Back to Search
Start Over
The binuclear dual emitter [Br(CO) 3 Re(PN)(NP)Re(CO) 3 Br] (PN): 3-chloro-6-(4-diphenylphosphinyl)butoxypyridazine, a new bridging P,N-bidentate ligand resulting from the ring opening of tetrahydrofuran.
- Source :
-
Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2017 Jan 31; Vol. 46 (5), pp. 1567-1576. - Publication Year :
- 2017
-
Abstract
- Lithium diphenylphosphide unexpectedly provokes the ring-opening of tetrahydrofuran (THF) and by reaction with 3,6-dichloropyridazine leads to the formation of the ligand 3-chloro-6-(4-diphenylphosphinyl)butoxypyridazine (P⋯N), which was isolated. The reaction of this ligand with the (Re(CO) <subscript>3</subscript> (THF)Br) <subscript>2</subscript> dimer yields the novel complex [Br(CO) <subscript>3</subscript> Re(μ-3-chloro-6-(4-diphenylphosphinyl)butoxypyridazine) <subscript>2</subscript> Re(CO) <subscript>3</subscript> Br] (BrRe(P⋯N)(N⋯P)ReBr), which was crystallized in the form of a chloroform solvate, (C <subscript>46</subscript> H <subscript>40</subscript> Br <subscript>2</subscript> Cl <subscript>2</subscript> N <subscript>4</subscript> O <subscript>8</subscript> P <subscript>2</subscript> Re <subscript>2</subscript> )·(CHCl <subscript>3</subscript> ). The monoclinic crystal (P2 <subscript>1</subscript> /n) displays a bimetallic cage structure with a symmetry inversion centre in the middle of the rhenium to rhenium line. The molecule shows two oxidation signals occurring at +1.50 V and +1.76 V which were assigned to the Re <superscript>I</superscript> /Re <superscript>II</superscript> and Re <superscript>II</superscript> /Re <superscript>III</superscript> metal-centered couples, respectively, while signals observed at -1.38 V and -1.68 V were assigned to ligand centered reductions. Experimental and DFT/TDDFT results indicate that the UV-Vis absorption maximum of BrRe(P⋯N)(N⋯P)ReBr occurring near 380 nm displays a metal to ligand charge transfer (MLCT) character, which is consistent with CV results. Upon excitation at this wavelength, a weak emission (Φ <subscript>em</subscript> < 1 × 10 <superscript>-3</superscript> ) is observed around 580 nm (in dichloromethane) which decays with two distinct lifetimes τ <subscript>1</subscript> and τ <subscript>2</subscript> of 24 and 4.7 ns, respectively. The prevalence of non-radiative deactivation pathways is consistent with efficient internal conversion induced by the high conformational flexibility of the P⋯N ligand's long carbon chain. Measurements in a frozen solvent at 77 K, where vibrational deactivation is hindered, show intense emission associated with the <superscript>3</superscript> MLCT state. These results demonstrate that BrRe(P⋯N)(N⋯P)ReBr preserves the dual emitting nature previously reported for the mononuclear complex RePNBr, with emission associated with and states.
Details
- Language :
- English
- ISSN :
- 1477-9234
- Volume :
- 46
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Dalton transactions (Cambridge, England : 2003)
- Publication Type :
- Academic Journal
- Accession number :
- 28091640
- Full Text :
- https://doi.org/10.1039/c6dt04158b