Rocío Aguilar-Sánchez

Rocío Aguilar-Sánchez


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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11 August 2020 in Symmetry
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RARocío Aguilar-Sánchez
Rocío Aguilar-Sánchez
IHIvan Herrera-González
Ivan Herrera-González
JMJ. A. Mendez-Bermudez
J. A. Mendez-Bermudez
José M. SigarretaJosé M. Sigarreta
José M. Sigarreta
We perform a detailed (computational) scaling study of well-known general indices (the first and second variable Zagreb indices, M1α(G) and M2α(G), and the general sum-connectivity index, χα(G)) as well as of general versions of indices of interest: the general inverse sum indeg index ISIα(G) and the general first geometric-arithmetic index GAα(G) (with α∈R). We apply these indices on two models of random networks: Erdös–Rényi (ER) random networks GER(nER,p) and random geometric (RG) graphs GRG(nRG,r). The ER random networks are formed by nER vertices connected independently with probability p∈[0,1]; while the RG graphs consist of nRG vertices uniformly and independently distributed on the unit square, where two vertices are connected by an edge if their Euclidean distance is less or equal than the connection radius r∈[0,2]. Within a statistical random matrix theory approach, we show that the average values of the indices normalized to the network size scale with the average degree k of the corresponding random network models, where kER=(nER−1)p and kRG=(nRG−1)(πr2−8r3/3+r4/2). That is, X(GER)/nER≈X(GRG)/nRG if kER=kRG, with X representing any of the general indices listed above. With this work, we give a step forward in the scaling of topological indices since we have found a scaling law that covers different network models. Moreover, taking into account the symmetries of the topological indices we study here, we propose to establish their statistical analysis as a generic tool for studying average properties of random networks. In addition, we discuss the application of specific topological indices as complexity measures for random networks.

24 October 2018 in Polymers
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SCSandra Castillejos
Sandra Castillejos
JCJorge Cerna
Jorge Cerna
FMFrancisco J. Melendez
Francisco J. Melendez
MCMaría Eugenia Castro
María Eugenia Castro
RARocío Aguilar-Sánchez
Rocío Aguilar-Sánchez
MTMaykel González Torres
Maykel González Torres
Copolymers of l-lactide and poly(propylene glycol) diglycidyl ether (PPGDGE380) were synthesized by ring opening polymerization (ROP). Stannous octoate was used as the catalyst and 1-dodecanol as the initiator. The effect of the variables on the thermal properties of the copolymers was investigated by differential scanning calorimetry (DSC). Contact angle measurements were made in order to study the wettability of the synthesized copolymers. The copolymers differed widely in their physical characteristics, ranging from weak elastomers to tougher thermoplastics, according to the ratio of l-lactide and PPGDGE380. The results showed that the copolymers were more hydrophilic than neat Poly(lactide) (PLA) and the monomer ratio had a strong influence on the hydrophilic properties.

20 March 2012 in Journal of Solid State Electrochemistry
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RARocío Aguilar-Sánchez
Rocío Aguilar-Sánchez
RDRodrigo J. Díaz-Caballeros
Rodrigo J. Díaz-Caballeros
JMJ. Antonio Méndez-Bermúdez
J. Antonio Méndez-Bermúdez
JGJ. Luis Gárate-Morales
J. Luis Gárate-Morales
GDGuadalupe Domínguez-Meneses
Guadalupe Domínguez-Meneses

12 September 2019 in Molecules
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ESEsteban Sánchez-Muñoz
Esteban Sánchez-Muñoz
JGJosé L. Gárate-Morales
José L. Gárate-Morales
JSJacinto Sandoval-Lira
Jacinto Sandoval-Lira
JHJulio Manuel Hernández-Pérez
Julio Manuel Hernández-Pérez
RARocío Aguilar-Sánchez
Rocío Aguilar-Sánchez
The formation of a binary porphyrinic self-assembled system between meso-tetrakis(4-carboxyphenyl) porphyrin (TCPP) and meso-tetrakis(4-dimethyl amino) porphyrin (TDAP) was easily designed through non-covalent interactions in solution and adsorbed on a gold substrate. It was found that non-covalent interactions and geometrical conformations between porphyrins allow their self-assembly into a well-defined arrangement, which was confirmed by UV-Vis spectroscopy, electrochemistry, atomic force microscopy and density functional theory (DFT) studies.