<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>Schindler, Kevin</dc:creator>
  <dc:creator>Crochet, Aurélien</dc:creator>
  <dc:creator>Zobi, Fabio</dc:creator>
  <dc:date>2021</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">New synthetic routes to aerobically stable and substitutionally labile α-diimine  rhenium(I) dicarbonyl complexes are described. The molecules are prepared in high  yield from the cis–cis–trans-[Re(CO)2(tBu2bpy)Br2]− anion (2, where tBu2bpy is 4,4′- di-tert-butyl-2,2′-bipyridine), which can be isolated from the one electron reduction of  the corresponding 17-electron complex (1). Compound 2 is stable in the solid state,  but in solution it is oxidized by molecular oxygen back to 1. Replacement of a single  bromide of 2 by σ-donor monodentate ligands (Ls) yields stable neutral 18-electron  cis–cis–trans-[Re(CO)2(tBu2bpy)Br(L)] species. In coordinating solvents like methanol  the halide is replaced giving the corresponding solvated cations.  [Re(CO)2(tBu2bpy)Br(L)] species can be further reacted with Ls to prepare stable cis– cis–trans-[Re(CO)2(tBu2bpy)(L)2]+ complexes in good yield. Ligand substitution of  Re(I) complexes proceeds via pentacoordinate intermediates capable of Berry  pseudorotation. In addition to the cis–cis–trans-complexes, cis–cis–cis- (all cis)  isomers are also formed. In particular, cis–cis–trans-[Re(CO)2(tBu2bpy)(L)2]+  complexes establish an equilibrium with all cis isomers in solution. The solid state  crystal structure of nearly all molecules presented could be elucidated. The molecules  adopt a slightly distorted octahedral geometry. In comparison to similar fac- [Re(CO)3]+complexes, Re(I) diacarbonyl species are characterized by a bend (ca. 7°)  of the axial ligands towards the α-diimine unit. [Re(CO)2(tBu2bpy)Br2]− and  [Re(CO)2(tBu2bpy)Br(L)] complexes may be considered as synthons for the  preparation of a variety of new stable diamagnetic dicarbonyl rhenium cis-[Re(CO)2]+  complexes, offering a convenient entry in the chemistry of the core.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/309288</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309288/files/zobi_et_al_2021_aerobically.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309288/files/zobi_et_al_2021_aerobically_suppl.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1039/D1RA00514F</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>RSC Advances. - 2021, vol. 11, p. 7511-7520</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Rhenium Chemistry</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns2="xml" ns2:lang="en">Aerobically stable and substitutionally labile α-diimine rhenium dicarbonyl complexes</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
