Manganese(i) complexes with metal-to-ligand charge transfer luminescence and photoreactivity
نویسندگان
چکیده
Precious metal complexes with the d6 valence electron configuration often exhibit luminescent metal-to-ligand charge transfer (MLCT) excited states, which form basis for many applications in lighting, sensing, solar cells and synthetic photochemistry. Iron(ii) has received much attention as a possible Earth-abundant alternative, but to date no iron(ii) complex been reported show MLCT emission upon continuous-wave excitation. Manganese(i) same that of iron(ii), until now typically overlooked search cheap luminophores. Here we report isocyanide chelate ligands give access air-stable manganese(i) luminescence solution at room temperature. These compounds were successfully used photosensitizers energy- electron-transfer reactions shown promote photoisomerization trans-stilbene. The observable photoreactivity occurred from emissive state, whereas triplet energy originated ligand-centred 3?–?* state. is isoelectronic development 3d6 emitters photosensitizers. Now, using chelating ligands, have obtained luminescence, well photoreactivity.
منابع مشابه
Rare Earth Nitrate Complexes with an ONO Schiff Base Ligand: Spectral, Thermal, Luminescence and Biological Studies
Five rare earth complexeslanthanum(III),praseodymium(III),neodymium(III), samarium(III) and europium(III) have been synthesized from Schiff base ligand (N,N-bis (2-hydroxy-1-naphthylidene) acetylhydrazone). The complexes were characterized based on elemental analysis, molar conductance, ultraviolet, infrared, mass, thermogravimetric and powder X-ray diffraction studies. Infrared spectra sug...
متن کاملMETAL-METAL CHARGE TRANSFER IN LnM-CN-FeCl3 COMPLEXES
By combining the organometallic cyanides L n M-CN [L n M = Cp(dppe)Fe, Cp(dppe)Ru, Cp(PPh 3 ) 2 Ru] with FeCl 3 the dinuclear complexes L n M-CN-FeCl 3 were obtained. Structure determinations have revealed configurations close to linear arrays Fe-C-N-Fe and Ru-CN-Fe. From the n(CN) band positions in their IR spectra it can be concluded that FeCl 3 is a very strong electron acceptor. Accordingly...
متن کاملSolvation-Driven Charge Transfer and Localization in Metal Complexes
In any physicochemical process in liquids, the dynamical response of the solvent to the solutes out of equilibrium plays a crucial role in the rates and products: the solvent molecules react to the changes in volume and electron density of the solutes to minimize the free energy of the solution, thus modulating the activation barriers and stabilizing (or destabilizing) intermediate states. In c...
متن کاملSynthesis and Characterization of Metal Complexes with New Unsymmetrical Schiff Base Ligand Derived from 2-Aminoethanethiol
A new unsymmetric thioether diamine N - ( 2 - ( 2 - aminophenylthio) ethyl) benzene - 1 , 2 - diamine was prepared through the nucleophilic substitution of cysteaminium chloride with 1 - chloro - 2 - nitrobenzene and then the nitro groups of prepared compuond converted to the amine by zinc powder and ammonium chloride. Then, unsymmetric Schiff bass ligand 2 - ((( 2 - (( 2 - (( 2 - (( 2 - hydrox...
متن کاملPressure and temperature effects on metal-to-metal charge transfer in cyano-bridged CoIII-FeII complexes.
The effects of pressure and temperature on the energy (Eop) of the metal-to-metal charge transfer (MMCT, FeII-->CoIII) transition of the cyano-bridged complexes trans-[L14CoNCFe(CN)5]- and cis-[L14CoNCFe(CN)5]- (where L14=6-methyl-1,4,8,11-tetraazacyclotetradecan-6-amine) were examined. The changes in the redox potentials of the cobalt and iron metal centres with pressure and temperature were a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Nature Chemistry
سال: 2021
ISSN: ['1755-4349', '1755-4330']
DOI: https://doi.org/10.1038/s41557-021-00744-9