MACCAGNO , Massimo

Donor-acceptor molecules have received an increasing interest in fields such as: dye-sensitized solar cells, molecular electronics and non-linear optics thanks to their specific spectroscopic and electronic properties, which are related to the intramolecular charge transfer that occurs in these systems. In particular, fullerene derivatives are...

A new symmetrical disulfide containing a diacetylenic unit and bearing a fluorescent carbazolyl end-group forming polymerizable self-assembled monolayers on metallic nanostructures has been synthesized. Suitable modifications of the synthetic steps involved in the synthesis of such derivatives were made in order to assure better synthetic...

Disulfide-functionalized fluorescent derivative of carbozole named 11-(9-carbazolyl)-1-undecyl disulfide (CBZDS) has been synthesized. Proton nuclear magnetic resonance spectroscopy was used to distinguish thiol from its corresponding symmetrical disulfide. Single step synthesis of gold nanoparticles coated with CBZDS was carried out which...

No description

No description

No description

No description

In this paper, we report the synthesis of novel diacetylenes bearing trimethylammonium end groups, their photochemical polymerization and the spectroscopic characterization of the polymers by different techniques (UV–vis, fluorescence, FT-IR, Raman). The obtained results shed light on the role of the trimethylammonium head group (and its...

No description

Stable hydrosols of gold and silver nanoparticles coated with the quaternary-ammonium group endowed diacetylene DAAMM (N,N,N-trimethyl-3-(pentacosa-10,12-diynamido)propan-1-ammonium) were obtained through a ligand-exchange reaction leaving the morphology of the pristine cores unmodified. Photopolymerization of the chemisorbed diacetylene shell...

No description

The unusual migration of a nitro group from the β- to the α-position of a β-aryl-α-nitroethenyl moiety, following a nitrocyclopropane to isoxazoline N-oxide isomerization, has been studied from a mechanistic and synthetic points of view. As a result, two series of isomeric isoxazoline N-oxides could be obtained under controlled conditions. When...

The conjugated bis(sulfonyl)nitrobutadienes 1 undergo, with primary amines, competitive MeSO2 replacement [vinylic substitution at C(1)] versus aza-Michael addition to the nitroethenyl C(3)–C(4) double bond. The latter pathway eventually leads to the trisubstituted pyrroles 2 and conditions have been optimized in order to maximize the yield of...

As a continuation of our research on the synthetic exploitation of the nitrobutadienic building-blocks obtained from the ring-opening of nitrothiophenes, we herein report about their reaction with the π-nucleophilic indole. Thanks to their double Michael-acceptor nature, 2,3-dinitro and 2-nitro-3-phenylsulfonyl substituted 1,3-butadienes...

No description