Vibrational spectroscopic studies of the chemical dynamics in charge transfer complexes of the type iodine-pyridine 1. Experimental results.

Saved in:
Bibliographic Details
Title: Vibrational spectroscopic studies of the chemical dynamics in charge transfer complexes of the type iodine-pyridine 1. Experimental results.
Authors: Tassaing, T., Besnard, M, Rwood, J. Ya
Source: Molecular Physics. 10/10/97, Vol. 92 Issue 2, p271-280. 10p.
Subjects: Pyridine, Iodine, Raman effect, Electron donor-acceptor complexes
Abstract: The far infrared and Raman spectra of the pyridine-I complex in solution in non-polar solvents have been investigated as functions of base concentration and temperature. Attempts have been made to assess the relative contribution of donor-acceptor and classical dipolar interactions to the spectral changes which occur with increasing medium polarity, temperature or donor strength (via the use of picolines as donors). It has been found that the overall evolution of band position, width and intensity is dependent mostly on the medium polarity, reflecting changes in complex stability induced by the surrounding dipoles. However, the irreversible appearance of the I anion seems to be associated with an increase in donor strength. Local dipole ordering, as a function of temperature lowering, clearly also is important for stabilizing the complex. 2 3. [ABSTRACT FROM AUTHOR]
Copyright of Molecular Physics is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Engineering Source
FullText Text:
  Availability: 0
Header DbId: egs
DbLabel: Engineering Source
An: 7612932
AccessLevel: 6
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Vibrational spectroscopic studies of the chemical dynamics in charge transfer complexes of the type iodine-pyridine 1. Experimental results.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Tassaing%2C+T%2E%22">Tassaing, T.</searchLink><br /><searchLink fieldCode="AR" term="%22Besnard%2C+M%22">Besnard, M</searchLink><br /><searchLink fieldCode="AR" term="%22Rwood%2C+J%2E+Ya%22">Rwood, J. Ya</searchLink>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Molecular+Physics%22">Molecular Physics</searchLink>. 10/10/97, Vol. 92 Issue 2, p271-280. 10p.
– Name: Subject
  Label: Subjects
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Pyridine%22">Pyridine</searchLink><br /><searchLink fieldCode="DE" term="%22Iodine%22">Iodine</searchLink><br /><searchLink fieldCode="DE" term="%22Raman+effect%22">Raman effect</searchLink><br /><searchLink fieldCode="DE" term="%22Electron+donor-acceptor+complexes%22">Electron donor-acceptor complexes</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: The far infrared and Raman spectra of the pyridine-I complex in solution in non-polar solvents have been investigated as functions of base concentration and temperature. Attempts have been made to assess the relative contribution of donor-acceptor and classical dipolar interactions to the spectral changes which occur with increasing medium polarity, temperature or donor strength (via the use of picolines as donors). It has been found that the overall evolution of band position, width and intensity is dependent mostly on the medium polarity, reflecting changes in complex stability induced by the surrounding dipoles. However, the irreversible appearance of the I anion seems to be associated with an increase in donor strength. Local dipole ordering, as a function of temperature lowering, clearly also is important for stabilizing the complex. 2 3. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Molecular Physics is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=egs&AN=7612932
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1080/002689797170464
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 10
        StartPage: 271
    Subjects:
      – SubjectFull: Pyridine
        Type: general
      – SubjectFull: Iodine
        Type: general
      – SubjectFull: Raman effect
        Type: general
      – SubjectFull: Electron donor-acceptor complexes
        Type: general
    Titles:
      – TitleFull: Vibrational spectroscopic studies of the chemical dynamics in charge transfer complexes of the type iodine-pyridine 1. Experimental results.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Tassaing, T.
      – PersonEntity:
          Name:
            NameFull: Besnard, M
      – PersonEntity:
          Name:
            NameFull: Rwood, J. Ya
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 10
              M: 10
              Text: 10/10/97
              Type: published
              Y: 1997
          Identifiers:
            – Type: issn-print
              Value: 00268976
          Numbering:
            – Type: volume
              Value: 92
            – Type: issue
              Value: 2
          Titles:
            – TitleFull: Molecular Physics
              Type: main
ResultId 1