Alessandro Sorrenti
Overview
Explore the profile of Alessandro Sorrenti 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
31
Citations
309
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.
Llaurado-Capdevila G, Veciana A, Guarducci M, Mayoral A, Pons R, Hertle L, et al.
Adv Mater
. 2023 Dec;
36(14):e2306345.
PMID: 38146105
Covalent organic frameworks (COFs) are crystalline materials with intrinsic porosity that offer a wide range of potential applications spanning diverse fields. Yet, the main goal in the COF research area...
3.
Mattera M, Sorrenti A, De Gregorio Perpina L, Oestreicher V, Sevim S, Arteaga O, et al.
Small
. 2023 Dec;
20(20):e2307621.
PMID: 38111987
Layered double hydroxides (LDHs) are a class of functional materials that exhibit exceptional properties for diverse applications in areas such as heterogeneous catalysis, energy storage and conversion, and bio-medical applications,...
4.
Sevim S, Sorrenti A, Vale J, El-Hachemi Z, Pane S, Flouris A, et al.
Nat Commun
. 2022 Apr;
13(1):1766.
PMID: 35365637
Homochirality is a fundamental feature of living systems, and its origin is still an unsolved mystery. Previous investigations showed that external physical forces can bias a spontaneous symmetry breaking process...
5.
Calvo Galve N, Abrishamkar A, Sorrenti A, Di Rienzo L, Satta M, DAbramo M, et al.
Angew Chem Int Ed Engl
. 2021 Mar;
60(29):15920-15927.
PMID: 33729645
Coordination polymers (CPs), including metal-organic frameworks (MOFs), are crystalline materials with promising applications in electronics, magnetism, catalysis, and gas storage/separation. However, the mechanisms and pathways underlying their formation remain largely...
6.
Sevim S, Franco C, Chen X, Sorrenti A, Rodriguez-San-Miguel D, Pane S, et al.
Adv Sci (Weinh)
. 2020 Jun;
7(12):1903172.
PMID: 32596108
Microfluidic technologies have emerged as advanced tools for surface-enhanced Raman spectroscopy (SERS). They have proved to be particularly appealing for in situ and real-time detection of analytes at extremely low...
7.
Dunne P, Adachi T, Dev A, Sorrenti A, Giacchetti L, Bonnin A, et al.
Nature
. 2020 May;
581(7806):58-62.
PMID: 32376963
When miniaturizing fluidic circuitry, the solid walls of the fluid channels become increasingly important because they limit the flow rates achievable for a given pressure drop, and they are prone...
8.
Sorrenti A, Jones L, Sevim S, Cao X, deMello A, Marti-Gastaldo C, et al.
J Am Chem Soc
. 2020 Apr;
142(20):9372-9381.
PMID: 32307978
Controlling and understanding the mechanisms that harness crystallization processes is of utmost importance in contemporary materials science and, in particular, in the realm of reticular solids where it still remains...
9.
Franco C, Rodriguez-San-Miguel D, Sorrenti A, Sevim S, Pons R, Platero-Prats A, et al.
J Am Chem Soc
. 2020 Jan;
142(7):3540-3547.
PMID: 31986022
Covalent organic frameworks (COFs) are commonly synthesized under harsh conditions yielding unprocessable powders. Control in their crystallization process and growth has been limited to studies conducted in hazardous organic solvents....
10.
Pi-Boleda B, Sorrenti A, Sans M, Illa O, Pons R, Branchadell V, et al.
Langmuir
. 2018 Sep;
34(38):11424-11432.
PMID: 30173523
Cationic bolaamphiphiles have been synthesized starting from meso cis- or chiral trans-1,2-difunctionalized cyclobutane derivatives. They include cis/trans pairs of diastereoisomers, of N- or C-centered bisamides. The goal of this work...