Publications by authors named "M B Natali"

Tris-(2-pyridylmethyl)amines (TPA or TPMA) are polipyrydine-based ligands extensively used in catalysis and supramolecular chemistry due their capability to form stable tetradentate complexes with a large variety of metals. The unsubstituted ligand, which is also commercially available, can be synthesised by consecutive alkylation of a picoline or by reductive amination of a pyridine aldehyde. In this article, we report a novel synthetic method which opens to the post-functionalisation of these ligands in the benzylic position.

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Article Synopsis
  • Photosynthetic hydrogen generation using cobalt(II) TPMA complexes faces challenges due to slow protonation and degradation processes.
  • The research highlights that while improving structural rigidity slightly boosts catalytic performance, incorporating ammonium groups near the cobalt enhances proton transfer, resulting in a fourfold increase in hydrogen production efficiency and a 22-fold increase in maximum turnover number.
  • The study emphasizes the importance of modifying the catalyst's surroundings to optimize its performance for solar fuel production, supported by transient absorption spectroscopy findings.
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Carbon/Phenolic Composites (CPCs) are essential to manufacture many portions of the nozzle assembly of Solid Rocket Motors (SRMs) which are essential both to preserve the independent access to space as well as for the homeland security. In our research, a feasible approach aimed at preliminary retrieving the in-plane and out-plane thermal diffusivity of CPCs through the Oxy-Acetylene Torch (OAT) tests was validated. The proposed approach showed to be effective and able to bypass some limitations of common protocols, especially in terms of capability to determine the thermal diffusivity of CPCs at high heating rates.

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In this work, we report on the synthesis and characterization of six new iridium(III) complexes of the type [Ir(C^N)(N^N)] using 2-phenylpyridine (-) and its fluorinated derivative (-) as cyclometalating ligands (C^N) and R-phenylimidazo(4,5-)1,10-phenanthroline (R = H, CH, F) as the ancillary ligand (N^N). These luminescent complexes have been fully characterized through optical and electrochemical studies. In solution, the - series exhibits quantum yields (Ф) twice as high as the - series, exceeding 60% in dichloromethane and where MLCT/LLCT and LC emissions participate in the phenomenon.

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A series of four novel heteroleptic Cu(I) complexes, bearing bis(1-indazol-1-yl)methane analogues as , ligands and DPEPhos as the ligand, were synthesised in high yields under mild conditions and characterised by spectroscopic and spectrometric techniques. In addition, the position of the carboxymethyl substituent in the complexes and its effect on the electrochemical and photophysical behaviour was evaluated. As expected, the homoleptic copper (I) complexes with the , ligands showed air instability.

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