H22 N2 O5P 15.108; 5.71; 14.903
79.659; 81.128; 89.62
422.4Dutt, Anita; Drew, Michael G. B.; Pramanik, Animesh
beta-Sheet mediated self-assembly of dipeptides of omega-amino acids and remarkable fibrillation in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2250-2254
7150173 CIFC17 H24 N2 O5P -15.448; 11.674; 14.81
79.936; 79.89; 85.346
911.8Dutt, Anita; Drew, Michael G. B.; Pramanik, Animesh
beta-Sheet mediated self-assembly of dipeptides of omega-amino acids and remarkable fibrillation in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2250-2254
7150174 CIFC22 H26 O6P 21 21 216.565; 8.698; 34.72
90; 90; 90
1983Cases, Manuel; Gonzalez-Lopez de Turiso, Felix; Hadjisoteriou, Maria S.; Pattenden, Gerald
Synthetic studies towards furanocembrane diterpenes. A total synthesis of bis-deoxylophotoxin.
Organic & biomolecular chemistry, 2005, 3, 2786-2804
7150175 CIFC18 H23 N O6P 21 21 2110.816; 16.904; 19.35
90; 90; 90
3537.8Cases, Manuel; Gonzalez-Lopez de Turiso, Felix; Hadjisoteriou, Maria S.; Pattenden, Gerald
Synthetic studies towards furanocembrane diterpenes. A total synthesis of bis-deoxylophotoxin.
Organic & biomolecular chemistry, 2005, 3, 2786-2804
7150176 CIFC24 H38 Na2 O14 PP 21 21 219.408; 11.05; 31.83
90; 90; 90
3309Babu, Ponnusamy; Chopra, D.; Row, T. N. Guru; Maitra, Uday
Micellar aggregates and hydrogels from phosphonobile salts.
Organic & biomolecular chemistry, 2005, 3, 3695-3700
7150177 CIFC54 H101 N9 O14 P2P 21 21 2117.059; 19.498; 19.657
90; 90; 90
6538Amendola, Valeria; Boiocchi, Massimo; Esteban-Gómez, David; Fabbrizzi, Luigi; Monzani, Enrico
Chiral receptors for phosphate ions.
Organic & biomolecular chemistry, 2005, 3, 2632-2639
7150178 CIFC22 H20 N4 O4 S2P 1 21/c 111.9376; 14.0036; 13.9101
90; 107.916; 90
2212.6Zahra, Jalal A.; Abu Thaher, Bassam A.; El-Abadelah, Mustafa M; Boese, Roland
3-Mercaptopropionic acid-nitrile imine adducts. An unprecedented cyclization into 1,3,4-thiadiazol-2(3H)-ones and -2(3H)-thiones.
Organic & biomolecular chemistry, 2005, 3, 2599-2603
7150179 CIFC31 H25 Cl N2 OP 3110.0175; 10.0175; 21.2378
90; 90; 120
1845.7Zhuang, Wei; Hazell, Rita G.; Jørgensen, Karl Anker
Enantioselective Friedel-Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst–synthesis of optically active tetrahydro-beta-carbolines.
Organic & biomolecular chemistry, 2005, 3, 2566-2571
7150180 CIFC12 H22 F6 N2 O4 S2P 41 2 212.2564; 12.2564; 13.4713
90; 90; 90
2023.65Zhuang, Wei; Hazell, Rita G.; Jørgensen, Karl Anker
Enantioselective Friedel-Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst–synthesis of optically active tetrahydro-beta-carbolines.
Organic & biomolecular chemistry, 2005, 3, 2566-2571
7150181 CIFC16 H26 F6 N2 O4 S2C 1 2/c 120.6214; 10.7987; 9.401
90; 95.972; 90
2082.1Zhuang, Wei; Hazell, Rita G.; Jørgensen, Karl Anker
Enantioselective Friedel-Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst–synthesis of optically active tetrahydro-beta-carbolines.
Organic & biomolecular chemistry, 2005, 3, 2566-2571
7150182 CIFC9.8 H12 F6 N2 O4 S2P 32 2 114.3841; 14.3841; 13.98
90; 90; 120
2504.97Zhuang, Wei; Hazell, Rita G.; Jørgensen, Karl Anker
Enantioselective Friedel-Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst‒synthesis of optically active tetrahydro-beta-carbolines.
Organic & biomolecular chemistry, 2005, 3, 2566-2571
7150183 CIFC16 H14 F6 N2 O4 S2P 65 2 211.6353; 11.6353; 52.806
90; 90; 120
6191.1Zhuang, Wei; Hazell, Rita G.; Jørgensen, Karl Anker
Enantioselective Friedel-Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst–synthesis of optically active tetrahydro-beta-carbolines.
Organic & biomolecular chemistry, 2005, 3, 2566-2571
7150184 CIFC30 H32 F6 N2 Ni O8 S2P 1 21/a 111.503; 15.7; 18.53
90; 92.82; 90
3342Fossey, John S.; Matsubara, Ryosuke; Vital, Paulo; Kobayashi, Shū
A C2-symmetric nickel diamine complex as an asymmetric catalyst for enecarbamate additions to butane-2,3-dione.
Organic & biomolecular chemistry, 2005, 3, 2910-2913
7150185 CIFC40 H44 Br2 O4P -110.055; 13.297; 15.802
75.124; 74.149; 69.449
1872.5Sýkora, Jan; Budka, Jan; Lhoták, Pavel; Stibor, Ivan; Císarová, Ivana
Two structural types of 1,3-alternate tetrapropoxycalix[4]arene derivatives in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2572-2578
7150186 CIFC26 H28 O2C 1 2/c 124.088; 12.665; 17.274
90; 126.477; 90
4237.5Sýkora, Jan; Budka, Jan; Lhoták, Pavel; Stibor, Ivan; Císarová, Ivana
Two structural types of 1,3-alternate tetrapropoxycalix[4]arene derivatives in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2572-2578
7150187 CIFC64 H64 O4P 1 21/c 114.921; 18.436; 19.88
90; 108.21; 90
5194.8Sýkora, Jan; Budka, Jan; Lhoták, Pavel; Stibor, Ivan; Císarová, Ivana
Two structural types of 1,3-alternate tetrapropoxycalix[4]arene derivatives in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2572-2578
7150188 CIFC20 H22 Br2 O2P n m a23.851; 12.333; 13.074
90; 90; 90
3845.77Sýkora, Jan; Budka, Jan; Lhoták, Pavel; Stibor, Ivan; Císarová, Ivana
Two structural types of 1,3-alternate tetrapropoxycalix[4]arene derivatives in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2572-2578
7150189 CIFC144 H192 O12P 1 21/c 113.9231; 35.1563; 25.7578
90; 94.5875; 90
12567.7Sýkora, Jan; Budka, Jan; Lhoták, Pavel; Stibor, Ivan; Císarová, Ivana
Two structural types of 1,3-alternate tetrapropoxycalix[4]arene derivatives in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2572-2578
7150190 CIFC20 H24 O2C 1 2/c 125.714; 8.002; 19.113
90; 121.009; 90
3370.71Sýkora, Jan; Budka, Jan; Lhoták, Pavel; Stibor, Ivan; Císarová, Ivana
Two structural types of 1,3-alternate tetrapropoxycalix[4]arene derivatives in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2572-2578
7150191 CIFC56 H80 O4P -110.3974; 13.0709; 19.4131
107.941; 93.567; 97.093
2476.72Sýkora, Jan; Budka, Jan; Lhoták, Pavel; Stibor, Ivan; Císarová, Ivana
Two structural types of 1,3-alternate tetrapropoxycalix[4]arene derivatives in the solid state.
Organic & biomolecular chemistry, 2005, 3, 2572-2578
7150192 CIFC16 H30 N2 O7 S2P 1 21/n 17.707; 17.374; 16.622
90; 92.17; 90
2224.1Wang, Wen-Jwu; Ganin, Eduard V.; Fonari, Marina S.; Simonov, Yurii A.; Bocelli, Gabriele
2,4-dithiouracil: the reproducible H-bonded structural motifs in the complexes with 18-membered crown ethers.
Organic & biomolecular chemistry, 2005, 3, 3054-3058
7150193 CIFC28 H44 N4 O6 S4P 1 21/n 111.624; 12.698; 12.093
90; 109.69; 90
1680.6Wang, Wen-Jwu; Ganin, Eduard V.; Fonari, Marina S.; Simonov, Yurii A.; Bocelli, Gabriele
2,4-dithiouracil: the reproducible H-bonded structural motifs in the complexes with 18-membered crown ethers.
Organic & biomolecular chemistry, 2005, 3, 3054-3058
7150194 CIFC24 H42 N2 O7 S2P 1 21/n 17.988; 21.627; 16.439
90; 93.17; 90
2835.6Wang, Wen-Jwu; Ganin, Eduard V.; Fonari, Marina S.; Simonov, Yurii A.; Bocelli, Gabriele
2,4-dithiouracil: the reproducible H-bonded structural motifs in the complexes with 18-membered crown ethers.
Organic & biomolecular chemistry, 2005, 3, 3054-3058
7150195 CIFC20 H30 N2 O7 S2P 21 21 217.973; 16.918; 17.566
90; 90; 90
2369.4Wang, Wen-Jwu; Ganin, Eduard V.; Fonari, Marina S.; Simonov, Yurii A.; Bocelli, Gabriele
2,4-dithiouracil: the reproducible H-bonded structural motifs in the complexes with 18-membered crown ethers.
Organic & biomolecular chemistry, 2005, 3, 3054-3058
7150196 CIFC26 H30 N6P 1 21/c 16.936; 16.389; 9.833
90; 92.78; 90
1116.4Gregoliński, Janusz; Lisowski, Jerzy; Lis, Tadeusz
New 2+2, 3+3 and 4+4 macrocycles derived from 1,2-diaminocyclohexane and 2,6-diformylpyridine.
Organic & biomolecular chemistry, 2005, 3, 3161-3166
7150197 CIFC52 H60 N12P 21 21 215.577; 30.563; 5.46
90; 90; 90
2599.4Gregoliński, Janusz; Lisowski, Jerzy; Lis, Tadeusz
New 2+2, 3+3 and 4+4 macrocycles derived from 1,2-diaminocyclohexane and 2,6-diformylpyridine.
Organic & biomolecular chemistry, 2005, 3, 3161-3166
7150198 CIFC13 H19 F2 N O4P 1 21/c 114.526; 7.068; 13.3397
90; 91.506; 90
1369.11Griffith, Gerry A.; Percy, Jonathan M.; Pintat, Stéphane; Smith, Clive A.; Spencer, Neil; Uneyama, Emi
Towards novel difluorinated sugar mimetics; syntheses and conformational analyses of highly-functionalised difluorinated cyclooctenones.
Organic & biomolecular chemistry, 2005, 3, 2701-2712
7150199 CIFC18 H15 N O2P -19.7709; 12.8905; 13.2494
70.822; 68.573; 76.36
1454.45O'Leary, Jane; Formosa, Xavier; Skranc, Wolfgang; Wallis, John D.
Structural studies of peri-interactions and bond formation between electron-rich atomic centres and N-phenylcarboxamides or nitroalkenyl groups.
Organic & biomolecular chemistry, 2005, 3, 3273-3283
7150200 CIFC19 H18 N2 OP 1 21/c 19.377; 9.7055; 16.7953
90; 91.3607; 90
1528.08O'Leary, Jane; Formosa, Xavier; Skranc, Wolfgang; Wallis, John D.
Structural studies of peri-interactions and bond formation between electron-rich atomic centres and N-phenylcarboxamides or nitroalkenyl groups.
Organic & biomolecular chemistry, 2005, 3, 3273-3283
7150201 CIFC26 H23 N3 O2P -19.8308; 9.664; 12.0688
85.4547; 68.6506; 78.8152
1047.58O'Leary, Jane; Formosa, Xavier; Skranc, Wolfgang; Wallis, John D.
Structural studies of peri-interactions and bond formation between electron-rich atomic centres and N-phenylcarboxamides or nitroalkenyl groups.
Organic & biomolecular chemistry, 2005, 3, 3273-3283
7150202 CIFC14 H14 N2 O2C 1 2/c 115.87; 5.4817; 28.7715
90; 101.03; 90
2456.73O'Leary, Jane; Formosa, Xavier; Skranc, Wolfgang; Wallis, John D.
Structural studies of peri-interactions and bond formation between electron-rich atomic centres and N-phenylcarboxamides or nitroalkenyl groups.
Organic & biomolecular chemistry, 2005, 3, 3273-3283
7150203 CIFC15 H16 N2 O2P 1 21/n 110.3347; 7.0992; 18.2556
90; 102.897; 90
1305.59O'Leary, Jane; Formosa, Xavier; Skranc, Wolfgang; Wallis, John D.
Structural studies of peri-interactions and bond formation between electron-rich atomic centres and N-phenylcarboxamides or nitroalkenyl groups.
