This paper discusses the effect mechanism of auxochrome of electronic spectrum. The study proves that the auxochrome does not invariably make the maximum absorption wavelength of chromophore shift towards lower photon energy. For the transition of n-->pi*, the p orbit of the auxochrome interacts with the minimum antibonding empty orbit(pi*), which will make the energy of pi* increase, while the p orbit of the auxochrome is perpendicular to the n orbit of chromophore, and the energy of the n orbit will remain steady ultimately, so the transition energy of n-->pi* will increase. For the transition of pi-->pi*, the interaction of p orbit of the auxochrome and maximum bonding orbit (pi) of the chromophore forms new orbits, so the energy of the maximum bonding orbit in new orbits will increase. In some compounds, the increase is higher than those of pi*, so the transition energy of pi-->pi* will decrease and absorption wavelength will shift towards lower photon energy, which, however, is reverse in other compounds.
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Phys Chem Chem Phys
January 2023
Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695-8204, USA.
Bacteriochlorophylls, nature's near-infrared absorbers, play an essential role in energy transfer in photosynthetic antennas and reaction centers. To probe energy-transfer processes akin to those in photosynthetic systems, nine synthetic bacteriochlorin-bacteriochlorin dyads have been prepared wherein the constituent pigments are joined at the -positions by a phenylethyne linker. The phenylethyne linker is an unsymmetric auxochrome, which differentially shifts the excited-state energies of the phenyl- or ethynyl-attached bacteriochlorin constituents in the dyad.
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June 2019
Department of Chemistry, King Fahd University of Petroleum and Minerals, Dhahran, Saudi Arabia.
1,1-Dimethyl-3-phenylurea (known as fenuron) which is a phenyl urea-based widely used herbicide exhibits interesting structural and conformational properties and a notable biological activity. A detailed analysis on the vibrational, molecular and electronic characteristics of fenuron has been carried out. Potential energy scans (PESs) performed at the B3LYP/6-311++G(d,p) level of theory predicted two possible minima corresponding to the optimized anti and synforms resulting from the internal rotation about the N-C bond.
View Article and Find Full Text PDFJ Phys Chem A
December 2014
Department of Chemistry, University of Florida, P.O. Box 117200, Gainesville, Florida 32611, United States.
A pair of diketopyrrolopyrrole (DPP) chromophores that are end-functionalized with platinum containing "auxochromes" were subjected to electrochemical and photophysical study. The chromophores contain either platinum acetylide or ortho-metalated 2-thienylpyridinyl(platinum) end-groups (DPP-Pt(CC) and DPP-Pt(acac), respectively). The ground state redox potentials of the chromophores were determined by solution electrochemistry, and the HOMO and LUMO levels were estimated.
View Article and Find Full Text PDFPhotochem Photobiol Sci
April 2014
Department of Chemistry, Washington University, St. Louis, Missouri 63130-4889, USA.
Synthetic chlorins can accommodate diverse substituents about the macrocycle perimeter. Simple auxochromes (e.g.
View Article and Find Full Text PDFPhotochem Photobiol
August 2012
Department of Chemistry, Washington University, St. Louis, MO, USA.
Assessing the effects of substituents on the spectra of chlorophylls is essential for gaining a deep understanding of photosynthetic processes. Chlorophyll a and b differ solely in the nature of the 7-substituent (methyl versus formyl), whereas chlorophyll a and d differ solely in the 3-substituent (vinyl versus formyl), yet have distinct long-wavelength absorption maxima: 665 (a) 646 (b) and 692 nm (d). Herein, the spectra, singlet excited-state decay characteristics, and results from DFT calculations are examined for synthetic chlorins and 13(1)-oxophorbines that contain ethynyl, acetyl, formyl and other groups at the 3-, 7- and/or 13-positions.
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