Charge-transfer complexes of dinuclear ruthenium compounds/polyoxometalates for multistate electrochromism covering ultraviolet, visible, and near-infrared region

2017 ◽  
Vol 5 (26) ◽  
pp. 6442-6449 ◽  
Author(s):  
Dandan Chong ◽  
Xinhua Wan ◽  
Jie Zhang
Keyword(s):  
Charge Transfer ◽  
Near Infrared ◽  
Infrared Region ◽  
Charge Transfer Complexes ◽  
Ruthenium Compounds ◽  
Dinuclear Ruthenium ◽  
Near Infrared Region ◽  
Full Absorption

Novel charge-transfer electrostatic complexes between the anionic polyoxometalates and cationic dinuclear ruthenium compounds display the full absorption covering ultraviolet, visible, and near-infrared region.

Schwingungs-und Elektronenspektren der bindungsisomeren Hexakis(thiocyanato(N)-thiocyanato(S))-osmate(III) und (IV) / Vibrational and Electronic Spectra of Bond-Isomeric Hexakis(thiocyanato(N)-thiocyanato(S))osmates(III) and (IV)

1988 ◽  
Vol 43 (4) ◽  
pp. 371-381 ◽  
Author(s):  
K. Bütje ◽  
W. Preetz
Keyword(s):  
Charge Transfer ◽  
Vibrational Spectra ◽  
Near Infrared ◽  
Bathochromic Shift ◽  
Infrared Region ◽  
Hypsochromic Shift ◽  
Linkage Isomers ◽  
Near Infrared Region ◽  
Ir And Raman ◽  
Metal Ligand

AbstractWell-resolved IR and Raman spectra of the two sets of all 10 isomeric complexes [Os(NCS)n(SCN)6-n]3-/2-, n = 0-6, have been recorded. For both series, νCS(N) > νCS(S) and δNCS > δSCN; for the Os(III) complexes, vCN(N) ~ vCN(S) and vOsN ≥ vOsS while for the Os(IV) compounds, vCN(N) < vCN(S) and vOsN ~ vOsS. The vibrational spectra of the n = 0 and n = 6 members of both sets are assigned according to D3d and Oh point symmetry, respectively. For the mixed linkage isomers the band pattern is strongly influenced by pseudo-octahedral coupling wherever frequencies of N- and S-bonded groups coincide. The metal-ligand stretching region is therefore assigned according rather to pseudo-Oh, pseudo-D3d and pseudo-D4h symmetry than to D4h, C4v, C3v and C2v microsymmetry. The charge-transfer spectra of both series are similar, showing a parallel hypsochromic shift with increasing n value. Upon oxidation, a bathochromic shift of the CT bands by an average of 5400 cm-1 is observed, and the intensity increases by a factor 2-2.5. Weak absorptions in the near infrared region are assigned to intraconfigurational transitions.

Ligand Influence Versus Electronic Configuration of d-metal Ion in Determining the Fate of NIR Emission from LnIII Ions: A Case Study with CuII, NiII and ZnII Complexes.

2021 ◽  
Author(s):  
Abhineet Verma ◽  
Sk Saddam Hossain ◽  
Sailaja S Sunkari ◽  
Joseph Reibenspies ◽  
Satyen Saha
Keyword(s):  
Metal Ion ◽  
Selection Rule ◽  
Near Infrared ◽  
Electronic Configuration ◽  
Infrared Region ◽  
Direct Excitation ◽  
Characteristic Emission ◽  
Nir Emission ◽  
Near Infrared Region

Lanthanides (LnIII) are well known for their characteristic emission in the Near-Infrared Region (NIR). However, direct excitation of lanthanides is not feasible as described by Laporte’s parity selection rule. Here,...

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