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Analysis of institutional authors

Martinez Diaz, VictoriaAuthorTorres Cebada, TomasAuthorTejerina Gonzalez, LaraAuthor

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October 19, 2020
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Convergent strategy for the regioselective synthesis of nonaggregated α-

Publicated to:ORGANIC LETTERS. 17 (3): 552-555 - 2015-02-06 17(3), DOI: 10.1021/ol503557c

Authors: Tejerina, Lara; Victoria Martinez-Diaz, M; Torres, Tomas

Affiliations

Departamento de Química Orgánica, Facultad de Ciencias, and ‡IMDEA Nanociencia, Universidad Autónoma de Madrid , c/Faraday 9, Campus de Cantoblanco, 28049 Madrid, Spain. - Author
Univ Autonoma Madrid, Fac Ciencias, Dept Quim Organ, E-28049 Madrid, Spain - Author
Univ Autonoma Madrid, IMDEA Nanociencia, E-28049 Madrid, Spain - Author
Universidad Autónoma de Madrid - Author

Abstract

© 2015 American Chemical Society. A new design of nonaggregated zinc(II) carboxyphthalocyanines with potential application in dye-sensitized solar cells has been developed. It is based on the introduction of bulky and rigid aryl groups at three α positions of the macrocycle. The synthesis has been carried out following a convergent route in which the bulky aryl groups are introduced by a Suzuki-Miyaura cross-coupling reaction on a preformed triiodophthalocyanine derivative. Two regioisomers of this α-triaryl-β-carboxyphthalocyanine could be isolated by column chromatography.

Keywords

BiochemistryBiodiversidadeBiotecnologíaChemistry, organicCiências agrárias iCiências biológicas iCiências biológicas iiFarmaciaGeneral medicineInterdisciplinarMateriaisMedicina iMedicina iiOrganic chemistryPhysical and theoretical chemistryQuímica

Quality index

Bibliometric impact. Analysis of the contribution and dissemination channel

The work has been published in the journal ORGANIC LETTERS due to its progression and the good impact it has achieved in recent years, according to the agency WoS (JCR), it has become a reference in its field. In the year of publication of the work, 2015, it was in position 4/59, thus managing to position itself as a Q1 (Primer Cuartil), in the category Chemistry, Organic.

From a relative perspective, and based on the normalized impact indicator calculated from the Field Citation Ratio (FCR) of the Dimensions source, it yields a value of: 1.93, which indicates that, compared to works in the same discipline and in the same year of publication, it ranks as a work cited above average. (source consulted: Dimensions Jul 2025)

Specifically, and according to different indexing agencies, this work has accumulated citations as of 2025-07-16, the following number of citations:

  • WoS: 15
  • Scopus: 17
  • Europe PMC: 1
  • Open Alex: 16

Impact and social visibility

From the perspective of influence or social adoption, and based on metrics associated with mentions and interactions provided by agencies specializing in calculating the so-called "Alternative or Social Metrics," we can highlight as of 2025-07-16:

  • The use of this contribution in bookmarks, code forks, additions to favorite lists for recurrent reading, as well as general views, indicates that someone is using the publication as a basis for their current work. This may be a notable indicator of future more formal and academic citations. This claim is supported by the result of the "Capture" indicator, which yields a total of: 28 (PlumX).

It is essential to present evidence supporting full alignment with institutional principles and guidelines on Open Science and the Conservation and Dissemination of Intellectual Heritage. A clear example of this is:

  • The work has been submitted to a journal whose editorial policy allows open Open Access publication.
  • Assignment of a Handle/URN as an identifier within the deposit in the Institutional Repository: https://repositorio.uam.es/handle/10486/673386

Leadership analysis of institutional authors

There is a significant leadership presence as some of the institution’s authors appear as the first or last signer, detailed as follows: First Author (Tejerina L) and Last Author (Torres T).