Crystallography Open Database

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7150447 CIFC60 H72 O4 S2P 1 21/c 117.511; 14.597; 22.804
90; 111.552; 90
5421Zeng, Xianshun; Sun, Hao; Chen, Langxing; Leng, Xuebing; Xu, Fengbo; Li, Qinshan; He, Xiwen; Zhang, Wenqin; Zhang, Zheng-Zhi
Synthesis of a tweezer-like bis(arylthiaalkoxy)calix[4]arene as a cation sensor for ion-selective electrodes: an investigation of the influence of neighboring halogen atoms on cation selectivity
Organic & Biomolecular Chemistry, 2003, 1, 1073-1079
7150448 CIFC6 F8P 1 21/c 18.134; 7.111; 12.699
90; 100.87; 90
721.34Lentz, Dieter; Patzschke, Mona; Bach, Ansgar; Scheins, Stephan; Luger, Peter
Experimental charge density of octafluoro-1,2-dimethylenecyclobutane: atomic volumes and charges in a perfluorinated hydrocarbon
Organic & Biomolecular Chemistry, 2003, 1, 409-414
7150449 CIFC27 H32 N2 O4 SP 1 21 111.1034; 11.9818; 9.9624
90; 109.214; 90
1251.6Miyabe, Hideto; Fujii, Kayoko; Naito, Takeaki
Radical addition to oxime ethers for asymmetric synthesis of β-amino acid derivatives
Organic & Biomolecular Chemistry, 2003, 1, 381
7150450 CIFC29 H38 N2 O4 SP 1 21 112.2395; 20.5642; 10.904
90; 94.209; 90
2737.1Miyabe, Hideto; Fujii, Kayoko; Naito, Takeaki
Radical addition to oxime ethers for asymmetric synthesis of β-amino acid derivatives
Organic & Biomolecular Chemistry, 2003, 1, 381
7150451 CIFC32 H28 N8 O7P 21 21 217.688; 13.2934; 31.112
90; 90; 90
3179.64Rosenbohm, Christoph; Christensen, Signe M.; Sørensen, Mads D.; Pedersen, Daniel Sejer; Larsen, Lotte-Emilie; Wengel, Jesper; Koch, Troels
Synthesis of 2'-amino-LNA: a new strategyElectronic supplementary information (ESI) available: further experimental details and the structure of compound S11 (.pdb file). See http://www.rsc.org/suppdata/ob/b2/b208864a/
Organic & Biomolecular Chemistry, 2003, 1, 655
7150452 CIFC18 H34 O5 SiP -112.677; 12.7397; 13.0974
102.147; 95.218; 91.166
2057.62Johnston, Derek; Couché, Emmanuel; Edmonds, David J.; Muir, Kenneth W.; Procter, David J.
The first synthetic studies on pestalotiopsin A. A stereocontrolled approach to the functionalised bicyclic coreElectronic supplementary information (ESI) available: crystal structure analysis of 18a. See http://www.rsc.org/suppdata/ob/b2/b209066j/
Organic & Biomolecular Chemistry, 2003, 1, 328
7150453 CIFC27 H35 N O2P 1 21 112.368; 17.711; 21.575
90; 92.382; 90
4721.9Chen, Yong-Jun; Gao, Ling-Jie; Murad, Ibrahim; Verstuyf, Annemieke; Verlinden, Lieve; Verboven, Christel; Bouillon, Roger; Viterbo, Davide; Milanesio, Marco; Van Haver, Dirk; Vandewalle, Maurits; De Clercq, Pierre J.
Synthesis, biological activity, and conformational analysis of CD-ring modified trans-decalin 1α,25-dihydroxyvitamin D analogsElectronic supplementary information (ESI) available: Further experimental details. See http://www.rsc.org/suppdata/ob/b2/b209147j/
Organic & Biomolecular Chemistry, 2003, 1, 257
7150454 CIFC9 H14 O2P 1 21 16.1182; 6.6921; 10.181
90; 94.019; 90
415.82Amelia García Fraile; David G. Morris; Antonio García Martínez; Santiago de la Moya Cerero; Kenneth W. Muir; Karl S. Ryder; Enrique Teso Vilar
Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols
Org. Biomol. Chem., 2003, 1, 700-704
7150455 CIFC10 H16 OP 21 21 215.9714; 20.5466; 22.5632
90; 90; 90
2768.32Amelia García Fraile; David G. Morris; Antonio García Martínez; Santiago de la Moya Cerero; Kenneth W. Muir; Karl S. Ryder; Enrique Teso Vilar
Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols
Org. Biomol. Chem., 2003, 1, 700-704
7150456 CIFC10 H16 OP 41 21 210.7633; 10.7633; 31.3398
90; 90; 90
3630.67Amelia García Fraile; David G. Morris; Antonio García Martínez; Santiago de la Moya Cerero; Kenneth W. Muir; Karl S. Ryder; Enrique Teso Vilar
Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols
Org. Biomol. Chem., 2003, 1, 700-704
7150457 CIFC48 H48 B20 N6 O4P 1 21/n 114.587; 7; 27.868
90; 105.047; 90
2748.01Frixa, Christophe; Mahon, Mary F.; Thompson, Andrew S.; Threadgill, Michael D.
