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Evaluation of MAA Analogues as Potential Candidates to Increase Photostability in Sunscreen Formulations 将 MAA 类似物作为提高防晒配方光稳定性的潜在候选物质进行评估
Photochem Pub Date : 2024-02-06 DOI: 10.3390/photochem4010007
Jacobo Soilán, Leonardo López-Cóndor, Beatriz Peñín, José Aguilera, M. V. de Gálvez, Diego Sampedro, R. Losantos
{"title":"Evaluation of MAA Analogues as Potential Candidates to Increase Photostability in Sunscreen Formulations","authors":"Jacobo Soilán, Leonardo López-Cóndor, Beatriz Peñín, José Aguilera, M. V. de Gálvez, Diego Sampedro, R. Losantos","doi":"10.3390/photochem4010007","DOIUrl":"https://doi.org/10.3390/photochem4010007","url":null,"abstract":"Avobenzone is one of the most widely used sunscreens in skin care formulations, but suffers from some drawbacks, including photo instability. To mitigate this critical issue, the use of octocrylene as a stabilizer is a common approach in these products. However, octocrylene has been recently demonstrated to show potential phototoxicity. The aim of this work is to analyze the performance of a series of mycosporine-like amino acid (MAA)-inspired compounds to act as avobenzone stabilizers as an alternative to octocrylene. Different avobenzone/MAA analogue combinations included in galenic formulations were followed under increasing doses of solar-simulated UV radiation. Some of the synthetic MAA analogues analyzed were able to increase by up to two times the UV dose required for 50% of avobenzone photobleaching. We propose some of these MAA analogues as new candidates to act as avobenzone-stabilizing compounds in addition to their UV absorbance and antioxidant properties, together with a facile synthesis.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"10 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139860673","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Physicochemical Properties of Tungsten Trioxide Photoanodes Fabricated by Wet Coating of Soluble, Particulate, and Mixed Precursors 通过湿法涂覆可溶性、颗粒状和混合前驱体制造的三氧化钨光阳极的物理化学特性
Photochem Pub Date : 2024-02-01 DOI: 10.3390/photochem4010006
Valli Kamala Laxmi Ramya Chittoory, Marketa Filipsika, Radim Bartoš, M. Králová, P. Dzik
{"title":"Physicochemical Properties of Tungsten Trioxide Photoanodes Fabricated by Wet Coating of Soluble, Particulate, and Mixed Precursors","authors":"Valli Kamala Laxmi Ramya Chittoory, Marketa Filipsika, Radim Bartoš, M. Králová, P. Dzik","doi":"10.3390/photochem4010006","DOIUrl":"https://doi.org/10.3390/photochem4010006","url":null,"abstract":"Advanced oxidation processes are emerging technologies for the decomposition of organic pollutants in various types of water by harnessing solar energy. The purpose of this study is to examine the physicochemical characteristics of tungsten(VI) oxide (WO3) photoanodes, with the aim of enhancing oxidation processes in the treatment of water. The fabrication of WO3 coatings on conductive fluorine-doped tin oxide (FTO) substrates was achieved through a wet coating process that utilized three different liquid formulations: a dispersion of finely milled WO3 particles, a fully soluble WO3 precursor (acetylated peroxo tungstic acid), and a combination of both (applying a brick-and-mortar strategy). Upon subjecting the WO3 coatings to firing at a temperature of 450 °C, it was observed that their properties exhibited marked variations. The fabricated photoanodes are examined using a range of analytical techniques, including profilometry, thermo-gravimetric analysis (TGA), X-ray diffraction (XRD), and voltammetry. The experimental data suggest that the layers generated through the combination of particulate ink and soluble precursor (referred to as the brick-and-mortar building approach) display advantageous physicochemical properties, rendering them suitable for use as photoanodes in photoelectrochemical cells.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"51 10","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139880993","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Physicochemical Properties of Tungsten Trioxide Photoanodes Fabricated by Wet Coating of Soluble, Particulate, and Mixed Precursors 通过湿法涂覆可溶性、颗粒状和混合前驱体制造的三氧化钨光阳极的物理化学特性
Photochem Pub Date : 2024-02-01 DOI: 10.3390/photochem4010006
Valli Kamala Laxmi Ramya Chittoory, Marketa Filipsika, Radim Bartoš, M. Králová, P. Dzik
