journal article·1998-01-19

Three-Dimensional Organic/Inorganic Hybrid Materials Constructed from One-Dimensional Copper Diamine Coordination Polymers Linked by Bridging Oxoanion Tetrahedra: [Cu(dpe)(MoO4)] and [Cu(dpe)(SO4)(H2O)] (dpe = 1,2-trans-(4-pyridyl)ethene)

Douglas Hagrman, Robert C. Haushalter, Jon Zubieta

Chemistry of Materials· Volume 10· Issue 1
Publisher page

Abstract

The hydrothermal reaction of CuSO 4 ·5H 2 O, dpe, MoO 3, and water in the mole ratio 1:2:2:900 at 120 °C for 111 h yielded [Cu(dpe)(MoO 4 )] ( 1 ). Upon omitting the molybdate component, the reaction of CuSO 4 ·5H 2 O, dpe and water in the mole ratio 1:1:1111 at 120 °C for 72 h yielded [Cu(dpe)(SO 4 )(H 2 O)] ( 2 ). The structure of 1 is constructed from {Cu(dpe)} 2+ linear chains bridged through {MoO 4 } 2 - tetrahedra into a three-dimensional framework, while that of 2 consists of {Cu(dpe)} 2+ chains bridged through {SO 4 } 2 - tetrahedra. However, while the {MoO 4 } 2 - units of 1 adopt the η 3 -coordination mode, each linking three adjacent chains, the {SO 4 } 2 - units of 2 assume η 2 -coordination and bridge only two neighboring chains. These differences in {EO 4 } 2 - coordination modes are reflected in the dramatically different three-dimensional structures displayed by 1 and 2 . Crystal data: C 12 H 10 CuMoN 2 O 4 ( 1 ), orthorhombic Pbcn, a = 22.0462(1) Å, b = 12.2957(2) Å, c = 9.7560(2) Å, V = 2644.59(7) Å, 3 Z = 8, D calc = 2.038 g cm - 3; 3202 reflections, R 1 = 0.056. C 12 H 12 CuN 2 O 5 S ( 2 ), monoclinic Pn, a = 7.2851(2) Å, b = 9.9062(3) Å, c = 9.1407(2) Å, β = 98.207(1)°, V = 652.91(3) Å, Z = 2, D calc = 1.830 g cm - 3; 1968 reflections, R 1 = 0.027.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Polyoxometalates: Synthesis and Applications · Chemical Synthesis and Characterization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, Syracuse University, Syracuse, New York 13244, and Symyx Technologies, 420 Oakmead Parkway, Sunnyvale, California 94086

References (40)

Show source-provided references
1. Hoskins B. F. · J. Am. Chem. Soc. · 1990 · 112 · 154610.1021/ja00160a038 ↗
2. Bowes C. L. · Adv. Mater. · 1996 · 8 · 1310.1002/adma.19960080103 ↗
3. Supramolecular Architecture · 1992
4. Magnetic Molecular Materials · NATO ASI Ser., Ser. E · 1991 · 198
5. Inorganic Materials · 1992
6. Introduction to Molecular Electronics; Petty, M., Bryce, M. R., Bloor, D., Eds.; Edward Arnold: London, 1995.
7. Fujita M. · J. Am. Chem. Soc. · 1995 · 117 · 728710.1021/ja00132a046 ↗
8. Gardner G. B. · J. Am. Chem. Soc. · 1996 · 118 · 694610.1021/ja960595r ↗
9. Blake A. J. · Chem. Commun. · 1997 · 100510.1039/a700866j ↗
10. Blake A. J. · J. Chem. Soc., Dalton Trans. · 1997 · 91310.1039/a700036g ↗
11. Carlucci L. · J. Chem. Soc., Dalton Trans. · 1997 · 180110.1039/a702146a ↗
12. Hoskins B. F. · J. Am. Chem. Soc. · 1997 · 119 · 295210.1021/ja9642626 ↗
13. Losier P. · J. Angew. Chem., Int. Ed. Engl. · 1996 · 35 · 277910.1002/anie.199627791 ↗
14. Subramanian S. · J. Angew. Chem., Int. Ed. Engl. · 1995 · 34 · 212710.1002/anie.199521271 ↗
15. Batsanov A. S. · J. Chem. Soc., Dalton Trans. · 1996 · 194710.1039/DT9960001947 ↗
16. Richardson H. W. · J. Am. Chem. Soc. · 1975 · 97 · 835
17. Chenggang C. · Acta Crystallogr. · 1992 · 48 · 1231
18. Yaghi O. M. · Angew. Chem., Int. Ed. Engl. · 1995 · 34 · 20710.1002/anie.199502071 ↗
19. Masciocchi N. · J. Chem. Soc., Dalton Trans. · 1996 · 273910.1039/DT9960002739 ↗
20. Kawata S. · Angew. Chem., Int. Ed. Engl. · 1994 · 33 · 175910.1002/anie.199417591 ↗
21. Chen Z. N. · J. Chem. Soc., Dalton Trans. · 1994 · 191710.1039/DT9940001917 ↗
22. MacGillivray L. R. · J. Chem. Soc., Chem. Commun. · 1994 · 132510.1039/c39940001325 ↗
23. Yaghi O. M. · J. Am. Chem. Soc. · 1995 · 117 · 1040110.1021/ja00146a033 ↗
24. Otieno T. · Inorg. Chem. · 1993 · 32 · 160710.1021/ic00061a015 ↗
25. Hennigar T. L. · J. Angew. Chem., Int. Ed. Engl. · 1997 · 36 · 97210.1002/anie.199709721 ↗
26. Robinson F. · J. Chem. Soc., Chem. Commun. · 1995 · 241310.1039/C39950002413 ↗
27. Carlucci J. · J. Chem. Soc., Chem. Commun. · 1996 · 2755
28. Hennigar T. L. · J. Angew. Chem., Int. Ed. Engl. · 1997 · 36 · 97210.1002/anie.199709721 ↗
29. Wu L. P. · Inorg. Chim. Acta · 1997 · 256 · 158
30. Pun · Angew. Chem., Int. Ed. Engl. · 1997 · 36 · 87310.1002/anie.199708731 ↗
31. SHELXTL, Version 5; Siemens Industrial Automation, Inc., 1994.
32. Software SMART · 1990
33. Cromer D. T. · 1974
34. Creagh D. C. · 1992 · 4
35. Laudise R. A. · 1987
36. Rabenau A. · Angew. Chem., Int. Ed. Engl. · 1985 · 24 · 102610.1002/anie.198510261 ↗
37. Haushalter R. C. · Chem. Mater. · 1982 · 4 · 3110.1021/cm00019a012 ↗
38. Khan M. I. · Prog. Inorg. Chem. · 1995 · 43 · 1
39. Stein A. · Science · 1993 · 259 · 155810.1126/science.259.5101.1558 ↗
40. Gopalakrishnan J. · Chem. Mater. · 1995 · 7 · 126510.1021/cm00055a001 ↗