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<title>UTas ePrints - 1H NMR Detection of Cationic Organopalladium(IV) Intermediates in Oxidative-Addition Reactions and the Structure of fac-PdBrMe2(CH2COPh)(bpy)</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="Skelton, B.W." name="eprints.creators_name" />
<meta content="Traill, P.R." name="eprints.creators_name" />
<meta content="Watson, A.A." name="eprints.creators_name" />
<meta content="White, A.H." name="eprints.creators_name" />
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<meta content="allan.canty@utas.edu.au" name="eprints.creators_id" />
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Intermediates in Oxidative-Addition Reactions and the Structure of fac-PdBrMe2(CH2COPh)(bpy)" name="eprints.title" />
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<meta content="Phenacyl bromides react with dimethylpalladium(I1) complexes PdMe2(L2) (L2 = bpy, phen) to form
the palladium(IV) complexes fac-PdBrMe2(CH2COAr)(L2) (Ar = Ph, p-C6H4Br), which have both methyl
groups trans to the bidentate nitrogen donor ligand. 1H NMR studies of the oxidative addition of phenacyl
bromides to PdMe2(bpy) in (CD3)2C0 at -5 C indicate the formation of two similar cationic intermediates,
prior to formation of the neutral product. As the cations have only one of the methyl groups trans to bpy,
configurational changes at palladium occur on cation formation and on conversion of the cations to the
neutral product. It is proposed that one of the cations may be stabilized via an intramolecularly coordinated
phenacyl group, [PdMe2(CH2COAr-C,0)(L2)]+. A single cation, exhibiting NMR spectra similar to those
of the cations of the bpy complexes, is detected as an intermediate in the reaction of PdMe2(phen) with
ArCOCH2Br. A cation has also been detected for the reaction of PdMe2(bpy) with CD3I in (CD3)2C0 at
-50 C, prior to formation of PdIMe2(CD3)(bpy). Both the cation, most likely [PdMe2(CD3)(bpy)((CD3)2CO)]+, and the neutral product display scrambled Me and CD3 groups, in contrast to the trans oxidative addition reported for the analogous reaction of PtMe2(bpy) with CD3I. Crystals of PdBrMe2(CH2COAr)(bpy) are orthorhombic, space group Pbca, with a = 19.554(3) A, b = 15.007(9) A, c = 13.282(4) 1, and Z = 8." name="eprints.abstract" />
<meta content="1992-09" name="eprints.date" />
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<meta content="Byers, P.K. and Canty, A.J. and Skelton, B.W. and Traill, P.R. and Watson, A.A. and White, A.H. (1992) 1H NMR Detection of Cationic Organopalladium(IV) Intermediates in Oxidative-Addition Reactions and the Structure of fac-PdBrMe2(CH2COPh)(bpy). Organometallics, 11 (9). pp. 3085-3088." name="eprints.citation" />
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Intermediates in Oxidative-Addition Reactions and the Structure of fac-PdBrMe2(CH2COPh)(bpy)" name="DC.title" />
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<meta content="Canty, A.J." name="DC.creator" />
<meta content="Skelton, B.W." name="DC.creator" />
<meta content="Traill, P.R." name="DC.creator" />
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<meta content="Phenacyl bromides react with dimethylpalladium(I1) complexes PdMe2(L2) (L2 = bpy, phen) to form
the palladium(IV) complexes fac-PdBrMe2(CH2COAr)(L2) (Ar = Ph, p-C6H4Br), which have both methyl
groups trans to the bidentate nitrogen donor ligand. 1H NMR studies of the oxidative addition of phenacyl
bromides to PdMe2(bpy) in (CD3)2C0 at -5 C indicate the formation of two similar cationic intermediates,
prior to formation of the neutral product. As the cations have only one of the methyl groups trans to bpy,
configurational changes at palladium occur on cation formation and on conversion of the cations to the
neutral product. It is proposed that one of the cations may be stabilized via an intramolecularly coordinated
phenacyl group, [PdMe2(CH2COAr-C,0)(L2)]+. A single cation, exhibiting NMR spectra similar to those
of the cations of the bpy complexes, is detected as an intermediate in the reaction of PdMe2(phen) with
ArCOCH2Br. A cation has also been detected for the reaction of PdMe2(bpy) with CD3I in (CD3)2C0 at
