Photoinduced Intramolecular Charge Transfer in Donor-Acceptor Biaryls and Resulting Applicational Aspects Regarding Fluorescent Probes and Solar Energy Conversion

This study is focused on the effects of photoinduced intramolecular charge transfer (CT) in three differently twisted donor-acceptor (D-A) biphenyls. Taking into account a further pair of differently twisted D-A biaryls new universal insights into the photoinduced electronic and conformation dynamics of D-A biaryls are obtained. Furthermore, possible applications in fields of solar energy conversion and fluorescence sensing of microenvironments are demonstrated.

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This study is focused on the effects of photoinduced intramolecular charge transfer (CT) in three differently twisted donor-acceptor (D-A) biphenyls. Taking into account a further pair of differently twisted D-A biaryls new universal insights into the photoinduced electronic and conformation dynamics of D-A biaryls are obtained. Furthermore, possible applications in fields of solar energy conversion and fluorescence sensing of microenvironments are demonstrated.

Experimental means of stationary and time-resolved (ps to s) luminescence, transient absorption (sub-ps), polarization spectroscopy, high pressure and low temperature techniques are employed in conjunction with quantum chemical calculations.

Twist angle and solvent dependent electron transfer (ET) interactions between the D and A aryl moieties are responsible for the low lying and solvatochromic intramolecular CT electron band which gains unusually high intensity through strong electronic coupling of the pure ¹ET with the ground (S₀) and ¹L_a state. As regards the class of biaryl compounds, for the first time, an excited state electron transfer from the D to the A could be monitored by dual spectrally separated stimulated fluorescence bands with precursor-successor relationship on a sub-ps timescale for the D-A biphenyls. It is concluded that, in additon to the electronic interaction of ¹ET with S₀ and ¹L_a, the electronic interaction with a close lying ¹L_b state plays a fundamental role in the ET dynamics and the ¹CT-S₀ transition probability in D-A biaryls.

The initial photoinduced conformational relaxation occurs towards planarity in all biaryls investigated. However, various results evidence that the highly twisted D-A biphenyl additionally performs a slow "excited state intramolecular back twist rotation" leading to a solvent polarity dependent conformational equilibrium between a more planar (CT) and a more twisted (CTR) conformer in S₁(¹CT). Using global analysis of the biexponential fluorescence decays as a function of temperature and pressure in medium polar solvents, the kinetics, thermodynamics, viscosity control and decomposed emission spectra associated with this adiabatic photoreaction are determined.

The twist angle dependent ability of the D-A biphenyls to serve as fluorescent probes of micropolarity, changes of microviscosity or matrix order, protic solvents and pH is investigated. In particular, fluorescence sensing of pH seems to be promising.