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Journal articles on the topic 'Alkanol'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Ives, H. E., and A. S. Verkman. "Effects of membrane fluidizing agents on renal brush border proton permeability." American Journal of Physiology-Renal Physiology 249, no. 6 (1985): F933—F940. http://dx.doi.org/10.1152/ajprenal.1985.249.6.f933.

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H+ permeability (PH) of brush border membrane vesicles isolated from rabbit renal cortex was measured from the rate of collapse of preformed pH gradients using acridine orange fluorescence quenching. n-Alkanols increased PH from 0.005 to 0.1 cm/s in a dose-dependent manner. At 25 degrees C, PH increased to 0.01 cm/s at [n-alkanol] = 90 mM (butanol), 30 mM (pentanol), 7 mM (hexanol), and 1.8 mM (heptanol). Activation energy (Ea) of PH was 21.6 kcal/mol (5-50 degrees C), which decreased to 18.5 kcal/mol in the presence of either 200 mM butanol or 12 mM hexanol. Membrane fluidity was estimated fr

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2

Koch, Daniel J., Mike M. Chen, Jan B. van Beilen, and Frances H. Arnold. "In Vivo Evolution of Butane Oxidation by Terminal Alkane Hydroxylases AlkB and CYP153A6." Applied and Environmental Microbiology 75, no. 2 (2008): 337–44. http://dx.doi.org/10.1128/aem.01758-08.

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ABSTRACT Enzymes of the AlkB and CYP153 families catalyze the first step in the catabolism of medium-chain-length alkanes, selective oxidation of the alkane to the 1-alkanol, and enable their host organisms to utilize alkanes as carbon sources. Small, gaseous alkanes, however, are converted to alkanols by evolutionarily unrelated methane monooxygenases. Propane and butane can be oxidized by CYP enzymes engineered in the laboratory, but these produce predominantly the 2-alkanols. Here we report the in vivo-directed evolution of two medium-chain-length terminal alkane hydroxylases, the integral

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3

González, Juan Antonio, I. García De La Fuente, and J. C. Cobos. "Thermodynamics of mixtures containing the CO and OH groups. II. DISQUAC predictions on VLE and HE for ternary mixtures containing 1-alkanols, n-alkanones, and one organic solvent." Canadian Journal of Chemistry 75, no. 10 (1997): 1424–33. http://dx.doi.org/10.1139/v97-171.

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Thermodynamic properties: vapour–liquid equilibria, VLE, or excess enthalpies, HE, for a set of 21 ternary mixtures of the type 1-alkanol + n-alkanone + organic solvent are studied in the framework of the DISQUAC group contribution model. This treatment is extended to the binaries involved. The DISQUAC analysis is developed on the basis of binary interactions only, that is, ternary interactions are neglected. Most of the interchange coefficients needed are available in the literature. The average relative standard deviations are 0.026 for pressure in the VLE (12 systems) and 0.098 in the HE (9

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4

Bhagat, Payal, and Sanjeev Maken. "Study of Intermolecular Interactions of Binary Mixture of sec- and tert-Amines with Alkanols (C1-C3): Refractive Indices." Asian Journal of Chemistry 32, no. 10 (2020): 2443–49. http://dx.doi.org/10.14233/ajchem.2020.22719.

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In this work, the refractive indices (nD) of binary mixture of diisopropylamine (DIPA) and tributylamine (TBA) (as sec- and tert-amines) with alkanol (methanol, ethanol, 1-propanol, 2-propanol) were measured from 298.15 K to 318.15 K. The sec- and tert-amines were selected to study the effect of branching at N-atom of amine on intermolecular interactions with alkanols having different chain length. It was found that the TBA interacts strongly with alkanol in comparison to DIPA due to steric hindrance offered by isopropyl group at N-atom. Various mixing rules were applied to evaluate the refrac

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5

Jetter, Reinhard, and Markus Riederer. "Cuticular waxes from the leaves and fruit capsules of eight Papaveraceae species." Canadian Journal of Botany 74, no. 3 (1996): 419–30. http://dx.doi.org/10.1139/b96-052.

