Dichloro(1,5-cyclooctadiene)palladium is the organopalladium compound with the formula PdCl2(C8H12) where C8H12 is cycloocta-1,5-diene (cod) or abbreviated PdCl2(cod). It is a yellow solid that is soluble in chloroform.[1] According to X-ray crystallography, the Pd center is square planar.[2] This complex can be synthesized by reaction of tetrachloropalladate in hydrochloric acid with cycloocta-1,5-diene.[3]
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3D model (JSmol)
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ECHA InfoCard | 100.031.953 |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C8H12Cl2Pd | |
Molar mass | 285.50 g·mol−1 |
Appearance | yellow solid |
Density | 2.045 g/cm3 |
Melting point | 210 °C (410 °F; 483 K) |
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H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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See also
editReferences
edit- ^ Shomir Ghosh; Xiang Wang; Anil Guram (2009). "Dichloro(1,5-cyclooctadiene)palladium(II)". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rd113.pub2. ISBN 978-0471936237.
- ^ R. Kumar; A. W. Maverick; F. R. Fronczek; J. R. Doyle; N. C. Baenziger; M. A. M. Howells (1993). "The Pbca polymorph of dichloro(η4-1,5-cyclooctadiene)palladium(II)". Acta Crystallogr. C. 49 (10): 1766–1767. Bibcode:1993AcCrC..49.1766K. doi:10.1107/S0108270193003889.
- ^ Drew, D.; Doyle, J. R.; Shaver, A. G. (1972). "Cyclic Diolefin Complexes of Platinum and Palladium". Inorganic Syntheses. Vol. 13. pp. 47–55. doi:10.1002/9780470132449.ch11. ISBN 978-0-470-13172-5.