@article {Belogorokhov:2011:1555-130X:478,
title = "Infrared Spectroscopy of Semiconductor Structures Based on Alkyl-Substituted Lanthanide (III) Clam-Shell Mono-, Di-, and Di-Trisphthalocyanine Complexes",
journal = "Journal of Nanoelectronics and Optoelectronics",
parent_itemid = "infobike://asp/jno",
publishercode ="asp",
year = "2011",
volume = "6",
number = "4",
publication date ="2011-12-01T00:00:00",
pages = "478-483",
itemtype = "ARTICLE",
issn = "1555-130X",
eissn = "1555-1318",
url = "https://www.ingentaconnect.com/content/asp/jno/2011/00000006/00000004/art00011",
doi = "doi:10.1166/jno.2011.1199",
keyword = "INFRARED SPECTROSCOPY, PHTHALOCYANINES, ORGANIC SEMICONDUCTORS",
author = "Belogorokhov, I. A. and Tikhonov, E. V. and Dronov, M. A. and Ryabchikov, Yu. V. and Neudachina, V. S. and Yashina, L. V. and Tomilova, L. G. and Khokhlov, D. R.",
abstract = "Optical properties of semiconductor structures based on clam-shell phthalocyanine complexes have been studied by Fourier Transform Infrared Spectrometry. Transmission spectra of metal-free monophthalocyanine, bis-phthalocyanine of Eu and Eu di-tris-phthalocyanine organic semiconductors
were have been obtained and analyzed. Comparison of spectral data from different clam-shell complexes revealed that magnetic ff interaction of Eu atoms increase the energy of vibronic states which is clearly indicated by the spectral shift of absorption lines position.
A new set of absorption lines in the 2360 \textdiv 2341 cm1 range was observed. It was suggested that these lines correspond to vibrations of orto-bis(oximetil)phenol group. It was found that vibronic modes of the phtalocyanine-ring reveal several absorption lines with spectral
coordinates 526 cm1, 502 cm1, 484 cm1, 467 cm1 in the far infrared region.",
}