Organic & biomolecular chemistry, 2005, 3, 3273-3283
7150204 CIFC21 H18 N2 O3P 1 21/c 17.7283; 13.6696; 15.7465
90; 95.5779; 90
1655.63O'Leary, Jane; Formosa, Xavier; Skranc, Wolfgang; Wallis, John D.
Structural studies of peri-interactions and bond formation between electron-rich atomic centres and N-phenylcarboxamides or nitroalkenyl groups.
Organic & biomolecular chemistry, 2005, 3, 3273-3283
7150205 CIFC172.23 H106 Cl3.11 F12 N6 O15 P2 RuP -116.1362; 17.4816; 30.711
77.635; 75.632; 65.267
7562.2Loren, Jon C.; Gantzel, Peter; Linden, Anthony; Siegel, Jay S.
Synthesis of achiral and racemic catenanes based on terpyridine and a directionalized terpyridine mimic, pyridyl-phenanthroline.
Organic & biomolecular chemistry, 2005, 3, 3105-3116
7150206 CIFC66 H64 F12 Fe N6 O5 P2P b c n23.3906; 11.4829; 23.2945
90; 90; 90
6256.7Loren, Jon C.; Gantzel, Peter; Linden, Anthony; Siegel, Jay S.
Synthesis of achiral and racemic catenanes based on terpyridine and a directionalized terpyridine mimic, pyridyl-phenanthroline.
Organic & biomolecular chemistry, 2005, 3, 3105-3116
7150207 CIFC66 H64 F12 N6 O5 P2 RuP b c n23.1733; 11.9603; 22.8083
90; 90; 90
6321.54Loren, Jon C.; Gantzel, Peter; Linden, Anthony; Siegel, Jay S.
Synthesis of achiral and racemic catenanes based on terpyridine and a directionalized terpyridine mimic, pyridyl-phenanthroline.
Organic & biomolecular chemistry, 2005, 3, 3105-3116
7150208 CIFC20 H28 Fe N2 O4P 1 21/n 110.8116; 11.8065; 40.9023
90; 91.049; 90
5220.19Chowdhury, Somenath; Mahmoud, Khaled A.; Schatte, Gabriele; Kraatz, Heinz-Bernhard
Amino acid conjugates of 1,1'-diaminoferrocene. Synthesis and chiral organization.
Organic & biomolecular chemistry, 2005, 3, 3018-3023
7150209 CIFC26 H38 Fe N4 O6C 1 2 115.479; 9.342; 11.04
90; 117.071; 90
1421.54Chowdhury, Somenath; Mahmoud, Khaled A.; Schatte, Gabriele; Kraatz, Heinz-Bernhard
Amino acid conjugates of 1,1'-diaminoferrocene. Synthesis and chiral organization.
Organic & biomolecular chemistry, 2005, 3, 3018-3023
7150210 CIFC26 H38 Fe N4 O6C 1 2 115.49; 9.339; 11.036
90; 117.09; 90
1421.3Chowdhury, Somenath; Mahmoud, Khaled A.; Schatte, Gabriele; Kraatz, Heinz-Bernhard
Amino acid conjugates of 1,1'-diaminoferrocene. Synthesis and chiral organization.
Organic & biomolecular chemistry, 2005, 3, 3018-3023
7150211 CIFC20 H22 N2 O5P 1 21/c 114.5548; 7.2083; 17.2662
90; 103.938; 90
1758.15Mateo Alonso, A.; Horcajada, Roberto; Groombridge, Helen J.; Chudasama Née Mandalia, Reshma; Motevalli, Majid; Utley, James H. P.; Wyatt, Peter B.
Synthesis of phenazine derivatives for use as precursors to electrochemically generated bases.
Organic & biomolecular chemistry, 2005, 3, 2832-2841
7150212 CIFC22 H26 N2 O2P 1 21/a 121.854; 10.992; 7.77
90; 90.01; 90
1867Mateo Alonso, A.; Horcajada, Roberto; Groombridge, Helen J.; Chudasama Née Mandalia, Reshma; Motevalli, Majid; Utley, James H. P.; Wyatt, Peter B.
Synthesis of phenazine derivatives for use as precursors to electrochemically generated bases.
Organic & biomolecular chemistry, 2005, 3, 2832-2841
7150213 CIFC30 H35 N O4P 21 21 218.6059; 11.6484; 25.9199
90; 90; 90
2598.34Davies, Stephen G.; Garner, A. Christopher; Long, Marcus J. C.; Morrison, Rachel M.; Roberts, Paul M.; Savory, Edward D.; Smith, Andrew D.; Sweet, Miles J.; Withey, Jonathan M.
Kinetic resolution and parallel kinetic resolution of methyl (+/-)-5-alkyl-cyclopentene-1-carboxylates for the asymmetric synthesis of 5-alkyl-cispentacin derivatives.
Organic & biomolecular chemistry, 2005, 3, 2762-2775
7150214 CIFC31 H37 N O2P 21 21 219.4415; 15.0875; 18.297
90; 90; 90
2606.38Davies, Stephen G.; Garner, A. Christopher; Long, Marcus J. C.; Morrison, Rachel M.; Roberts, Paul M.; Savory, Edward D.; Smith, Andrew D.; Sweet, Miles J.; Withey, Jonathan M.
Kinetic resolution and parallel kinetic resolution of methyl (+/-)-5-alkyl-cyclopentene-1-carboxylates for the asymmetric synthesis of 5-alkyl-cispentacin derivatives.
Organic & biomolecular chemistry, 2005, 3, 2762-2775
7150215 CIFC28 H31 N O2P 1 21/c 110.0421; 9.1315; 25.1731
90; 95.1151; 90
2299.17Davies, Stephen G.; Garner, A. Christopher; Long, Marcus J. C.; Morrison, Rachel M.; Roberts, Paul M.; Savory, Edward D.; Smith, Andrew D.; Sweet, Miles J.; Withey, Jonathan M.
Kinetic resolution and parallel kinetic resolution of methyl (+/-)-5-alkyl-cyclopentene-1-carboxylates for the asymmetric synthesis of 5-alkyl-cispentacin derivatives.
Organic & biomolecular chemistry, 2005, 3, 2762-2775
7150216 CIFC58 H48 O4P 1 21/c 110.54; 25.92; 16.25
90; 100.15; 90
4370Ohta, Eisuke; Higuchi, Hiroki; Kawai, Hidetoshi; Fujiwara, Kenshu; Suzuki, Takanori
Butane-1,4-diyl dications stabilized by steric factors: electrochiroptical response systems based on reversible interconversion between dihydro[5]helicene-type electron acceptors and electron-donating 1,1'-binaphthyls.
Organic & biomolecular chemistry, 2005, 3, 3024-3031
7150217 CIFC48 H30 O2P 1 21/n 111.977; 24.465; 12.25
90; 110.328; 90
3365.9Ohta, Eisuke; Higuchi, Hiroki; Kawai, Hidetoshi; Fujiwara, Kenshu; Suzuki, Takanori
Butane-1,4-diyl dications stabilized by steric factors: electrochiroptical response systems based on reversible interconversion between dihydro[5]helicene-type electron acceptors and electron-donating 1,1'-binaphthyls.
Organic & biomolecular chemistry, 2005, 3, 3024-3031
7150218 CIFC52 H42 Cl12 O4 Sb2C 1 2/m 118.425; 34.5; 10.674
90; 115.457; 90
6126Ohta, Eisuke; Higuchi, Hiroki; Kawai, Hidetoshi; Fujiwara, Kenshu; Suzuki, Takanori
Butane-1,4-diyl dications stabilized by steric factors: electrochiroptical response systems based on reversible interconversion between dihydro[5]helicene-type electron acceptors and electron-donating 1,1'-binaphthyls.
Organic & biomolecular chemistry, 2005, 3, 3024-3031
7150219 CIFC50 H32 Cl6 O3P -111.219; 12.48; 16.557
86.02; 89.83; 64.63
2088.7Ohta, Eisuke; Higuchi, Hiroki; Kawai, Hidetoshi; Fujiwara, Kenshu; Suzuki, Takanori
Butane-1,4-diyl dications stabilized by steric factors: electrochiroptical response systems based on reversible interconversion between dihydro[5]helicene-type electron acceptors and electron-donating 1,1'-binaphthyls.
Organic & biomolecular chemistry, 2005, 3, 3024-3031
7150220 CIFC49.5 H30 Cl15 O2 Sb2F d d 257.17; 35.88; 10.483
90; 90; 90
21503Ohta, Eisuke; Higuchi, Hiroki; Kawai, Hidetoshi; Fujiwara, Kenshu; Suzuki, Takanori
Butane-1,4-diyl dications stabilized by steric factors: electrochiroptical response systems based on reversible interconversion between dihydro[5]helicene-type electron acceptors and electron-donating 1,1'-binaphthyls.
Organic & biomolecular chemistry, 2005, 3, 3024-3031
7150221 CIFC120 H138 N8 O17P -114.9686; 17.0315; 24.6488
102.373; 91.482; 107.245
5835.1Ghosh, Pradyut; Federwisch, Guido; Kogej, Michael; Schalley, Christoph A.; Haase, Detlev; Saak, Wolfgang; Lützen, Arne; Gschwind, Ruth M.
Controlling the rate of shuttling motions in [2]rotaxanes by electrostatic interactions: a cation as solvent-tunable brake.
Organic & biomolecular chemistry, 2005, 3, 2691-2700
7150222 CIFC12 H19 N3P b c a10.805; 10.863; 19.502
90; 90; 90
2289Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150223 CIFC33.33 H37.33 Cl N3 O6 S3P -110.0306; 13.513; 14.3379
108.817; 104.119; 103.132
1682Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150224 CIFC14 H28 Cl3 N3 O13P -18.7647; 11.2725; 12.7812
82.1469; 71.7511; 69.0389
1119.48Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150225 CIFC35 H41 N3 O6 S3P 1 21/c 116.6393; 12.0999; 18.0854
90; 115.568; 90
3284.6Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150226 CIFC14 H26 Br3 N3P 1 21/n 111.0558; 11.6209; 15.1984
90; 107.842; 90
1858.75Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150227 CIFC14 H26 Cl3 N3P 1 21/n 19.5996; 10.1003; 17.1572
90; 93.8496; 90
1659.79Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150228 CIFC14 H30 F5 N3 OP 1 21/c 15.4382; 16.5549; 19.6525
90; 91.581; 90
1768.62Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150229 CIFC16 H28 N4C 1 2/c 112.5482; 14.9721; 17.298
90; 91.7346; 90
3248.3Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150230 CIFC16 H34 Br Cl3 N4 O13P n a 2114.893; 18.055; 10.0567
90; 90; 90
2704.2Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150231 CIFC44 H52 N4 O8 S4P -111.8732; 13.1219; 15.1537
88.4512; 86.6823; 68.4241
2191.8Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150232 CIFC16 H39 F5 N4 O3C 1 2/c 121.1345; 11.3695; 19.3298
90; 111.385; 90
4324.9Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150233 CIFC16 H32 Br4 N4P -19.4815; 11.0386; 11.4504
88.5738; 68.2659; 86.0713
1110.62Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150234 CIFC14 H30 Cl4 N4 O1.5C 1 2/c 129.725; 6.348; 22.054
90; 93.999; 90
4151.3Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150235 CIFC44 H50 Cl4 N4 O8 S4P 1 21/n 110.0881; 30.6387; 15.8038
90; 94.292; 90
4871Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150236 CIFC16 H34 I7 N5C 1 2/c 133.7945; 11.5702; 15.8028
90; 103.859; 90
5999.1Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150237 CIFC16 H38 Br5 N5 O2P -18.4897; 11.1914; 14.9026
82.7077; 81.8566; 69.501
1308.3Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150238 CIFC16 H39 Cl5 N5 O2.5P -110.5378; 11.8423; 20.8415
81.0248; 78.1161; 87.7689
2513.9Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150239 CIFC16 H38 Cl5 N5 OP -19.862; 10.525; 12.113
97.654; 100.99; 103.968
1176.4Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150240 CIFC51 H59 N5 O10 S5P 1 21/n 113.925; 16.012; 22.88
90; 98.651; 90
5043.4Ilioudis, Christos A.; Steed, Jonathan W.
Polyaza metacyclophanes as ditopic anion receptors.
Organic & biomolecular chemistry, 2005, 3, 2935-2945
7150241 CIFC15 H21 F2 N O5P b c a9.319; 12.579; 27.029
90; 90; 90
3168.4Crowley, Patrick J.; Fawcett, John; Griffith, Gerry A.; Moralee, Andrew C.; Percy, Jonathan M.; Salafia, Vittoria
Highly-functionalised difluorinated cyclohexane polyols via the Diels-Alder reaction: regiochemical control via the phenylsulfonyl group.