{"title":"Physicochemical Properties of Tungsten Trioxide Photoanodes Fabricated by Wet Coating of Soluble, Particulate, and Mixed Precursors","authors":"Valli Kamala Laxmi Ramya Chittoory, Marketa Filipsika, Radim Bartoš, M. Králová, P. Dzik","doi":"10.3390/photochem4010006","DOIUrl":"https://doi.org/10.3390/photochem4010006","url":null,"abstract":"Advanced oxidation processes are emerging technologies for the decomposition of organic pollutants in various types of water by harnessing solar energy. The purpose of this study is to examine the physicochemical characteristics of tungsten(VI) oxide (WO3) photoanodes, with the aim of enhancing oxidation processes in the treatment of water. The fabrication of WO3 coatings on conductive fluorine-doped tin oxide (FTO) substrates was achieved through a wet coating process that utilized three different liquid formulations: a dispersion of finely milled WO3 particles, a fully soluble WO3 precursor (acetylated peroxo tungstic acid), and a combination of both (applying a brick-and-mortar strategy). Upon subjecting the WO3 coatings to firing at a temperature of 450 °C, it was observed that their properties exhibited marked variations. The fabricated photoanodes are examined using a range of analytical techniques, including profilometry, thermo-gravimetric analysis (TGA), X-ray diffraction (XRD), and voltammetry. The experimental data suggest that the layers generated through the combination of particulate ink and soluble precursor (referred to as the brick-and-mortar building approach) display advantageous physicochemical properties, rendering them suitable for use as photoanodes in photoelectrochemical cells.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"278 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139820931","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Inverse Problems in Pump–Probe Spectroscopy 泵浦探针光谱学中的逆问题
Photochem Pub Date : 2024-01-31 DOI: 10.3390/photochem4010005
Denis S. Tikhonov, Diksha Garg, Melanie Schnell
{"title":"Inverse Problems in Pump–Probe Spectroscopy","authors":"Denis S. Tikhonov, Diksha Garg, Melanie Schnell","doi":"10.3390/photochem4010005","DOIUrl":"https://doi.org/10.3390/photochem4010005","url":null,"abstract":"Ultrafast pump–probe spectroscopic studies allow for deep insights into the mechanisms and timescales of photophysical and photochemical processes. Extracting valuable information from these studies, such as reactive intermediates’ lifetimes and coherent oscillation frequencies, is an example of the inverse problems of chemical kinetics. This article describes a consistent approach for solving this inverse problem that avoids the common obstacles of simple least-squares fitting that can lead to unreliable results. The presented approach is based on the regularized Markov Chain Monte-Carlo sampling for the strongly nonlinear parameters, allowing for a straightforward solution of the ill-posed nonlinear inverse problem. The software to implement the described fitting routine is introduced and the numerical examples of its application are given. We will also touch on critical experimental parameters, such as the temporal overlap of pulses and cross-correlation time and their connection to the minimal reachable time resolution.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"433 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140473140","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Rhodamine–Perylene Compact Electron Donor–Acceptor Dyad: Spin-Orbit Charge-Transfer Intersystem Crossing and the Energy Balance of the Triplet Excited States 罗丹明-苝紧密电子供体-受体二元体:自旋轨道电荷转移系统间交叉和三重激发态的能量平衡
Photochem Pub Date : 2024-01-29 DOI: 10.3390/photochem4010004
M. Imran, Dongyi Liu, Kaiyue Ye, Xue Zhang, Jianzhang Zhao
{"title":"The Rhodamine–Perylene Compact Electron Donor–Acceptor Dyad: Spin-Orbit Charge-Transfer Intersystem Crossing and the Energy Balance of the Triplet Excited States","authors":"M. Imran, Dongyi Liu, Kaiyue Ye, Xue Zhang, Jianzhang Zhao","doi":"10.3390/photochem4010004","DOIUrl":"https://doi.org/10.3390/photochem4010004","url":null,"abstract":"We prepared a rhodamine (RB)–perylene (Pery) compact electron donor/acceptor dyad (RB–Pery) to study the spin-orbit charge-transfer intersystem crossing (SOCT–ISC). The UV–vis absorption spectrum indicates a negligible electronic interaction between the donor and acceptor at ground state. However, the fluorescence of both the RB and Pery units are quenched in the dyad, which is attributed to the photoinduced electron transfer, supported by the electrochemical studies. Nanosecond transient absorption (ns-TA) spectra show delocalized triplet states, i.e., there is an excited-state equilibrium between Pery and the RB triplet states. The triplet state lifetime was determined as 109.8 μs. With intermolecular triplet–triplet energy transfer, monitored using ns-TA spectra, the triplet-state energy balance between RB and Pery in RB–Pery was confirmed. The proposed cascade photophysical processes of the dyad are 1RB*-Pery→RB–Pery+•→[3RB*-Pery↔RB-3Pery*]. Moreover, long-lived rhodamine radical cation (in milliseconds) was detected in both deaerated/aerated non-polar or low-polarity solvents (i.e., p-xylene, toluene). The potential energy curve of the dyad against the variation in the dihedral angle between the two units indicates large torsional freedom (53°~128°) in RB–Pery, which leads to inefficient SOCT–ISC; consequently, low singlet-oxygen quantum yields (ΦΔ = 2~8%) were observed.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"58 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140487206","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interactions of CdSe Nanocrystals with Cationic Proteins Extracted from Moringa oleifera Seeds 硒化镉纳米晶体与从辣木籽中提取的阳离子蛋白的相互作用
