Low-dimensional framework constructed by silver(I) trifluoromethylsulfonate with 1,5-bis(benzimidazol-2-yl)-3-oxapentane or 1,6-bis(benzimidazol-2-yl)-2,5-dioxahexane

Inorganica Chimica Acta

Volumn 342, Issue , 2003, Pages 107-113

  Cai, Yue Peng ^a,b   Chen, Chun Long ^a   Zhang, Li ^a   Shi, Jun Ling ^a   Xu, An Wu ^a   Su, Cheng Yong ^a   Kang, Bei Sheng ^a,b  

^a SUN YAT SEN UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

1,5 bis(benzimidazol 2 yl) 3 oxapentane (OEBIm); 1,6 bis(benzimidazol 2 yl) 2,5 dioxahexane (DEBIm); Crystal structures; Low dimensional network; Silver(I) complexes

Indexed keywords

COMPLEX NETWORKS; CRYSTAL STRUCTURE; HYDROGEN BONDS; LIGANDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

1,5-BIS(BENZIMIDAZOL-2-YL)-3-OXAPENTANE (OEBIM); 1,6-BIS(BENZIMIDAZOL-2-YL)-2,5-DIOXAHEXANE (DEBIM); 1H NMR SPECTROSCOPY; COORDINATION BONDS; CRYSTALLOGRAPHIC ANALYSIS; LOW DIMENSIONAL; NON-BONDING INTERACTIONS; SILVER COMPLEXES;

SILVER COMPOUNDS;

1,5 BIS(BENZIMIDAZOL 2 YL) 3 OXAPENTANE; 1,6 BIS(BENZIMIDAZOL 2 YL) 2,5 DIOXAHEXANE; ALKANE DERIVATIVE; LIGAND; OXYGEN; SILVER; SULFONIC ACID DERIVATIVE; TRIFLUOROMETHYLSULFONATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL BOND; CHEMICAL REACTION; CRYSTALLOGRAPHY; HYDROGEN BOND; INFRARED SPECTROSCOPY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SPECTROSCOPY;

EID: 0037427929     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0020-1693(02)01153-2     Document Type: Article

References (18)

1. Roderick W.R., Nordeen C.W., von Esch A.M., Appell R.N. J. Med. Chem. 15:1972;655.
2. van Berkel P.M., Driessen W.L., Koolhaas G.J.A.A., Reedijk J., Sherington D.C. Polymer. 28:1995;39.
3. Min K.S., Suh M.P. J. Am. Chem. Soc. 122:2000;6834.
4. Piquet C., Bünzli J.-C.G., Williams A.F. J. Ally Comp. 225:1995;324.
5. Hennigar T.L., MacQuarrie D., Losier P., Rogers R.D. Agew. Chem., Int. Ed. Engl. 36:1992;972.
6. Gardner G.B., Venkataraman D., Moore J.S., Lee S. Nature. 374:1995;792.
7. Holliday B.J., Mirkin C.A. Agew. Chem., Int. Ed. Engl. 40:2001;2023.
8. Desiraju G.R. Agew. Chem., Int. Ed. Engl. 34:1995;2311.
9. Su C.-Y., Kang B.-S., Du C.-X., Yang Q.-G., Thomas Q.-G., Mak C.W. Inorg. Chem. 39:2000;4843.
10. C.-Y. Su, B.-S. Kang, H.-Q. Liu, Q.-G. Yang and Thomas, C.W. Mak, Chem. Commun. (1998) 1551 C.-Y. Su, B.-S. Kang, Q.-G. Yang and Thomas, C.W. Mak, J. Chem. Soc., Dalton Trans. (2000) 1858.
11. Y.-P. Cai, X.-H. Zhang, A.-W. Xu, C.-Y. Su, B.-S. Kang, J. Chem. Soc., Dalton Trans. (2001) 2429.
12. Y.-P. Cai, C.-Y. Su, H.X. Zhang, L.X. Zhu, A.S.C. Chan, H.-Q. Liu, B.-S. Kang, Zeit. Anorg. Allgem. Chem. (2002) in press.
13. Thompson L.K., Ramaswamy B.S., Seymour E.A. Can. J. Chem. 55:1977;878.
14. Sheldrick G.M. SADABS, Program for Scaling and Correction of Area Detector Data. 1996;University of Göttingen, Göttingen, Germany.
15. SHELXTL, Ver. 5.10, Bruker Analytical X-ray Systems, Madision, WI, 1998.
16. Xu A.-W., Su C.-Y., Zhang Z.-F., Cai Y.-P., Chen C.-L. New J. Chem. 25:2001;480.
17. Su C.-Y., Yang X.-P., Kang B.-S., Liu H.-Q. Inorg. Chem. Commun. 2:1999;383.
18. Thalladi V.R., Weiss H.-C., Blaser D., Boese R., Nangia A., Desiraju G.R. J. Am. Chem. Soc. 120:1998;8702.