Organic & biomolecular chemistry, 2005, 3, 3297-3310
7150242 CIFC18 H19 F2 N O5 SP 1 21/n 110.4325; 11.7993; 14.7171
90; 92.051; 90
1810.5Crowley, Patrick J.; Fawcett, John; Griffith, Gerry A.; Moralee, Andrew C.; Percy, Jonathan M.; Salafia, Vittoria
Highly-functionalised difluorinated cyclohexane polyols via the Diels-Alder reaction: regiochemical control via the phenylsulfonyl group.
Organic & biomolecular chemistry, 2005, 3, 3297-3310
7150243 CIFC17 H16 F2 O6 SP 1 21/c 19.9999; 8.3226; 19.8738
90; 94.609; 90
1648.65Crowley, Patrick J.; Fawcett, John; Griffith, Gerry A.; Moralee, Andrew C.; Percy, Jonathan M.; Salafia, Vittoria
Highly-functionalised difluorinated cyclohexane polyols via the Diels-Alder reaction: regiochemical control via the phenylsulfonyl group.
Organic & biomolecular chemistry, 2005, 3, 3297-3310
7150244 CIFC21 H27 F2 N O6 SP 1 21/c 18.806; 22.25; 11.795
90; 98.871; 90
2283.4Crowley, Patrick J.; Fawcett, John; Griffith, Gerry A.; Moralee, Andrew C.; Percy, Jonathan M.; Salafia, Vittoria
Highly-functionalised difluorinated cyclohexane polyols via the Diels-Alder reaction: regiochemical control via the phenylsulfonyl group.
Organic & biomolecular chemistry, 2005, 3, 3297-3310
7150245 CIFC18 H20 F2 O5 SP 1 21/c 117.875; 6.5609; 15.029
90; 93.158; 90
1759.9Crowley, Patrick J.; Fawcett, John; Griffith, Gerry A.; Moralee, Andrew C.; Percy, Jonathan M.; Salafia, Vittoria
Highly-functionalised difluorinated cyclohexane polyols via the Diels-Alder reaction: regiochemical control via the phenylsulfonyl group.
Organic & biomolecular chemistry, 2005, 3, 3297-3310
7150246 CIFC18 H22 F2 O4P -110.5327; 11.552; 16.158
75.465; 71.827; 68.79
1720.1Crowley, Patrick J.; Fawcett, John; Griffith, Gerry A.; Moralee, Andrew C.; Percy, Jonathan M.; Salafia, Vittoria
Highly-functionalised difluorinated cyclohexane polyols via the Diels-Alder reaction: regiochemical control via the phenylsulfonyl group.
Organic & biomolecular chemistry, 2005, 3, 3297-3310
7150247 CIFC14 H18 I N O3P 21 21 2114.113; 12.461; 8.528
90; 90; 90
1499.8Adler, Thomas; Bonjoch, Josep; Clayden, Jonathan; Font-Bardía, Mercè; Pickworth, Mark; Solans, Xavier; Solé, Daniel; Vallverdú, Lluís
Slow interconversion of enantiomeric conformers or atropisomers of anilide and urea derivatives of 2-substituted anilines.
Organic & biomolecular chemistry, 2005, 3, 3173-3183
7150248 CIFC46 H48 N4 O8P -19.7073; 10.569; 10.9986
92.126; 109.791; 101.734
1032.7Danila, Crenguta; Böhmer, Volker; Bolte, Michael
Conformational properties of cyanomethoxy calix[4]arenes.
Organic & biomolecular chemistry, 2005, 3, 3508-3513
7150249 CIFC41 H43 Cl N4 O8.5P -111.4637; 18.3534; 19.8397
74.256; 85.809; 83.824
3990.1Danila, Crenguta; Böhmer, Volker; Bolte, Michael
Conformational properties of cyanomethoxy calix[4]arenes.
Organic & biomolecular chemistry, 2005, 3, 3508-3513
7150250 CIFC46 H48 N4 O8P -110.3157; 12.4728; 17.753
99.611; 103.81; 99.245
2138.5Danila, Crenguta; Böhmer, Volker; Bolte, Michael
Conformational properties of cyanomethoxy calix[4]arenes.
Organic & biomolecular chemistry, 2005, 3, 3508-3513
7150251 CIFC54 H66 N2 O4P -110.4041; 10.6679; 11.557
105.672; 91.147; 108.061
1166.6Danila, Crenguta; Böhmer, Volker; Bolte, Michael
Conformational properties of cyanomethoxy calix[4]arenes.
Organic & biomolecular chemistry, 2005, 3, 3508-3513
7150252 CIFC32 H34P 1 21/c 17.6807; 13.2365; 24.25
90; 93.2; 90
2461.55Nehls, Benjamin S.; Galbrecht, Frank; Bilge, Askin; Brauer, David J.; Lehmann, Christian W.; Scherf, Ullrich; Farrell, Tony
Synthesis and spectroscopy of an oligophenyl based cruciform with remarkable pi-pi assisted folding.
Organic & biomolecular chemistry, 2005, 3, 3213-3219
7150253 CIFC52 H58C 1 2/c 126.1849; 15.839; 10.076
90; 103.728; 90
4059.57Nehls, Benjamin S.; Galbrecht, Frank; Bilge, Askin; Brauer, David J.; Lehmann, Christian W.; Scherf, Ullrich; Farrell, Tony
Synthesis and spectroscopy of an oligophenyl based cruciform with remarkable pi-pi assisted folding.
Organic & biomolecular chemistry, 2005, 3, 3213-3219
7150254 CIFC5 H3 Cl2 N S5P -18.7805; 9.1484; 13.906
79.21; 87.892; 84.473
1092Amelichev, Stanislav A.; Konstantinova, Lidia S.; Lyssenko, Konstantin A.; Rakitin, Oleg A.; Rees, Charles W.
Direct synthesis of fused 1,2,3,4,5-pentathiepins.
Organic & biomolecular chemistry, 2005, 3, 3496-3501
7150255 CIFC8 H9 Cl2 N S5P 1 21/c 18.7306; 9.4354; 16.064
90; 93.761; 90
1320.4Amelichev, Stanislav A.; Konstantinova, Lidia S.; Lyssenko, Konstantin A.; Rakitin, Oleg A.; Rees, Charles W.
Direct synthesis of fused 1,2,3,4,5-pentathiepins.
Organic & biomolecular chemistry, 2005, 3, 3496-3501
7150256 CIFC12 H14 N2 O SP 1 21/c 17.569; 18.652; 8.388
90; 103.69; 90
1150.6Pesquet, Anthony; Daïch, Adam; Decroix, Bernard; Van Hijfte, Luc
Acid-catalysed formation of tricyclic N,S-acetals in imidazolinone series based on the use of the unprecedented N-acyliminium ion cascade reaction involving transposition, heterocyclisation and pi-cyclisation.
Organic & biomolecular chemistry, 2005, 3, 3937-3947
7150257 CIFC13 H16 N2 O SP n a 2119.225; 10.95; 6.047
90; 90; 90
1273Pesquet, Anthony; Daïch, Adam; Decroix, Bernard; Van Hijfte, Luc
Acid-catalysed formation of tricyclic N,S-acetals in imidazolinone series based on the use of the unprecedented N-acyliminium ion cascade reaction involving transposition, heterocyclisation and pi-cyclisation.
Organic & biomolecular chemistry, 2005, 3, 3937-3947
7150260 CIFC12 H10 N O5 SP -17.6162; 9.1924; 10.6592
107.647; 97.265; 110.172
644.88Nikolaev, Vsevolod; Hennig, Lothar; Sieler, Jochim; Rodina, Ludmila; Schulze, Barbel; Nikolaev, Valerij
Cyclic and acyclic sulfonimides in reactions with Rh(II)-ketocarbenoids: a new access to chemoselective O-functionalization of the imidic carbonyl groups.
Organic & biomolecular chemistry, 2005, 3, 4108-4116
7150261 CIFC13 H14 Cl N O7 SP -18.0512; 8.7739; 11.745
91.894; 105.771; 90.555
797.9Nikolaev, Vsevolod; Hennig, Lothar; Sieler, Jochim; Rodina, Ludmila; Schulze, Barbel; Nikolaev, Valerij
Cyclic and acyclic sulfonimides in reactions with Rh(II)-ketocarbenoids: a new access to chemoselective O-functionalization of the imidic carbonyl groups.
Organic & biomolecular chemistry, 2005, 3, 4108-4116
7150262 CIFC27 H33 Cl O9 SiP 6114.153; 14.153; 25.881
90; 90; 120
4489.6Bailey, Simon; Helliwell, Madeleine; Teerawutgulrag, Aphiwat; Thomas, Eric J.
A total synthesis of milbemycin G: approaches to the C1-C10-fragment and completion of the synthesis.
Organic & biomolecular chemistry, 2005, 3, 3654-3677
7150263 CIFC35 H44 O10 SiP 21 21 2114.792; 28.3; 8.5666
90; 90; 90
3586.1Bailey, Simon; Helliwell, Madeleine; Teerawutgulrag, Aphiwat; Thomas, Eric J.
A total synthesis of milbemycin G: approaches to the C1-C10-fragment and completion of the synthesis.
Organic & biomolecular chemistry, 2005, 3, 3654-3677
7150264 CIFC23 H24 N4 O4P 1 21/c 17.6072; 24.695; 11.851
90; 108.06; 90
2116.6Schmid, Sylvia; Röttgen, Martin; Thewalt, Ulf; Austel, Volkhard
Synthesis and conformational properties of 2,6-bis-anilino-3-nitropyridines.
Organic & biomolecular chemistry, 2005, 3, 3408-3421
7150265 CIFC18 H16 N4 O2P -110.113; 12.417; 14.105
107.48; 95.21; 102.18
1628.7Schmid, Sylvia; Röttgen, Martin; Thewalt, Ulf; Austel, Volkhard
Synthesis and conformational properties of 2,6-bis-anilino-3-nitropyridines.
Organic & biomolecular chemistry, 2005, 3, 3408-3421
7150266 CIFC22 H22 N4 O4P -18.5952; 9.79; 13.308
72.57; 83.91; 75.36
1033.2Schmid, Sylvia; Röttgen, Martin; Thewalt, Ulf; Austel, Volkhard
Synthesis and conformational properties of 2,6-bis-anilino-3-nitropyridines.
Organic & biomolecular chemistry, 2005, 3, 3408-3421
7150267 CIFC15 H17 F3 N2 O3 Pd SP 1 21/c 19.1402; 12.351; 15.852
90; 97.942; 90
1772.4Lu, Zhong-Lin; Neverov, Alexei A.; Brown, R. Stan
An ortho-palladated dimethylbenzylamine complex as a highly efficient turnover catalyst for the decomposition of P=S insecticides. Mechanistic studies of the methanolysis of some P=S-containing phosphorothioate triesters.
Organic & biomolecular chemistry, 2005, 3, 3379-3387
7150268 CIFC14 H17 Cl N2 PdP b c a9.5463; 16.258; 18.117
90; 90; 90
2811.8Lu, Zhong-Lin; Neverov, Alexei A.; Brown, R. Stan
An ortho-palladated dimethylbenzylamine complex as a highly efficient turnover catalyst for the decomposition of P=S insecticides. Mechanistic studies of the methanolysis of some P=S-containing phosphorothioate triesters.
Organic & biomolecular chemistry, 2005, 3, 3379-3387
7150269 CIFC12 H14 O5C 1 2/c 129.189; 4.9244; 19.8157
90; 123.921; 90
2363.5Rodriguez, Raphaël; Moses, John E.; Adlington, Robert M.; Baldwin, Jack E.
A new and efficient method for o-quinone methide intermediate generation: application to the biomimetic synthesis of the benzopyran derived natural products (+/-)-lucidene and (+/-)-alboatrin.
Organic & biomolecular chemistry, 2005, 3, 3488-3495
7150270 CIFC23 H32 O2P 1 21/c 119.4765; 9.6966; 21.0587
90; 94.5151; 90
3964.72Rodriguez, Raphaël; Moses, John E.; Adlington, Robert M.; Baldwin, Jack E.
A new and efficient method for o-quinone methide intermediate generation: application to the biomimetic synthesis of the benzopyran derived natural products (+/-)-lucidene and (+/-)-alboatrin.
Organic & biomolecular chemistry, 2005, 3, 3488-3495
7150271 CIFC14 H18 O3P 1 21/n 18.8435; 13.404; 10.6982
90; 105.571; 90
1221.6Rodriguez, Raphaël; Moses, John E.; Adlington, Robert M.; Baldwin, Jack E.
A new and efficient method for o-quinone methide intermediate generation: application to the biomimetic synthesis of the benzopyran derived natural products (+/-)-lucidene and (+/-)-alboatrin.
Organic & biomolecular chemistry, 2005, 3, 3488-3495
7150272 CIFC36 H44 O8P 1 21/n 116.999; 11.735; 17.495
90; 112.405; 90
3227Larsen, Lesley; Benn, Michael H.; Parvez, Masood; Perry, Nigel B.
