Joaquim Crusats
Overview
Explore the profile of Joaquim Crusats including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
40
Citations
219
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Dardouri N, Hrichi S, Torres P, Chaabane-Banaoues R, Sorrenti A, Roisnel T, et al.
Molecules
. 2024 Jul;
29(13).
PMID: 38999116
The present article describes the synthesis of an isonicotinate-derived -arylporphyrin, that has been fully characterized by spectroscopic methods (including fluorescence spectroscopy), as well as elemental analysis and HR-MS. The structure...
2.
Torres P, Guillen M, Escriba M, Crusats J, Moyano A
Molecules
. 2023 Feb;
28(4).
PMID: 36838985
The design, synthesis, and initial study of amino-functionalized porphyrins as a new class of bifunctional catalysts for asymmetric organophotocatalysis is described. Two new types of amine-porphyrin hybrids derived from 5,10,15,20-tetraphenylporphyrin...
3.
Buhse T, Cruz J, Noble-Teran M, Hochberg D, Ribo J, Crusats J, et al.
Chem Rev
. 2021 Jan;
121(4):2147-2229.
PMID: 33464058
Spontaneous deracemizations is a challenging, multidisciplinary subject in current chirality research. In the absence of any chiral inductors, an achiral substance or a racemic composition is driven into an enantioenriched...
4.
Arlegui A, Torres P, Cuesta V, Crusats J, Moyano A
Molecules
. 2020 Aug;
25(15).
PMID: 32731520
Two chiral proline-derived amphiphilic 5-substituted-10,15,20-tris(4-sulfonatophenyl)porphyrins were prepared, and their pH-dependent supramolecular behavior was studied. In neutral aqueous solutions, the free-base form of the hybrids is highly soluble, allowing enamine-based organocatalysis...
5.
Arlegui A, Soler B, Galindo A, Arteaga O, Canillas A, Ribo J, et al.
Chem Commun (Camb)
. 2019 Sep;
55(81):12219-12222.
PMID: 31553004
This report shows how the net supramolecular chirality that emerged by spontaneous mirror-symmetry breaking (SMSB) at the mesoscale level can be transferred towards asymmetric solution chemistry. The J-aggregates obtained by...
6.
El-Hachemi Z, Crusats J, Troyano C, Ribo J
ACS Omega
. 2019 Aug;
4(3):4804-4813.
PMID: 31459664
The comparison between nanoparticle morphologies of the J-aggregates of different -4-sulfonatophenylporphyrins showing non-sulfonato groups at some of the -positions constitutes an ultimate proof of the 2D crystal-like character of the...
7.
Arlegui A, El-Hachemi Z, Crusats J, Moyano A
Molecules
. 2018 Dec;
23(12).
PMID: 30572589
A convenient protocol for the preparation of 5-phenyl-10,15,20-tris(4-sulfonatophenyl)porphyrin, a water-soluble porphyrin with unique aggregation properties, is described. The procedure relies on the one-pot reductive deamination of 5-(4-aminophenyl)-10,15,20-tris(4-sulfonatophenyl)porphyrin, that can be...
8.
Ribo J, Hochberg D, Crusats J, El-Hachemi Z, Moyano A
J R Soc Interface
. 2017 Dec;
14(137).
PMID: 29237824
Recent reports on both theoretical simulations and on the physical chemistry basis of spontaneous mirror symmetry breaking (SMSB), that is, asymmetric synthesis in the absence of any chiral polarizations other...
9.
Ribo J, Crusats J, El-Hachemi Z, Moyano A, Hochberg D
Chem Sci
. 2017 Apr;
8(1):763-769.
PMID: 28451224
Chiral hypercycle replicators (first-order autocatalysis together with mutual cross-catalysis) formed from achiral or racemizing resources may lead to spontaneous mirror symmetry breaking (SMSB) without the need for additional heterochiral inhibition...
10.
Ribo J, El-Hachemi Z, Arteaga O, Canillas A, Crusats J
Chem Rec
. 2017 Jan;
17(7):713-724.
PMID: 28105702
Chiral J-aggregates of achiral amphiphilic porphyrins (4-sulfonatophenyl and aryl meso-substituted porphyrins) show several effects under the hydrodynamic forces of common stirring. These effects can be classified as pure mechanic (e. ...