Synthesis of meso-substituted porphyrins carrying carboranes and oligo(ethylene glycol) units for potential applications in boron neutron capture therapyElectronic supplementary information (ESI) available: experimental details for the synthesis of compounds 12‒15, 31 and 32. See http://www.rsc.org/suppdata/ob/b2/b209534c/
Organic & Biomolecular Chemistry, 2003, 1, 306
7150458 CIFC22 H23 B F4 OP 1 21/m 19.8532; 6.9944; 14.504
90; 105.737; 90
962.11Laus, Gerhard; Schottenberger, Herwig; Wurst, Klaus; Schütz, Johannes; Ongania, Karl-Hans; Horvath, Ulrike Erika Ida; Schwärzler, Alexander
Solvatochromism, halochromism, and preferential solvation of new dipolar guaiazulenyl 1,4-benzoquinone methidesElectronic supplementary information (ESI) available: Absorption maxima of the dyes 6‒10 in seven binary solvent mixtures. See http://www.rsc.org/suppdata/ob/b2/b209555f/
Organic & Biomolecular Chemistry, 2003, 1, 1409
7150459 CIFC30 H38 OP 1 21/c 114.324; 12.5501; 14.623
90; 100; 90
2588.8Laus, Gerhard; Schottenberger, Herwig; Wurst, Klaus; Schütz, Johannes; Ongania, Karl-Hans; Horvath, Ulrike Erika Ida; Schwärzler, Alexander
Solvatochromism, halochromism, and preferential solvation of new dipolar guaiazulenyl 1,4-benzoquinone methidesElectronic supplementary information (ESI) available: Absorption maxima of the dyes 6‒10 in seven binary solvent mixtures. See http://www.rsc.org/suppdata/ob/b2/b209555f/
Organic & Biomolecular Chemistry, 2003, 1, 1409
7150460 CIFC20 H22 N2 O2P 1 21/n 111.1081; 12.6796; 11.6659
90; 101.259; 90
1611.48Banwell, Martin G.; Edwards, Alison J.; Jolliffe, Katrina A.; Smith, Jason A.; Hamel, Ernest; Verdier-Pinard, Pascal
Total synthesis of (±)-rhazinal, an alkaloidal spindle toxin from Kopsia teoi
Organic & Biomolecular Chemistry, 2003, 1, 296
7150461 CIFC22 H23 N O7P 21 21 219.3201; 12.5782; 17.9679
90; 90; 90
2106.38Anat Reizelman; Suzanne C. M. Wigchert; Cinzia del-Bianco; Binne Zwanenburg
Synthesis and bioactivity of labelled germination stimulants for the isolation and identification of the strigolactone receptor
Org. Biomol. Chem., 2003, 1, 950-959
7150462 CIFC30 H21 N5 O6P b c n32.285; 11.8982; 19.8475
90; 90; 90
7624.1Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.
Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/
Organic & Biomolecular Chemistry, 2003, 1, 741
7150463 CIFC36 H36 N5 O9 S3P -111.0659; 12.04; 15.9608
84.462; 81.333; 64.306
1893.21Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.
Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/
Organic & Biomolecular Chemistry, 2003, 1, 741
7150464 CIFC34 H31 N7 O12 S2P -18.608; 15.212; 15.257
67.786; 84.475; 73.886
1776.8Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.
Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/
Organic & Biomolecular Chemistry, 2003, 1, 741
7150465 CIFC30 H19 N7 O10P 1 21/c 120.3034; 10.1636; 13.457
90; 104.057; 90
2693.8Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.
Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/
Organic & Biomolecular Chemistry, 2003, 1, 741
7150466 CIFC62 H90 Cl N9 O10P -113.408; 15.847; 17.023
73.042; 74.733; 68.046
3159.9Camiolo, Salvatore; Gale, Philip A.; Hursthouse, Michael B.; Light, Mark E.
Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonationElectronic supplementary information (ESI) available: 1H NMR, 13C NMR and mass spectra for compounds 2 and 3, NMR anion titration profiles in DMSO-d6‒0.5% water. See http://www.rsc.org/suppdata/ob/b2/b210848h/
Organic & Biomolecular Chemistry, 2003, 1, 741
7150467 CIFC19 H16 O2 Se2P 1 21/c 110.516; 18.569; 8.832
90; 100.21; 90
1697.3Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150468 CIFC14 H14 O SeP -17.2242; 7.9556; 11.007
83.594; 73.236; 86
601.47Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150469 CIFC18 H14 O2 Se2P 1 21/n 115.0339; 5.642; 18.9279
90; 101.673; 90
1572.3Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150470 CIFC22 H22 O2 Se2P -18.5958; 11.37; 12.388
116.25; 100.28; 104.48
991.4Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150471 CIFC20 H18 O2 Se2P 1 21/c 17.1618; 15.132; 8.2912
90; 103.609; 90
873.3Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150472 CIFC15 H16 O SeP 1 21/n 17.2789; 9.4958; 19.043
90; 97.047; 90
1306.3Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150473 CIFC12 H10 O2 SeP -18.7061; 10.3054; 11.8008
92.369; 90.07; 94.027
1055.2Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150474 CIFC14 H14 O SeP b c a14.991; 9.9673; 15.93
90; 90; 90
2380.3Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150475 CIFC14 H14 O SeP 1 21/c 19.0416; 7.8911; 17.6103
90; 102.406; 90
1227.1Oddershede, Jette; Henriksen, Lars; Larsen, Sine
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Organic & Biomolecular Chemistry, 2003, 1, 1053
7150476 CIFC32 H39 N O12P 21 21 217.917; 19.736; 21.32
90; 90; 90
3331.2Liao, Jian; Peng, Xiaohua; Zhang, Juhua; Yu, Kaibei; Cui, Xin; Zhu, Jin; Deng, Jingen
Facile resolution of racemic terbutaline and a study of molecular recognition through chiral supramolecules based on enantiodifferentiating self-assemblyElectronic supplementary information (ESI) available: 1) 1H and 13C NMR analyses of (R)-1·4 and (S)-1·4; 2) ORTEP views and stacking structures of crystals 5, 7 and 8; 3) DSC and TG analyses of the more- and less-soluble salts. See http://www.rsc.org/suppdata/ob/b2/b211327a/
Organic & Biomolecular Chemistry, 2003, 1, 1080
7150477 CIFC32 H37 N O11P 1 21 17.512; 18.733; 11.599
90; 103.1; 90
1589.8Liao, Jian; Peng, Xiaohua; Zhang, Juhua; Yu, Kaibei; Cui, Xin; Zhu, Jin; Deng, Jingen
Facile resolution of racemic terbutaline and a study of molecular recognition through chiral supramolecules based on enantiodifferentiating self-assemblyElectronic supplementary information (ESI) available: 1) 1H and 13C NMR analyses of (R)-1·4 and (S)-1·4; 2) ORTEP views and stacking structures of crystals 5, 7 and 8; 3) DSC and TG analyses of the more- and less-soluble salts. See http://www.rsc.org/suppdata/ob/b2/b211327a/
Organic & Biomolecular Chemistry, 2003, 1, 1080
7150478 CIFC32 H37 N O11P 1 21 17.506; 18.714; 11.59
90; 103.03; 90
1586.1Liao, Jian; Peng, Xiaohua; Zhang, Juhua; Yu, Kaibei; Cui, Xin; Zhu, Jin; Deng, Jingen
Facile resolution of racemic terbutaline and a study of molecular recognition through chiral supramolecules based on enantiodifferentiating self-assemblyElectronic supplementary information (ESI) available: 1) 1H and 13C NMR analyses of (R)-1·4 and (S)-1·4; 2) ORTEP views and stacking structures of crystals 5, 7 and 8; 3) DSC and TG analyses of the more- and less-soluble salts. See http://www.rsc.org/suppdata/ob/b2/b211327a/
Organic & Biomolecular Chemistry, 2003, 1, 1080
7150479 CIFC35 H45 N O13P 21 21 217.81; 21.431; 21.948
90; 90; 90
3673.6Liao, Jian; Peng, Xiaohua; Zhang, Juhua; Yu, Kaibei; Cui, Xin; Zhu, Jin; Deng, Jingen