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Cuticular waxes from leaves and fruit capsules of Papaver alpinum sensu Markgr., P. bracteatum Lindl., P. dubium L., P. nudicaule L., P. orientale L., P. rhoeas L., P. somniferum L., and Eschscholtzia californica Cham. were investigated. They consisted of n-alkanes (< 19%), alk-1-ylesters (< 18%), alk-2-ylesters (< 6%), alkanals (< 19%), secondary alkanols (21–71%, mainly nonacosan-10-ol), triglycerides (< 6%), primary alkanols (2–33%), alkanediols (2–23%, mainly isomeric nonacosanediols), alkanoic acids (< 8%), and alkaloids (< 12%). In addition, minor amounts of iso- and

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6

Bui, Huong Thi. "\(\textit{n}\)-alkanol stress-induced cell envelope injury of \(σ^{E}\) promoter in \(\textit{Escherichia coli}\)". Academia Journal of Biology 44, № 2 (2022): 91–104. http://dx.doi.org/10.15625/2615-9023/17136.

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To characterize the cellular stress by n-alkanols with different alkyl chain lengths in Escherichia coli, we investigated how n-alkanols damage cell envelope permeability and whether they enhance the promoter activity of the envelope stress response regulator, σE, by using variants of green fluorescent protein (GFP). By using E. coli cells having GFPuv expressing and localizing in the cytoplasm, the inner membrane, and the periplasm, after exposure to n-alkanols, the fluorescent intensity of GFPuv released from cells was examined. Our data showed that at the similar levels of cell death of abo

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7

Ortega, J., JA Pena, and MI Pazandrade. "Excess Molar Volumes of Binary Mixtures of Ethyl Acetate and Propyl Acetate With Normal Alkanols." Australian Journal of Chemistry 39, no. 10 (1986): 1685. http://dx.doi.org/10.1071/ch9861685.

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This article reports measurements of VE/m at 298.15 K for binary mixtures of n- alkanols CnH2n+1OH (from n = 2 to n = 10) with ethyl and propyl acetates. All the excess volumes are positive over the entire concentration range, with VE/m increasing with the length of the alkanol chain. Suitable equations have been fitted to the data for each mixture. The results are compared with data previously published.

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8

Wolf, Jeremy R. "Main Chain Noncentrosymmetric Hydrogen Bonded Macromolecules Incorporating Aniline, Alkanol, and Alkanoic Acid Hydrogen Bond Donors." Journal of Polymers 2014 (April 27, 2014): 1–7. http://dx.doi.org/10.1155/2014/472901.

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The syntheses and characterization of three noncentrosymmetric main chain hydrogen bonded macromolecules which incorporate aniline, alkanoic acid, and alkanol hydrogen bond donor units are reported. These macromolecules participate in weak intermolecular hydrogen bonding as demonstrated using attenuated total reflectance (ATR) FTIR. The phase transitions of these macromolecules depend on the identity of the hydrogen bond donor.

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9

Piekarski, Henryk, and Gus Somsen. "Enthalpies of solution of urea in water–alkanol mixtures and the enthalpic pair interaction coefficients of urea and several nonelectrolytes in water." Canadian Journal of Chemistry 64, no. 9 (1986): 1721–24. http://dx.doi.org/10.1139/v86-284.

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Enthalpies of solution of urea in binary mixtures of isopropanol, s-butanol, and ethoxyethanol with water have been measured at high water content. Those in the binaries isopropanol + water and ethoxyethanol + water show endothermic maxima at 8 and 4 mol% alkanol, respectively. Enthalpic pair interaction coefficients are calculated for the interactions between urea and the alkanols and discussed in connection with these coefficients for interactions between urea and other nonelectrolytes and between N,N-dimethylformamide and several nonelectrolytes. The enthalpic pair interaction coefficients

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10

Munk, Petr, Anwei Qin, and Dolly E. Hoffman. "Excess Volumes of Mixtures of Alkanols with Aromatic Hydrocarbons." Collection of Czechoslovak Chemical Communications 58, no. 11 (1993): 2612–24. http://dx.doi.org/10.1135/cccc19932612.

