Photocatalytic Dehydrogenation of Primary Alcohols: Selectivity Goes against Adsorptivity

Dongge Ma; Anan Liu; Chichong Lu; Chuncheng Chen

doi:10.1021/acsomega.7b00754

Photocatalytic Dehydrogenation of Primary Alcohols: Selectivity Goes against Adsorptivity

ACS Omega. 2017 Aug 2;2(8):4161-4172. doi: 10.1021/acsomega.7b00754. eCollection 2017 Aug 31.

Authors

Dongge Ma^{1

2

3}, Anan Liu^{2

3}, Chichong Lu¹, Chuncheng Chen^{2

3}

Affiliations

¹ School of Science, Beijing Technology and Business University, 100048 Beijing, P. R. China.
² Key Laboratory of Photochemistry, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, 100190 Beijing, P. R. China.
³ University of Chinese Academy of Sciences, Beijing 100049, P. R. China.

Abstract

Solid/liquid heterogeneous photocatalysis was often considered to occur on the active sites of a solid catalyst surface. Herein, we report that the selectivity of photocatalytic dehydrogenative oxidations of aliphatic primary alcohols in acetonitrile solution into corresponding aldehydes exhibits an anomalous relationship with adsorption behavior of the alcohols. By using Pt-loaded TiO₂ photocatalyst in an inert atmosphere under UV light illumination, primary short-chain alcohols (SCAs) with strong adsorption were dehydrogenated into aldehydes in very poor selectivity, whereas weak-adsorbable long-chain alcohols (LCAs) were transformed into corresponding aldehydes with much higher selectivity. More than 20 examples of primary LCAs (C₄-C₁₀) were successfully transformed into their corresponding aldehydes with satisfactory selectivity and yield. Both solid-state magic-angle-spinning ¹³C NMR and attenuated total reflectance-Fourier transform infrared spectroscopy studies provided concrete differences in adsorption behaviors on the Pt-TiO₂ photocatalyst surface between SCA ethanol and LCA n-octanol. To further uncover the mechanism for different selectivities of SCAs and LCAs in photodehydrogenation, in situ electron paramagnetic resonance (EPR) experiments (at 8 K temperature) were employed to observe the oxidation features of photogenerated hole in the valance band of Pt-TiO₂ (h_vb ⁺). The EPR experimental studies exhibited that unlike ethanol, either n-octanol or solvent acetonitrile alone all could not scavenge photogenerated h_vb ⁺ on Pt-P25 photocatalyst and only n-octanol dissolved in acetonitrile solvent could smoothly react with photoinduced hole. This indicated that selective oxidations of LCAs were achieved by solvent-delivered oxidation rather than directly destructive oxidation of photogenerated h_vb ⁺. Our results may open an alternative way in selective dehydrogenative oxidation of various substrates sensitive to both dioxygen and high-temperature treatments.