Electronic spectroscopy organic molecules

Ultraviolet (UV) spectroscopy (Section 14.7) An optical spectroscopy employing ultraviolet irradiation. UV spectroscopy provides structural information about the extent of 7r electron conjugation in organic molecules. 

Bifunctional spacer molecules of different sizes have been used to construct nanoparticle networks formed via self-assembly of arrays of metal colloid particles prepared via reductive stabilization [88,309,310]. A combination of physical methods such as TEM, XAS, ASAXS, metastable impact electron spectroscopy (MIES), and ultraviolet photoelectron spectroscopy (UPS) has revealed that the particles are interlinked through rigid spacer molecules with proton-active functional groups to bind at the active aluminium-carbon sites in the metal-organic protecting shells [88]. 

Many techniques are available for the determination of the geometry of organic molecules in their ground states, such as microwave spectroscopy, infrared and Raman spectroscopy, and electron and x-ray diffraction. 

In ultraviolet and visible region, electronic transition of atoms and molecules are observed. This is why it is called electronic spectroscopy. In infrared region the absorption of radiation by an organic compound causes molecular vibrations and so it is called vibrational spectroscopy. 

In contrast to the minimal activity in infrared reflection studies the technique of inelastic electron tunneling spectroscopy (IETS) recently has contributed a large amount of information on monolayer adsorption of organic molecules on smooth metal oxide surfaces,Q),aluminum oxide layers on evaporated aluminum. These results indicate that a variety of organic molecules with acidic hydrogens, such as carboxylic acids and phenols chemisorb on aluminum Oxide overlayers by proton dissociation - 1 — and that monolayer coverage can be attained quite repro-ducibly by solution doping techniques. - The IETS technique is sensitive to both infrared and Raman modes. — However, almost no examples exist in which Raman il and or infrared spectra have been taken for an adsorbate/substrate system for which IETS spectra have been observed. 

The principles of electronic spectroscopy have been discussed by Herzberg (1950) for diatomic molecules, and in a classic review by Sponer and Teller (1941) for the more general case of polyatomic structures. Recent developments are described in articles appearing regularly in the Annual Reviews of Physical Chemistry. Triatomic molecules and radicals have been intensively studied, the latter by the powerful method of flash photolysis (Herzberg, 1959). As triatomic structures have been comprehensively reviewed recently (Ramsay, 1962) we include in this article only those triatomic systems that are of particular interest in organic chemistry. Otherwise attention will be directed to molecules of four or more atoms, including all known representatives of the important chromophores. 

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