Facile resolution of racemic terbutaline and a study of molecular recognition through chiral supramolecules based on enantiodifferentiating self-assemblyElectronic supplementary information (ESI) available: 1) 1H and 13C NMR analyses of (R)-1·4 and (S)-1·4; 2) ORTEP views and stacking structures of crystals 5, 7 and 8; 3) DSC and TG analyses of the more- and less-soluble salts. See http://www.rsc.org/suppdata/ob/b2/b211327a/
Organic & Biomolecular Chemistry, 2003, 1, 1080
7150480 CIFC7 H7 N3 O5P 1 21/n 16.4904; 16.785; 8.2216
90; 102.454; 90
874.6Crampton, Michael R.; Emokpae, Thomas A.; Howard, Judith A. K.; Isanbor, Chukwuemeka; Mondal, Raju
Kinetic and equilibrium studies of σ-adduct formation and nucleophilic substitution in the reactions of 2-phenoxy-3,5-dinitropyridine and 2-ethoxy-3,5-dinitropyridine with aliphatic amines in dipolar aprotic solventsElectronic supplementary information (ESI) available: Tables 10‒15. See http://www.rsc.org/suppdata/ob/b2/b211639c/
Organic & Biomolecular Chemistry, 2003, 1, 1004
7150481 CIFC10 H12 N4 O4P -15.9847; 7.3833; 12.375
94.29; 95.28; 91.8
542.6Crampton, Michael R.; Emokpae, Thomas A.; Howard, Judith A. K.; Isanbor, Chukwuemeka; Mondal, Raju
Kinetic and equilibrium studies of σ-adduct formation and nucleophilic substitution in the reactions of 2-phenoxy-3,5-dinitropyridine and 2-ethoxy-3,5-dinitropyridine with aliphatic amines in dipolar aprotic solventsElectronic supplementary information (ESI) available: Tables 10‒15. See http://www.rsc.org/suppdata/ob/b2/b211639c/
Organic & Biomolecular Chemistry, 2003, 1, 1004
7150482 CIFC24 H20 N4 O4P b c m9.1922; 7.1341; 31.75
90; 90; 90
2082.1Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150483 CIFC30 H24 N4 O5A m a 235.743; 9.285; 7.338
90; 90; 90
2435.3Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150484 CIFC18 H16 N4 O4P n m a7.281; 24.097; 8.919
90; 90; 90
1564.8Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150485 CIFC26 H32 N4 O4P 1 21/m 15.492; 34.585; 6.318
90; 102.81; 90
1170.2Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150486 CIFC20 H16 N4 O4P n m a7.251; 24.325; 9.185
90; 90; 90
1620.1Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150487 CIFC20 H20 N4 O4P 1 21/m 15.7015; 26.821; 6.1015
90; 104.708; 90
902.47Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150488 CIFC20 H17 N4 O2P 1 21/n 110.268; 15.529; 11.158
90; 105.47; 90
1714.7Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150489 CIFC30 H24 N4 O4P b c n9.117; 14.433; 19.312
90; 90; 90
2541.2Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150490 CIFC19 H18 N4 O4C 1 2/c 117.29; 4.0427; 24.72
90; 93.121; 90
1725.3Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150491 CIFC26 H32 N4 O4P -18.4312; 10.1438; 15.0064
85.842; 73.025; 78.006
1200.6Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150492 CIFC20 H16 N4 O4P -13.842; 9.062; 12.098
87.23; 81.25; 78.18
407.41Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150493 CIFC24 H20 N4 O4P -17.767; 8.8044; 9.1959
62.048; 71.921; 70.707
515.1Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150494 CIFC29 H29 N4 O3P -18.783; 10.6035; 13.8087
88.06; 87.645; 86.861
1282.4Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150495 CIFC30 H26 N4 O6P -110.3442; 11.7028; 12.6687
78.461; 65.91; 73.925
1338.68Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425
7150496 CIFC24 H20 N4 O3C 1 2/c 128.8097; 7.8866; 18.5925
90; 98.004; 90
4183.3Bensemann, Igor; Gdaniec, Maria; Łakomecka, Karina; Milewska, Maria J.; Połoński, Tadeusz
Creation of hydrogen bonded 1D networks by co-crystallization of N,N'-bis(2-pyridyl)aryldiamines with dicarboxylic acidsSupramolecular structures formed by 2-aminopyridine derivatives. Part II.5
Organic & Biomolecular Chemistry, 2003, 1, 1425

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