Viológeno (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Viológeno" in Spanish language version.

refsWebsite

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9doi.org

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2nih.gov

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1iupac.org

538^th place

297^th place

1sciencedirect.com

149^th place

128^th place

1issn.org

57^th place

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doi.org

dx.doi.org

Bockman T. M.; Kochi J. K. (1990). «Isolation and oxidation-reduction of methylviologen cation radicals. Novel disproportionation in charge-transfer salts by X-ray crystallography». J. Org. Chem. 55 (13): 4127-4135. doi:10.1021/jo00300a033.
Mortimer, R. J. Electrochromic Materials 41. pp. 241-268. doi:10.1146/annurev-matsci-062910-100344.
Bravo, José A.; Raymo, Françisco M.; Stoddart, J. Fraser; White, Andrew J. P.; Williams, David J. (1998). «High Yielding Template-Directed Syntheses of [2]Rotaxanes». Eur. J. Org. Chem. 1998 (11): 2565-2571. doi:10.1002/(SICI)1099-0690(199811)1998:11<2565::AID-EJOC2565>3.0.CO;2-8.
Burgess, Mark; Moore, Jeffrey S.; Rodriguez-Lopez, Joaquin (2016), «Redox Active Polymers as Soluble Nanomaterials for Energy Storage», Accounts of Chemical Research 49: 2649-2657, doi:10.1021/acs.accounts.6b00341 .
Dean R. Wheeler; Joseph Nichols; Dane Hansen; Merritt Andrus; Sang Choi; Gerald D. Watt (2009). «Viologen Catalysts for a Direct Carbohydrate Fuel Cell». J. Electrochem. Soc. 156 (10): B1201-B1207. doi:10.1149/1.3183815.
W. W. Porter, T. P. Vaid and A. L. Rheingold (2005). «Synthesis and Characterization of a Highly Reducing Neutral "Extended Viologen" and the Isostructural Hydrocarbon 4,4' '-Di-n-octyl-p-quaterphenyl». J. Am. Chem. Soc. 127 (47): 16559-16566. PMID 16305245. doi:10.1021/ja053084q.
Moreland, D. E. (1 de enero de 1980). «Mechanisms of Action of Herbicides». Annual Review of Plant Physiology 31 (1): 597-638. doi:10.1146/annurev.pp.31.060180.003121.
Roede, J. R.; Miller, G. W. (1 de enero de 2014). Diquat. pp. 202-204. ISBN 9780123864550. doi:10.1016/B978-0-12-386454-3.00137-8.
Bus, J S; Aust, S D; Gibson, J E (1 de agosto de 1976). «Paraquat toxicity: proposed mechanism of action involving lipid peroxidation.». Environmental Health Perspectives 16: 139-146. ISSN 0091-6765. PMC 1475222. PMID 1017417. doi:10.1289/ehp.7616139.

issn.org

portal.issn.org

Bus, J S; Aust, S D; Gibson, J E (1 de agosto de 1976). «Paraquat toxicity: proposed mechanism of action involving lipid peroxidation.». Environmental Health Perspectives 16: 139-146. ISSN 0091-6765. PMC 1475222. PMID 1017417. doi:10.1289/ehp.7616139.

iupac.org

goldbook.iupac.org

Unión Internacional de Química Pura y Aplicada. «viologens». Compendium of Chemical Terminology. Versión en línea (en inglés).

nih.gov

ncbi.nlm.nih.gov

W. W. Porter, T. P. Vaid and A. L. Rheingold (2005). «Synthesis and Characterization of a Highly Reducing Neutral "Extended Viologen" and the Isostructural Hydrocarbon 4,4' '-Di-n-octyl-p-quaterphenyl». J. Am. Chem. Soc. 127 (47): 16559-16566. PMID 16305245. doi:10.1021/ja053084q.
Bus, J S; Aust, S D; Gibson, J E (1 de agosto de 1976). «Paraquat toxicity: proposed mechanism of action involving lipid peroxidation.». Environmental Health Perspectives 16: 139-146. ISSN 0091-6765. PMC 1475222. PMID 1017417. doi:10.1289/ehp.7616139.

sciencedirect.com

Roede, J. R.; Miller, G. W. (1 de enero de 2014). Diquat. pp. 202-204. ISBN 9780123864550. doi:10.1016/B978-0-12-386454-3.00137-8.