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The excess volumes of twenty binary mixtures of four aromatic hydrocarbons (benzene, toluene, ethylbenzene, and p-xylene) and five linear alkanols (methanol, ethanol, 1-propanol, 1-butanol, and 1-pentanol) at 20 °C are reported. The excess volume of systems with the same alkanol increases with increasing size and number of substituents on the benzene ring. For systems with the same aromatic hydrocarbon it increases with the length of the alkanols. The dependence of ∆V/φ1ϑ2 values on composition is noticeably asymmetric. Systems with benzene as one of the component show larger ∆V/φ1ϑ2 values th

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11

Krzan, Marcel, Pradipta Chattopadhyay, Sandra Orvalho, and Maria Zednikova. "Effects of N-Alkanol Adsorption on Bubble Acceleration and Local Velocities in Solutions of the Homologous Series from Ethanol to N-Decanol." Materials 16, no. 5 (2023): 2125. http://dx.doi.org/10.3390/ma16052125.

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The influence of n-alkanol (C2–C10) water solutions on bubble motion was studied in a wide range of concentrations. Initial bubble acceleration, as well as local, maximal and terminal velocities during motion were studied as a function of motion time. Generally, two types of velocity profiles were observed. For low surface-active alkanols (C2–C4), bubble acceleration and terminal velocities diminished with the increase in solution concentration and adsorption coverage. No maximum velocities were distinguished. The situation is much more complicated for higher surface-active alkanols (C5–C10).

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12

Abraham, Michael H., Joelle le, and William E. Acree. "The Solvation Properties of the Aliphatic Alcohols." Collection of Czechoslovak Chemical Communications 64, no. 11 (1999): 1748–60. http://dx.doi.org/10.1135/cccc19991748.

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Solubilities of solute gases and vapours, as log L, where L is the Ostwald solubility coefficient, in the alkan-1-ols from methanol to decan-1-ol have been correlated through the solvation equation of Abraham. It is shown that there is a regular progression of solvent properties from methanol to decan-1-ol, except for the solvent hydrogen-bond basicity that remains the same along the series, and, indeed, is the same as that of water. A slightly different solvation equation is used to correlate the partition of solutes from water to the dry alkanols. For the longer chain alkanols, the coefficie

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13

García, Begoña, Francisco J. Hoyuelos, Rafael Alcalde, and José M. Leal. "Molar excess volumes of binary liquid mixtures: 2-pyrrolidinone with C6–C10n-alkanols." Canadian Journal of Chemistry 74, no. 1 (1996): 121–27. http://dx.doi.org/10.1139/v96-016.

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The excess volumes VE of the binary mixtures 2-pyrrolidinone–(C6–C10) n-alkanols have been calculated from density measurements over the whole composition range and the 298.15–318.15 K temperature range. The excess volumes were independent of temperature, but changed noticeably with the chain length of the alkanol. The VE values were only positive starting from heptanol, with the maximum value, 0.239 cm3 mol−1, for equimolar decanol. The observed changeover VE < 0 to VE > 0 suggests that the steric effect is primarily responsible for the positive contributions to VE. The thermal expansio

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14

Kochergin, P. M., I. S. Mikhailova, and E. V. Aleksandrova. "The synthesis of (aminophenyl)alkanols by hydrogenation of (nitrophenyl)alkanol nitroesters." Pharmaceutical Chemistry Journal 32, no. 11 (1998): 598–99. http://dx.doi.org/10.1007/bf02465833.

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15

Oswal, S. L., K. D. Prajapati, P. Oswal, N. Y. Ghael, and S. P. Ijardar. "Viscosity of binary mixtures of 1-alkanol+cyclohexane, 2-alkanol+cyclohexane and 1-alkanol+methylcyclohexane at 303.15 K." Journal of Molecular Liquids 116, no. 2 (2005): 73–82. http://dx.doi.org/10.1016/j.molliq.2004.05.004.

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16

González, Juan Antonio, Ángela Mediavilla, Isaías García de la Fuente, José Carlos Cobos, Cristina Alonso Tristán, and Nicolás Riesco. "Orientational Effects and Random Mixing in 1-Alkanol + Alkanone Mixtures." Industrial & Engineering Chemistry Research 52, no. 30 (2013): 10317–28. http://dx.doi.org/10.1021/ie4019269.