A cytotoxic triketone-phloroglucinol-bullatenone hybrid from Lophomyrtus bullata.
Organic & biomolecular chemistry, 2005, 3, 3236-3241
7150273 CIFC30 H54 N4 O10 S2C 1 2 125.41; 5.071; 15.318
90; 106.77; 90
1890Das, Apurba Kumar; Drew, Michael G. B.; Haldar, Debasish; Banerjee, Arindam
The role of the disulfide bond in amyloid-like fibrillogenesis in a model peptide system.
Organic & biomolecular chemistry, 2005, 3, 3502-3507
7150274 CIFC26 H31 N O6P 1 21 19.934; 5.408; 22.042
90; 96.59; 90
1176.3Dhavale, Dilip D.; Kumar, K. S. Ajish; Chaudhari, Vinod D.; Sharma, Tarun; Sabharwal, Sushma G.; Prakashareddy, J.
Aziridine carboxylate from D-glucose: synthesis of polyhydroxylated piperidine, pyrrolidine alkaloids and study of their glycosidase inhibition.
Organic & biomolecular chemistry, 2005, 3, 3720-3726
7150275 CIFC32 H34 O8 S2P -19.3831; 9.6997; 10.247
117.46; 95.447; 106.754
763.39Müller, Petra U; Weber, Edwin; Rheinwald, Gerd; Seichter, Wilhelm
Oligofunctional amphiphiles featuring geometric core group preorganization: synthesis and study of Langmuir and Langmuir-Blodgett films.
Organic & biomolecular chemistry, 2005, 3, 3757-3766
7150276 CIFC52 H70 O6P -18.8583; 9.1667; 15.4654
88.41; 80.604; 65.605
1127.25Müller, Petra U; Weber, Edwin; Rheinwald, Gerd; Seichter, Wilhelm
Oligofunctional amphiphiles featuring geometric core group preorganization: synthesis and study of Langmuir and Langmuir-Blodgett films.
Organic & biomolecular chemistry, 2005, 3, 3757-3766
7150277 CIFC11 H10 O3P 1 21/a 18.72; 12.944; 8.918
90; 100.47; 90
989.8Müller, Petra U; Weber, Edwin; Rheinwald, Gerd; Seichter, Wilhelm
Oligofunctional amphiphiles featuring geometric core group preorganization: synthesis and study of Langmuir and Langmuir-Blodgett films.
Organic & biomolecular chemistry, 2005, 3, 3757-3766
7150278 CIFC20 H24 O SP 21 21 219.932; 11.5642; 14.7502
90; 90; 90
1694.14Hitchcock, Peter B.; Rowlands, Gareth J.; Seacome, Richard J.
The synthesis and directed ortho-lithiation of 4-tert-butylsulfinyl[2.2]paracyclophane.
Organic & biomolecular chemistry, 2005, 3, 3873-3876
7150279 CIFC20 H24 O SP 21 21 219.9622; 11.5421; 14.9696
90; 90; 90
1721.28Hitchcock, Peter B.; Rowlands, Gareth J.; Seacome, Richard J.
The synthesis and directed ortho-lithiation of 4-tert-butylsulfinyl[2.2]paracyclophane.
Organic & biomolecular chemistry, 2005, 3, 3873-3876
7150280 CIFC27 H30 O2 SP -110.8751; 13.6785; 16.9532
74.165; 75.054; 69.839
2239.71Hitchcock, Peter B.; Rowlands, Gareth J.; Seacome, Richard J.
The synthesis and directed ortho-lithiation of 4-tert-butylsulfinyl[2.2]paracyclophane.
Organic & biomolecular chemistry, 2005, 3, 3873-3876
7150281 CIFC24 H32 O2 SP 42/n :221.1744; 21.1744; 9.5008
90; 90; 90
4259.7Hitchcock, Peter B.; Rowlands, Gareth J.; Seacome, Richard J.
The synthesis and directed ortho-lithiation of 4-tert-butylsulfinyl[2.2]paracyclophane.
Organic & biomolecular chemistry, 2005, 3, 3873-3876
7150282 CIFC17 H16 N4P b c n25.1991; 8.6736; 12.6158
90; 90; 90
2757.4Wong, Wallace W. H.; Vickers, Matthew S.; Cowley, Andrew R.; Paul, Rowena L.; Beer, Paul D.
Tetrakis(imidazolium) macrocyclic receptors for anion binding.
Organic & biomolecular chemistry, 2005, 3, 4201-4208
7150283 CIFC46 H54 F24 N10 P4P -19.6741; 12.6292; 13.1081
65.7093; 71.7542; 83.9297
1385.83Wong, Wallace W. H.; Vickers, Matthew S.; Cowley, Andrew R.; Paul, Rowena L.; Beer, Paul D.
Tetrakis(imidazolium) macrocyclic receptors for anion binding.
Organic & biomolecular chemistry, 2005, 3, 4201-4208
7150284 CIFC14 H10 O4C 1 2/c 117.771; 10.833; 15.115
90; 124.564; 90
2396.2Lion, Cedric J.; Vasselin, David A.; Schwalbe, Carl H.; Matthews, Charles S.; Stevens, Malcolm F. G.; Westwell, Andrew D.
Novel reaction products from the hypervalent iodine oxidation of hydroxylated stilbenes and isoflavones.
Organic & biomolecular chemistry, 2005, 3, 3996-4001
7150285 CIFC20 H19 Cl2 N O3 SP 1 21/c 18.7617; 12.4255; 37.845
90; 94.123; 90
4109.5Zhao, Gui-Ling; Shi, Min
Baylis-Hillman reactions of N-tosyl aldimines and aryl aldehydes with 3-methylpenta-3,4-dien-2-one.
Organic & biomolecular chemistry, 2005, 3, 3686-3694
7150286 CIFC14 H12 B Cl4 F4 N3P 1 21/c 17.7703; 20.6759; 11.1315
90; 95.594; 90
1779.85Schmidt, Andreas; Mordhorst, Thorsten; Nieger, Martin
From uncharged to decacationic molecules: syntheses and spectroscopic properties of heteroarenium-substituted pyridines.
Organic & biomolecular chemistry, 2005, 3, 3788-3793
7150287 CIFC10 H9 N O4P 1 21/n 110.244; 13.92; 13.155
90; 92.4243; 90
1874.2Palmer, Francine N.; Lach, Franck; Poriel, Cyril; Pepper, Adrian G.; Bagley, Mark C.; Slawin, Alexandra M. Z.; Moody, Christopher J.
The diazo route to diazonamide A: studies on the tyrosine-derived fragment.
Organic & biomolecular chemistry, 2005, 3, 3805-3811
7150288 CIFC18 H26 SeP n a 218.418; 13.169; 15.523
90; 90; 90
1721Ford, Susan; Hofmann, Marco; Morley, Christopher P.; Roberts, John L.; Di Vaira, Massimo
Tetramethylcyclopentadienylselenium derivatives.
Organic & biomolecular chemistry, 2005, 3, 3990-3995
7150289 CIFC9 H12 SeP -17.325; 8.283; 8.758
62.64; 84.18; 67.59
434.5Ford, Susan; Hofmann, Marco; Morley, Christopher P.; Roberts, John L.; Di Vaira, Massimo
Tetramethylcyclopentadienylselenium derivatives.
Organic & biomolecular chemistry, 2005, 3, 3990-3995
7150290 CIFC21 H22 N2 O5P 1 21 16.7593; 7.8597; 18.4268
90; 90.99; 90
978.8Basak, Amit; Ghosh, Subhash C.; Das, Amit K.; Bertolasi, Valerio
A novel azetidinyl gamma-lactam based peptide with a preference for beta-turn conformation.
Organic & biomolecular chemistry, 2005, 3, 4050-4052
7150291 CIFC23 H25 N O2 SP 21 21 2110.712; 13.782; 14.26
90; 90; 90
2105.24Betson, Mark S.; Clayden, Jonathan; Helliwell, Madeleine; Mitjans, David
Kinetic and thermodynamic stereocontrol in the atroposelective formation of sulfoxides by oxidation of 2-sulfanyl-1-naphthamides.
Organic & biomolecular chemistry, 2005, 3, 3898-3904
7150292 CIFC24 H22 N2 OP -19.413; 10.281; 11.618
101.32; 109.63; 112.28
909.9Khlebnikov, Alexander F.; Novikov, Mikhail S.; Shinkevich, Ekaterina Yu; Vidovic, Denis
Selective transannular ring transformations in azirino-fused eight-membered O,N- or S,N-heterocycles.
Organic & biomolecular chemistry, 2005, 3, 4040-4042
7150293 CIFC20 H26 O8P 1 21/c 19.8194; 20.3687; 10.7783
90; 116.445; 90
1930.18Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150294 CIFC21 H27 N O9P 1 21 16.4142; 13.0225; 12.6626
90; 91.031; 90
1057.52Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150295 CIFC21.5 H28 Cl N O9P -16.8253; 12.1456; 15.2031
113.501; 93.419; 92.824
1150.02Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150296 CIFC32 H32 O8P 1 21/n 112.0281; 17.769; 14.0771
90; 114.804; 90
2731.1Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150297 CIFC22 H30 Cl2 O9P -16.6987; 13.8444; 14.0583
105.07; 101.138; 95.648
1219.91Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150298 CIFC23 H29 N O9P 1 21/n 114.6048; 7.954; 19.9249
90; 99.051; 90
2285.79Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150299 CIFC21 H30 O10P 1 21/n 110.4467; 11.4334; 18.614
90; 91.264; 90
2222.74Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150300 CIFC20 H34 O7P 21 21 219.2857; 10.4352; 21.127
90; 90; 90
2047.17Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150301 CIFC16 H21 N O7P b c a19.0707; 13.0777; 27.3853
90; 90; 90
6829.9Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150302 CIFC14 H23 N O7P 1 21/c 114.2904; 10.495; 11.2184
90; 108.84; 90
1592.37Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150303 CIFC17 H28 O6P 21 21 217.9383; 14.4423; 15.4979
90; 90; 90
1776.79Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150304 CIFC14 H22 O6P 21 21 218.5902; 10.0809; 16.5589
90; 90; 90
1433.95Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150305 CIFC17 H27.5 Br O6.25P 1 21 110.4635; 9.3926; 10.5987
90; 111.888; 90
966.55Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150306 CIFC13 H20 O7C 1 c 19.9656; 17.1331; 8
90; 100.757; 90
1341.93Ley, Steven V.; Dixon, Darren J.; Guy, Richard T.; Rodríguez, Félix; Sheppard, Tom D.
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & biomolecular chemistry, 2005, 3, 4095-4107
7150307 CIFC24 H27 N O7 SP -18.9592; 9.2569; 15.3512
79.472; 83.129; 69.351
1169.19Mitchell, Judith M.; Finney, Nathaniel S.
Synthetic studies of pseurotin A: preparation of an advanced lactam aldehyde intermediate.
Organic & biomolecular chemistry, 2005, 3, 4274-4281
7150308 CIFC33 H29 N O2C 1 c 115.3223; 12.7909; 14.0095
90; 104.82; 90
2654.34Robertson, Jeremy; Bell, Stephen J.; Krivokapic, Alexander
On the reaction of diphenylketene with isocyanides.
Organic & biomolecular chemistry, 2005, 3, 4246-4251
7150309 CIFC32 H27 N O2P 1 21/n 19.6597; 14.5094; 17.0652
90; 95.093; 90
2382.35Robertson, Jeremy; Bell, Stephen J.; Krivokapic, Alexander
On the reaction of diphenylketene with isocyanides.
Organic & biomolecular chemistry, 2005, 3, 4246-4251
7150310 CIFC46 H37 N O3P 1 21/c 111.608; 17.2569; 17.9855
90; 103.702; 90
3500.29Robertson, Jeremy; Bell, Stephen J.; Krivokapic, Alexander
On the reaction of diphenylketene with isocyanides.
Organic & biomolecular chemistry, 2005, 3, 4246-4251
7150311 CIFC32 H27 N O2P 1 21/c 117.7513; 5.9105; 23.5922
90; 96.6068; 90
2458.83Robertson, Jeremy; Bell, Stephen J.; Krivokapic, Alexander
On the reaction of diphenylketene with isocyanides.
Organic & biomolecular chemistry, 2005, 3, 4246-4251
7150312 CIFC36 H27 N O2P 1 21/a 122.3209; 5.822; 22.4854
90; 116.634; 90
2611.97Robertson, Jeremy; Bell, Stephen J.; Krivokapic, Alexander
On the reaction of diphenylketene with isocyanides.
Organic & biomolecular chemistry, 2005, 3, 4246-4251
7151345 CIFC13 H15 Cl O5 SP 21 21 216.853; 9.6726; 21.2802
90; 90; 90
1410.59Alonso, A. Mateo; Horcajada, Roberto; Motevalli, Majid; Utley, James H. P.; Wyatt, Peter B.