-50 C, prior to formation of PdIMe2(CD3)(bpy). Both the cation, most likely [PdMe2(CD3)(bpy)((CD3)2CO)]+, and the neutral product display scrambled Me and CD3 groups, in contrast to the trans oxidative addition reported for the analogous reaction of PtMe2(bpy) with CD3I. Crystals of PdBrMe2(CH2COAr)(bpy) are orthorhombic, space group Pbca, with a = 19.554(3) A, b = 15.007(9) A, c = 13.282(4) 1, and Z = 8." name="DC.description" />
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<meta content="Byers, P.K. and Canty, A.J. and Skelton, B.W. and Traill, P.R. and Watson, A.A. and White, A.H. (1992) 1H NMR Detection of Cationic Organopalladium(IV) Intermediates in Oxidative-Addition Reactions and the Structure of fac-PdBrMe2(CH2COPh)(bpy). Organometallics, 11 (9). pp. 3085-3088." name="DC.identifier" />
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<h1 class="ep_tm_pagetitle">1H NMR Detection of Cationic Organopalladium(IV) Intermediates in Oxidative-Addition Reactions and the Structure of fac-PdBrMe2(CH2COPh)(bpy)</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">Skelton, B.W.</span> and <span class="person_name">Traill, P.R.</span> and <span class="person_name">Watson, A.A.</span> and <span class="person_name">White, A.H.</span> (1992) <xhtml:em>1H NMR Detection of Cationic Organopalladium(IV) Intermediates in Oxidative-Addition Reactions and the Structure of fac-PdBrMe2(CH2COPh)(bpy).</xhtml:em> Organometallics, 11 (9). pp. 3085-3088.</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/2079/1/om00045a023.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/2079/1/om00045a023.pdf"><span class="ep_document_citation">PDF</span></a> - Full text restricted - Requires a PDF viewer<br />498Kb</td><td><form method="get" accept-charset="utf-8" action="http://eprints.utas.edu.au/cgi/request_doc"><input value="2615" 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/10.1021/om00045a023">http://dx.doi.org/10.1021/om00045a023</a></p><div class="not_ep_block"><h2>Abstract</h2><p style="padding-bottom: 16px; text-align: left; margin: 1em auto 0em auto">Phenacyl bromides react with dimethylpalladium(I1) complexes PdMe2(L2) (L2 = bpy, phen) to form
the palladium(IV) complexes fac-PdBrMe2(CH2COAr)(L2) (Ar = Ph, p-C6H4Br), which have both methyl
groups trans to the bidentate nitrogen donor ligand. 1H NMR studies of the oxidative addition of phenacyl
bromides to PdMe2(bpy) in (CD3)2C0 at -5 C indicate the formation of two similar cationic intermediates,
prior to formation of the neutral product. As the cations have only one of the methyl groups trans to bpy,
configurational changes at palladium occur on cation formation and on conversion of the cations to the
neutral product. It is proposed that one of the cations may be stabilized via an intramolecularly coordinated
phenacyl group, [PdMe2(CH2COAr-C,0)(L2)]+. A single cation, exhibiting NMR spectra similar to those
of the cations of the bpy complexes, is detected as an intermediate in the reaction of PdMe2(phen) with
ArCOCH2Br. A cation has also been detected for the reaction of PdMe2(bpy) with CD3I in (CD3)2C0 at
-50 C, prior to formation of PdIMe2(CD3)(bpy). Both the cation, most likely [PdMe2(CD3)(bpy)((CD3)2CO)]+, and the neutral product display scrambled Me and CD3 groups, in contrast to the trans oxidative addition reported for the analogous reaction of PtMe2(bpy) with CD3I. Crystals of PdBrMe2(CH2COAr)(bpy) are orthorhombic, space group Pbca, with a = 19.554(3) A, b = 15.007(9) A, c = 13.282(4) 1, and Z = 8.</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">Additional Information:</th><td valign="top" class="ep_row">Definitive version is available online at http://pubs.acs.org/journals/orgnd7/index.html</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 > 259900 Other Chemical Sciences > 259901 Organometallic Chemistry</a></td></tr><tr><th valign="top" class="ep_row">Collections:</th><td valign="top" class="ep_row">UNSPECIFIED</td></tr><tr><th valign="top" class="ep_row">ID Code:</th><td valign="top" class="ep_row">2079</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">11 Oct 2007 12:01</td></tr><tr><th valign="top" class="ep_row">Last Modified:</th><td valign="top" class="ep_row">01 Feb 2008 14:42</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=2079;">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&eprintid=2079">item control page</a></p>
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