Mechanistic Investigations Towards a Successful PET with Breslow-Intermediates

Experimental mechanistic studies to learn about suitable conditions for a successful photocatalytic oxidation of Breslow intermediates.<div>Key findings </div><div>a) address the effect of additives (oxidative, reductive) and assembly effects on PET and the dark reaction, </div><div>b) include the experimental support of a SET + HAT sequence directly connecting the primary adduct of aldhyde and NHC and the Breslow intermediate.</div>

Mechanistic Investigations Towards a Successful PET with Breslow-Intermediates

Experimental mechanistic studies to learn about suitable conditions for a successful photocatalytic oxidation of Breslow intermediates.<div>Key findings </div><div>a) address the effect of additives (oxidative, reductive) and assembly effects on PET and the dark reaction, </div><div>b) include the experimental support of a SET + HAT sequence directly connecting the primary adduct of aldhyde and NHC and the Breslow intermediate.</div>

Mechanistic Investigations Towards a Successful PET with Breslow-Intermediates

Experimental mechanistic studies to learn about suitable conditions for a successful photocatalytic oxidation of Breslow intermediates.<div>Key findings </div><div>a) address the effect of additives (oxidative, reductive) and assembly effects on PET and the dark reaction, </div><div>b) include the experimental support of a SET + HAT sequence directly connecting the primary adduct of aldhyde and NHC and the Breslow intermediate.</div>

Utilization of iron sludge resulted from electro-coagulation in heterogeneous photo-Fenton process

The iron sludge generated from an electrocoagulation process was employed for the degradation of phenol through photo-Fenton process instead of iron salts. The morphology, functional groups and chemical composition of the iron sludge were investigated using scanning electron microscopy, Fourier infrared spectroscopy, and energy-dispersive X-ray spectroscopy. The effects of iron dose, H2O2 concentration, reaction time and initial concentration of phenol on photo-Fenton process performance were studied. The degradation efficiency of phenol reached 100% in the case of light compared to 68.6% in the case of dark reaction at pH of 3, iron dose of 150 mg/L and H2O2 concentration of 1.5 g/L. The degradation efficiencies of phenol were 100%, 71.3 and 51% at initial phenol concentrations of 50 mg/L, 100 mg/L and 150 mg/L, respectively. The expected cost for the treatment of one cubic meter of the contaminated wastewater was estimated to be 0.6224 $/m3.

Photosynthetic Function and the Photoprotective Mechanism of Leaves of Morus alba L. Seedlings under NaCl and NaHCO3 Stress Revealed by Proteomics

Photosynthetic function, photoprotection, and the response of related proteomics of mulberry (Morus alba L.) seedling leaves under NaCl and NaHCO3 stress with the same Na+ concentration (100 mmol&bull;L-1) were studied by using photosynthetic gas exchange and chlorophyll fluorescence techniques combined with TMT proteomics. The results showed that NaCl stress had no significant effect on photosystem II (PSII) activity in mulberry seedling leaves, and the expressions of the related proteins, OEE3-1 and PPD4, of the PSII oxygen-evolving complex (OEC) and the antenna proteins, CP24 10A, CP26, and CP29, of LHCII in the leaves also increased to varying degrees. The photosystem I (PSI) activity in the leaves of mulberry seedling also increased, and the expressions of some proteins, PsaF, PsaG, PsaH, PsaL, PsaN, and Ycf4, in PSI increased significantly under NaCl stress. Under NaHCO3 stress, the activity of PSII and PSI and the expression of their protein complexes and the electron transfer-related proteins significantly decreased. NaCl stress had little effect on RuBP regeneration during dark reaction in the leaves and the expressions of glucose synthesis related proteins and net photosynthetic rate (Pn) did not decrease significantly. The leaves could adapt to NaCl stress by reducing stomatal conductance (Gs) to increase water use efficiency (WUE). Under NaHCO3 stress, the expression of dark reaction-related proteins was mostly down-regulated, and Gs was significantly reduced, which indicated that non-stomatal factors were important reasons for the significant inhibition of carbon assimilation. In the photoprotective mechanism under NaCl stress, the expression of cyclic electron flow (CEF) related proteins, ndhH, ndhI, ndhK, and ndhM, involved in NAD(P)H dehydrogenase (NDH) and the key enzyme of the xanthophyll cycle, violaxanthin de-epoxidase (VDE) were up-regulated. In addition, the ratio of xanthophyll cycle components (A+Z)/(V+A+Z) was increased. The expressions of proteins FTR and Fd-NiR, which are related to Fd-dependent ROS metabolism and nitrogen metabolism, were also significant up-regulated under NaCl stress, which can effectively reduce the electronic pressure on Fd. Under NaHCO3 stress, the expressions of CEF-related proteins, VDE, ZE, FTR, Fd-NiR, Fd-GOGAT, SGAT, and GGAT, were significant down-regulated, and the photoprotective mechanism, like the xanthophyll cycle, CEF, and photorespiration, might be damaged, resulting in the inhibition of PSII activity and carbon assimilation in leaves of mulberry seedling under NaHCO3 stress.

Light-driven charge accumulation of a molecular Cu(I) complex for storage of photoredox equivalents

The diurnal day/night cycle is presently of great interest for harvesting solar energy aimed at rendering suitable energy storage schemes. To this end we present a noble-metal free system based on a Cu(I) 4H-imidazolate complex, that is efficiently photoreduced in the presence of a sacrificial donor. The two-electron reduced species obtained can be stored in the dark for more than 14 hours. In a dark reaction, the photoredox equivalents can subsequently be transferred to the electron acceptors methyl viologen or oxygen, while the starting Cu(I) complex is almost completely regained. Repetition of this process revealed a charging capacity of 72% after four cycles. The implications of light-driven charge accumulation and prolonged storage times for solar battery and photoredox catalysis are discussed

Light-driven charge accumulation of a molecular Cu(I) complex for storage of photoredox equivalents

The diurnal day/night cycle is presently of great interest for harvesting solar energy aimed at rendering suitable energy storage schemes. To this end we present a noble-metal free system based on a Cu(I) 4H-imidazolate complex, that is efficiently photoreduced in the presence of a sacrificial donor. The two-electron reduced species obtained can be stored in the dark for more than 14 hours. In a dark reaction, the photoredox equivalents can subsequently be transferred to the electron acceptors methyl viologen or oxygen, while the starting Cu(I) complex is almost completely regained. Repetition of this process revealed a charging capacity of 72% after four cycles. The implications of light-driven charge accumulation and prolonged storage times for solar battery and photoredox catalysis are discussed