Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V)
Autor(a) principal: | |
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Data de Publicação: | 1982 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFBA |
Texto Completo: | http://www.repositorio.ufba.br/ri/handle/ri/8632 |
Resumo: | p. 3310 - 3316 |
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Giacomelli, AmbrogioFloriani, CarloDuarte, Adalcindo Ofir de SouzaChiesi-Villa, AngiolaGuastini, CarloGiacomelli, AmbrogioFloriani, CarloDuarte, Adalcindo Ofir de SouzaChiesi-Villa, AngiolaGuastini, Carlo2013-02-21T19:00:04Z2013-02-21T19:00:04Z19820020-1669http://www.repositorio.ufba.br/ri/handle/ri/8632v. 21, n. 9p. 3310 - 3316Basic hydrolysis, under mild conditions, of (~-oxo)bis[bis(8-quinolinato)oxovanadium(V)], [(Q2VO)20]( Q = 8-quinolinato anion), obtained by a one-step synthesis, gave a dioxovanadium(V) complex, [Q2V02]-, containing the V02- unit. The structure of this anionic species was determined by an X-ray analysis carried out on the corresponding salts ( [Q2V02Na(H20)2]2(pDMF)()V I) and ([Q2V02(]n -Bu4N).H201( VII). The VQ2 unit has similar structural characteristics in both complexes, with the two N donor atoms trans to the oxo groups, which have a cis configuration. The V-N bonds, as a consequence, have the longest distances so far encountered (V-Na, = 2.33 A). Complex VI is a dimer, where two V02 units are bridged by two Na' ions sharing the oxygen of a DMF molecule. In complex VI1 the oxygen is only weakly bonded to a H20 molecule, via hydrogen bonding. In both complexes the structural data concerning the V02 units are very close, with a V-0-V angle varying from 105.7 (2)' in complex VI to 106.1 (5)' in com lex VII, while the V-0 bond distances have a double-bond character [1.647 (4) and 1.628 (2) 8, in complex VI; 1.62 (1) 1in complex VII]. The 0-0 bite values are 2.610 (4) A (complex VI) and 2.58 (1) A (complex VII). These results invite comparison of the V02- unit with the carboxylato group RCOC. The relationship between other vanadium(V) derivatives and organic functional groups related to a carboxylic acid is reported. The inorganic analogue of a carboxylic acid itself is obtained on acidifying an aqueous solution of [Q2VOz]-. [QzV(O)(OH)], which is a very well-known analytical reagent for organic compounds, was found to be a weak acid with a pKA of 6.3. Crystallographic details for ([Q2V02Na(H20)2]2(p-DMF)}:s pace group Pbcn (orthorhombic); a = 30.245 (2), b = 9.744 (l), c = 14.167 (1) A; V = 4175.1 A,; Z = 4. The final R factor was 4.7% for 2867 observed data. Crystallographic details for ( [QzV02](n-Bu4N).H20]}: space group Z42d (tetragonal); a = b = 19.04 (3), c = 19.486 (3) A; V = 7064.1 .A3; Z = 8. The final R factor was 5.9% for 568 observed data.Submitted by Santiago Fabio (fabio.ssantiago@hotmail.com) on 2013-02-21T19:00:04Z No. of bitstreams: 1 11111.pdf: 804308 bytes, checksum: 79a3cd0b62464cf1096d8b844774c208 (MD5)Made available in DSpace on 2013-02-21T19:00:04Z (GMT). No. of bitstreams: 1 11111.pdf: 804308 bytes, checksum: 79a3cd0b62464cf1096d8b844774c208 (MD5) Previous issue date: 1982SalvadorInorganic Chemistry10.1021/ic00139a012reponame:Repositório Institucional da UFBAinstname:Universidade Federal da Bahia (UFBA)instacron:UFBAChemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V)Inorganic Chemistryinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleenginfo:eu-repo/semantics/openAccessORIGINAL11111.pdf11111.pdfapplication/pdf804308https://repositorio.ufba.br/bitstream/ri/8632/1/11111.pdf79a3cd0b62464cf1096d8b844774c208MD51LICENSElicense.txtlicense.txttext/plain1762https://repositorio.ufba.br/bitstream/ri/8632/2/license.txt1b89a9a0548218172d7c829f87a0eab9MD52TEXT11111.pdf.txt11111.pdf.txtExtracted texttext/plain7https://repositorio.ufba.br/bitstream/ri/8632/3/11111.pdf.txt212b0306580d4f0044d18f9a3edcc832MD53ri/86322022-07-05 14:04:14.227oai:repositorio.ufba.br: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Repositório InstitucionalPUBhttp://192.188.11.11:8080/oai/requestopendoar:19322022-07-05T17:04:14Repositório Institucional da UFBA - Universidade Federal da Bahia (UFBA)false |
dc.title.pt_BR.fl_str_mv |
Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V) |
dc.title.alternative.pt_BR.fl_str_mv |
Inorganic Chemistry |
title |
Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V) |
spellingShingle |
Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V) Giacomelli, Ambrogio |
title_short |
Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V) |
title_full |
Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V) |
title_fullStr |
Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V) |
title_full_unstemmed |
Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V) |
title_sort |
Chemistry and Structure of an Inorganic Analogue of a Carboxylic Acid: Hydroxobis (8-quinolinato) oxovanadium (V) |
author |
Giacomelli, Ambrogio |
author_facet |
Giacomelli, Ambrogio Floriani, Carlo Duarte, Adalcindo Ofir de Souza Chiesi-Villa, Angiola Guastini, Carlo |
author_role |
author |
author2 |
Floriani, Carlo Duarte, Adalcindo Ofir de Souza Chiesi-Villa, Angiola Guastini, Carlo |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Giacomelli, Ambrogio Floriani, Carlo Duarte, Adalcindo Ofir de Souza Chiesi-Villa, Angiola Guastini, Carlo Giacomelli, Ambrogio Floriani, Carlo Duarte, Adalcindo Ofir de Souza Chiesi-Villa, Angiola Guastini, Carlo |
description |
p. 3310 - 3316 |
publishDate |
1982 |
dc.date.issued.fl_str_mv |
1982 |
dc.date.accessioned.fl_str_mv |
2013-02-21T19:00:04Z |
dc.date.available.fl_str_mv |
2013-02-21T19:00:04Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://www.repositorio.ufba.br/ri/handle/ri/8632 |
dc.identifier.issn.none.fl_str_mv |
0020-1669 |
dc.identifier.number.pt_BR.fl_str_mv |
v. 21, n. 9 |
identifier_str_mv |
0020-1669 v. 21, n. 9 |
url |
http://www.repositorio.ufba.br/ri/handle/ri/8632 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Inorganic Chemistry |
publisher.none.fl_str_mv |
Inorganic Chemistry |
dc.source.pt_BR.fl_str_mv |
10.1021/ic00139a012 |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFBA instname:Universidade Federal da Bahia (UFBA) instacron:UFBA |
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Universidade Federal da Bahia (UFBA) |
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UFBA |
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UFBA |
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Repositório Institucional da UFBA |
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Repositório Institucional da UFBA |
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