The reactivity, as electrogenerated bases, of chiral and achiral phenazine radical-anions, including application in asymmetric deprotonation.
Organic & biomolecular chemistry, 2005, 3, 2842-2847
7151346 CIFC14 H16 O4 SP 1 21/c 121.102; 10.963; 5.929
90; 92.57; 90
1370.2Alonso, A. Mateo; Horcajada, Roberto; Motevalli, Majid; Utley, James H. P.; Wyatt, Peter B.
The reactivity, as electrogenerated bases, of chiral and achiral phenazine radical-anions, including application in asymmetric deprotonation.
Organic & biomolecular chemistry, 2005, 3, 2842-2847
7151347 CIFC16 H15 N O4P c a 2123.051; 7.509; 7.739
90; 90; 90
1339.5Kataeva, Olga; Krahl, Micha P.; Knölker, Hans-Joachim
First total synthesis of the biologically active 2,7-dioxygenated tricyclic carbazole alkaloids 7-methoxy-O-methylmukonal, clausine H (clauszoline-C), clausine K (clauszoline-J) and clausine O.
Organic & biomolecular chemistry, 2005, 3, 3099-3101
7151348 CIFC25 H28 Cl2 N2 O2 SP n a 2124.2176; 14.582; 14.204
90; 90; 90
5016Karpov, Alexei S.; Rominger, Frank; Müller, Thomas J J
A diversity oriented four-component approach to tetrahydro-beta-carbolines initiated by Sonogashira coupling.
Organic & biomolecular chemistry, 2005, 3, 4382-4391
7151349 CIFC26 H27 N3 O4P 1 21/c 111.762; 13.0069; 14.7316
90; 97.724; 90
2233.3Karpov, Alexei S.; Rominger, Frank; Müller, Thomas J J
A diversity oriented four-component approach to tetrahydro-beta-carbolines initiated by Sonogashira coupling.
Organic & biomolecular chemistry, 2005, 3, 4382-4391
7151350 CIFC27 H30 N2 O3C 1 2/c 115.6913; 16.5338; 18.142
90; 99.574; 90
4641.15Karpov, Alexei S.; Rominger, Frank; Müller, Thomas J J
A diversity oriented four-component approach to tetrahydro-beta-carbolines initiated by Sonogashira coupling.
Organic & biomolecular chemistry, 2005, 3, 4382-4391
7151351 CIFC25 H26 N2 O2 SP 1 21/n 19.8924; 10.3918; 23.1132
90; 95.472; 90
2365.21Karpov, Alexei S.; Rominger, Frank; Müller, Thomas J J
A diversity oriented four-component approach to tetrahydro-beta-carbolines initiated by Sonogashira coupling.
Organic & biomolecular chemistry, 2005, 3, 4382-4391
7151352 CIFC25 H28 N2 O2 SP 1 21/n 18.6239; 22.0514; 13.2225
90; 100.164; 90
2475.05Karpov, Alexei S.; Rominger, Frank; Müller, Thomas J J
A diversity oriented four-component approach to tetrahydro-beta-carbolines initiated by Sonogashira coupling.
Organic & biomolecular chemistry, 2005, 3, 4382-4391
7151353 CIFC18 H20 N2 O3P 1 21/c 111.5257; 12.9651; 10.7417
90; 94.77; 90
1599.59Karpov, Alexei S.; Rominger, Frank; Müller, Thomas J J
A diversity oriented four-component approach to tetrahydro-beta-carbolines initiated by Sonogashira coupling.
Organic & biomolecular chemistry, 2005, 3, 4382-4391
7151354 CIFC27 H26 N2 O7P -111.25; 11.291; 11.708
76.459; 64.71; 64.809
1214.28Heaney, Frances; McCarthy, Tomas; Mahon, Mary; McKee, V.
Bridgehead nitrogen heterocycles which contain the quinazoline moiety – synthesis and cycloaddition of 1,2-dihydroquinazoline 3-oxides.
Organic & biomolecular chemistry, 2005, 3, 4351-4361
7151355 CIFC39 H38 N2 O17P 1 21/n 111.1011; 21.952; 15.9307
90; 103.285; 90
3778.3Heaney, Frances; McCarthy, Tomas; Mahon, Mary; McKee, V.
Bridgehead nitrogen heterocycles which contain the quinazoline moiety – synthesis and cycloaddition of 1,2-dihydroquinazoline 3-oxides.
Organic & biomolecular chemistry, 2005, 3, 4351-4361
7151356 CIFC16 H26 N2 O9P b c a10.675; 10.8521; 33.594
90; 90; 90
3891.7Calvet, Géraldine; Guillot, Régis; Blanchard, Nicolas; Kouklovsky, Cyrille
Intermolecular nitroso Diels-Alder cycloaddition of alpha-acetoxynitroso derivatives in aqueous medium.
Organic & biomolecular chemistry, 2005, 3, 4395-4401
7204165 CIFC80 H98 N2 O16P -111.2391; 12.889; 14.478
90.734; 110.956; 112.21
1786.49Brett A. Roberts; Gareth W. V. Cave; Colin L. Raston; Janet L. Scott
Solvent-free synthesis of calix[4]resorcinarenes
Green Chem., 3, 280-284
7204218 CIFC15 H17 N O5P n a 219.1435; 27.8109; 5.8488
90; 90; 90
1487.3Correa, Waldo H.; Scott, Janet L.
Solvent-free, two-step synthesis of some unsymmetrical 4-aryl-1,4-dihydropyridines
Green Chemistry, 2001, 3, 296-301
7204901 CIFC5 H6 Bi Cl4 NC 1 c 112.717; 12.894; 7.274
90; 118.49; 90
1048.3Jóźków, Jolanta; Medycki, Wojciech; Zaleski, Jacek; Jakubas, Ryszard; Bator, Grażyna; Ciunik, Zbigniew
Structure, phase transition and molecular motions in (C5H5NH)BiCl4
Physical Chemistry Chemical Physics, 2001, 3, 3222
7204902 CIFC80 H91 Cl N Na O14P 1 21/n 119.8693; 13.459; 30.405
90; 108.422; 90
7714.3Danil de Namor, Angela F.; Kowalska, Dorota; Castellano, Eduardo E.; Piro, Oscar E.; Sueros Velarde, Felix J.; Villanueva Salas, Jose
Lower rim calix(4)arene ketone derivatives and their interaction with alkali metal cations. Structural and thermodynamic (solution and complexation) characterisation of the tetraphenyl ketone derivative and its sodium complex
Physical Chemistry Chemical Physics, 2001, 3, 4010
7204903 CIFC76 H80 O8C 1 2/c 129.487; 24.884; 20.322
90; 115.49; 90
13460Danil de Namor, Angela F.; Kowalska, Dorota; Castellano, Eduardo E.; Piro, Oscar E.; Sueros Velarde, Felix J.; Villanueva Salas, Jose
Lower rim calix(4)arene ketone derivatives and their interaction with alkali metal cations. Structural and thermodynamic (solution and complexation) characterisation of the tetraphenyl ketone derivative and its sodium complex
Physical Chemistry Chemical Physics, 2001, 3, 4010
7204905 CIFC14 H10 I2 N2 O7 RuP 1 21/c 16.8645; 19.7584; 13.7107
90; 95.978; 90
1849.49Luukkanen, Saija; Haukka, Matti; Eskelinen, Esa; Pakkanen, Tapani A.; Lehtovuori, Viivi; Kallioinen, Jani; Myllyperkiö, Pasi; Korppi-Tommola, Jouko
Photochemical reactivity of halogen-containing ruthenium‒dcbpy (dcbpy = 4,4'-dicarboxylic acid-2,2'-bipyridine) compounds, trans(Br)-[Ru(dcbpy)(CO)2Br2] and trans(I)-[Ru(dcbpy)(CO)2I2]
Physical Chemistry Chemical Physics, 2001, 3, 1992
7216696 CIFC24 H12 F6P -19.624; 9.777; 10.267
89.282; 73.95; 86.894
927Shigeyuki Yamada; Keita Kinoshita; Shota Iwama; Takashi Yamazaki; Toshio Kubota; Tomoko Yajima
Development of novel synthetic routes to bis(perfluoroalkyl)-substituted anthracene derivatives
RSC Advances, 2013, 3, 6803-6806
7216697 CIFC28 H16 F6P -19.7598; 9.8853; 11.7566
71.537; 81.277; 76.796
1043.6Shigeyuki Yamada; Keita Kinoshita; Shota Iwama; Takashi Yamazaki; Toshio Kubota; Tomoko Yajima
Development of novel synthetic routes to bis(perfluoroalkyl)-substituted anthracene derivatives
RSC Advances, 2013, 3, 6803-6806
7216698 CIFC24 H14 F6 S2C 1 2/c 121.785; 5.4006; 16.888
90; 104.112; 90
1926.9Shigeyuki Yamada; Keita Kinoshita; Shota Iwama; Takashi Yamazaki; Toshio Kubota; Tomoko Yajima
Development of novel synthetic routes to bis(perfluoroalkyl)-substituted anthracene derivatives
RSC Advances, 2013, 3, 6803-6806
7216699 CIFC34 H20 F6 O2P 1 21/n 111.8145; 8.9218; 12.4651
90; 95.06; 90
1308.78Shigeyuki Yamada; Keita Kinoshita; Shota Iwama; Takashi Yamazaki; Toshio Kubota; Tomoko Yajima
Development of novel synthetic routes to bis(perfluoroalkyl)-substituted anthracene derivatives
RSC Advances, 2013, 3, 6803-6806
7216700 CIFC21 H8 F16P 1 21/c 115.259; 11.705; 12.681
90; 113.096; 90
2083.4Shigeyuki Yamada; Keita Kinoshita; Shota Iwama; Takashi Yamazaki; Toshio Kubota; Tomoko Yajima
Development of novel synthetic routes to bis(perfluoroalkyl)-substituted anthracene derivatives
RSC Advances, 2013, 3, 6803-6806
7216701 CIFC23 H8 F20P 1 21/c 128.388; 5.7555; 14.35
90; 76.509; 90
2279.9Shigeyuki Yamada; Keita Kinoshita; Shota Iwama; Takashi Yamazaki; Toshio Kubota; Tomoko Yajima
Development of novel synthetic routes to bis(perfluoroalkyl)-substituted anthracene derivatives
RSC Advances, 2013, 3, 6803-6806
7221497 CIFAl Na Si4P 4/n m m :14.13; 4.13; 7.4
90; 90; 90
126.221Nowotny, H.; Scheil, E.
Ueber eine ternaere Verbindung im System Aluminium-Silicium- Natrium
Metallforschung, 1947, 3, 76-80
7221940 CIF
HKL
Al0.05 Ca0.475 Ce0.025 Li0.025 O2 Si0.45 Sr0.475P n m a6.94901; 5.59224; 9.46525
90; 90; 90
367.82Shihai Miao; Zhiguo Xia; Maxim S. Molokeev; Mingyue Chen; Jie Zhang; Quanlin Liu
Effect of Al/Si Substitution on the Structure and Luminescence Properties of CaSrSiO4:Ce3+ Phosphor: Analysis based on the Polyhedral Distortion
Journal of Materials Chemistry C, 2015, 3, 4616-4622
7221941 CIF
HKL
Al0.005 Ca0.475 Ce0.025 Li0.025 O2 Si0.495 Sr0.475P n m a6.95269; 5.58722; 9.45515
90; 90; 90
367.3Shihai Miao; Zhiguo Xia; Maxim S. Molokeev; Mingyue Chen; Jie Zhang; Quanlin Liu
Effect of Al/Si Substitution on the Structure and Luminescence Properties of CaSrSiO4:Ce3+ Phosphor: Analysis based on the Polyhedral Distortion
Journal of Materials Chemistry C, 2015, 3, 4616-4622
7221942 CIF
HKL
Ca3.8 Ce0.2 Li0.2 O16 Si4 Sr3.8P n m a6.95409; 5.58264; 9.45199
90; 90; 90
366.95Shihai Miao; Zhiguo Xia; Maxim S. Molokeev; Mingyue Chen; Jie Zhang; Quanlin Liu
Effect of Al/Si Substitution on the Structure and Luminescence Properties of CaSrSiO4:Ce3+ Phosphor: Analysis based on the Polyhedral Distortion
Journal of Materials Chemistry C, 2015, 3, 4616-4622
7221943 CIF
HKL
Ca19.81 Eu1.2 O48 Si12 Sr3P n a 2120.4644; 9.31815; 5.54812
90; 90; 90
1057.97Shihai Miao; Zhiguo Xia; Maxim Molokeev; Jie Zhang; QuanLin Liu
Crystal Structure Refinement and Luminescence Property of Blue-Green-Emitting CaSrAl2SiO7:Ce3+,Li+,Eu2+ Phosphors
Journal of Materials Chemistry C, 2015, 3, 8322-8328
7221944 CIF
HKL
Ca17.4 Ce1.2 Li1.2 O48 Si12 Sr4.2P n a 2120.5411; 9.34901; 5.55337
90; 90; 90
1066.46Shihai Miao; Zhiguo Xia; Maxim Molokeev; Jie Zhang; QuanLin Liu
Crystal Structure Refinement and Luminescence Property of Blue-Green-Emitting CaSrAl2SiO7:Ce3+,Li+,Eu2+ Phosphors
Journal of Materials Chemistry C, 2015, 3, 8322-8328
7224688 CIF
HKL
Ba7.69 Ce0.14 Eu0.03 Li0.14 O32 Si12P 1 21/c 112.4859; 4.69043; 13.94982
90; 93.558; 90
815.39Mingyue Chen; Zhiguo Xia; Maxim S. Molokeev; Quanlin Liu
Insights into Ba4Si6O16 structure and photoluminescence tuning of Ba4Si6O16:Ce3+,Eu2+ phosphors
Journal of Materials Chemistry C, 2015, 3, 12477-12483
7224689 CIF
HKL
Ba7.72 Ce0.14 Li0.14 O32 Si12P 1 21/c 112.48631; 4.69045; 13.94852
90; 93.5664; 90
815.33Mingyue Chen; Zhiguo Xia; Maxim S. Molokeev; Quanlin Liu
Insights into Ba4Si6O16 structure and photoluminescence tuning of Ba4Si6O16:Ce3+,Eu2+ phosphors
Journal of Materials Chemistry C, 2015, 3, 12477-12483
7228257 CIFCu2.667 Li2.667 Nb8 O24I 2 37.5286; 7.5286; 7.5286
90; 90; 90
426.72Mineo Sato; Yoshiki Hama
Structure of new perovskite-related compounds, LiCuM3O9 (M = Nb, Ta)
Journal of Materials Chemistry, 1993, 3, 233-236
7228258 CIFCu2.667 Li2.667 O24 Ta8I m -37.5178; 7.5178; 7.5178
90; 90; 90
424.886Mineo Sato; Yoshiki Hama
Structure of new perovskite-related compounds, LiCuM3O9 (M = Nb, Ta)
Journal of Materials Chemistry, 1993, 3, 233-236
7228542 CIFFe S2P c a 215.42; 5.42; 5.42
90; 90; 90
159.22El Mendili, Y.; Abdelouas, A.; Bardeau, J.-F.
