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- Organic sensitizers featuring thiophene derivative based donors with improved stability and photovoltaic performance. Kai Miao, Mao Liang, Zhihui Wang, Chunyao Zhang, Zhe Sun, Song Xue
, Phys. Chem. Chem. Phys.
, 2017
, 19
, 1927
- Effect of processing Verdejo grape must by UHPH using non-Saccharomyces yeasts in the absence of SO2. Carlos Escott, Cristian Vaquero, Juan Manuel del Fresno, Angelo Topo, Piergiorgio Comuzzo, Carmen Gonzalez, Antonio Morata
, Sustainable Food Technol.
, 2024
, 2
, 437
- Phenothiazine and amide-ornamented novel nitrogen heterocyclic hybrids: synthesis, biological and molecular docking studies. Ramar Sivaramakarthikeyan, Ayyanar Karuppasamy, Shunmugam Iniyaval, Krishnaraj Padmavathy, Wei-Meng Lim, Chun-Wai Mai, Chennan Ramalingan
, New J. Chem.
, 2020
, 44
, 4049
- Structures and hydrogen bonding of 1,7-dioxaspiro[5.5]undecane and its hydrates. Yugao Xu, Zhi-You Wei, Wenqin Li, Jiaqi Zhang, Tao Lu, Yan Jin, Wei-Jun Zheng, Gang Feng
, Phys. Chem. Chem. Phys.
, 2021
, 23
, 19289
- Physical, antioxidant and antimicrobial properties of modified peanut protein isolate based films incorporating thymol. Tianchen Zhong, Yue Liang, Shan Jiang, Lulu Yang, Yimo Shi, Siwen Guo, Chunhong Zhang
, RSC Adv.
, 2017
, 7
, 41610
- The colorimetric determination of boron in carbon and stainless steels. D. Bell, K. McArthur
, Analyst
, 1968
, 93
, 298
- CCXXXV.—Electromotive forces in alcohol. Part III. Further experiments with the hydrogen electrode in dry and moist alcoholic hydrogen chloride. Robert Taylor Hardman, Arthur Lapworth
, J. Chem. Soc., Trans.
, 1912
, 101
, 2249
- 698. Molecular polarisation and molecular interaction. Part IV. The molecular polarisation of diphenylamine in solution in benzene, dioxan, and mixtures of benzene with nitrobenzene, triethylamine, and pyridine. J. W. Smith
, J. Chem. Soc.
, 1950
, 3532
- CXVIII.—The ternary system sodium sulphidesodium sulphate–water. Arthur Robert Hogg
, J. Chem. Soc.
, 1926
, 129
, 855
- 718. The Hammett acidity function in aqueous nitric acid. J. G. Dawber, P. A. H. Wyatt
, J. Chem. Soc.
, 1960
, 3589