The unexpected formation of a mixed bis(η 5-pentamethylcyclopentadienyl)tetracarbonyl(μ 3-ethylidene)triangulotricobalt compound and its structural characterization
The title compound was first obtained photolytically from (η 5-Me 5C 5)Co(CO) 2 (by a mechanism not understood) and later by refluxing C 5Me 5H with Co 3(CO) 9CCH 3. It was identified and characterized structurally by X-ray crystallography. The crystals belong to space group P2 1/n with a 9.529(2),...
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Published in | Journal of organometallic chemistry Vol. 173; no. 3; pp. 317 - 324 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.01.1979
|
Online Access | Get full text |
ISSN | 0022-328X 1872-8561 |
DOI | 10.1016/S0022-328X(00)84786-5 |
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Abstract | The title compound was first obtained photolytically from (η
5-Me
5C
5)Co(CO)
2 (by a mechanism not understood) and later by refluxing C
5Me
5H with Co
3(CO)
9CCH
3. It was identified and characterized structurally by X-ray crystallography. The crystals belong to space group
P2
1/n with
a 9.529(2),
b 18.325(4),
c 14.801(3) Å, β 95.69(2)° with
Z = 4, making one entire molecule the asymmetric unit. Using 2641 reflections with F
0
2 > 3σ (F
0
2 the structure was solved and refined to R
1 = 0.051 and R
2 = 0.067. It consists of a triangular pyramid with two (η
5-C
5Me
5)Co groups and one Co(CO)
3 group in the base and CCH
3 at the apex. The basal edge between the (η
5-C
5Me
5)Co groups has a bridging CO group and a Co—Co distance of 2.405(1) Å, while the other two unbridged Co—Co distances are 2.484(1) and 2.501(1) Å. The distances from the apical C atom to the bridged Co atoms are 1.857(6) and 1.866(6) but 1.932(6) Å to the unique Co atom. The C—C distance in the ethylidyne group is 1.497(9) Å. The structure is closely similar to that of the analogous (η
5-C
5H
5)
2Co
3(CO)
4CCH
3 compound. |
---|---|
AbstractList | The title compound was first obtained photolytically from (η
5-Me
5C
5)Co(CO)
2 (by a mechanism not understood) and later by refluxing C
5Me
5H with Co
3(CO)
9CCH
3. It was identified and characterized structurally by X-ray crystallography. The crystals belong to space group
P2
1/n with
a 9.529(2),
b 18.325(4),
c 14.801(3) Å, β 95.69(2)° with
Z = 4, making one entire molecule the asymmetric unit. Using 2641 reflections with F
0
2 > 3σ (F
0
2 the structure was solved and refined to R
1 = 0.051 and R
2 = 0.067. It consists of a triangular pyramid with two (η
5-C
5Me
5)Co groups and one Co(CO)
3 group in the base and CCH
3 at the apex. The basal edge between the (η
5-C
5Me
5)Co groups has a bridging CO group and a Co—Co distance of 2.405(1) Å, while the other two unbridged Co—Co distances are 2.484(1) and 2.501(1) Å. The distances from the apical C atom to the bridged Co atoms are 1.857(6) and 1.866(6) but 1.932(6) Å to the unique Co atom. The C—C distance in the ethylidyne group is 1.497(9) Å. The structure is closely similar to that of the analogous (η
5-C
5H
5)
2Co
3(CO)
4CCH
3 compound. |
Author | Bailey, Webb I. Cotton, F.Albert Jamerson, Jackie D. |
Author_xml | – sequence: 1 givenname: Webb I. surname: Bailey fullname: Bailey, Webb I. – sequence: 2 givenname: F.Albert surname: Cotton fullname: Cotton, F.Albert – sequence: 3 givenname: Jackie D. surname: Jamerson fullname: Jamerson, Jackie D. |
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Cites_doi | 10.1021/ic50156a046 10.1016/S0022-328X(00)95110-6 10.1039/dt9750001771 10.1107/S0567740878006342 10.1063/1.1674266 10.1021/ja01557a018 |
