journal article·2009-07-28

A Platinum(II) Extended Linear Chain Material That Selectively Uptakes Benzene

Steven M. Drew, Lisa I. Smith, Kari A. McGee, Kent R. Mann

Chemistry of Materials· Volume 21· Issue 14
Publisher page

Abstract

cis -Bis(isopropyl isocyanide)dicyanoplatinum(II), Pt II (CN- i -C 3 H 7 ) 2 (CN) 2, has been synthesized, and its solid-state characteristics have been investigated. X-ray crystallographic data show that Pt II (CN- i -C 3 H 7 ) 2 (CN) 2 forms an extended linear chain (ELC) material in the solid state that is yellow and luminescent. Exposure of crystalline films of Pt II (CN- i -C 3 H 7 ) 2 (CN) 2 to benzene vapor leads to a solid-state luminescence color change from yellow to blue and a loss of crystallinity. Single-crystal X-ray data obtained for a benzene solvate of Pt II (CN- i -C 3 H 7 ) 2 (CN) 2 suggest that the luminescent blue form observed in the thin film results from a structural rearrangement. In the benzene solvate single crystal the lattice is changed from a staggered to an eclipsed ELC material in which the unit cell has expanded by 20% in volume and contains one benzene molecule for every two Pt II (CN- i -C 3 H 7 ) 2 (CN) 2 molecules. The selectivity, kinetics, and reversibility of this transformation have been studied to determine if crystalline films of Pt II (CN- i -C 3 H 7 ) 2 (CN) 2 would make a useful benzene sensor.
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Research context

OpenAlex topics: Analytical Chemistry and Sensors · Conducting polymers and applications · Inorganic and Organometallic Chemistry

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

Affiliations

Department of Chemistry, Carleton College, One North College Street, Northfield, Minnesota 55057

Department of Chemistry, University of Minnesota, 207 Pleasant Street SE, Minneapolis, Minnesota 55455

References (37)

Show source-provided references
1. Miller J. S. · 1982 · 110.1007/978-1-4613-3249-7 ↗
2. Bera J. K. · Angew. Chem., Int. Ed. · 2002 · 41 · 445310.1002/1521-3773(20021202)41:23<4453::AID-ANIE4453>3.0.CO;2-1 ↗
3. Atoji M. · J. Am. Chem. Soc. · 1957 · 79 · 301710.1021/ja01569a009 ↗
4. Krogmann K. · Angew. Chem., Int. Ed. · 1969 · 8 · 3510.1002/anie.196900351 ↗
5. Shriver D. F. · Inorg. Synth. · 1979 · 19 · 110.1002/9780470132500.ch1 ↗
6. Williams J. M. · Adv. Inorg. Chem. Radiochem. · 1983 · 26 · 23510.1016/S0898-8838(08)60095-1 ↗
7. Daws C. A. · Chem. Mater. · 1997 · 9 · 36310.1021/cm960397z ↗
8. Exstrom C. L. · Chem. Mater. · 1998 · 10 · 94210.1021/cm970788t ↗
9. Exstrom C. L. · Chem. Mater. · 1995 · 7 · 1510.1021/cm00049a005 ↗
10. Buss C. E. · J. Am. Chem. Soc. · 1998 · 120 · 778310.1021/ja981218c ↗
11. Buss C. E. · J. Am. Chem. Soc. · 2002 · 124 · 103110.1021/ja011986v ↗
12. Dylla A. G. · Organometallics · 2007 · 26 · 624310.1021/om7008167 ↗
13. Drew S. M. · J. Am. Chem. Soc. · 2001 · 123 · 841410.1021/ja016010x ↗
14. Drew S. M. · Anal. Chem. · 2002 · 74 · 254710.1021/ac011255d ↗
15. Drew S. M. · Sens. Actuators, B · 2004 · 97 · 30710.1016/j.snb.2003.09.005 ↗
16. Centers for Disease Control web site:http://www.cdc.gov/niosh/npg/npgd0049.html.
17. Jeffers J. D. · Anal. Chem. · 2004 · 76 · 42410.1021/ac0345392 ↗
18. Hubalek J. · Sens. Actuators, B · 2004 · 101 · 27710.1016/j.snb.2004.01.015 ↗
19. Nicoletti S. · Sens. Actuators, B · 1999 · 60 · 9010.1016/S0925-4005(99)00261-0 ↗
20. Zampolli S. · Chem. Commun. · 2007 · 279010.1039/b703747c ↗
21. Albert K. J. · Chem. Rev. · 2000 · 100 · 259510.1021/cr980102w ↗
22. Stitzel S. E. · Anal. Chem. · 2001 · 73 · 526610.1021/ac010111w ↗
23. Lewis N. S. · Acc. Chem. Res. · 2004 · 37 · 66310.1021/ar030120m ↗
24. Suslick K. S. · Quim. Nova · 2007 · 30 · 67710.1590/S0100-40422007000300029 ↗
25. Pang J. · Angew. Chem. · 2001 · 113 · 416610.1002/1521-3757(20011105)113:21<4166::AID-ANGE4166>3.0.CO;2-J ↗
26. Das S. · Inorg. Chem. · 2006 · 45 · 525710.1021/ic060518p ↗
27. Das S. · Cryst. Growth Des. · 2007 · 7 · 119210.1021/cg060531k ↗
28. McGee K. A. · Inorg. Chem. · 2008 · 47 · 914310.1021/ic801287p ↗
29. Wendt O. F. · J. Chem. Soc., Dalton Trans. · 1997 · 473310.1039/a705048h ↗
30. Kukushkin V. Y. · Inorg. Synth. · 1997 · 31 · 27910.1002/9780470132623.ch48 ↗
31. Mason W. R. · J. Am. Chem. Soc. · 1968 · 90 · 572110.1021/ja01023a012 ↗
32. Jackson J. E. · 199110.1002/0471725331 ↗
33. Beebe K. R. · 1998
34. Khawam A. · J. Phys. Chem. B · 2006 · 110 · 1731510.1021/jp062746a ↗
35. Bruno I. J. · Acta Crystallogr. · 2002 · 58 · 38910.1107/S0108768102003324 ↗
36. Martellaro P. J. · Inorg. Chim. Acta · 2005 · 358 · 337710.1016/j.ica.2005.06.024 ↗
37. Sun Y. · Angew. Chem., Int. Ed. · 2006 · 45 · 561010.1002/anie.200601588 ↗