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Syntheses, Structures, and Bonding of NgF 2 ⋅CrOF 4 , NgF 2 ⋅2CrOF 4 (Ng=Kr, Xe), and (CrOF 4 )

The noble-gas difluoride adducts, NgF ⋅CrOF and NgF ⋅2CrOF (Ng=Kr and Xe), have been synthesized and structurally characterized at low temperatures by Raman spectroscopy and single-crystal X-ray diffraction. The low fluoride ion affinity of CrOF renders it incapable of inducing fluoride ion transfer...

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Published in:Chemistry : a European journal 2019-09, Vol.25 (52), p.12105-12119
Main Authors: Mercier, Hélène P A, Breddemann, Ulf, Brock, David S, Bortolus, Mark R, Schrobilgen, Gary J
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creator Mercier, Hélène P A
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description The noble-gas difluoride adducts, NgF ⋅CrOF and NgF ⋅2CrOF (Ng=Kr and Xe), have been synthesized and structurally characterized at low temperatures by Raman spectroscopy and single-crystal X-ray diffraction. The low fluoride ion affinity of CrOF renders it incapable of inducing fluoride ion transfer from NgF (Ng=Kr and Xe) to form ion-paired salts of the [NgF] cations having either the [CrOF ] or [Cr O F ] anions. The crystal structures show the NgF ⋅CrOF adducts are comprised of F -Ng-F - - -Cr(O)F structural units in which NgF is weakly coordinated to CrOF by means of a fluorine bridge, F , in which Ng-F is elongated relative to the terminal Ng-F bond. In contrast with XeF ⋅2MOF (M=Mo or W) and KrF ⋅2MoOF , in which the Lewis acidic, F (O)M- - -F - - -M(O)F moiety coordinates to Ng through a single M- - -F -Ng bridge, both fluorine ligands of NgF coordinate to CrOF molecules to form F (O)Cr- - -F -Ng-F - - -Cr(O)F adducts in which both Ng-F bonds are only marginally elongated relative to the Ng-F bonds of free NgF . Quantum-chemical calculations show that the Cr-F bonds of NgF ⋅CrOF and NgF ⋅2CrOF are predominantly electrostatic with a small degree of covalent character that accounts for their nonlinear Cr- - -F -Ng bridge angles and staggered O-Cr- - -F -Ng-F dihedral angles. The crystal structures and Raman spectra of two CrOF polymorphs have also been obtained. Both are comprised of fluorine-bridged chains that are cis- and trans-fluorine-bridged with respect to oxygen.
doi_str_mv 10.1002/chem.201902005
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The low fluoride ion affinity of CrOF renders it incapable of inducing fluoride ion transfer from NgF (Ng=Kr and Xe) to form ion-paired salts of the [NgF] cations having either the [CrOF ] or [Cr O F ] anions. The crystal structures show the NgF ⋅CrOF adducts are comprised of F -Ng-F - - -Cr(O)F structural units in which NgF is weakly coordinated to CrOF by means of a fluorine bridge, F , in which Ng-F is elongated relative to the terminal Ng-F bond. In contrast with XeF ⋅2MOF (M=Mo or W) and KrF ⋅2MoOF , in which the Lewis acidic, F (O)M- - -F - - -M(O)F moiety coordinates to Ng through a single M- - -F -Ng bridge, both fluorine ligands of NgF coordinate to CrOF molecules to form F (O)Cr- - -F -Ng-F - - -Cr(O)F adducts in which both Ng-F bonds are only marginally elongated relative to the Ng-F bonds of free NgF . Quantum-chemical calculations show that the Cr-F bonds of NgF ⋅CrOF and NgF ⋅2CrOF are predominantly electrostatic with a small degree of covalent character that accounts for their nonlinear Cr- - -F -Ng bridge angles and staggered O-Cr- - -F -Ng-F dihedral angles. The crystal structures and Raman spectra of two CrOF polymorphs have also been obtained. Both are comprised of fluorine-bridged chains that are cis- and trans-fluorine-bridged with respect to oxygen.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.201902005</identifier><identifier>PMID: 31172609</identifier><language>eng</language><publisher>Germany</publisher><ispartof>Chemistry : a European journal, 2019-09, Vol.25 (52), p.12105-12119</ispartof><rights>2019 Wiley-VCH Verlag GmbH &amp; Co. 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Quantum-chemical calculations show that the Cr-F bonds of NgF ⋅CrOF and NgF ⋅2CrOF are predominantly electrostatic with a small degree of covalent character that accounts for their nonlinear Cr- - -F -Ng bridge angles and staggered O-Cr- - -F -Ng-F dihedral angles. The crystal structures and Raman spectra of two CrOF polymorphs have also been obtained. 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The low fluoride ion affinity of CrOF renders it incapable of inducing fluoride ion transfer from NgF (Ng=Kr and Xe) to form ion-paired salts of the [NgF] cations having either the [CrOF ] or [Cr O F ] anions. The crystal structures show the NgF ⋅CrOF adducts are comprised of F -Ng-F - - -Cr(O)F structural units in which NgF is weakly coordinated to CrOF by means of a fluorine bridge, F , in which Ng-F is elongated relative to the terminal Ng-F bond. In contrast with XeF ⋅2MOF (M=Mo or W) and KrF ⋅2MoOF , in which the Lewis acidic, F (O)M- - -F - - -M(O)F moiety coordinates to Ng through a single M- - -F -Ng bridge, both fluorine ligands of NgF coordinate to CrOF molecules to form F (O)Cr- - -F -Ng-F - - -Cr(O)F adducts in which both Ng-F bonds are only marginally elongated relative to the Ng-F bonds of free NgF . Quantum-chemical calculations show that the Cr-F bonds of NgF ⋅CrOF and NgF ⋅2CrOF are predominantly electrostatic with a small degree of covalent character that accounts for their nonlinear Cr- - -F -Ng bridge angles and staggered O-Cr- - -F -Ng-F dihedral angles. The crystal structures and Raman spectra of two CrOF polymorphs have also been obtained. Both are comprised of fluorine-bridged chains that are cis- and trans-fluorine-bridged with respect to oxygen.</abstract><cop>Germany</cop><pmid>31172609</pmid><doi>10.1002/chem.201902005</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-8716-2330</orcidid><orcidid>https://orcid.org/0000-0002-1671-381X</orcidid><orcidid>https://orcid.org/0000-0003-3101-0706</orcidid><orcidid>https://orcid.org/0000-0001-5109-6979</orcidid></addata></record>
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title Syntheses, Structures, and Bonding of NgF 2 ⋅CrOF 4 , NgF 2 ⋅2CrOF 4 (Ng=Kr, Xe), and (CrOF 4 )
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