1979
DOI: 10.1021/ic50197a015
|View full text |Cite
|
Sign up to set email alerts
|

Thermal intramolecular cobalt(III)-iron(II) and cobalt(III)-titanium(III) electron-transfer reactions involving outer-sphere and inner-sphere precursor complexes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0
1

Year Published

1979
1979
2005
2005

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 12 publications
(3 citation statements)
references
References 10 publications
0
2
0
1
Order By: Relevance
“…Arguments for and against the involvement of the peripheral moieties, such as the carboxylates of TCPP complexes, in electron-transfer reactions have been put forth. There are significant precedents for OH and other groups to act as bridging ligands for electron transfer with Ti III and Cr II as the reducing agents. We, currently, do not favor an inner-sphere pathway involving the peripheral carboxylates. Evidence against a peripheral inner-sphere mechanism comes from the pH dependence data (where no dehalogenation was observed despite the presence of free carboxylates) and dehalogenation experiments using Cr II as the bulk electron source.…”
Section: Discussionmentioning
confidence: 99%
“…Arguments for and against the involvement of the peripheral moieties, such as the carboxylates of TCPP complexes, in electron-transfer reactions have been put forth. There are significant precedents for OH and other groups to act as bridging ligands for electron transfer with Ti III and Cr II as the reducing agents. We, currently, do not favor an inner-sphere pathway involving the peripheral carboxylates. Evidence against a peripheral inner-sphere mechanism comes from the pH dependence data (where no dehalogenation was observed despite the presence of free carboxylates) and dehalogenation experiments using Cr II as the bulk electron source.…”
Section: Discussionmentioning
confidence: 99%
“…Much is known on the preparation, crystalline structure, and properties of the Cu(II) [5][6][7][8], Fe(II) [9], Fe(III) [9][10][11][12], Mn(II) [6,13], Mn(III) [14,15], Ag(I) [1,16], Co(II) [5,6], Co(III) [17], Pt(II) [18], Ti(III) [19], Ni(II) [5,6], and Zn(II) [5,6] complexes. The metal-to-ligand stoichiometry 1:1 was found for complexes of Cu(II) [8] and Fe(II) [9], dinuclear and polymeric complexes were determined in the case of Ag(I) complexes [1,16], whereas 1:2 complexes were observed for Cu(II) [5][6][7], Fe(II) and Fe(III) [9][10][11][12], Mn(II) and Mn(III) [6,[13][14][15], Co(II) and Co(III) [5,6,17], Pt(II) [18], Ti(III) [19], Ni(II) [5,6], and Zn(II) [5,…”
Section: Introductionmentioning
confidence: 99%
“…Ti[21], Cr[13], Mn[ll, 221, Fe[lO], Co[9], Rh[23] bzw. Ru[16] sind in wal3riger Losung hervorragend stabil.…”
unclassified