Raman Spectroscopic Characteristics of Phthalocyanine and Naphthalocyanine in Sandwich-Type Phthalocyaninato and Porphyrinato Rare Earth Complexes. Part 5.Raman Spectroscopic Characteristics of Naphthalocyanine in Mixed [tetrakis(4-tert-butylphenyl)p

Sun, Xuan, , Biang, Yongzhong, , Wang, Rongming, & Jiang, Jianzhuang (2003) Raman Spectroscopic Characteristics of Phthalocyanine and Naphthalocyanine in Sandwich-Type Phthalocyaninato and Porphyrinato Rare Earth Complexes. Part 5.Raman Spectroscopic Characteristics of Naphthalocyanine in Mixed [tetrakis(4-tert-butylphenyl)p. Journal of Raman Spectroscopy, 34, pp. 306-314.

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Raman spectra were recorded in the range 400–1800 cm−1 for a series of 15 mixed [tetrakis(4-tert-butylphenyl)porphyrinato](2,3-naphthalocyaninato) rare earth double-deckers M(TBPP)(Nc) (M = Y; La–Lu except Pm) using laser excitation at 632.8 and 785 nm. Comparisons with bis(naphthalocyaninato) rare earth counterparts reveal that the vibrations of the metallonaphthalocyanine M(Nc) fragment dominate the Raman features of M(TBPP)(Nc). When excited with radiation of 632.8 nm, the most intense vibration appears at about 1595 cm−1, due to the naphthalene stretching. These complexes exhibit the marker Raman band for Nc•− as a medium-intense band in the range 1496–1507 cm−1, attributed to the coupling of pyrrole and aza stretching, while the marker Raman band of Nc2− in intermediate-valence Ce(TBPP)(Nc) appears as a strong band at 1493 cm−1 and is due to the isoindole stretchings. By contrast, when excited with radiation of 785 nm that is in close resonance with the main Q absorption band of the naphthalocyanine ligand, the ring radial vibrations at ca 680 and 735 cm−1 for MIII(TBPP)(Nc) are selectively intensified and are the most intense bands. For the cerium double-decker, the most intense vibration also acting as the marker Raman band of Nc2− appears at 1497 cm−1 with contributions from both pyrrole CC and aza CN stretches. The same vibrational modes show weak to medium intensity scattering at 1506–1509 cm−1 for MIII(TBPP)(Nc) and this is the marker Raman band of Nc•− when thus excited. The scatterings due to the Nc breathings, ring radial vibration, aza group stretchings, naphthalene stretchings, benzoisoindole stretchings and the coupling of pyrrole CC and aza CN stretchings in MIII(TBPP)(Nc) are all slightly blue shifted along with the decrease in rare earth ionic radius, confirming the effects of increased ring–ring interactions on the Raman characteristics of naphthalocyanine in the mixed ring double-deckers.

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ID Code: 23616
Item Type: Contribution to Journal (Journal Article)
Refereed: Yes
ORCID iD:
Rintoul, Llewellynorcid.org/0000-0003-0489-4446
Measurements or Duration: 9 pages
DOI: 10.1002/jrs.997
ISSN: 0377-0486
Pure ID: 34121045
Divisions: Past > QUT Faculties & Divisions > Faculty of Science and Technology
Past > QUT Faculties & Divisions > Science & Engineering Faculty
Current > Research Centres > Australian Research Centre for Aerospace Automation
Copyright Owner: Consult author(s) regarding copyright matters
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Deposited On: 17 Jun 2009 14:01
Last Modified: 03 Mar 2024 16:29