Sandra and Juan Carlos received their awards for best academic record, last Monday during the San Alberto Magno ceremony, at the Faculty of Sciences. Well done!! Congratulations!!


Sandra and Juan Carlos received their awards for best academic record, last Monday during the San Alberto Magno ceremony, at the Faculty of Sciences. Well done!! Congratulations!!


CSIC organices this week an interesting event dedicated to children from schools of Aragon and surprise them with Science (“Semana de la Ciencia”). Sandra, Christian, Guillermo and Fanny from HOCA lab, have been awakening scientific vocations. Maybe some of them will incorporated to our Institute, the ISQCH, in the near future 😉


Last Tuesday, Sandra Ardevines, PhD student in our group, gave her talk about the “Synthesis of 1,4-dihydropyridine derivatives and the study of their biological properties” during the first session of the IV NanoOncology Workshop (October, 19-20th) celebrated in Zaragoza.
Well done!!

Today we said goodbye to Devan, a student from the TUM who got a DAAD internship and joined the HOCA lab for 6 weeks working very hard.
We hope you learnt with us and you had enjoyed.
Good luck and come back to visit us soon! Thank you 😉



Single-crystal-to-single-crystal transformation and catalytic properties of new organically template perhalidometallates, Rayes, A.; Zárate-Roldán, S.; Ara, I.; Moncer, M.; Dege, N.; Gimeno, M. C.; Ayed, B.; Herrera, R. P. Catalysts 2021, 11, 758. https://doi.org/10.3390/catal11070758.
Abstract. Two new organic–inorganic salts of perhalidometallates with protonated organic amine cations have been synthesized and characterized by X-ray diffraction and thermal analysis. (CHBMAH2)ZnBr4·3/2H2O 1 and (CHBMAH2)ZnCl44 [(CHBMAH2)2+: 1,3-cyclohexanebis(methylammonium)] were obtained in single-crystal form. The crystal packing in all of the obtained compounds is governed by the formation of various non-covalent intermolecular forces between tetrahalidometallate anions and organic cations, assisted by water molecules in the hydrates. Hirshfeld surface analysis denotes that the most important contributions to the crystal packing are X···H/H···X (X: Cl, Br, I) and H···H interactions. Interestingly, the compound 1,3-cyclohexanebis(methylammonium)tetrachloridozincate (II) dihydrate, (CHBMAH2)ZnCl4·2H2O 2, undergoes thermally-triggered single-crystal-to-single-crystal (SCSC) transformation upon dehydration to produce a supramolecular solid compound, 1,3-cyclohexanebis(methylammonium) tetrachloridozincate (II), (CHBMAH2)ZnCl44. The SCSC transformation causes changes in the lattice parameters and a structural rearrangement. Furthermore, the catalytic properties of (CHBMAH2)ZnCl4·2H2O 2 and (CHBMAH2)CdI4·2H2O 3 have been explored in the acetalization process using various uncommon alcohols, beyond methanol or ethanol, for the first time in the literature, with outstanding results, and opening the door to the formation of alternative acetals.
Keywords: perhalidometallates; X-ray crystal structure; thermal analysis; Hirshfeld surface analysis; catalysis; acetalization
Effort has reward… congrats!! 😉
Unconventional Gold-Catalyzed One-Pot/Multicomponent Synthesis of Propargylamines Starting from Benzyl Alcohols, Zárate-Roldán, S.; Gimeno, M. C.; Herrera, R. P. Catalysts 2021, 11, 513. https://doi.org/10.3390/catal11040513.
Abstract. A formal homogeneous gold-catalyzed A3-coupling, starting from benzyl alcohols, is reported for the straightforward synthesis of propargylamines. This is the first process where these highly valuable compounds have been synthesized, starting from the corresponding alcohols in a one-pot oxidation procedure using MnO2, followed by a HAuCl4·3H2O catalyzed multicomponent reaction. The final products are obtained with very good yields in short reaction times, which is of fundamental interest for the synthesis of pharmaceuticals. The usefulness and efficiency of our methodology is successfully compared against the same reaction starting from aldehydes.
Keywords. benzyl alcohols; gold; multicomponent; one-pot; propargylamine