Triplet states molecular spectroscopy

Typical singlet lifetimes are measured in nanoseconds while triplet lifetimes of organic molecules in rigid solutions are usually measured in milliseconds or even seconds. In liquid media where drfifiision is rapid the triplet states are usually quenched, often by tire nearly iibiqitoiis molecular oxygen. Because of that, phosphorescence is seldom observed in liquid solutions. In the spectroscopy of molecules the tenn fluorescence is now usually used to refer to emission from an excited singlet state and phosphorescence to emission from a triplet state, regardless of the actual lifetimes. 

McGlynn, S. P., Azumi, T., and Kinoshita, M. (1969). Molecular Spectroscopy of the Triplet State , Prentice Hall, Englewood Cliffs, N.J. 

The functionalization of zinc porphyrin complexes has been studied with respect to the variation in properties. The structure and photophysics of octafluorotetraphenylporphyrin zinc complexes were studied.762 Octabromoporphyrin zinc complexes have been synthesized and the effects on the 11 NMR and redox potential of 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetraarylporphyrin were observed.763 The chiral nonplanar porphyrin zinc 3,7,8,12,13,17,18-heptabromo-2-(2-methoxyphenyl)-5,10,15,20-tetraphenylporphyrin was synthesized and characterized.764 X-ray structures for cation radical zinc 5,10,15,20-tetra(2,6-dichlorophenyl)porphyrin and the iodinated product that results from reaction with iodine and silver(I) have been reported.765 Molecular mechanics calculations, X-ray structures, and resonance Raman spectroscopy compared the distortion due to zinc and other metal incorporation into meso dialkyl-substituted porphyrins. Zinc disfavors ruffling over doming with the total amount of nonplanar distortion reduced relative to smaller metals.766 Resonance Raman spectroscopy has also been used to study the lowest-energy triplet state of zinc tetraphenylporphyrin.767... 

A molecular structure, similar to that of hexasilylated benzene derivative 229, was obtained from tetracyclic hexasilylbenzene 230 by Kira, Sakurai and coworkers, where the six silicon centres are incorporated in three five-membered ring systems (Scheme 80) °. In dimetalated compound 231, two lithium centres, coordinated by a quinuclidine ligand each, are capping the phenyl ring plane from both sides in the solid state. Moreover, it could be found that compound 231 has a thermally accessible triplet state, investigated by temperature-dependent ESR spectroscopy °°. 

R. S.P. McGlynn, T. Azumi and M. Kinoshita, Molecular Spectroscopy of the Triplet States. Englewood Cliff, N.J. Prentice-Hall, 1969. 

McGlynn SP, Azumi T, Kinoshita M (1969) In Molecular spectroscopy of the triplet state. Prentice-Hall, Englewood Cliffs, p 17... 

Molecular nitrogen, N2, is one of the most extensively studied diatomic molecules and optical spectroscopy has provided a wealth of information about its ground and excited electronic states. Molecular beam magnetic resonance studies of N2 in its ground state have yielded information about 14N nuclear spin dipolar and quadrupole interactions. Similar studies of N2 in its electronically excited A 3LU state were described in two very extensive papers by Freund, Miller, De Santis and Lurio [43] (paper I) and De Santis, Lurio, Miller and Freund [44] (paper II). We will describe their results and analysis in detail, but first note in passing that, strictly speaking, the lowest excited triplet state should be labelled the a state the label A has been used by all concerned in the past, so we will continue to do so. 

Photolysis of FL at a silica gel/air interface leads to the generation of 9-fluorenone (FLO) as the only isolable product. No dark reactions were observed and singlet molecular oxygen is not involved in the reaction. Transient spectroscopy shows that both the triplet state and the radical cation of FL are formed, thus indicating that an electron transfer mechanism is involved. Loss of a proton from the radical cation and subsequent reaction with molecular oxygen yields FL peroxide radicals, leading to the formation of 9-hydroxyfluorene. The latter readily photolyzes on the silica surface to produce FLO. 

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