Physical and Chemical Response of FeCl3/FeCl4 – Spin Probes on the Functionalizing of Ionic Liquids
Fe(III) compounds FeCl3 and FeCl4 – have been used as ESR spin probes in ionic liquids (ILs) at 293 and 77 K for the first time. They showed characteristic spectral patterns, which could be separated from each other by simulation. The largest contribution originates from aggregated FeCl4 – and other...
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Veröffentlicht in: | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2013-05, Vol.117 (19), p.3960-3971 |
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description | Fe(III) compounds FeCl3 and FeCl4 – have been used as ESR spin probes in ionic liquids (ILs) at 293 and 77 K for the first time. They showed characteristic spectral patterns, which could be separated from each other by simulation. The largest contribution originates from aggregated FeCl4 – and other exchange coupled species at g′ ≈ 2.6. FeCl4 – has been shown to be an identifiable, changeable, customizable, transferable, and extractable probe with contributions to a characteristic ESR fine structure. For simulation a spin Hamiltonian with up to fourth order and statistic distributions of spin coupling parameters has been used. The different Fe(III) signals coexist being dependent on the functionalization of the IL, i.e., on changing the chain length of the substituent at the imidazolium cation as well as varying the respective anion (BF4 –, PF6 –, Cl–, and FeCl4 –). From the molecular structure and occurrence of the Fe(III) species conclusions could be drawn concerning their locations and reactions in polar and nonpolar compartments of the ILs. Their contributions could be purposefully adjusted via the molecular control of the properties of the ILs. The conversion of FeCl3 into FeCl4 – and [FeCl4X2]3‑ species could be observed to be dependent on the formation of polar and nonpolar domains in ILs. |
doi_str_mv | 10.1021/jp403260r |
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They showed characteristic spectral patterns, which could be separated from each other by simulation. The largest contribution originates from aggregated FeCl4 – and other exchange coupled species at g′ ≈ 2.6. FeCl4 – has been shown to be an identifiable, changeable, customizable, transferable, and extractable probe with contributions to a characteristic ESR fine structure. For simulation a spin Hamiltonian with up to fourth order and statistic distributions of spin coupling parameters has been used. The different Fe(III) signals coexist being dependent on the functionalization of the IL, i.e., on changing the chain length of the substituent at the imidazolium cation as well as varying the respective anion (BF4 –, PF6 –, Cl–, and FeCl4 –). From the molecular structure and occurrence of the Fe(III) species conclusions could be drawn concerning their locations and reactions in polar and nonpolar compartments of the ILs. Their contributions could be purposefully adjusted via the molecular control of the properties of the ILs. The conversion of FeCl3 into FeCl4 – and [FeCl4X2]3‑ species could be observed to be dependent on the formation of polar and nonpolar domains in ILs.</description><identifier>ISSN: 1089-5639</identifier><identifier>EISSN: 1520-5215</identifier><identifier>DOI: 10.1021/jp403260r</identifier><identifier>PMID: 23597290</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Atomic and molecular physics ; Chlorides - chemistry ; Electron resonance and relaxation ; Electron Spin Resonance Spectroscopy ; Exact sciences and technology ; Ferric Compounds - chemistry ; Hydrophobic and Hydrophilic Interactions ; Imidazoles - chemistry ; Ionic Liquids - chemistry ; Kinetics ; Molecular Dynamics Simulation ; Molecular Probes - chemistry ; Molecular properties and interactions with photons ; Molecular Structure ; Physics ; Spin Labels ; Temperature</subject><ispartof>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2013-05, Vol.117 (19), p.3960-3971</ispartof><rights>Copyright © 2013 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jp403260r$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jp403260r$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28203632$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23597290$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stößer, Reinhard</creatorcontrib><creatorcontrib>Herrmann, Werner</creatorcontrib><title>Physical and Chemical Response of FeCl3/FeCl4 – Spin Probes on the Functionalizing of Ionic Liquids</title><title>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</title><addtitle>J. Phys. Chem. A</addtitle><description>Fe(III) compounds FeCl3 and FeCl4 – have been used as ESR spin probes in ionic liquids (ILs) at 293 and 77 K for the first time. They showed characteristic spectral patterns, which could be separated from each other by simulation. The largest contribution originates from aggregated FeCl4 – and other exchange coupled species at g′ ≈ 2.6. FeCl4 – has been shown to be an identifiable, changeable, customizable, transferable, and extractable probe with contributions to a characteristic ESR fine structure. For simulation a spin Hamiltonian with up to fourth order and statistic distributions of spin coupling parameters has been used. The different Fe(III) signals coexist being dependent on the functionalization of the IL, i.e., on changing the chain length of the substituent at the imidazolium cation as well as varying the respective anion (BF4 –, PF6 –, Cl–, and FeCl4 –). From the molecular structure and occurrence of the Fe(III) species conclusions could be drawn concerning their locations and reactions in polar and nonpolar compartments of the ILs. Their contributions could be purposefully adjusted via the molecular control of the properties of the ILs. The conversion of FeCl3 into FeCl4 – and [FeCl4X2]3‑ species could be observed to be dependent on the formation of polar and nonpolar domains in ILs.