Abstract
The properties of two series of oligo(2,3-dioxyfunctionalized)naphthalenes which are connected at the 1,4-positions, that is, methoxy derivatives 1-4 and derivatives that possess two pyrene groups on the central scaffolding oxygen functions 5-8, are described. In 1-4, the fluorescence quantum yields increased by about 20-80% as the number of naphthalene units increased. The intramolecular energy transfer quantum yields of 5-8 were around 20% regardless of the number of naphthalene units.
| Original language | English |
|---|---|
| Pages (from-to) | 1241-1244 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 47 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 2006 Feb 20 |
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ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
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Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes. / Tsubaki, Kazunori; Miura, Masaya; Nakamura, Asao; Kawabata, Takeo.
In: Tetrahedron Letters, Vol. 47, No. 8, 20.02.2006, p. 1241-1244.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes
AU - Tsubaki, Kazunori
AU - Miura, Masaya
AU - Nakamura, Asao
AU - Kawabata, Takeo
PY - 2006/2/20
Y1 - 2006/2/20
N2 - The properties of two series of oligo(2,3-dioxyfunctionalized)naphthalenes which are connected at the 1,4-positions, that is, methoxy derivatives 1-4 and derivatives that possess two pyrene groups on the central scaffolding oxygen functions 5-8, are described. In 1-4, the fluorescence quantum yields increased by about 20-80% as the number of naphthalene units increased. The intramolecular energy transfer quantum yields of 5-8 were around 20% regardless of the number of naphthalene units.
AB - The properties of two series of oligo(2,3-dioxyfunctionalized)naphthalenes which are connected at the 1,4-positions, that is, methoxy derivatives 1-4 and derivatives that possess two pyrene groups on the central scaffolding oxygen functions 5-8, are described. In 1-4, the fluorescence quantum yields increased by about 20-80% as the number of naphthalene units increased. The intramolecular energy transfer quantum yields of 5-8 were around 20% regardless of the number of naphthalene units.
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UR - http://www.scopus.com/inward/citedby.url?scp=30944459020&partnerID=8YFLogxK
U2 - 10.1016/j.tetlet.2005.12.095
DO - 10.1016/j.tetlet.2005.12.095
M3 - Article
VL - 47
SP - 1241
EP - 1244
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 8
ER -