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    <title>UTas ePrints - Co-ordination Chemistry of Pyridyl and N-Methyl imidazolyl Ketones. Synthetic and X-Ray Structural t Studies of Copper(II), Nickel(II), and Dimethylgold(III) Complexes</title>
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    <meta content="Byers, P.K." name="eprints.creators_name" />
<meta content="Canty, A.J." name="eprints.creators_name" />
<meta content="Engelhardt, L.M." name="eprints.creators_name" />
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<meta content="White, A.H." name="eprints.creators_name" />
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<meta content="Co-ordination Chemistry of Pyridyl and N-Methyl imidazolyl Ketones. Synthetic and X-Ray Structural t Studies of Copper(II), Nickel(II), and Dimethylgold(III) Complexes" name="eprints.title" />
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<meta content="Di-2-pyridyl ketone (dpk) reacts with dimethylgold(III) nitrate in water to form the complex [AuMe2(dpk.H2O)]NO3 in which the ligand has been hydrated to form a geminal diol. The closely related ketones 2-pyridyl-N-methyl-2-imidazolyl ketone (pik) and di(N-methyl-2-imidazolyl)
ketone (dik) react with Au(III)Me3 nitrate to form complexes that do not involve hydration of the ligand, [AuMe3(L)]NO3 (L = pik or dik). They react similarly with copper(II) sulphate and nickel(II) nitrate, forming [Cu(pik)(SO4)].0.5H2O, [Cu(dik)(SO4)].2H2O, [Ni(pik)(N03)2].0.5H2O and [Ni(dik)2(NO3)2].l.5Me0H; dpk forms [Ni(dpk.H2O)2(NO3)2].0.5H2O on reaction with nickel(II)
nitrate. The crystal structures of [AuMe2(dpk.H2O)]NO3 and [Cu(dik)(SO4)].2H2O have been determined by single-crystal X-ray diffraction at 295 K and refined by least-squares methods to R = 0.045 and 0.032 for 2 031 and 4 754 independent 'observed' reflections, respectively. The
cation [AuMe2(dpk.H2O)]+ has the ligand N,N-chelated with cis-square-planar co-ordination for gold(III), with an intramolecular hydroxy group positioned 2.850(8) A from the gold atom. The complex [Cu(dik)(SO4)].2H2O has square-pyramidal co-ordination for copper(II), with the
N,N-chelated ligand in the basal plane together with a water molecule and unidentate sulphate ion, and a water molecule co-ordinated axially. There is an intermolecular Cu...0 contact of 3.254(2) A with a ketone oxygen. Possible reasons for different behaviour of the ligands toward hydration are discussed." name="eprints.abstract" />
<meta content="1985" name="eprints.date" />
<meta content="published" name="eprints.date_type" />
<meta content="Journal of the Chemical Society, Dalton Transactions" name="eprints.publication" />
<meta content="5" name="eprints.volume" />
<meta content="981-986" name="eprints.pagerange" />
<meta content="10.1039/DT9850000981" name="eprints.id_number" />
<meta content="TRUE" name="eprints.refereed" />
<meta content="1477-9226" name="eprints.issn" />
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1 R. R. Osborne and W. R. McWhinnie, J. Chem. Soc. A, 1967,2075.
2 M. C. Feller and R. Robson, Aust. J. Chem., 1968,21,2919.
3 M. C. Feller and R. Robson, Aust. J. Chem., 1970,23, 1997.

4 I. J. Bakker, M. C. Feller, and R. Robson, J. Inorg. Nucl. Chem., 1971,
5 J. D. Ortego and D. L. Perry, J. Inorg. Nucl. Chem., 1973,35,3031
6 J. D. Ortego, D. D. Waters, and C. S. Steele, J. Inorg. Nucl. Chem.,
1974,36,751.
7 J. D. Ortego, S. Upalawanna, and S. Amanollahi, J. Inorg. Nucl.
Chem., 1979,41,593.
8 R. Jagannathan and S. Soundararajan, J. Inorg. Nucl. Chem., 1980,
42, 145.
9 G. Annibale, L. Canovese, L. Cattalini, G. Natile, M. Biagini-Cingi,
A-M. Manotti-Lanfredi, and A. Tiripicchio, J. Chem. Soc., Dalton
Trans., 1981,2280.
33,747.