Photochem Pub Date : 2024-01-15 DOI: 10.3390/photochem4010003
L. Daniel, Salatiel Kapofi, Martha Kandawa-Schulz, H. Kwaambwa
{"title":"Interactions of CdSe Nanocrystals with Cationic Proteins Extracted from Moringa oleifera Seeds","authors":"L. Daniel, Salatiel Kapofi, Martha Kandawa-Schulz, H. Kwaambwa","doi":"10.3390/photochem4010003","DOIUrl":"https://doi.org/10.3390/photochem4010003","url":null,"abstract":"Even with significant developments in nanoscience, relatively little is known about the interactions of nanocrystal semiconducting materials with bio-macromolecules. To investigate the interfacial phenomena of cadmium selenide quantum dot (CdSe QD) nanocrystals with proteins extracted from Moringa oleifera seeds, different concentrations of cadmium selenide quantum dots–Moringa oleifera seed protein (CdSe–MSP) complexes were prepared. Respective CdSe QDs with hexagonal phase and crystalline size in the range of 4–7 nm were synthesized and labelled with the purified mesoporous MSP having a surface area of 8.4 m2/g. The interaction mechanism between CdSe QDs and MSP was studied using UV–Vis absorption, fluorescence emission and Fourier Transform Infrared spectroscopies. The UV–Vis absorption spectra showed absorption bands of CdSe–MSP complexes at 546.5 nm. The fluorescence intensity of CdSe QDs was found to decrease with increasing concentration of MSP. The thermodynamic potentials ∆Hθ (−321.3 × 103 Jmol−1); ∆Sθ (156.0 JK−1mol−1) and ∆Gθ (−46.6 × 103 Jmol−1) were also calculated. The stability of the complex found is strongly influenced by electrostatics interaction and surface-bound complexation equilibrium attraction. This information can help to elucidate the surface characteristics of MSP and its potential interactions with other molecules or nanoparticles.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":" 7","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139622071","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Survey of T1 and T2 Energies of Intramolecular Singlet Fission Chromophores 分子内单子裂变色团的 T1 和 T2 能量调查
Photochem Pub Date : 2024-01-10 DOI: 10.3390/photochem4010002
Guoying Yao, Zhenyu Yang, T. Zeng
{"title":"Survey of T1 and T2 Energies of Intramolecular Singlet Fission Chromophores","authors":"Guoying Yao, Zhenyu Yang, T. Zeng","doi":"10.3390/photochem4010002","DOIUrl":"https://doi.org/10.3390/photochem4010002","url":null,"abstract":"Singlet fission is a desired process in photovoltaics since it enhances photoelectric conversion efficiency. Intramolecular singlet fission is of special interest as the fission efficiency can be improved through tuning configurations between chromophore units that are covalently connected. However, intramolecular singlet fission chromophores feature a large tetraradical character, and may tend to dissatisfy the ET2>2ET1 criterion for all singlet fission chromophores, intramolecular or not. We performed spin-flip time-dependent density functional theory calculations for a collection of representative intramolecular singlet fission chromophores to show that this is indeed the case.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"78 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139440708","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Twisted 8-Acyl-1-dialkyl-amino-naphthalenes Emit from a Planar Intramolecular Charge Transfer Excited State 扭曲的 8-酰基-1-二烷基氨基萘发出平面分子内电荷转移激发态
Photochem Pub Date : 2024-01-04 DOI: 10.3390/photochem4010001
Christopher Abelt, Kirsten Sweigart
{"title":"Twisted 8-Acyl-1-dialkyl-amino-naphthalenes Emit from a Planar Intramolecular Charge Transfer Excited State","authors":"Christopher Abelt, Kirsten Sweigart","doi":"10.3390/photochem4010001","DOIUrl":"https://doi.org/10.3390/photochem4010001","url":null,"abstract":"Fluorescence from dialkylamino donor–acyl acceptor substituted 1,8-naphthalene derivatives can occur either from a planar (PICT) or a twisted (TICT) intramolecular charge transfer excited state. The photophysical properties of 8-acetyl-1-(dimethyl-amino)naphthalene (3) and 8-pivaloyl-1-(dimethyl-amino)naphthalene (4) are compared with 1-methyl-2,3-dihydronaphtho[1,8-bc]azepin-4(1H)-one (5). In 3 and 4, both the carbonyl and amino groups are forced to twist out of the plane of the naphthalene ring. In 5, these groups are nearly coplanar with the naphthalene. Neither 3 nor 4 fluoresce as strongly as 5, but all three show similar degrees of solvato-chromism and all are strongly quenched by alcohol solvents. Nitrile 6, 8-cyano-1-(dimethyl-amino)naphthalene, does not show the same degree of solvato-chromism as 3–5, nor is it as affected by alcohols. Calculations corroborate the experimental results, indicating that 3–5 emit from a PICT excited state.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"71 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139386078","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recent Advances in Visible Light Photoinitiating Systems Based on Flavonoids 基于黄酮类化合物的可见光光引发体系的最新进展