Impact of a sulphidogenic environment on the corrosion behavior of carbon steel at 90 °C
RSC Advances, 2013, 3, 15148-15156
7233954 CIFC34 H38 N2P 1 21/n 112.6244; 14.8163; 14.6426
90; 91.253; 90
2738.2Yiliu Lin; Gan Chen; Lifang Zhao; Wang Zhang Yuan; Yongming Zhang; Ben Zhong Tang
Diethylamino functionalized tetraphenylethenes: structural and electronic modulation of photophysical properties, implication for the CIE mechanism and application to cell imaging
Journal of Materials Chemistry C, 2015, 3, 112-120
7233955 CIFC34 H36 F2 N2P -19.6825; 10.7418; 14.3568
73.476; 76.694; 88.074
1392.3Yiliu Lin; Gan Chen; Lifang Zhao; Wang Zhang Yuan; Yongming Zhang; Ben Zhong Tang
Diethylamino functionalized tetraphenylethenes: structural and electronic modulation of photophysical properties, implication for the CIE mechanism and application to cell imaging
Journal of Materials Chemistry C, 2015, 3, 112-120
7233956 CIFC31.5 H29 B Cl Cu F4 N5 PP 1 21/c 110.47; 15.697; 39.879
90; 91.893; 90
6550Fengshou Wu; Jie Li; Hongbo Tong; Zaoying Li; Chihaya Adachi; Adam Langlois; Pierre D. Harvey; Li Liu; Wai-Yeung Wong; Wai-Kwok Wong; Xunjin Zhu
Phosphorescent Cu(I) complexes based on bis(pyrazol-1-yl-methyl)-pyridine derivatives for organic light-emitting diodes
Journal of Materials Chemistry C, 2015, 3, 138-146
7233957 CIFC35 H36 B Cu F4 N5 PP n a 2120.5475; 10.2304; 32.811
90; 90; 90
6897.2Fengshou Wu; Jie Li; Hongbo Tong; Zaoying Li; Chihaya Adachi; Adam Langlois; Pierre D. Harvey; Li Liu; Wai-Yeung Wong; Wai-Kwok Wong; Xunjin Zhu
Phosphorescent Cu(I) complexes based on bis(pyrazol-1-yl-methyl)-pyridine derivatives for organic light-emitting diodes
Journal of Materials Chemistry C, 2015, 3, 138-146
7233958 CIFC43 H52 B Cu F4 N5 PP 1 21/n 116.775; 16.685; 18.348
90; 112.177; 90
4756Fengshou Wu; Jie Li; Hongbo Tong; Zaoying Li; Chihaya Adachi; Adam Langlois; Pierre D. Harvey; Li Liu; Wai-Yeung Wong; Wai-Kwok Wong; Xunjin Zhu
Phosphorescent Cu(I) complexes based on bis(pyrazol-1-yl-methyl)-pyridine derivatives for organic light-emitting diodes
Journal of Materials Chemistry C, 2015, 3, 138-146
7233959 CIFC55 H44 B Cu F4 N5 PP -113.96; 14.57; 14.67
117.544; 99.86; 95.08
2558Fengshou Wu; Jie Li; Hongbo Tong; Zaoying Li; Chihaya Adachi; Adam Langlois; Pierre D. Harvey; Li Liu; Wai-Yeung Wong; Wai-Kwok Wong; Xunjin Zhu
Phosphorescent Cu(I) complexes based on bis(pyrazol-1-yl-methyl)-pyridine derivatives for organic light-emitting diodes
Journal of Materials Chemistry C, 2015, 3, 138-146
7233960 CIFC34 H38 N4 O2P -14.7039; 9.3029; 16.8491
100.068; 92.587; 99.396
714.16Mina Kim; Dong Ryeol Whang; Johannes Gierschner; Soo Young Park
A distyrylbenzene based highly efficient deep red/near-infrared emitting organic solid
Journal of Materials Chemistry C, 2015, 3, 231-234
7233961 CIFC6 H18 Cl6 Si6C 1 2/c 117.7183; 9.8193; 13.5232
90; 109.717; 90
2214.8Sung Jin Park; Hyeon Mo Cho; Myong Euy Lee; Miyoung Kim; Kwenwoo Han; Seunghee Hong; Sanghak Lim; Hansong Lee; Byeonggyu Hwang; Sang Kyun Kim; Sangdeok Shim; Philjae Kang; Moon-Gun Choi
Soluble polycyclosilane-polysiloxane hybrid material and silicon thin film with optical properties at 193 nm and etch selectivity
Journal of Materials Chemistry C, 2015, 3, 239-242
7233962 CIFC18 H48 O6 Si6I -4 3 d23.3514; 23.3514; 23.3514
90; 90; 90
12733.2Sung Jin Park; Hyeon Mo Cho; Myong Euy Lee; Miyoung Kim; Kwenwoo Han; Seunghee Hong; Sanghak Lim; Hansong Lee; Byeonggyu Hwang; Sang Kyun Kim; Sangdeok Shim; Philjae Kang; Moon-Gun Choi
Soluble polycyclosilane-polysiloxane hybrid material and silicon thin film with optical properties at 193 nm and etch selectivity
Journal of Materials Chemistry C, 2015, 3, 239-242
7233963 CIFC12 H10 Br2 N2 O2 ZnC 1 2/c 120.94; 9.168; 16.491
90; 114.673; 90
2877Pei-Xin Li; Ming-Sheng Wang; Li-Zhen Cai; Guan-E. Wang; Guo-Cong Guo
Rare electron-transfer photochromic and thermochromic difunctional compounds
Journal of Materials Chemistry C, 2015, 3, 253-256
7233964 CIFC12 H10 Cl2 N2 O2 ZnC 1 2/c 121.042; 8.881; 16.352
90; 113.67; 90
2799Pei-Xin Li; Ming-Sheng Wang; Li-Zhen Cai; Guan-E. Wang; Guo-Cong Guo
Rare electron-transfer photochromic and thermochromic difunctional compounds
Journal of Materials Chemistry C, 2015, 3, 253-256
7233965 CIFC12 H10 Br2 N2 O2 ZnC 1 2/c 121.005; 9.1974; 16.531
90; 114.679; 90
2901.9Pei-Xin Li; Ming-Sheng Wang; Li-Zhen Cai; Guan-E. Wang; Guo-Cong Guo
Rare electron-transfer photochromic and thermochromic difunctional compounds
Journal of Materials Chemistry C, 2015, 3, 253-256
7233966 CIFC12 H10 Cl2 N2 O2 ZnC 1 2/c 121.004; 8.861; 16.329
90; 113.747; 90
2781.8Pei-Xin Li; Ming-Sheng Wang; Li-Zhen Cai; Guan-E. Wang; Guo-Cong Guo
Rare electron-transfer photochromic and thermochromic difunctional compounds
Journal of Materials Chemistry C, 2015, 3, 253-256
7233993 CIFC16 H6 N4 S3P 1 21/n 17.1953; 17.8923; 11.5414
90; 103.832; 90
1442.76Abby Casey; Yang Han; Zhuping Fei; Andrew J. P. White; Thomas D. Anthopoulos; Martin Heeney
Cyano substituted benzothiadiazole: a novel acceptor inducing n-type behaviour in conjugated polymers
Journal of Materials Chemistry C, 2015, 3, 265-275
7233994 CIFC42 H36 N4 S2P -17.2133; 14.5623; 16.4041
91.618; 97.367; 98.76
1686.96Masahiro Nakano; Itaru Osaka; Kazuo Takimiya
Dibenzo[a,e]pentalene-embedded dicyanomethylene-substituted thienoquinoidals for n-channel organic semiconductors: synthesis, properties, and device characteristics
Journal of Materials Chemistry C, 2015, 3, 283-290
7233995 CIFC30 H19 Cl3 N4 S4P -17.7895; 11.882; 17.8299
84.474; 78.079; 80.66
1589.9Francois Baert; Clement Cabanetos; Antoine Leliege; Eva Kirchner; Olivier Segut; Olivier Aleveque; Magali Allain; Gijun Seo; Sungyeop Jung; Denis Tondelier; Bernard Geffroy; Jean Roncali; Philippe Leriche; Philippe Blanchard
A bridged low band gap A-D-A quaterthiophene as efficient donor for organic solar cells
Journal of Materials Chemistry C, 2015, 3, 390-398
7233996 CIFC62 H111 O25.5 S12 Ti6P 1 21/n 121.0421; 32.775; 28.371
90; 91.981; 90
19555Jing-Xue Yin; Peng Huo; Sheng Wang; Jing Wu; Qin-Yu Zhu; Jie Dai
A tetrathiafulvalene-grafted titanium-oxo-cluster material: self-catalyzed crystal exfoliation and photocurrent response properties
Journal of Materials Chemistry C, 2015, 3, 409-415
7233997 CIFC30 H30 N OP -17.73; 11.04; 14.68
79.75; 87.94; 89.29
1232Anil Kuwar; Rahul Patil; Amanpreet Singh; Suban K. Sahoo; Jaromir Marek; Narinder Singh
A two-in-one dual channel chemosensor for Fe3+ and Cu2+ with nanomolar detection mimicking the IMPLICATION logic gate
Journal of Materials Chemistry C, 2015, 3, 453-460
7233998 CIFC32 H16 N8 O VP -18.7236; 12.0048; 12.6103
68.024; 83.699; 85.6
1216.35Alexandra J. Ramadan; Luke A. Rochford; Dean S. Keeble; Paul Sullivan; Mary P. Ryan; Tim S. Jones; Sandrine Heutz
Exploring high temperature templating in non-planar phthalocyanine/copper iodide (111) bilayers
Journal of Materials Chemistry C, 2015, 3, 461-465
7233999 CIFC31 H31 B N2 O2P 1 21/n 115.136; 8.9997; 20.207
90; 104.56; 90
2664.2Lu Wang; Zhenyu Zhang; Xiao Cheng; Kaiqi Ye; Feng Li; Yue Wang; Hongyu Zhang
Red emissive diarylboron diketonate crystals: aggregation-induced color change and amplified spontaneous emission
Journal of Materials Chemistry C, 2015, 3, 499-505
7234000 CIFC31 H31 B N2 O2P 110.62; 10.757; 18.073
79.44; 88.37; 76.63
1974.5Lu Wang; Zhenyu Zhang; Xiao Cheng; Kaiqi Ye; Feng Li; Yue Wang; Hongyu Zhang
Red emissive diarylboron diketonate crystals: aggregation-induced color change and amplified spontaneous emission
Journal of Materials Chemistry C, 2015, 3, 499-505
7234001 CIFC31 H21 B F10 N2 O2P -19.0631; 11.578; 14.74
70.07; 80.02; 84.06
1430.4Lu Wang; Zhenyu Zhang; Xiao Cheng; Kaiqi Ye; Feng Li; Yue Wang; Hongyu Zhang
Red emissive diarylboron diketonate crystals: aggregation-induced color change and amplified spontaneous emission
Journal of Materials Chemistry C, 2015, 3, 499-505
7234002 CIFC20 H16 N2C 1 2/c 116.8377; 5.6889; 15.3882
90; 106.671; 90
1412.05Marta Reig; Joaquim Puigdollers; Dolores Velasco
Molecular order of air-stable p-type organic thin-film transistors by tuning the extension of the pi-conjugated core: the cases of indolo[3,2-b]carbazole and triindole semiconductors
Journal of Materials Chemistry C, 2015, 3, 506-513
7234003 CIFC29 H22 N2P -110.2279; 11.9024; 19.51
106.347; 95.623; 102.023
2197.8Lin Kong; Yu-peng Tian; Qi-yu Chen; Qiong Zhang; Hui Wang; Dong-qin Tan; Zhao-ming Xue; Jie-ying Wu; Hong-ping Zhou; Jia-xiang Yang
Self-assembly of metal ion induced highly emissive fluorophore-triphenylamine nanostructures: enhanced two-photon action cross-section for bioimaging applications
Journal of Materials Chemistry C, 2015, 3, 570-581
7234004 CIFC28 H14 S4P b c n6.0452; 7.701; 43.405
90; 90; 90
2020.7Claude Niebel; Yeongin Kim; Christian Ruzie; Jolanta Karpinska; Basab Chattopadhyay; Guillaume Schweicher; Audrey Richard; Vincent Lemaur; Yoann Olivier; Jerome Cornil; Alan R. Kennedy; Ying Diao; Wen-Ya Lee; Stefan Mannsfeld; Zhenan Bao; Yves H. Geerts
Thienoacene dimers based on the thieno[3,2-b]thiophene moiety: synthesis, characterization and electronic properties
