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Article: Synthesis, electrochemistry and X-ray crystal structure of cis-[RuIIIL1(Cl)(H2O)][ClO4] 2·2H2O [L1 = N,N′-dimethyl- N,N′-bis(2-pyridylmethyl)ethylenediamine]; Electrochemical oxidation of alcohols and tetrahydrofuran by cis-[RuVL1(Cl)O]2+
Title | Synthesis, electrochemistry and X-ray crystal structure of cis-[RuIIIL1(Cl)(H2O)][ClO4] 2·2H2O [L1 = N,N′-dimethyl- N,N′-bis(2-pyridylmethyl)ethylenediamine]; Electrochemical oxidation of alcohols and tetrahydrofuran by cis-[RuVL1(Cl)O]2+ |
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Authors | |
Issue Date | 1991 |
Publisher | Royal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/dalton |
Citation | Journal Of The Chemical Society, Dalton Transactions, 1991 n. 8, p. 1909-1914 How to Cite? |
Abstract | Reaction of K2[RuCl5(H2O)] with N,N′-dimethyl-N,N′-bis(2-pyridylmethyl)ethylenediamine (L1) in ethanol gave cis-[RuIIIL1Cl2]+ and then cis-[RuIIIL1(Cl)(H2O)]2+ upon reaction with AgI in water. The structure of cis-[RuIIIL1(Cl)(H2O)][ClO4] 2·2H2O has been established by X-ray crystallography: space group Pbca, a = 10.863(1), b = 21.548(2), c = 21.912(2) Å. The measured Ru-Cl and Ru-OH2 distances are 2.307(4) Å and 2.070(9) Å respectively. A cyclic voltammogram of cis- [RuIIIL1(Cl)-(H2O)]2+ in 0.1 mol dm-3 CF3CO2H shows three reversible/quasi-reversible couples at 1.29, 0.93 and 0.23 V vs. saturated calomel electrode assigned to the couples RuV-RuIV, RuIV-RuIII and RuIII-RuII. The complex cis-[RuIIIL1(Cl)(H2O)]2+ is an active catalyst for the electrochemical oxidation of alcohols and tetrahydrofuran. The second-order rate constant for the oxidation of benzyl alcohol by electrochemically generated cis-[RuVL1(Cl)O]2+ is estimated to be 8.4 × 104 dm3 mol-1 s-1. |
Persistent Identifier | http://hdl.handle.net/10722/168193 |
ISSN | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Li, CK | en_US |
dc.contributor.author | Tang, WT | en_US |
dc.contributor.author | Che, CM | en_US |
dc.contributor.author | Wong, KY | en_US |
dc.contributor.author | Wang, RJ | en_US |
dc.contributor.author | Mak, TCW | en_US |
dc.date.accessioned | 2012-10-08T03:16:09Z | - |
dc.date.available | 2012-10-08T03:16:09Z | - |
dc.date.issued | 1991 | en_US |
dc.identifier.citation | Journal Of The Chemical Society, Dalton Transactions, 1991 n. 8, p. 1909-1914 | en_US |
dc.identifier.issn | 1472-7773 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168193 | - |
dc.description.abstract | Reaction of K2[RuCl5(H2O)] with N,N′-dimethyl-N,N′-bis(2-pyridylmethyl)ethylenediamine (L1) in ethanol gave cis-[RuIIIL1Cl2]+ and then cis-[RuIIIL1(Cl)(H2O)]2+ upon reaction with AgI in water. The structure of cis-[RuIIIL1(Cl)(H2O)][ClO4] 2·2H2O has been established by X-ray crystallography: space group Pbca, a = 10.863(1), b = 21.548(2), c = 21.912(2) Å. The measured Ru-Cl and Ru-OH2 distances are 2.307(4) Å and 2.070(9) Å respectively. A cyclic voltammogram of cis- [RuIIIL1(Cl)-(H2O)]2+ in 0.1 mol dm-3 CF3CO2H shows three reversible/quasi-reversible couples at 1.29, 0.93 and 0.23 V vs. saturated calomel electrode assigned to the couples RuV-RuIV, RuIV-RuIII and RuIII-RuII. The complex cis-[RuIIIL1(Cl)(H2O)]2+ is an active catalyst for the electrochemical oxidation of alcohols and tetrahydrofuran. The second-order rate constant for the oxidation of benzyl alcohol by electrochemically generated cis-[RuVL1(Cl)O]2+ is estimated to be 8.4 × 104 dm3 mol-1 s-1. | en_US |
dc.language | eng | en_US |
dc.publisher | Royal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/dalton | en_US |
dc.relation.ispartof | Journal of the Chemical Society, Dalton Transactions | en_US |
dc.title | Synthesis, electrochemistry and X-ray crystal structure of cis-[RuIIIL1(Cl)(H2O)][ClO4] 2·2H2O [L1 = N,N′-dimethyl- N,N′-bis(2-pyridylmethyl)ethylenediamine]; Electrochemical oxidation of alcohols and tetrahydrofuran by cis-[RuVL1(Cl)O]2+ | en_US |
dc.type | Article | en_US |
dc.identifier.email | Che, CM:cmche@hku.hk | en_US |
dc.identifier.authority | Che, CM=rp00670 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1039/DT9910001909 | en_US |
dc.identifier.scopus | eid_2-s2.0-37049073381 | en_US |
dc.identifier.issue | 8 | en_US |
dc.identifier.spage | 1909 | en_US |
dc.identifier.epage | 1914 | en_US |
dc.identifier.isi | WOS:A1991GB33400009 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Li, CK=8714186500 | en_US |
dc.identifier.scopusauthorid | Tang, WT=15121154000 | en_US |
dc.identifier.scopusauthorid | Che, CM=7102442791 | en_US |
dc.identifier.scopusauthorid | Wong, KY=7404760030 | en_US |
dc.identifier.scopusauthorid | Wang, RJ=7405340385 | en_US |
dc.identifier.scopusauthorid | Mak, TCW=7401931058 | en_US |
dc.identifier.issnl | 1364-5447 | - |