Dergiler / Turkish Journal of Chemistry / 2004 / Cilt: 28 - Sayı: 4

Photophysical Properties and Electrochemistry of the N,N'-bis-n-butyl Derivative of Naphthalene Diimide

Sayfa
415–424
Yayın Tarihi
2004-04-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

It has been found that, in contrast to perylene diimide derivatives, which form p-electron donor-acceptor complexes with aromatic donor molecules of naphthalene, phenanthrene, pyrene and perylene, BBND does not form p-electron-donor acceptor complexes with aromatic donor molecules.

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Amaç & Hipotez:The spectral-luminescent properties and electrochemistry of the N,N'-bis-n-butyl derivative of naphthalene diimide were studied.
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Temel Bulgular & Veri:The main photophysical parameters (quantum yield, rate constants of fluorescence and of non-radiative deactivation and fluorescence lifetime) were determined.
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Sonuç & Katkı:It has been found that, in contrast to perylene diimide derivatives, which form p-electron donor-acceptor complexes with aromatic donor molecules of naphthalene, phenanthrene, pyrene and perylene, BBND does not form p-electron-donor acceptor complexes with aromatic donor molecules.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Spectral-luminescent properties · cyclic voltammetry · N'-bis-n-butyl derivative of naphthalene diimide

Özet

The spectral-luminescent properties and electrochemistry of the N,N'-bis-n-butyl derivative of naphthalene diimide were studied. The main photophysical parameters (quantum yield, rate constants of fluorescence and of non-radiative deactivation and fluorescence lifetime) were determined. The LUMO value (-3.51 eV) was determined by cyclic voltammetry. The N,N'-bis-n-butyl derivative of naphthalene diimide (BBND) shows 2 reversible reduction steps (-1.19 V and -1.75 V vs. Ferrocene) in chloroform. Quenching the fluorescence emissions of aromatic donor molecules in acetonitrile revealed the electron acceptor ability of the studied naphthalene diimide derivative. It has been found that, in contrast to perylene diimide derivatives, which form p-electron donor-acceptor complexes with aromatic donor molecules of naphthalene, phenanthrene, pyrene and perylene, BBND does not form p-electron-donor acceptor complexes with aromatic donor molecules.

Abstract

The spectral-luminescent properties and electrochemistry of the N,N'-bis-n-butyl derivative of naphthalene diimide were studied. The main photophysical parameters (quantum yield, rate constants of fluorescence and of non-radiative deactivation and fluorescence lifetime) were determined. The LUMO value (-3.51 eV) was determined by cyclic voltammetry. The N,N'-bis-n-butyl derivative of naphthalene diimide (BBND) shows 2 reversible reduction steps (-1.19 V and -1.75 V vs. Ferrocene) in chloroform. Quenching the fluorescence emissions of aromatic donor molecules in acetonitrile revealed the electron acceptor ability of the studied naphthalene diimide derivative. It has been found that, in contrast to perylene diimide derivatives, which form p-electron donor-acceptor complexes with aromatic donor molecules of naphthalene, phenanthrene, pyrene and perylene, BBND does not form p-electron-donor acceptor complexes with aromatic donor molecules.

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Bu Makaleye Atıf Yap

POSOKHOV, Y., ALP, S., KÖZ, B. (2004). Photophysical Properties and Electrochemistry of the N,N'-bis-n-butyl Derivative of Naphthalene Diimide. Turkish Journal of Chemistry, Cilt: 28 - Sayı: 4, 415–424. https://ajindex.com/articles/722898

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