New Members of the 1,3-Di(2-pyridyl)benzene Pro-Ligand Family Bearing Tri- or Tetra-Phenylethylene and Related Platinum(II) Complexes
4 affiliations
- 1Department of Chemistry, Università degli Studi di Milano, UdR dell’INSTM, Via Golgi 19, 20133 Milano, Italy
- 2Laboratoire de Chimie, ENS de Lyon, 46, Allée d’Italie, 69364 Lyon, France
- 3Institut des Sciences Chimiques de Rennes, University Rennes, Centre National de la Recherche Scientifique, 35000 Rennes, France
- 4Institute of Chemical Sciences and Technologies “Giulio Natta” (SCITEC) of CNR, Via Golgi 19, 20133 Milano, Italy
Abstract
1,3-di(2-pyridyl)benzene (dpybH) is a fascinating pro-ligand which is structurally similar to terpyridine but the central N atom is replaced by a CH moiety; when CH deprotonation occurs upon binding to a metal atom, then a cyclometallated compound is formed in which the N^C^N-bound ligand is isoelectronic with terpyridine, but it is an anionic ligand rather than a neutral ligand. In this study we prepared and thoroughly characterized two new pro-ligands, namely 1,3-bis(4-triphenylethylene-pyridin-2-yl)-4,6-difluoro-benzene and 1,3-bis(4-tetraphenylethylene-pyridin-2-yl)-4,6-difluoro-benzene, which open the doors for new N^C^N metal complexes. The related platinum(II) complexes, characterized by a weak emission in solution, were also synthesized.
Related
- Silica‐Supported Mononuclear Methyl‐Platinum Complexes Stabilized by Trimethylphosphine—Synthesis, Structure, and Reactions Under Reducing Conditions
- Probing the electronic origins of heterometallic tuning in platinum complexes by 195Pt NMR spectroscopy
- Molecular Heptazine-Platinum Complexes to Model Metal-Support Coordination in Platinized Graphitic Carbon Nitride: Insights into Catalyst Stability and Support Suitability.
- Meta-Pyridyl Substitution for New Blue Host Materials with Enhanced Thermal Stability and Electron-Injection Properties
- Isolable silyl- and germyl-thioketones dearomatize their own benzene rings at room temperature
BibTeX
@article{soricellis2026members,
title = {{New Members of the 1,3-Di(2-pyridyl)benzene Pro-Ligand Family Bearing Tri- or Tetra-Phenylethylene and Related Platinum(II) Complexes}},
author = {Giulia De Soricellis and Véronique Guerchais and Alessia Colombo and Claudia Dragonetti and Francesco Fagnani and Dominique Roberto and Daniele Marinotto},
journal = {Inorganics},
year = {2026},
month = oct,
doi = {10.3390/inorganics14110281},
url = {https://www.mdpi.com/2304-6740/14/11/281},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - New Members of the 1,3-Di(2-pyridyl)benzene Pro-Ligand Family Bearing Tri- or Tetra-Phenylethylene and Related Platinum(II) Complexes
AU - Giulia De Soricellis
AU - Véronique Guerchais
AU - Alessia Colombo
AU - Claudia Dragonetti
AU - Francesco Fagnani
AU - Dominique Roberto
AU - Daniele Marinotto
PY - 2026
DA - 2026/10/30
JO - Inorganics
DO - 10.3390/inorganics14110281
UR - https://www.mdpi.com/2304-6740/14/11/281
AB - 1,3-di(2-pyridyl)benzene (dpybH) is a fascinating pro-ligand which is structurally similar to terpyridine but the central N atom is replaced by a CH moiety; when CH deprotonation occurs upon binding to a metal atom, then a cyclometallated compound is formed in which the N^C^N-bound ligand is isoelectronic with terpyridine, but it is an anionic ligand rather than a neutral ligand. In this study we prepared and thoroughly characterized two new pro-ligands, namely 1,3-bis(4-triphenylethylene-pyridin-2-yl)-4,6-difluoro-benzene and 1,3-bis(4-tetraphenylethylene-pyridin-2-yl)-4,6-difluoro-benzene, which open the doors for new N^C^N metal complexes. The related platinum(II) complexes, characterized by a weak emission in solution, were also synthesized.
SN - 2304-6740
ER -