2000
DOI: 10.1002/(sici)1099-0682(200001)2000:1<205::aid-ejic205>3.0.co;2-1
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis, Spectroscopic, and Electrochemical Properties of Rare Earth Double-Deckers with Tetra(tert-butyl)-2,3-naphthalocyaninato Ligands

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

4
33
0

Year Published

2001
2001
2015
2015

Publication Types

Select...
9

Relationship

6
3

Authors

Journals

citations
Cited by 62 publications
(38 citation statements)
references
References 34 publications
4
33
0
Order By: Relevance
“…S1. Due to remarkable rare earth size effect, the visible Q bands at 708-725 nm may be attributed to characteristic p-radical anion bands of Nc ring [18, [21][22][23]. It should be mentioned that the Q band of naphthalocyanine splits into two bands, which is the result of the introduction of thiophenyl on the naphthalocyanine ring, and the second Q band at 792-812 nm becomes stronger with the decrease of rare earth ion radius.…”
Section: Resultsmentioning
confidence: 99%
“…S1. Due to remarkable rare earth size effect, the visible Q bands at 708-725 nm may be attributed to characteristic p-radical anion bands of Nc ring [18, [21][22][23]. It should be mentioned that the Q band of naphthalocyanine splits into two bands, which is the result of the introduction of thiophenyl on the naphthalocyanine ring, and the second Q band at 792-812 nm becomes stronger with the decrease of rare earth ion radius.…”
Section: Resultsmentioning
confidence: 99%
“…As shown in Table 1, the ionic radii of Ce(Ⅲ), Sm(Ⅲ) and Lu(Ⅲ) are 114 pm, 109 pm and 97 pm respectively [47,48], and the 2PA cross-section of Ce(OOPc) 2 (1), Sm(OOPc) 2 (2), Lu(OOPc) 2 (3) is 3.5×10 4 GM (1), 9.3×10 4 GM (2) and 1.2×10 5 GM (3) at the wavelength of 800 nm respectively. Previous research has proved that the π-π interaction between the two phthalocyaninato rings becomes stronger with the decrease of the rare earth atomic radius.…”
Section: A C C E P T E D Accepted Manuscriptmentioning
confidence: 99%
“…This method considerably differs from the synthesis in solution [11][12][13] since the starting nitrile serves simultaneously as the reagent and the reaction medium. According to this method, the synthesis of dinaphthalocyanines 2-4 was performed by melting of a mixture of dinitrile 1 with the corresponding lanthanide acetates by the gradual increase of temperature from 220 to 310 °C and by keeping at this temperature until the reaction mixture was solidified (~2 h).…”
Section: Synthesismentioning
confidence: 99%
“…Using of this approach allowed us to decrease the time of reaction and increase the yields of target complexes comparing to their analogues, which were obtained by the synthesis in solution. [13] Sandwich-Type Lanthanide(III) Dinaphthalocyanine Complexes In addition to the melting method, the europium and erbium dinaphthalocyanine complexes were synthesized using microwave irradiation (MW). This method has been suggested for the first time for the synthesis of unsubstituted and octa-tert-butyl-substituted lanthanide diphthalocyanines [15] and so far has not been used for preparation of naphthalocyanine complexes.…”
Section: Synthesismentioning
confidence: 99%