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References | Cromer, Liberman (BIB8) 1970; 53 Elder, Robinson, Simpson (BIB1) 1975 Markby, Wender, Friedel, Cotton, Sternberg (BIB4) 1958; 80 McCallum, Penfold (BIB2) 1978; B34 Cotton, Frenz, Deganello, Shaver (BIB5) 1973; 50 Cromer, Waber (BIB7) 1974; IV Feitler, Whitesides (BIB3) 1976; 15 The initial work was performed on an Amdahl 470 computer using the followins programs: DATARED, a data reduction program by Frenz; FAME, by Dewar for generating E's; MULTAN, by Main, Woolfson, and Germain for direct methods; FOURIER, a crystallographic summation program by Dellaca and Robinson based on Zalkin's FORDAP; NUCLS, a least-squares program by Ibers and Doedens: and SADIAN, program for calculating atomic distances and angles by Baur. The final refinement of the structure and the production of the derived results were done using the Molecular Structure Corporation PDP-11/45 computer and the Enraf-Nonius Structure Determination Package with programs written chiefly by Frenz and Okaya. McCallum (10.1016/S0022-328X(00)84786-5_BIB2) 1978; B34 Elder (10.1016/S0022-328X(00)84786-5_BIB1) 1975 10.1016/S0022-328X(00)84786-5_BIB6 Cotton (10.1016/S0022-328X(00)84786-5_BIB5) 1973; 50 Cromer (10.1016/S0022-328X(00)84786-5_BIB7) 1974; IV Markby (10.1016/S0022-328X(00)84786-5_BIB4) 1958; 80 Cromer (10.1016/S0022-328X(00)84786-5_BIB8) 1970; 53 Feitler (10.1016/S0022-328X(00)84786-5_BIB3) 1976; 15 |
References_xml | – volume: 15 start-page: 466 year: 1976 ident: BIB3 publication-title: Inorg. Chem. – start-page: 1771 year: 1975 ident: BIB1 publication-title: J. Chem. Soc. Dalton – reference: The initial work was performed on an Amdahl 470 computer using the followins programs: DATARED, a data reduction program by Frenz; FAME, by Dewar for generating E's; MULTAN, by Main, Woolfson, and Germain for direct methods; FOURIER, a crystallographic summation program by Dellaca and Robinson based on Zalkin's FORDAP; NUCLS, a least-squares program by Ibers and Doedens: and SADIAN, program for calculating atomic distances and angles by Baur. The final refinement of the structure and the production of the derived results were done using the Molecular Structure Corporation PDP-11/45 computer and the Enraf-Nonius Structure Determination Package with programs written chiefly by Frenz and Okaya. – volume: IV year: 1974 ident: BIB7 publication-title: International Tables for X-Ray Crystallography – volume: 53 start-page: 1891 year: 1970 ident: BIB8 publication-title: J. Chem. Phys. – volume: 80 start-page: 529 year: 1958 ident: BIB4 publication-title: J. Amer. Chem. Soc. – volume: 50 start-page: 227 year: 1973 ident: BIB5 publication-title: J. Organometal. Chem. – volume: B34 start-page: 1688 year: 1978 ident: BIB2 publication-title: Acta Cryst. – ident: 10.1016/S0022-328X(00)84786-5_BIB6 – volume: 15 start-page: 466 year: 1976 ident: 10.1016/S0022-328X(00)84786-5_BIB3 publication-title: Inorg. Chem. doi: 10.1021/ic50156a046 – volume: 50 start-page: 227 year: 1973 ident: 10.1016/S0022-328X(00)84786-5_BIB5 publication-title: J. Organometal. Chem. doi: 10.1016/S0022-328X(00)95110-6 – start-page: 1771 year: 1975 ident: 10.1016/S0022-328X(00)84786-5_BIB1 publication-title: J. Chem. Soc. Dalton doi: 10.1039/dt9750001771 – volume: B34 start-page: 1688 year: 1978 ident: 10.1016/S0022-328X(00)84786-5_BIB2 publication-title: Acta Cryst. doi: 10.1107/S0567740878006342 – volume: 53 start-page: 1891 year: 1970 ident: 10.1016/S0022-328X(00)84786-5_BIB8 publication-title: J. Chem. Phys. doi: 10.1063/1.1674266 – volume: 80 start-page: 529 year: 1958 ident: 10.1016/S0022-328X(00)84786-5_BIB4 publication-title: J. Amer. Chem. Soc. doi: 10.1021/ja01557a018 – volume: IV year: 1974 ident: 10.1016/S0022-328X(00)84786-5_BIB7 |
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Snippet | The title compound was first obtained photolytically from (η
5-Me
5C
5)Co(CO)
2 (by a mechanism not understood) and later by refluxing C
5Me
5H with Co
3(CO)... |
SourceID | crossref elsevier |
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StartPage | 317 |
Title | The unexpected formation of a mixed bis(η 5-pentamethylcyclopentadienyl)tetracarbonyl(μ 3-ethylidene)triangulotricobalt compound and its structural characterization |
URI | https://dx.doi.org/10.1016/S0022-328X(00)84786-5 |
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