10 J. D. Ortego and M. Seymour, Polyhedron, 1982,1,21.
11 B. E. Fischer and H. Sigel, J. Inorg. Nucl. Chem., 1975,37,2127.
12 A. J. Canty, E. E. George, and C. V. Lee, Aust. J. Chem., 1983,36,415.
13 E. Regel and K-H. Buchel, Liebigs Ann. Chem., 1977,145.
14 A. J. Canty, N. J. Minchin, P. C. Healy, and A. H. White, J. Chem.
15 F. H. Brain and C. S. Gibson, J. Chem. Soc., 1931,762.
16 D. T. Cromer and J. B. Mann, Acta Crystallogr., 1968,24,321.
17 D. T. Cromer and D. Liberman, J. Chem. Phys., 1970,53,1891.
18 R. F. Stewart, E. R. Davidson, and W. T. Simpson, J. Chem. Phys.,
1965,42,3175.
19 'The X-RAY System, Version of March 1976,' Technical Report TR-
446, ed. J. M. Stewart, Computer Science Center, University of
Maryland.
20 J. C. Tedenac and E. Philip, J. Inorg. Nucl. Chem., 1975,37,846; Acta
Crystallogr., Sect B, 1974,30,2286.
21 P. C. Healy, C. H. L. Kennard, G. Smith, and A. H. White, Cryst.
Struct. Commun., 1978,7, 565.
22 P. C. Healy, J. M. Patrick, and A. H. White, Aust. J. Chem., 1984,37,
1111.
23 R. J. Read and M. N. G. James, Acta Crystallogr., Sect. B, 1980,36,
3 100." name="eprints.referencetext" />
<meta content="Byers, P.K. and Canty, A.J. and Engelhardt, L.M. and Patrick, J.M. and White, A.H. (1985) Co-ordination Chemistry of Pyridyl and N-Methyl imidazolyl Ketones. Synthetic and X-Ray Structural t Studies of Copper(II), Nickel(II), and Dimethylgold(III) Complexes. Journal of the Chemical Society, Dalton Transactions, 5 . pp. 981-986. ISSN 1477-9226" name="eprints.citation" />
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<meta content="Canty, A.J." name="DC.creator" />
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<meta content="Di-2-pyridyl ketone (dpk) reacts with dimethylgold(III) nitrate in water to form the complex [AuMe2(dpk.H2O)]NO3 in which the ligand has been hydrated to form a geminal diol. The closely related ketones 2-pyridyl-N-methyl-2-imidazolyl ketone (pik) and di(N-methyl-2-imidazolyl)
ketone (dik) react with Au(III)Me3 nitrate to form complexes that do not involve hydration of the ligand, [AuMe3(L)]NO3 (L = pik or dik). They react similarly with copper(II) sulphate and nickel(II) nitrate, forming [Cu(pik)(SO4)].0.5H2O, [Cu(dik)(SO4)].2H2O, [Ni(pik)(N03)2].0.5H2O and [Ni(dik)2(NO3)2].l.5Me0H; dpk forms [Ni(dpk.H2O)2(NO3)2].0.5H2O on reaction with nickel(II)
nitrate. The crystal structures of [AuMe2(dpk.H2O)]NO3 and [Cu(dik)(SO4)].2H2O have been determined by single-crystal X-ray diffraction at 295 K and refined by least-squares methods to R = 0.045 and 0.032 for 2 031 and 4 754 independent 'observed' reflections, respectively. The
cation [AuMe2(dpk.H2O)]+ has the ligand N,N-chelated with cis-square-planar co-ordination for gold(III), with an intramolecular hydroxy group positioned 2.850(8) A from the gold atom. The complex [Cu(dik)(SO4)].2H2O has square-pyramidal co-ordination for copper(II), with the
N,N-chelated ligand in the basal plane together with a water molecule and unidentate sulphate ion, and a water molecule co-ordinated axially. There is an intermolecular Cu...0 contact of 3.254(2) A with a ketone oxygen. Possible reasons for different behaviour of the ligands toward hydration are discussed." name="DC.description" />
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    <h1 class="ep_tm_pagetitle">Co-ordination Chemistry of Pyridyl and N-Methyl imidazolyl Ketones. Synthetic and X-Ray Structural t Studies of Copper(II), Nickel(II), and Dimethylgold(III) Complexes</h1>