Journal of Materials Chemistry C, 2015, 3, 674-685
7234005 CIFC14 H8 S2P 1 21/c 111.8095; 5.8538; 7.9599
90; 105.99; 90
528.98Claude Niebel; Yeongin Kim; Christian Ruzie; Jolanta Karpinska; Basab Chattopadhyay; Guillaume Schweicher; Audrey Richard; Vincent Lemaur; Yoann Olivier; Jerome Cornil; Alan R. Kennedy; Ying Diao; Wen-Ya Lee; Stefan Mannsfeld; Zhenan Bao; Yves H. Geerts
Thienoacene dimers based on the thieno[3,2-b]thiophene moiety: synthesis, characterization and electronic properties
Journal of Materials Chemistry C, 2015, 3, 674-685
7234006 CIFC40 H32 F8 N8 O2C 1 2/c 114.7987; 12.0088; 20.0244
90; 90.598; 90
3558.4Marco Saccone; Valentina Dichiarante; Alessandra Forni; Alexis Goulet-Hanssens; Gabriella Cavallo; Jaana Vapaavuori; Giancarlo Terraneo; Christopher J. Barrett; Giuseppe Resnati; Pierangelo Metrangolo; Arri Priimagi
Supramolecular hierarchy among halogen and hydrogen bond donors in light-induced surface patterning
Journal of Materials Chemistry C, 2015, 3, 759-768
7234007 CIFC44 H38 I2 N8C 1 2/m 117.6158; 7.4356; 14.8281
90; 98.184; 90
1922.5Marco Saccone; Valentina Dichiarante; Alessandra Forni; Alexis Goulet-Hanssens; Gabriella Cavallo; Jaana Vapaavuori; Giancarlo Terraneo; Christopher J. Barrett; Giuseppe Resnati; Pierangelo Metrangolo; Arri Priimagi
Supramolecular hierarchy among halogen and hydrogen bond donors in light-induced surface patterning
Journal of Materials Chemistry C, 2015, 3, 759-768
7234008 CIFAl2 O4 SrP -3 1 c6.1456; 6.1456; 10.5585
90; 90; 120
345.35Xufan Li; John D. Budai; Feng Liu; Yu-Sheng Chen; Jane Y. Howe; Chengjun Sun; Jonathan Z. Tischler; Richard S. Meltzer; Zhengwei Pan
Crystal structures and optical properties of new quaternary strontium europium aluminate luminescent nanoribbons
Journal of Materials Chemistry C, 2015, 3, 778-788
7234009 CIFC10 H8 F N3P -16.4282; 8.584; 8.968
108.015; 103.788; 92.762
453N. Venkatramaiah; Deisy M. G. C. Rocha; P. Srikanth; Filipe A. Almeida Paz; Joao P. C. Tome
Synthesis and photophysical characterization of dimethylamine-derived Zn(ii)phthalocyanines: exploring their potential as selective chemosensors for trinitrophenol
Journal of Materials Chemistry C, 2015, 3, 1056-1067
7234010 CIFC10 H8 Cl N3P -17.0606; 7.0918; 10.4983
76.075; 71.33; 77.999
478.45N. Venkatramaiah; Deisy M. G. C. Rocha; P. Srikanth; Filipe A. Almeida Paz; Joao P. C. Tome
Synthesis and photophysical characterization of dimethylamine-derived Zn(ii)phthalocyanines: exploring their potential as selective chemosensors for trinitrophenol
Journal of Materials Chemistry C, 2015, 3, 1056-1067
7234011 CIFC12 H12 F2 N4P 1 21/n 16.7161; 16.551; 11.136
90; 92.593; 90
1236.6N. Venkatramaiah; Deisy M. G. C. Rocha; P. Srikanth; Filipe A. Almeida Paz; Joao P. C. Tome
Synthesis and photophysical characterization of dimethylamine-derived Zn(ii)phthalocyanines: exploring their potential as selective chemosensors for trinitrophenol
Journal of Materials Chemistry C, 2015, 3, 1056-1067
7234012 CIFC58 H49 B Cu F4 N4 O0.5 P2P 1 21/n 126.6146; 14.2867; 27.576
90; 99.038; 90
10355.2Xu-Lin Chen; Chen-Sheng Lin; Xiao-Yuan Wu; Rongming Yu; Teng Teng; Qi-Kai Zhang; Qing Zhang; Wen-Bing Yang; Can-Zhong Lu
Highly efficient cuprous complexes with thermally activated delayed fluorescence and simplified solution process OLEDs using the ligand as host
Journal of Materials Chemistry C, 2015, 3, 1187-1195
7234013 CIFC56 H42 B Cu F4 N4 O P2P 1 21/n 113.5909; 22.0914; 15.8659
90; 92.711; 90
4758.3Xu-Lin Chen; Chen-Sheng Lin; Xiao-Yuan Wu; Rongming Yu; Teng Teng; Qi-Kai Zhang; Qing Zhang; Wen-Bing Yang; Can-Zhong Lu
Highly efficient cuprous complexes with thermally activated delayed fluorescence and simplified solution process OLEDs using the ligand as host
Journal of Materials Chemistry C, 2015, 3, 1187-1195
7234014 CIFC34 H23 O PP -19.0088; 9.6445; 14.0042
96.309; 98.175; 92.359
1195.1Godumala Mallesham; Chidirala Swetha; Surukonti Niveditha; Maneesha Esther Mohanty; Nanubolu Jagadeesh Babu; Arunandan Kumar; Kotamarthi Bhanuprakash; Vaidya Jayathirtha Rao
Phosphine oxide functionalized pyrenes as efficient blue light emitting multifunctional materials for organic light emitting diodes
Journal of Materials Chemistry C, 2015, 3, 1208-1224
7234036 CIFC119 H96 N2 O3C 1 2 142.9951; 9.1135; 12.2084
90; 106.498; 90
4586.7Qingyun Lu; Xiaofang Li; Jun Li; Zhiyong Yang; Bingjia Xu; Zhenguo Chi; Jiarui Xu; Yi Zhang
Influence of cyano groups on the properties of piezofluorochromic aggregation-induced emission enhancement compounds derived from tetraphenylvinyl-capped ethane
Journal of Materials Chemistry C, 2015, 3, 1225-1234
7234037 CIFC61 H48P -19.6852; 11.1199; 21.963
93.231; 95.749; 112.722
2159.2Qingyun Lu; Xiaofang Li; Jun Li; Zhiyong Yang; Bingjia Xu; Zhenguo Chi; Jiarui Xu; Yi Zhang
Influence of cyano groups on the properties of piezofluorochromic aggregation-induced emission enhancement compounds derived from tetraphenylvinyl-capped ethane
Journal of Materials Chemistry C, 2015, 3, 1225-1234
7234038 CIFC30 H20 B2 N2 O2P 1 21/c 19.5948; 20.3932; 11.8402
90; 98.68; 90
2290.22Krzysztof Durka; Ireneusz Glowacki; Sergiusz Lulinski; Beata Luszczynska; Jaromir Smetek; Pawel Szczepanik; Janusz Serwatowski; Urszula E. Wawrzyniak; Grzegorz Wesela-Bauman; Ewelina Witkowska; Gabriela Wiosna-Salyga; Krzysztof Wozniak
Efficient 8-oxyquinolinato emitters based on a 9,10-dihydro-9,10-diboraanthracene scaffold for applications in optoelectronic devices
Journal of Materials Chemistry C, 2015, 3, 1354-1364
7234039 CIFC30 H18 B2 F2 N2 O2P -110.3718; 10.6554; 11.367
90.027; 96.603; 113.011
1147.19Krzysztof Durka; Ireneusz Glowacki; Sergiusz Lulinski; Beata Luszczynska; Jaromir Smetek; Pawel Szczepanik; Janusz Serwatowski; Urszula E. Wawrzyniak; Grzegorz Wesela-Bauman; Ewelina Witkowska; Gabriela Wiosna-Salyga; Krzysztof Wozniak
Efficient 8-oxyquinolinato emitters based on a 9,10-dihydro-9,10-diboraanthracene scaffold for applications in optoelectronic devices
Journal of Materials Chemistry C, 2015, 3, 1354-1364
7234040 CIFC32 H20 B2 Cl6 F2 N2 O2P 1 21/c 19.5314; 14.0687; 12.3085
90; 107.299; 90
1575.84Krzysztof Durka; Ireneusz Glowacki; Sergiusz Lulinski; Beata Luszczynska; Jaromir Smetek; Pawel Szczepanik; Janusz Serwatowski; Urszula E. Wawrzyniak; Grzegorz Wesela-Bauman; Ewelina Witkowska; Gabriela Wiosna-Salyga; Krzysztof Wozniak
Efficient 8-oxyquinolinato emitters based on a 9,10-dihydro-9,10-diboraanthracene scaffold for applications in optoelectronic devices
Journal of Materials Chemistry C, 2015, 3, 1354-1364
7234041 CIFC30 H18 B2 Cl2 N2 O2P 1 21/c 19.9401; 12.5613; 19.659
90; 91.6; 90
2453.68Krzysztof Durka; Ireneusz Glowacki; Sergiusz Lulinski; Beata Luszczynska; Jaromir Smetek; Pawel Szczepanik; Janusz Serwatowski; Urszula E. Wawrzyniak; Grzegorz Wesela-Bauman; Ewelina Witkowska; Gabriela Wiosna-Salyga; Krzysztof Wozniak
Efficient 8-oxyquinolinato emitters based on a 9,10-dihydro-9,10-diboraanthracene scaffold for applications in optoelectronic devices
Journal of Materials Chemistry C, 2015, 3, 1354-1364
7234042 CIFC30 H16 B2 F4 N2 O2P -110.9289; 11.3491; 12.0394
64.416; 64.811; 84.204
1212.51Krzysztof Durka; Ireneusz Glowacki; Sergiusz Lulinski; Beata Luszczynska; Jaromir Smetek; Pawel Szczepanik; Janusz Serwatowski; Urszula E. Wawrzyniak; Grzegorz Wesela-Bauman; Ewelina Witkowska; Gabriela Wiosna-Salyga; Krzysztof Wozniak
Efficient 8-oxyquinolinato emitters based on a 9,10-dihydro-9,10-diboraanthracene scaffold for applications in optoelectronic devices
Journal of Materials Chemistry C, 2015, 3, 1354-1364
7234043 CIFC26 H16 B2 N2 O2 S2P -17.9127; 9.325; 9.806
92.99; 101.3; 113.32
644.76Krzysztof Durka; Ireneusz Glowacki; Sergiusz Lulinski; Beata Luszczynska; Jaromir Smetek; Pawel Szczepanik; Janusz Serwatowski; Urszula E. Wawrzyniak; Grzegorz Wesela-Bauman; Ewelina Witkowska; Gabriela Wiosna-Salyga; Krzysztof Wozniak
Efficient 8-oxyquinolinato emitters based on a 9,10-dihydro-9,10-diboraanthracene scaffold for applications in optoelectronic devices
Journal of Materials Chemistry C, 2015, 3, 1354-1364
7234044 CIFC23 H16 B Cl6 N O2P 1 21/c 119.3536; 12.1881; 20.5126
90; 93.794; 90
4827.98Krzysztof Durka; Ireneusz Glowacki; Sergiusz Lulinski; Beata Luszczynska; Jaromir Smetek; Pawel Szczepanik; Janusz Serwatowski; Urszula E. Wawrzyniak; Grzegorz Wesela-Bauman; Ewelina Witkowska; Gabriela Wiosna-Salyga; Krzysztof Wozniak
Efficient 8-oxyquinolinato emitters based on a 9,10-dihydro-9,10-diboraanthracene scaffold for applications in optoelectronic devices
Journal of Materials Chemistry C, 2015, 3, 1354-1364
7234045 CIFC23 H16 Cu N4 S16P 1 21 115.9296; 8.569; 12.7261
90; 111.355; 90
1617.9Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234046 CIFC23 H16 Cu N4 S16P 1 21 115.938; 8.5815; 12.7618
90; 111.243; 90
1626.9Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234047 CIFC23 H16 Cu N4 S16P 1 21 115.947; 8.5931; 12.7978
90; 111.133; 90
1635.8Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234048 CIFC23 H16 Cu N4 S16P 1 21 115.964; 8.608; 12.8406
90; 111.006; 90
