Please use this identifier to cite or link to this item:
http://hdl.handle.net/10261/19106
Share/Export:
SHARE CORE BASE | |
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |
Title: | Reactivity of the Pyrazolatopalladium(II) complexes [Pd(dmpz)2(Hdmpz)2] and [Pd2(-dmpz)2(dmpz)2(Hdmpz)2] towards carboxylic acids: Hydrogen bonds as the driving force that determines the nature of the final products |
Authors: | Ara, Irene CSIC; Forniés, Juan CSIC; Lasheras, Roberto; Martín, Antonio CSIC ORCID; Sicilia, Violeta CSIC ORCID | Keywords: | Carboxylate ligands Heterometallic complexes Hydrogen bonds N ligands Palladium |
Issue Date: | 10-Jan-2006 | Publisher: | Wiley-Blackwell | Citation: | European Journal of Inorganic Chemistry 2006(5): 948-957 (2006) | Abstract: | The compound [Pd(Hdmpz)4](O2CCH2NHCOCH3)2 (1; (Hdmpz = 3,5-dimethylpyrazole) has been obtained by treatment of [Pd(dmpz)2(Hdmpz)2] (A) with two equivalents of N-acetylglycine (HO2CCH2NHCOCH3). The X-ray study on a crystal of 1 revealed that the N-acetylglycinate anion links to the cationic complex [Pd(Hdmpz)4]2+ through the carboxylate group by charge assisted N-H(+)···O(-) hydrogen bonds. Additionally, the remaining N-H and C=O groups allow the N-acetylglycinate anions to self-assemble through N-H···O hydrogen bonds to generate infinite chains. The compounds [Pd2(-dmpz)2(O2CCH2NHCOCH3-O)2(Hdmpz)2] (2) and [Pd2(-dmpz)2(O2CC6H4-R-O)2(Hdmpz)2] [R = m-NO2 (3a), p-N(CH3)2 (3b), p-NH2 (3c), p-OCH3 (3d), p-OH (3e)] have been obtained by treatment of [Pd2(-dmpz)2(dmpz)2(Hdmpz)2] (B) with two equivalents of the monocarboxylic acids N-acetylglycine (HO2CCH2NHCOCH3) and the benzoic derivatives HO2CC6H4R [R = m-NO2, p-N(CH3)2, p-NH2, p-OCH3, p-OH] respectively. The X-ray study on complexes 3d and 3e shows that in these complexes the carboxylate anion bonded to one Pd atom and the terminal Hdmpz group bonded to the other one have the right arrangement to establish an N-H···O hydrogen bond. The H···O and N···O distances are in the range of those corresponding to charge-assisted N-H(+)···O(-) interactions. In complexes 3a-3e, the H atoms of the terminal Hdmpz groups can be replaced by Ag+ to give the mixed-metal complexes [Pd2Ag2(-dmpz)4(-O2CC6H4-R-O)2(Hdmpz)2] [R = m-NO2 (4a), p-N(CH3)2 (4b), p-NH2 (4c), p-OCH3 (4d), p-OH (4e)]. Compounds 4a-4e, which exhibit a transoid conformation of the carboxylate groups with respect to the Pd···Pd line, isomerise to the cisoid species (4a-4e). The X-ray structure of the DMSO adduct of 4d is also reported. | Description: | 10 pages, 5 tables, 6 figures, 3 schemes. | Publisher version (URL): | http://dx.doi.org/10.1002/ejic.200500791 | URI: | http://hdl.handle.net/10261/19106 | DOI: | 10.1002/ejic.200500791 | ISSN: | 1434-1948 | E-ISSN: | 1099-0682 |
Appears in Collections: | (ICMA) Artículos |
Show full item record
CORE Recommender
SCOPUSTM
Citations
23
checked on Mar 13, 2024
WEB OF SCIENCETM
Citations
24
checked on Feb 24, 2024
Page view(s)
294
checked on Mar 18, 2024
Google ScholarTM
Check
Altmetric
Altmetric
WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.