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17

Pardo, J., V. Rodríguez, M. C. López, F. M. Royo, and J. S. Urieta. "Excess molar volumes VEm of (an alkanol + another alkanol) or (hexane + an alkanol) or (an alkanediol + an alkanol or another alkanediol) at the temperature 303.15 K." Journal of Chemical Thermodynamics 24, no. 2 (1992): 113–17. http://dx.doi.org/10.1016/s0021-9614(05)80039-4.

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18

de Ruiz Holgado, M. EF, J. Fernandez, M. I. Paz Andrade, and E. L. Arancibia. "Excess molar enthalpies of mixtures of methyl derivatives of polyethylene glycol with 1-alkanol at 298.15 K and 101.3 kPa." Canadian Journal of Chemistry 80, no. 5 (2002): 462–66. http://dx.doi.org/10.1139/v02-044.

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Excess molar enthalpies (H E) of the binary mixtures containing tetraethylene glycol dimethyl ether (TEGDME) or polyethylene glycol 350 monomethyl ether with a 1-alkanol (1-propanol, 1-butanol, or 1-pentanol) at 298.15 K and atmospheric pressure were measured using a Calvet microcalorimeter. All the H E experimental values were positive and increase as the 1-alkanol length increases. The results are discussed qualitatively in terms of molecular interactions. The UNIFAC and DISQUAC group contribution models have been used to compare the predicted and the experimental values.Key words: excess en

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19

Casal, Margarida, Helena Cardoso, and Cecília Leão. "Effects of Ethanol and Other Alkanols on Transport of Acetic Acid in Saccharomyces cerevisiae." Applied and Environmental Microbiology 64, no. 2 (1998): 665–68. http://dx.doi.org/10.1128/aem.64.2.665-668.1998.

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ABSTRACT In glucose-grown cells of Saccharomyces cerevisiae IGC 4072, acetic acid enters only by simple diffusion of the undissociated acid. In these cells, ethanol and other alkanols enhanced the passive influx of labelled acetic acid. The influx of the acid followed first-order kinetics with a rate constant that increased exponentially with the alcohol concentration, and an exponential enhancement constant for each alkanol was estimated. The intracellular concentration of labelled acetic acid was also enhanced by alkanols, and the effect increased exponentially with alcohol concentration. Ac

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20

Bao, Xuefei, Xu Li, Chunfeng Jiang, Wei Xiao, and Guoliang Chen. "Recent advances in catalysts for the Henry reaction." Australian Journal of Chemistry 75, no. 10 (2022): 806–19. http://dx.doi.org/10.1071/ch22136.

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The Henry reaction, the coupling of a nitro alkane and a carbonyl group, is an important C–C bond-forming reaction giving nitro alkanols, which are useful, versatile intermediates in synthetic organic chemistry and for the pharmaceutical industry. Among the catalysts employed in the Henry reaction, transition metal complex catalysts play an important role. Transition metal complexes, including small molecules and nanoparticles, catalyze the asymmetric Henry reaction efficiently and in most of the cases give chiral nitro alkanol products in good yield and enantiomeric excess. This review summar

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21

Marcus, Y. "Extraction of alkanol isomers." Journal of Organic Chemistry 55, no. 7 (1990): 2224–26. http://dx.doi.org/10.1021/jo00294a044.

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22

Yudha, Sandy. "Pengembangan Lembar Kerja Peserta Didik (LKPD) Berbasis Problem Based Learning pada Materi Alkanol dan Alkoksi Alkana Untuk Kelas XII SMA/MA." Jurnal Ilmu Manajemen dan Pendidikan (JIMPIAN) 3, no. 2 (2023): 61–70. http://dx.doi.org/10.30872/jimpian.v3i2.2263.

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Alkanol dan Alkoksi Alkana merupakan komponen senyawa karbon yang dipelajari pada semester kedua kelas XII SMA/MA. Salah satu model pembelajaran yang dapat digunakan dalam materi alkanol dan alkoksi alkana adalah model Problem Based Learning. Tujuan penelitian ini adalah mengembangkan LKPD dan menentukan kategori validitasnya. Research and Development (R&D) merupakan jenis penelitian ini karena menggunakan model pengembangan 4-D. Adapun tahap-tahapnya yaitu define, design, develop dan disseminate. Namun, untuk penelitian ini tahapnya dibatasi pada tahap ketiga yaitu pengembangan (Develop).

