<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Zobi, Fabio</dc:creator>
  <dc:creator>Blacque, Olivier</dc:creator>
  <dc:creator>Steyl, Gideon</dc:creator>
  <dc:creator>Spingler, Bernhard</dc:creator>
  <dc:creator>Alberto, Roger</dc:creator>
  <dc:date>2009</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The chemistry of [(tacn)-N-CO-Re(III)(CO)(2)Br]X (X = Cl or Br), obtained in good  yield from the reaction of fac-[(tacn)Re(I)(CO)(3)]Br (1, tacn = 1,4,7- triazacyclononane) with X(2) in water, is described. The [(tacn)-N-CO-Re(III)(CO) (2)Br]X complex (2 with X = Br(-); 2a with X = BrCl(2)(-)), which we have previously  communicated, is characterized by an unusual three-membered ring acyl amide bond.  Complex 2 is stable as a solid but is reactive in aqueous solution. Under basic  conditions (1 M NaOH), reductive decarbonylation was observed, and the bis-carbonyl  complex [(tacn)Re(I)(CO)(2)Br] (3) was obtained in quantitative yield. The Br(-) ligand  in 3 could be replaced by CN(-), giving the neutral complex [(tacn)Re(I)(CO)(2)(CN)]  (4). In acidic media (1 M HBr), complex 2 partially converted to the monocarbonyl mu- oxo bridged dinuclear complex {[(tacn)Re(III)(CO)Br](2)O}(2+) (5 as [PF(6)](-) salt).  Under mild oxidative conditions the trioxo [(tacn)Re(VII)O(3)](ReO(4)(-)) (6) was  formed almost quantitatively, and small amounts of the uncommon Re(VI) complex  [(tacn)Re(VI)O(2)Br](ReO(4)(-)) (7) were identified. Mechanistic investigations at the  density functional level of theory (DFT) showed that the elementary steps in the  formation of 2 from 1 and 3 from 2 involved reactions of the complexes with  hydroxide. The calculated pathway is strongly exothermic (ca. -137 kcal/mol),  confirming the energetically and kinetically highly favored formation of 3. The X-ray  structures of 2a and 3-5 are reported and discussed.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/309264</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309264/files/zobi_et_al_2009_formation.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/ic9002803</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Inorganic Chemistry. - 2009, vol. 48, no. 11, p. 4963-4970</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Rhenium Chemistry</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Solution chemistry</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Metals</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Ligands</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Crystal structure</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Molecules</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Formation and Reactivity of [(tacn)-N-CO-Re(III)Br(CO)(2)](+) in Water : a Theoretical and Experimental Study</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
