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The coordination chemistry of thioet...

DuPont, Julie A.

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The coordination chemistry of thioether-supported, low-valent cobalt complexes.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	The coordination chemistry of thioether-supported, low-valent cobalt complexes./
作者:	DuPont, Julie A.
面頁冊數:	165 p.
附註:	Source: Dissertation Abstracts International, Volume: 66-12, Section: B, page: 6610.
Contained By:	Dissertation Abstracts International66-12B.
標題:	Chemistry, Inorganic. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3200521
ISBN:	9780542449864

The coordination chemistry of thioether-supported, low-valent cobalt complexes.
DuPont, Julie A.

The coordination chemistry of thioether-supported, low-valent cobalt complexes. - 165 p.

Source: Dissertation Abstracts International, Volume: 66-12, Section: B, page: 6610.

Thesis (Ph.D.)--University of Delaware, 2006.

The tridentate S3- donor ligand, phenyltris((tert-butylthio)methyl)borate, [PhTttBu]-, has been used to investigate the coordination chemistry of cobalt. A series of coordinatively and electronically unsaturated organocobalt(II) complexes [PhTttBu]Co(R) (R = CH3, CH2CH3, C6H5, CH2C6H5, C3H5) was synthesized through reaction of the starting material [PhTttBu]COCl, with the appropriate Grignard reagent. The resultant pseudotetrahedral complexes (allyl derivative is square pyramidal) proved to be both air and moisture sensitive. The complexes were characterized spectroscopically and crystal lographically. The small molecule reactivity of these complexes was assayed through reactions with CO and NO. The former reagent showed sensitivity to the identity of the organocobalt while the latter gave rise to the same product, regardless of the organic ligand. When R = CH3, CH2CH 3, C6H5, reaction of [PhTttBu]Co(R) with CO yielded red, five-coordinate [PhTttBu]Co(CO)(C(O)R). These square-pyramidal complexes contain apical thioether ligation with the remaining four ligands in the basal plane. Alternatively, when R = CH 2C6H5, C3H5, reaction with CO resulted in Co-C bond homolysis with formation of the brown Co(I) complex, [PhTtBu]Co(CO)2. In all cases, reaction of the organocobalt(II) complexes with NO resulted in the formation of the kappa2-dinitrosyl complex, [kappa2-PhTttBu]Co(NO)2. These results were confirmed both spectroscopically and crystallographically.

ISBN: 9780542449864Subjects--Topical Terms:

517253
Chemistry, Inorganic.

The coordination chemistry of thioether-supported, low-valent cobalt complexes.
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245 1 4 $a The coordination chemistry of thioether-supported, low-valent cobalt complexes.
300 $a 165 p.
500 $a Source: Dissertation Abstracts International, Volume: 66-12, Section: B, page: 6610.
500 $a Adviser: Charles G. Riordan.
502 $a Thesis (Ph.D.)--University of Delaware, 2006.
520 $a The tridentate S3- donor ligand, phenyltris((tert-butylthio)methyl)borate, [PhTttBu]-, has been used to investigate the coordination chemistry of cobalt. A series of coordinatively and electronically unsaturated organocobalt(II) complexes [PhTttBu]Co(R) (R = CH3, CH2CH3, C6H5, CH2C6H5, C3H5) was synthesized through reaction of the starting material [PhTttBu]COCl, with the appropriate Grignard reagent. The resultant pseudotetrahedral complexes (allyl derivative is square pyramidal) proved to be both air and moisture sensitive. The complexes were characterized spectroscopically and crystal lographically. The small molecule reactivity of these complexes was assayed through reactions with CO and NO. The former reagent showed sensitivity to the identity of the organocobalt while the latter gave rise to the same product, regardless of the organic ligand. When R = CH3, CH2CH 3, C6H5, reaction of [PhTttBu]Co(R) with CO yielded red, five-coordinate [PhTttBu]Co(CO)(C(O)R). These square-pyramidal complexes contain apical thioether ligation with the remaining four ligands in the basal plane. Alternatively, when R = CH 2C6H5, C3H5, reaction with CO resulted in Co-C bond homolysis with formation of the brown Co(I) complex, [PhTtBu]Co(CO)2. In all cases, reaction of the organocobalt(II) complexes with NO resulted in the formation of the kappa2-dinitrosyl complex, [kappa2-PhTttBu]Co(NO)2. These results were confirmed both spectroscopically and crystallographically.
520 $a A series of cobalt(I) phosphine complexes, [PhTttBu ]Co(PR3), PR3 = PMe3, PEt3, PMe2Ph, PMePh2, PPh3, P(OPh3), was prepared by reduction of [PhTttBu]COCl in the presence of the phosphine. These four-coordinate complexes were characterized spectroscopically and crystal lographically. The structures may be grouped into two classes, pseudo-tetrahedral and cis-divacant (i.e. an octahedron where two cis ligands have been removed, alpha = 54.7° for this complex; aalpha is the degree to which L lies off of the linear vector). The former class, for which PR 3 = PMe3, PEt3, PMe2Ph, the phosphine donor resides approximately on the B...Co vector. The latter class, for which PR3 = PMePh2, PPh3, P(OPh) 3, the phosphine is significantly "off-axis." These complexes exhibited varying a angles allowing for insight into the structural choice of the complex based on the sigma-donating and pi-accepting properties of the phosphine donor.
520 $a The cobalt and nickel isocyanide complexes, [PhTttBu]M(CNBu t) are readily alkylated with MeI, leading to the corresponding cationic iminoacyl complexes, {[PhTttBu]M(C(Me)NBut)}I.
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