6533b858fe1ef96bd12b5a2b

RESEARCH PRODUCT

Supramolecular assemblies and photophysical properties of ionic homo- and heteronuclear metallophilic complexes

Laura RodríguezNoora SvahnIngrid SanzKari Rissanen

subject

010405 organic chemistryOrganic ChemistryIntermolecular forceSupramolecular chemistryIonic bondingOr010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryHeteronuclear moleculeHexafluorophosphateCompostos d'orMaterials ChemistryGoldPhysical and Theoretical ChemistryNonaneLuminescenceTrifluoromethanesulfonateGold compounds

description

Abstract The synthesis of two dinuclear ionic complexes with chemical formula [Au(PR 3 ) 2 ][Au(C ≡ CC 5 H 4 N-4) 2 ] that contain the water soluble phosphines, PR 3 , PTA (1, 3,5-triaza-7-phosphaadamantane, 1 ) and DAPTA (3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane, 2 ) is herein described. The differences on their intermolecular reorganization have been analyzed and compared with the previously reported for the neutral complexes [Au(PR 3 )(C ≡ CC 5 H 4 N-4)]. It has been evidenced that the reorganization of the ligands giving rise to the dinuclear ionic complexes produces a complete change in the properties giving rise to Au⋯Au intermolecular assemblies. These aurophilic contacts are the responsible for the resulting luminescence which is not displayed for the parent compounds [Au(PR 3 ) 2 ]Cl and [PPh 4 ][Au(C ≡ CC 5 H 4 N-4) 2 ]. Compounds 1 and 2 were made react with three different silver salts (nitrate, triflate and hexafluorophosphate) giving rise to 1:1 heterometallic assemblies with some changes both on the wavelength and emission intensity.

10.1016/j.jorganchem.2019.07.001http://hdl.handle.net/2445/152750