</description><subject>Atomic and molecular physics</subject><subject>Chlorides - chemistry</subject><subject>Electron resonance and relaxation</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Exact sciences and technology</subject><subject>Ferric Compounds - chemistry</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Imidazoles - chemistry</subject><subject>Ionic Liquids - chemistry</subject><subject>Kinetics</subject><subject>Molecular Dynamics Simulation</subject><subject>Molecular Probes - chemistry</subject><subject>Molecular properties and interactions with photons</subject><subject>Molecular Structure</subject><subject>Physics</subject><subject>Spin Labels</subject><subject>Temperature</subject><issn>1089-5639</issn><issn>1520-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkctOwzAQRS0EouWx4AeQN0hsQseexEmWKKJQqRIVj3XkJA51ldhpnCzKin_gD_kSUih0Mw_pzFzpXkIuGNww4GyyanxALqA9IGMWcPACzoLDYYYo9gKB8YicOLcCAIbcPyYjjkEc8hjGRC2WG6dzWVFpCposVf2zPCnXWOMUtSWdqqTCybb69Ovjkz432tBFazPlqDW0Wyo67U3eaWtkpd-1edtezazROZ3rda8Ld0aOSlk5db7rp-R1eveSPHjzx_tZcjv3JA9Z5_GIFYLHWezngYQwLlSEoFDwsgCWIRZRiILxADNAiEIVi1BGiJIJLlGWBZ6S69-_TWvXvXJdWmuXq6qSRtnepQwDBB8i4AN6uUP7rFZF2rS6lu0m_bNmAK52gHSDJWUrTa7dnos4oEC-52Tu0pXt28GFQQnSbTTpfzT4DZKBe-E</recordid><startdate>20130516</startdate><enddate>20130516</enddate><creator>Stößer, Reinhard</creator><creator>Herrmann, Werner</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20130516</creationdate><title>Physical and Chemical Response of FeCl3/FeCl4 – Spin Probes on the Functionalizing of Ionic Liquids</title><author>Stößer, Reinhard ; Herrmann, Werner</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a271t-281d629b94c5a079de830e362fd01b33d87361253b03087e967a833a162a3afd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Atomic and molecular physics</topic><topic>Chlorides - chemistry</topic><topic>Electron resonance and relaxation</topic><topic>Electron Spin Resonance Spectroscopy</topic><topic>Exact sciences and technology</topic><topic>Ferric Compounds - chemistry</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Imidazoles - chemistry</topic><topic>Ionic Liquids - chemistry</topic><topic>Kinetics</topic><topic>Molecular Dynamics Simulation</topic><topic>Molecular Probes - chemistry</topic><topic>Molecular properties and interactions with photons</topic><topic>Molecular Structure</topic><topic>Physics</topic><topic>Spin Labels</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stößer, Reinhard</creatorcontrib><creatorcontrib>Herrmann, Werner</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stößer, Reinhard</au><au>Herrmann, Werner</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physical and Chemical Response of FeCl3/FeCl4 – Spin Probes on the Functionalizing of Ionic Liquids</atitle><jtitle>The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory</jtitle><addtitle>J. Phys. Chem. A</addtitle><date>2013-05-16</date><risdate>2013</risdate><volume>117</volume><issue>19</issue><spage>3960</spage><epage>3971</epage><pages>3960-3971</pages><issn>1089-5639</issn><eissn>1520-5215</eissn><abstract>Fe(III) compounds FeCl3 and FeCl4 – have been used as ESR spin probes in ionic liquids (ILs) at 293 and 77 K for the first time. They showed characteristic spectral patterns, which could be separated from each other by simulation. The largest contribution originates from aggregated FeCl4 – and other exchange coupled species at g′ ≈ 2.6. FeCl4 – has been shown to be an identifiable, changeable, customizable, transferable, and extractable probe with contributions to a characteristic ESR fine structure. For simulation a spin Hamiltonian with up to fourth order and statistic distributions of spin coupling parameters has been used. The different Fe(III) signals coexist being dependent on the functionalization of the IL, i.e., on changing the chain length of the substituent at the imidazolium cation as well as varying the respective anion (BF4 –, PF6 –, Cl–, and FeCl4 –). From the molecular structure and occurrence of the Fe(III) species conclusions could be drawn concerning their locations and reactions in polar and nonpolar compartments of the ILs. Their contributions could be purposefully adjusted via the molecular control of the properties of the ILs. The conversion of FeCl3 into FeCl4 – and [FeCl4X2]3‑ species could be observed to be dependent on the formation of polar and nonpolar domains in ILs.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>23597290</pmid><doi>10.1021/jp403260r</doi><tpages>12</tpages></addata></record> |
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subjects | Atomic and molecular physics Chlorides - chemistry Electron resonance and relaxation Electron Spin Resonance Spectroscopy Exact sciences and technology Ferric Compounds - chemistry Hydrophobic and Hydrophilic Interactions Imidazoles - chemistry Ionic Liquids - chemistry Kinetics Molecular Dynamics Simulation Molecular Probes - chemistry Molecular properties and interactions with photons Molecular Structure Physics Spin Labels Temperature |
title | Physical and Chemical Response of FeCl3/FeCl4 – Spin Probes on the Functionalizing of Ionic Liquids |
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