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DC Field | Value | Language |
---|---|---|
dc.citation.endPage | 8850 | - |
dc.citation.number | 21 | - |
dc.citation.startPage | 8843 | - |
dc.citation.title | JOURNAL OF PHYSICAL CHEMISTRY | - |
dc.citation.volume | 99 | - |
dc.contributor.author | RUOFF, RS | - |
dc.contributor.author | KADISH, KM | - |
dc.contributor.author | BOULAS, P | - |
dc.contributor.author | CHEN, ECM | - |
dc.date.accessioned | 2023-12-22T12:41:57Z | - |
dc.date.available | 2023-12-22T12:41:57Z | - |
dc.date.created | 2021-10-19 | - |
dc.date.issued | 1995-05 | - |
dc.description.abstract | Differences in energy for neutral molecule and negative ions upon going from the gas phase to solution, -Delta Delta G(sol), have been calculated from gas phase electron affinities and half-wave reduction potentials for a series of fullerenes, aromatic hydrocarbons, metalloporphyrins, and metal complexes in dimethylformamide (DMF). For those compounds with similar charge delocalization, the value of -Delta Delta G(sol) is constant and equal to 1.76 +/- 0.06 eV for the fullerenes, 1.99 +/- 0.05 eV for the aromatic hydrocarbons and the metalloporphyrins, and 2.19 +/- 0.14 eV for the metal acetylacetonates. The fullerenes form a new class of molecules in which the charge is highly delocalized, and this is demonstrated by the relatively low value of -Delta Delta G(sol). A procedure for determining adiabatic electron affinities from reduction potentials, and vice versa, is established. This procedure is applied to benzene to give an electron affinity of -0.7 +/- 0.14 eV, to La@C-82 to give an electron affinity of 3.21 +/- 0.06 eV, and to Y@C-82 to give an electron affinity of 3.32 +/- 0.06 eV. On the other hand, a value of E(1/2) = 0.09 +/- 0.14 V vs SCE is predicted for the reduction of Ca@C-60 in DMF based upon a reported electron affinity of 3.0 +/- 0.1 eV. | - |
dc.identifier.bibliographicCitation | JOURNAL OF PHYSICAL CHEMISTRY, v.99, no.21, pp.8843 - 8850 | - |
dc.identifier.doi | 10.1021/j100021a060 | - |
dc.identifier.issn | 0022-3654 | - |
dc.identifier.scopusid | 2-s2.0-0029309264 | - |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/54540 | - |
dc.identifier.url | https://pubs.acs.org/doi/abs/10.1021/j100021a060 | - |
dc.identifier.wosid | A1995RA14700060 | - |
dc.language | 영어 | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | THE RELATIONSHIP BETWEEN THE ELECTRON-AFFINITIES AND HALF-WAVE REDUCTION POTENTIALS OF FULLERENES, AROMATIC-HYDROCARBONS, AND METAL-COMPLEXES | - |
dc.type | Article | - |
dc.description.isOpenAccess | FALSE | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | TRANSFER EQUILIBRIA | - |
dc.subject.keywordPlus | APROTIC-SOLVENTS | - |
dc.subject.keywordPlus | GAS-PHASE | - |
dc.subject.keywordPlus | C-60 | - |
dc.subject.keywordPlus | BUCKMINSTERFULLERENE | - |
dc.subject.keywordPlus | ELECTROSYNTHESIS | - |
dc.subject.keywordPlus | CARBON | - |
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