Molecular complexes of substituted diphenyl sulphides with π acceptors. Charge transfer spectra and ionization potentials of the donors

1974 ◽  
Vol 70 (0) ◽  
pp. 1908 ◽  
Author(s):  
G. Gaetano Aloisi ◽  
Sergio Santini ◽  
Salvatore Sorriso
Keyword(s):  
Charge Transfer ◽  
Molecular Complexes ◽  
Ionization Potentials

Molecular Complexes of p-Chloranil with Aniline, Phenol and their Derivatives

2015 ◽  
Vol 670 ◽  
pp. 89-94
Author(s):  
Boris S. Pryalkin ◽  
Yulia S. Bodagova
Keyword(s):  
Charge Transfer ◽  
Electron Acceptor ◽  
Photoelectron Spectroscopy ◽  
Spectral Properties ◽  
Molecular Complexes ◽  
Ionization Potentials ◽  
Wide Range ◽  
Vertical Ionization Potentials ◽  
Vertical Ionization Energies

Classification of simple supramolecular structures (for example molecular complexes), which has been introduced and described by Mulliken [1], is based on types of molecular orbitals of the components. In the paper [2], disadvantages of such classification are shown, which motivate us to return to the re-examination properties of molecular complexes. By this reason, there is a need to research the molecular complexes of one electron acceptor with a wide range of electron donor molecules. This paper have continued work (Part I [3]) on the chloranil complexes by studying the spectral properties complexes of N- and O-unsubstituting anilines and phenols. The present work aimed at analyzing linear relation the energies of charge-transfer bands of molecular complexes are related to ionization potentials of the donor components. All complexes conform to linear relations like involving both adiabatic and vertical ionization potentials of donor components. Mulliken [1] has been proposed to apply the vertical ionization potentials of donor components only. The development of photoelectron spectroscopy has led to the measurement of adiabatic and vertical ionization energies for thousands of molecules, which allow theirs to the present analysis of spectral properties molecular complexes.

Complexes moléculaires d'hétérocycles soufrés et oxygénés. Étude spectrophotométrique de bandes de transfert de charge multiples

1982 ◽  
Vol 60 (7) ◽  
pp. 862-871 ◽  
Author(s):  
Jean-Paul Canselier ◽  
Serge Domenech ◽  
Štefan Stankovsky ◽  
Sabine Gautier
Keyword(s):  
Charge Transfer ◽  
Absorption Spectra ◽  
Electronic Absorption ◽  
Electronic Absorption Spectra ◽  
Molecular Complexes ◽  
The Other ◽  
Ionization Potentials ◽  
Nonpolar Solvents ◽  
Other Hand ◽  
The One

As with benzenoid donors, the electronic absorption spectra of the molecular complexes of simple or condensed sulfur or oxygen-containing five-membered heterocycles with TCNE (or DDQ) often show two charge-transfer bands. In many cases, the knowledge of the actual frequencies requires a technique of resolution. The results so obtained are correlated with the ionization potentials of donors on the one hand, and the refractivity of nonpolar solvents on the other hand.

Charge Transfer Molecular Complexes of 4-(Dimethylamino)pyridine with Some Conventional and Unconventional Acceptors Involving Fluoroarenes

2006 ◽  
Vol 71 (9) ◽  
pp. 1359-1370 ◽  
Author(s):  
Usama M. Rabie
Keyword(s):  
Charge Transfer ◽  
Nmr Spectra ◽  
Molecular Complexes ◽  
Outer Sphere ◽  
Formation Constants ◽  
Stoichiometric Ratio ◽  
Spectral Bands ◽  
Elemental Analyses ◽  
Ct Complexes ◽  
Solid Complexes

Charge transfer (CT) complexes of 4-(dimethylamino)pyridine (DMAP) with iodine as a typical σ-type acceptor and with typical π-type acceptor, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), have been synthesized and characterized. Octafluorotoluene (OFT), octafluoronaphthalene (OFN), perfluorophenanthrene (PFP), and 2,3,5,6-tetrafluoropyridine-4-carbonitrile (TFP) were also used as acceptors for interaction with DMAP. Properties of such CT complexes were investigated by UV/VIS and IR spectra, and elemental analyses of the isolated complexes. The systems DMAP-iodine and DMAP-DDQ are characterized by formation of triiodide ions (I3-) and DDQ•- anion radicals, respectively, which is proposed to occur via initial formation of outer-sphere CT complexes. The systems (DMAP-OFT, DMAP-OFN, DMAP-PFP and DMAP-TFP) are characterized by the appearance of new UV/VIS spectral bands assigned as CT bands; they also furnished the corresponding solid complexes with the stoichiometric ratio 1:1. 1H and 19F NMR spectra were used on confirming the formation of the DMAP-PFP CT complexes. The formation constants (KCT) and molar absorption coefficients (εCT) of the latter complex were obtained.

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