Light intensity effects on photoinduced charge separation parameters in a molecular triad based on an Iridium(III) bis(terpyridine) unit.

نویسندگان

  • Lucia Flamigni
  • Etienne Baranoff
  • Jean-Paul Collin
  • Jean-Pierre Sauvage
  • Barbara Ventura
چکیده

The effect of photon flux on the yield and lifetime of charge separation over the extreme components of a D-Ir-A triad, where D is a triphenyl amine electron donor, A is a naphthalene bis(imide) electron acceptor and Ir is an Ir(III) bis(terpyridine) complex, has been investigated. In usual laboratory conditions, with nanosecond and picosecond laser pulses in the 4-8 mJ range, biphotonic processes take place. Biphotonic products and their evolution can introduce complications in reaction mechanisms and their interpretation but can also drastically reduce the yield and the lifetime of the charge-separated state. In the present case, after discussion of several possible mechanisms, the process detrimental to charge separation is ascribed to absorption of a photon by the photogenerated charge-separated state D(+)-Ir-A(-).

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A photoinduced mixed-valence state in an organic bis-triarylamine mixed-valence compound with an iridium-metal-bridge.

Upon irradiation a mixed-valence (MV) state is formed in a donor-iridium(III)-acceptor triad by a photoinduced electron transfer process. The resulting radical and intervalence charge transfer (IV-CT) absorptions cover a wide spectral range (3200-400 nm). These results were supported by spectroelectrochemistry, fs-time resolved pump-probe spectroscopy and assisted by TD-DFT calculations.

متن کامل

Optimising the synthesis, polymer membrane encapsulation and photoreduction performance of Ru(II)- and Ir(III)-bis(terpyridine) cytochrome c bioconjugates.

Ruthenium(II) and iridium(III) bis(terpyridine) complexes were prepared with maleimide functionalities in order to site-specifically modify yeast iso-1 cytochrome c possessing a single cysteine residue available for modification (CYS102). Single X-ray crystal structures were solved for aniline and maleimide Ru(II) 3 and Ru(II) 4, respectively, providing detailed structural detail of the complex...

متن کامل

Ultrafast photoinduced electron transfer reactions in supramolecular arrays: From charge separation and storage to molecular switches

Photochemical electron transfer reactions on a picosecond time scale have been studied in two covalently-linked donor-acceptor systems. The first molecule is a chlorophyll-porphyrin-quinone triad that closely mimics photosynthetic charge separation by undergoing picosecond electron transfer in low temperature glasses to yield a radical ion pair that lives for 2 ms and exhibits spin-polarization...

متن کامل

b308983e doc..b308983e chapter .. Page147

In order to mimic the photosynthetic reaction centre and better understand photoinduced electron transfer processes, a family of compounds has been studied for the past 15 years. These are transition metal complexes, M(tpy)2 where tpy is a 2,2A:6A,2B terpyridine based ligand, bearing on one side a donor group and on the other side an acceptor group. The resulting triad molecules or their two-co...

متن کامل

The influence of numbers and ligation positions of the triphenylamine unit on the photophysical and electroluminescent properties of homoleptic iridium(III) complexes: a theoretical perspective.

A DFT/TDDFT investigation was carried out on a series of homoleptic triphenylamine-featured Ir(iii) complexes [: (fac-tris[2-phenyl-4-(2-(N,N-diphenylamino)phenyl)pyridine]iridium(iii)); : (fac-tris[2-phenyl-4-(3-(N,N-diphenylamino)phenyl)pyridine]iridium(iii)); : (fac-tris[2-phenyl-4-(4-(N,N-diphenylamino)phenyl)pyridine]iridium(iii))] with one triphenylamine unit in the 2-phenylpyridine (ppy)...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Chemphyschem : a European journal of chemical physics and physical chemistry

دوره 8 13  شماره 

صفحات  -

تاریخ انتشار 2007