1647.3Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234049 CIFC23 H16 Cu N4 S16P 1 21 115.975; 8.6198; 12.885
90; 110.882; 90
1657.7Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234050 CIFC22 H16 Cu N2 S18P 1 21 116.3427; 8.3968; 12.8302
90; 111.229; 90
1641.17Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234051 CIFC22 H16 Cu N2 S18P 1 21 116.3129; 8.4112; 12.9105
90; 111.028; 90
1653.5Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234052 CIFC22 H16 Cu N2 S18P 1 21 116.2671; 8.421; 13.0072
90; 110.715; 90
1666.6Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234053 CIFC22 H16 Cu N2 S18P 1 21 116.2426; 8.4301; 13.0764
90; 110.455; 90
1677.61Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234054 CIFC22 H16 Cu N2 S18P 1 21 116.2397; 8.4425; 13.1293
90; 110.276; 90
1688.5Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234055 CIFC22 H16 Br Cu N3 S16P n m a12.8965; 29.651; 8.4826
90; 90; 90
3243.7Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234056 CIFC22 H16 Br Cu N3 S16P n m a12.8991; 29.754; 8.5025
90; 90; 90
3263.3Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234057 CIFC22 H16 Br Cu N3 S16P n m a12.9117; 29.845; 8.5178
90; 90; 90
3282.3Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234058 CIFC22 H16 Br Cu N3 S16P n m a12.9342; 29.937; 8.5325
90; 90; 90
3303.9Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234059 CIFC22 H16 Br Cu N3 S16P n m a12.9653; 30.028; 8.5444
90; 90; 90
3326.5Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234060 CIFC22 H16 Cl Cu N3 S16P n m a12.8852; 29.5759; 8.4161
90; 90; 90
3207.3Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234061 CIFC22 H16 Cl Cu N3 S16P n m a12.8917; 29.6686; 8.4335
90; 90; 90
3225.6Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234062 CIFC22 H16 Cl Cu N3 S16P n m a12.9062; 29.7595; 8.4509
90; 90; 90
3245.8Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234063 CIFC22 H16 Cl Cu N3 S16P n m a12.9262; 29.848; 8.4661
90; 90; 90
3266.4Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234064 CIFC22 H16 Cl Cu N3 S16P n m a12.955; 29.9368; 8.4811
90; 90; 90
3289.2Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234065 CIFC20 H16 I3 S16P 1 21/c 116.2595; 8.4332; 12.7668
90; 109.091; 90
1654.3Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234066 CIFC20 H16 I3 S16P 1 21/c 116.2944; 8.4439; 12.7917
90; 108.93; 90
1664.8Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234067 CIFC20 H16 I3 S16P 1 21/c 116.3364; 8.4593; 12.813
90; 108.773; 90
1676.49Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234068 CIFC20 H16 I3 S16P 1 21/c 116.3793; 8.4773; 12.836
90; 108.624; 90
1689Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234069 CIFC20 H16 I3 S16P 1 21/c 116.4227; 8.4972; 12.8688
90; 108.493; 90
1703.1Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234070 CIFC22 H18 Ag N2 O S16P 1 21 115.9984; 8.5499; 12.4594
90; 109.846; 90
1603Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234071 CIFC22 H18 Ag N2 O S16P 1 21 116.0164; 8.5758; 12.4828
90; 109.747; 90
1613.7Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234072 CIFC22 H18 Ag N2 O S16P 1 21 116.0283; 8.5985; 12.5042
90; 109.62; 90
1623.27Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234073 CIFC22 H18 Ag N2 O S16P 1 21 116.0442; 8.6241; 12.5341
90; 109.452; 90
1635.31Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234074 CIFC22 H18 Ag N2 O S16P 1 21 116.0579; 8.6445; 12.5766
90; 109.254; 90
1648.1Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234075 CIFC23 H16 Cu2 N3 S16P 1 21/c 116.075; 8.5801; 13.2856
90; 114.772; 90
1663.8Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234076 CIFC23 H16 Cu2 N3 S16P 1 21/c 116.0598; 8.5797; 13.2802
90; 114.516; 90
1664.9Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234077 CIFC23 H16 Cu2 N3 S16P 1 21/c 116.0681; 8.5852; 13.307
90; 114.2; 90
1674.4Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234078 CIFC23 H16 Cu2 N3 S16P 1 21/c 116.082; 8.5906; 13.3532
90; 113.794; 90
1688Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234079 CIFC23 H16 Cu2 N3 S16P 1 21/c 116.08; 8.5837; 13.3946
90; 113.349; 90
1697.4Takaaki Hiramatsu; Yukihiro Yoshida; Gunzi Saito; Akihiro Otsuka; Hideki Yamochi; Mitsuhiko Maesato; Yasuhiro Shimizu; Hiroshi Ito; Hideo Kishida
Quantum spin liquid: design of a quantum spin liquid next to a superconducting state based on a dimer-type ET Mott insulator
Journal of Materials Chemistry C, 2015, 3, 1378-1388
7234080 CIFC57 H63 N3 O6P -111.3178; 21.3745; 21.9731
70.045; 76.206; 88.942
4840.8Michael Giese; Tim Krappitz; Ronald Y. Dong; Carl A. Michal; Wadood Y. Hamad; Brian O. Patrick; Mark J. MacLachlan
Tuning the photonic properties of chiral nematic mesoporous organosilica with hydrogen-bonded liquid-crystalline assemblies
Journal of Materials Chemistry C, 2015, 3, 1537-1545
7234081 CIFC48 H51 N9 O6P 1 21/n 112.4651; 14.1037; 24.879
90; 98.502; 90
4325.8Michael Giese; Tim Krappitz; Ronald Y. Dong; Carl A. Michal; Wadood Y. Hamad; Brian O. Patrick; Mark J. MacLachlan
Tuning the photonic properties of chiral nematic mesoporous organosilica with hydrogen-bonded liquid-crystalline assemblies
Journal of Materials Chemistry C, 2015, 3, 1537-1545
7234082 CIFC22 H16 O4P 21 21 214.557; 18.5706; 18.986
90; 90; 90
1606.7Toshiki Higashino; Shohei Kumeta; Sumika Tamura; Yoshio Ando; Ken Ohmori; Keisuke Suzuki; Takehiko Mori
Ambipolar transistor properties of 2,2'-binaphthosemiquinones
Journal of Materials Chemistry C, 2015, 3, 1588-1594
7234083 CIFC24 H20 O4P 1 21/n 112.2447; 4.98276; 15.1193
90; 93.2547; 90
920.98Toshiki Higashino; Shohei Kumeta; Sumika Tamura; Yoshio Ando; Ken Ohmori; Keisuke Suzuki; Takehiko Mori
Ambipolar transistor properties of 2,2'-binaphthosemiquinones
Journal of Materials Chemistry C, 2015, 3, 1588-1594
7234084 CIFC26 H24 O4C 1 2/c 129.3578; 4.3053; 18.6433
90; 118.437; 90
2072.08Toshiki Higashino; Shohei Kumeta; Sumika Tamura; Yoshio Ando; Ken Ohmori; Keisuke Suzuki; Takehiko Mori
Ambipolar transistor properties of 2,2'-binaphthosemiquinones
Journal of Materials Chemistry C, 2015, 3, 1588-1594
7234085 CIFC32 H32 O4C 1 2/c 123.0134; 16.386; 15.4408
90; 119.532; 90
5066.2Toshiki Higashino; Shohei Kumeta; Sumika Tamura; Yoshio Ando; Ken Ohmori; Keisuke Suzuki; Takehiko Mori
Ambipolar transistor properties of 2,2'-binaphthosemiquinones
Journal of Materials Chemistry C, 2015, 3, 1588-1594
7234086 CIFC40 H52 N4 Si2P -17.5919; 13.551; 18.32
89.808; 87.902; 81.114
1860.8Fabian Paulus; Benjamin D. Lindner; Hilmar Reiss; Frank Rominger; Andreas Leineweber; Yana Vaynzof; Henning Sirringhaus; Uwe H. F. Bunz
N,N'-Dihydrotetraazapentacenes (DHTA) in thin film transistors
Journal of Materials Chemistry C, 2015, 3, 1604-1609
7234087 CIFC40 H50 N4 Si2C 1 2/c 133.88; 15.837; 14.074
90; 100.068; 90
7435Fabian Paulus; Benjamin D. Lindner; Hilmar Reiss; Frank Rominger; Andreas Leineweber; Yana Vaynzof; Henning Sirringhaus; Uwe H. F. Bunz
N,N'-Dihydrotetraazapentacenes (DHTA) in thin film transistors
Journal of Materials Chemistry C, 2015, 3, 1604-1609
7234088 CIFC40 H50 F2 N4 Si2P 1 21/c 118.845; 13.5519; 16.4737
90; 107.673; 90
4008.6Fabian Paulus; Benjamin D. Lindner; Hilmar Reiss; Frank Rominger; Andreas Leineweber; Yana Vaynzof; Henning Sirringhaus; Uwe H. F. Bunz
N,N'-Dihydrotetraazapentacenes (DHTA) in thin film transistors
Journal of Materials Chemistry C, 2015, 3, 1604-1609
7234089 CIFC40 H52 N4 Si2P 1 21/n 17.7626; 29.864; 34.922
90; 95.412; 90
8059.6Fabian Paulus; Benjamin D. Lindner; Hilmar Reiss; Frank Rominger; Andreas Leineweber; Yana Vaynzof; Henning Sirringhaus; Uwe H. F. Bunz
N,N'-Dihydrotetraazapentacenes (DHTA) in thin film transistors
Journal of Materials Chemistry C, 2015, 3, 1604-1609
7234090 CIFC40 H50 F2 N4 Si2P 1 21/c 116.4266; 39.893; 36.045
90; 99.223; 90
23315Fabian Paulus; Benjamin D. Lindner; Hilmar Reiss; Frank Rominger; Andreas Leineweber; Yana Vaynzof; Henning Sirringhaus; Uwe H. F. Bunz
N,N'-Dihydrotetraazapentacenes (DHTA) in thin film transistors
Journal of Materials Chemistry C, 2015, 3, 1604-1609
7234091 CIFC25 H22 N2 O2 PtP 1 21/c 19.928; 17.328; 11.79
90; 95.749; 90
2018.1Alexander Tronnier; Ute Heinemeyer; Stefan Metz; Gerhard Wagenblast; Ingo Muenster; Thomas Strassner
Heteroleptic platinum(ii) NHC complexes with a C/C* cyclometalated ligand - synthesis, structure and photophysics
Journal of Materials Chemistry C, 2015, 3, 1680-1693
7234092 CIFC30 H32 N2 O2 PtP 1 21/c 112.228; 13.642; 16.074
90; 98.842; 90
2649.5Alexander Tronnier; Ute Heinemeyer; Stefan Metz; Gerhard Wagenblast; Ingo Muenster; Thomas Strassner
Heteroleptic platinum(ii) NHC complexes with a C/C* cyclometalated ligand - synthesis, structure and photophysics
Journal of Materials Chemistry C, 2015, 3, 1680-1693
7234093 CIFC34 H24 N2 O2 PtR -3 :H40.894; 40.894; 9.173
90; 90; 120
13285Alexander Tronnier; Ute Heinemeyer; Stefan Metz; Gerhard Wagenblast; Ingo Muenster; Thomas Strassner
Heteroleptic platinum(ii) NHC complexes with a C/C* cyclometalated ligand - synthesis, structure and photophysics
Journal of Materials Chemistry C, 2015, 3, 1680-1693

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