Photochem Pub Date : 2023-12-12 DOI: 10.3390/photochem3040030
F. Dumur
{"title":"Recent Advances in Visible Light Photoinitiating Systems Based on Flavonoids","authors":"F. Dumur","doi":"10.3390/photochem3040030","DOIUrl":"https://doi.org/10.3390/photochem3040030","url":null,"abstract":"The design of biosourced and/or bioinspired photoinitiators is an active research field as it offers a unique opportunity to develop photoinitiating systems exhibiting better biocompatibility as well as reduced toxicity. In this field, flavonoids can be found in numerous fruits and vegetables so these structures can be of interest for developing, in the future, polymerization processes, offering a reduced environmental impact but also better biocompatibility of the polymers. In this review, the different flavonoids reported to date as photoinitiators of polymerization are presented. Over the years, different modifications of the flavonoid scaffold have been examined including the grafting of well-known chromophores, the preparation of Type II photoinitiators or the introduction of photocleavable groups enabling the generation of Type I photoinitiators. Different families of flavonoids have also been investigated, enabling to design of high-performance photoinitiating systems.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"58 13","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139007136","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Photolytic Degradation of the Insecticide Clothianidin in Hydrochar Aquatic Suspensions and Extracts 水生生物悬浮液和萃取物中杀虫剂噻虫胺的光解降解
Photochem Pub Date : 2023-11-07 DOI: 10.3390/photochem3040027
Artemis Pappa, Feidias Bairamis, Ioannis Konstantinou
{"title":"Photolytic Degradation of the Insecticide Clothianidin in Hydrochar Aquatic Suspensions and Extracts","authors":"Artemis Pappa, Feidias Bairamis, Ioannis Konstantinou","doi":"10.3390/photochem3040027","DOIUrl":"https://doi.org/10.3390/photochem3040027","url":null,"abstract":"In this study, the aqueous photolytic degradation of the neonicotinoid pesticide clothianidin was studied in suspensions and aqueous extracts of hydrochar produced from olive kernels. A slight and nonsignificant decrease in the photodegradation rate of clothianidin in aqueous extracts of hydrochar (HCw) with an initial concentration of hydrochar ranged from 50 to 400 mg L−1 (rate constants ranged between k = 0.0034 and 0.0039 min−1) was observed in comparison to the respective rate in the bi-distilled water (k = 0.0040 min−1). On the contrary, in the presence of hydrochar suspensions (HCp), a significant decrease was observed for 50 mg L−1 hydrochar particle concentration (k = 0.020 min−1), while for higher concentrations (100 to 400 mg L−1), rate constants increased but with nonsignificant differences compared with the kinetics followed in the absence of them. Generally, the photodegradation rate of clothianidin, in the presence of HCw and HCp, is reduced compared to the photodegradation rate in bi-distilled aqueous solutions, except in the case of the aqueous suspension with an HCp concentration of 200 mg L−1. The transformation products (TPs) of clothianidin formed in the photolytic degradation processes were identified using ultrahigh-performance liquid chromatography coupled with accurate high-resolution mass spectrometry technique (UHPLC-LTQ-ORBITRAP). The formation profiles of TPs varied according to the matrix showing different degrees of participation of direct and indirect (photosensitized) phototransformation pathways. Photolytic degradation of clothianidin takes place mainly through denitration, hydroxylation and dechlorination pathways. Finally, the toxicity of the identified TPs was studied using the Vibrio fischeri bioassay. Toxicity was slightly reduced after 300 min of irradiation while maximum value was observed after 180–240 min of irradiation showing the formation of more toxic TPs along the photochemical degradation.","PeriodicalId":74440,"journal":{"name":"Photochem","volume":"67 5","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135474596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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