Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Charge Transfer arenes

Structural Features of Arene Charge-Transfer Complexes... [Pg.445]

Quantitative Evaluation of Arenes as Electron Donors 437 Spectral (UV/vis) Probe for the Formation of CT Complexes 438 IR Spectroscopic Studies of Charge-Transfer Complexation 442 Thermodynamics of Charge-Transfer Complexation 443 Structural Features of Arene Charge-Transfer Complexes 445 Bonding Distance of the Donor/Acceptor Dyad in Arene Complexes 446 Relationship Between Hapticity and Charge Transfer in Arene Complexes 447 Effect of Charge Transfer on the Structural Features of Coordinated Arenes 448... [Pg.631]

NMR signals of the amino acid ligand that are induced by the ring current of the diamine ligand" ". From the temperature dependence of the stability constants of a number of ternary palladium complexes involving dipeptides and aromatic amines, the arene - arene interaction enthalpies and entropies have been determined" ". It turned out that the interaction is generally enthalpy-driven and counteracted by entropy. Yamauchi et al. hold a charge transfer interaction responsible for this effect. [Pg.89]

Indeed, the charge-transfer absorption energies of dibromine complexes with various arenes [65] and alkenes [45] both show clear correlations with the ionization potentials of various donors (Fig. 5). [Pg.155]

Fig. 5 Mulliken dependence of the charge-transfer energy in the series of dibromine complexes with alkyl and chloro-substituted arenes and alkene donors (data from [45,65])... Fig. 5 Mulliken dependence of the charge-transfer energy in the series of dibromine complexes with alkyl and chloro-substituted arenes and alkene donors (data from [45,65])...
Rosokha SV, Kochi JK (2002) Charge-transfer effects on arene structure and reactivity. In Astruc D (ed) Modern arene chemistry. Wiley-VCH, New York, pp 435-478... [Pg.169]

Similar vivid colorations are observed when other aromatic donors (such as methylbenzenes, naphthalenes and anthracenes) are exposed to 0s04.218 The quantitative effect of such dramatic colorations is illustrated in Fig. 13 by the systematic spectral shift in the new electronic absorption bands that parallels the decrease in the arene ionization potentials in the order benzene 9.23 eV, naphthalene 8.12 eV, anthracene 7.55 eV. The progressive bathochromic shift in the charge-transfer transitions (hvct) in Fig. 13 is in accord with the Mulliken theory for a related series of [D, A] complexes. [Pg.271]

Electron-transfer activation. Time-resolved spectroscopy establishes that irradiation of the charge-transfer band (hvCj) of various arene/0s04 complexes directly leads to the contact ion pair. For example, 25-ps laser excitation of the [anthracene, 0s04] charge-transfer complex results in the ion-radical pair instantaneously, as shown in Fig. 14218 (equation 76). [Pg.273]

Supramolecular chirality can be introduced in columns of discotic molecules by using specific interactions, apart from the arene-arene interactions. To achieve this, a study with chiral dopants has been performed.73 Hexa-n-hexyloxytriphenylenes were mixed in dodecane solutions with a variety of chiral electron-deficient dopants and the resulting charge transfer complexes... [Pg.399]

Carbocations as electron acceptors in aromatic EDA complexes 192 Bis(arene)iron(II) complexes with arene and ferrocene donors 198 Carbonylmetallate anions as electron donors in charge-transfer salts 204 Aromatic EDA complexes with osmium tetroxide 219... [Pg.185]

Fig. 2 Direct relationship of the charge-transfer absorption bands of various arene-iodine complexes (ordinate) with those of the corresponding aromatic complexes with different acceptors (abscissa) as indicated, T,... [Pg.189]

Fig. 5 (A) Typical time-resolved picosecond absorption spectrum following the charge-transfer excitation of tropylium EDA complexes with arenes (anthracene-9-carbaldehyde) showing the bleaching (negative absorbance) of the charge-transfer absorption band and the growth of the aromatic cation radical. (B) Temporal evolution of ArH+- monitored at Amax. The inset shows the first-order plot of the ion... Fig. 5 (A) Typical time-resolved picosecond absorption spectrum following the charge-transfer excitation of tropylium EDA complexes with arenes (anthracene-9-carbaldehyde) showing the bleaching (negative absorbance) of the charge-transfer absorption band and the growth of the aromatic cation radical. (B) Temporal evolution of ArH+- monitored at Amax. The inset shows the first-order plot of the ion...

See other pages where Charge Transfer arenes is mentioned: [Pg.421]    [Pg.503]    [Pg.144]    [Pg.421]    [Pg.421]    [Pg.503]    [Pg.144]    [Pg.421]    [Pg.97]    [Pg.100]    [Pg.92]    [Pg.93]    [Pg.1097]    [Pg.1097]    [Pg.147]    [Pg.155]    [Pg.166]    [Pg.39]    [Pg.284]    [Pg.93]    [Pg.126]    [Pg.129]    [Pg.131]    [Pg.155]    [Pg.207]    [Pg.297]    [Pg.8]    [Pg.296]    [Pg.662]    [Pg.673]    [Pg.238]    [Pg.186]    [Pg.188]    [Pg.195]    [Pg.197]    [Pg.198]    [Pg.198]   
See also in sourсe #XX -- [ Pg.865 ]

See also in sourсe #XX -- [ Pg.865 ]

See also in sourсe #XX -- [ Pg.865 ]




SEARCH



Arenes charge-transfer complexes

© 2024 chempedia.info