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Design, Synthesis, Characterization of Novel Ruthenium(II) Catalysts: Highly Efficient and Selective Hydrogenation of Cinnamaldehyde to (E)-3-Phenylprop-2-en-1-ol
In this contribution, two novel supported and non-supported ruthenium(II) complexes of type [RuCl(2)(dppme)(NN)] where [dppme is H(2)C=C(CH(2)PPh(2))(2) and NN is N1-(3-(trimethoxysilyl)propyl)ethane-1,2-diamine] were prepared. The NN co-ligand caused release of one of the dppme ligands from [RuCl(2...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271071/ https://www.ncbi.nlm.nih.gov/pubmed/24818576 http://dx.doi.org/10.3390/molecules19055965 |
Sumario: | In this contribution, two novel supported and non-supported ruthenium(II) complexes of type [RuCl(2)(dppme)(NN)] where [dppme is H(2)C=C(CH(2)PPh(2))(2) and NN is N1-(3-(trimethoxysilyl)propyl)ethane-1,2-diamine] were prepared. The NN co-ligand caused release of one of the dppme ligands from [RuCl(2)(dppme)(2)] precursor to yield complex 1. The process of substitution of dppme by NN was monitored by (31)P{(1)H}-NMR. Taking advantage of the presence of trimethoxysilane group in the backbone of complex 1, polysiloxane xerogel counterpart, X1, was prepared via sol-gel immobilization using tetraethoxysilane as cross-linker. Both complexes 1 and X1 have been characterized via elemental analysis, CV and a number of spectroscopic techniques including FT-IR, (1)H-, (13)C-, and (31)P-NMR, and mass spectrometry. Importantly, carbonyl selective hydrogenation was successfully accomplished under mild conditions using complex 1 as a homogenous catalyst and X1 as a heterogeneous catalyst, respectively. |
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