    <p style="margin-bottom: 1em" class="not_ep_block"><span class="person_name">Byers, P.K.</span> and <span class="person_name">Canty, A.J.</span> and <span class="person_name">Engelhardt, L.M.</span> and <span class="person_name">Patrick, J.M.</span> and <span class="person_name">White, A.H.</span> (1985) <xhtml:em>Co-ordination Chemistry of Pyridyl and N-Methyl imidazolyl Ketones. Synthetic and X-Ray Structural t Studies of Copper(II), Nickel(II), and Dimethylgold(III) Complexes.</xhtml:em> Journal of the Chemical Society, Dalton Transactions, 5 . pp. 981-986. ISSN 1477-9226</p><p style="margin-bottom: 1em" class="not_ep_block"></p><table style="margin-bottom: 1em" class="not_ep_block"><tr><td valign="top" style="text-align:center"><a href="http://eprints.utas.edu.au/2831/1/Dalton1985_2C_981.pdf"><img alt="[img]" src="http://eprints.utas.edu.au/style/images/fileicons/application_pdf.png" border="0" class="ep_doc_icon" /></a></td><td valign="top"><a href="http://eprints.utas.edu.au/2831/1/Dalton1985_2C_981.pdf"><span class="ep_document_citation">PDF</span></a> - Full text restricted - Requires a PDF viewer<br />661Kb</td><td><form method="get" accept-charset="utf-8" action="http://eprints.utas.edu.au/cgi/request_doc"><input value="4072" name="docid" accept-charset="utf-8" type="hidden" /><div class=""><input value="Request a copy" name="_action_null" class="ep_form_action_button" onclick="return EPJS_button_pushed( '_action_null' )" type="submit" /> </div></form></td></tr></table><p style="margin-bottom: 1em" class="not_ep_block">Official URL: <a href="http://dx.doi.org/10.1039/DT9850000981">http://dx.doi.org/10.1039/DT9850000981</a></p><div class="not_ep_block"><h2>Abstract</h2><p style="padding-bottom: 16px; text-align: left; margin: 1em auto 0em auto">Di-2-pyridyl ketone (dpk) reacts with dimethylgold(III) nitrate in water to form the complex [AuMe2(dpk.H2O)]NO3 in which the ligand has been hydrated to form a geminal diol. The closely related ketones 2-pyridyl-N-methyl-2-imidazolyl ketone (pik) and di(N-methyl-2-imidazolyl)&#13;
ketone (dik) react with Au(III)Me3 nitrate to form complexes that do not involve hydration of the ligand, [AuMe3(L)]NO3 (L = pik or dik). They react similarly with copper(II) sulphate and nickel(II) nitrate, forming [Cu(pik)(SO4)].0.5H2O, [Cu(dik)(SO4)].2H2O, [Ni(pik)(N03)2].0.5H2O and [Ni(dik)2(NO3)2].l.5Me0H; dpk forms [Ni(dpk.H2O)2(NO3)2].0.5H2O on reaction with nickel(II)&#13;
nitrate. The crystal structures of [AuMe2(dpk.H2O)]NO3 and [Cu(dik)(SO4)].2H2O have been determined by single-crystal X-ray diffraction at 295 K and refined by least-squares methods to R = 0.045 and 0.032 for 2 031 and 4 754 independent 'observed' reflections, respectively. The&#13;
cation [AuMe2(dpk.H2O)]+ has the ligand N,N-chelated with cis-square-planar co-ordination for gold(III), with an intramolecular hydroxy group positioned 2.850(8) A from the gold atom. The complex [Cu(dik)(SO4)].2H2O has square-pyramidal co-ordination for copper(II), with the&#13;
N,N-chelated ligand in the basal plane together with a water molecule and unidentate sulphate ion, and a water molecule co-ordinated axially. There is an intermolecular Cu...0 contact of 3.254(2) A with a ketone oxygen. Possible reasons for different behaviour of the ligands toward hydration are discussed.</p></div><table style="margin-bottom: 1em" border="0" cellpadding="3" class="not_ep_block"><tr><th valign="top" class="ep_row">Item Type:</th><td valign="top" class="ep_row">Article</td></tr><tr><th valign="top" class="ep_row">Subjects:</th><td valign="top" class="ep_row"><a href="http://eprints.utas.edu.au/view/subjects/259901.html">250000 Chemical Sciences &gt; 259900 Other Chemical Sciences &gt; 259901 Organometallic Chemistry</a></td></tr><tr><th valign="top" class="ep_row">ID Code:</th><td valign="top" class="ep_row">2831</td></tr><tr><th valign="top" class="ep_row">Deposited By:</th><td valign="top" class="ep_row"><span class="ep_name_citation"><span class="person_name">Prof Allan J Canty</span></span></td></tr><tr><th valign="top" class="ep_row">Deposited On:</th><td valign="top" class="ep_row">14 Jan 2008 08:47</td></tr><tr><th valign="top" class="ep_row">Last Modified:</th><td valign="top" class="ep_row">14 Jan 2008 08:47</td></tr><tr><th valign="top" class="ep_row">ePrint Statistics:</th><td valign="top" class="ep_row"><a target="ePrintStats" href="/es/index.php?action=show_detail_eprint;id=2831;">View statistics for this ePrint</a></td></tr></table><p align="right">Repository Staff Only: <a href="http://eprints.utas.edu.au/cgi/users/home?screen=EPrint::View&amp;eprintid=2831">item control page</a></p>
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