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23

Lissi, E. A., and E. B. Abuin. "HYDROPHOBIC EFFECTS IN WATER AND WATER/UREA SOLUTIONS A COMPARISON." SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 2, no. 2 (1994): 71–82. http://dx.doi.org/10.48141/sbjchem.v2.n2.1994.72_1994.pdf.

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The partition of several n-alkanols, from methanol to n-nonanol, between n-hexane and water and between n-hexane and water containing 20 % (w/v) urea has been measured at temperatures ranging from 0 °C to 60 °C. The standard free energy of transfer from water to the urea-containing solution decreases with the length of the alkyl chain, being positive for the small alcohols and negative for the higher alkanols. The same tendency is observed upon all the temperature range considered. On the other hand, the standard entropy of transfer from water to the urea-containing solution increases with the

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24

Bommel, Andrew van, Andrew Glennie, Danielle Chisholm, and Rama M. Palepu. "Dynamics of percolation and energetics in the clustering of water/AOT/oil microemulsions in the presence of ethanol amines." Canadian Journal of Chemistry 84, no. 3 (2006): 412–20. http://dx.doi.org/10.1139/v06-011.

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Temperature-induced percolation in water/AOT/oil microemulsions in the presence of mono-, di-, and tri-ethanol amines have been studied using conductometric measurements. The percolation temperature of water/AOT/oil microemulsions depends on the nature of the alkanol amine added. Mono- and di-ethanol amines hinder the percolation process, while triethanol amine promotes the process. Percolation studies were also conducted with varying ω = [H2O]/[AOT] values and varying chain lengths of continuous oil phase (C6C10). The results indicate that increases in both ω and the chain length of the oil

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25

Aspée, Alexis, and Eduardo Lissi. "Solubilization of Alkanols in DPPC LUVs: Dependence on the Alkanol Concentration and Topology." Journal of Colloid and Interface Science 175, no. 1 (1995): 225–29. http://dx.doi.org/10.1006/jcis.1995.1450.

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26

González, J. A., U. Domanska, and J. Lachwa. "Thermodynamics of binary mixtures containing a very strongly polar compound — Part 3: DISQUAC characterization of NMP + organic solvent mixtures." Canadian Journal of Chemistry 81, no. 12 (2003): 1451–61. http://dx.doi.org/10.1139/v03-159.

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Binary mixtures of 1-methyl pyrrolidin-2-one (NMP) with alkanes, benzene, toluene, 1-alkanol, or 1-alkyne have been investigated in the framework of the DISQUAC model. The reported interaction parameters change regularly with the molecular structure of the mixture components. The model consistently describes a set of thermodynamic properties, including liquid–liquid equilibria, vapor–liquid equilibria, solid–liquid equilibria, and molar excess enthalpies. A brief comparison of the DISQUAC results and those obtained from the UNIFAC and ERAS models is presented. The experimental excess enthalpie

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27

Qin, Anwei, Dolly E. Hoffman, and Petr Munk. "Excess Volumes of Mixtures of Some Alkyl Esters and Ketones with Alkanols." Collection of Czechoslovak Chemical Communications 58, no. 11 (1993): 2625–41. http://dx.doi.org/10.1135/cccc19932625.

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Excess volumes were calculated from measured densities of binary mixtures of five linear alkanols (methanol, ethanol, 1-propanol, 1-butanol, and 1-pentanol) with five n-alkyl acetates (methyl, ethyl, propyl, butyl, and pentyl acetates) and with two ketones (acetone and 2-butanone) at 20 °C. The whole composition range was studied for all thirty-five binary systems. For a given alcohol, the ∆V/φ1ϑ2 value decreases with increasing size of the carbonyl compound. For a given carbonyl compound, it increases with the length of the alkanol. Systems with methyl acetate as one component have relatively

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28

Carmona, F. J., F. J. Arroyo, I. García de la Fuente, J. A. González, and J. C. Cobos. "Excess molar volumes of methanol or ethanol + n-polyethers at 298.15 K." Canadian Journal of Chemistry 77, no. 10 (1999): 1608–16. http://dx.doi.org/10.1139/v99-189.

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Excess molar volumes VmE at 298.15 K and atmospheric pressure for methanol and ethanol + 2,5-dioxahexane, + 3,6-dioxaoctane, + 2,5,8-trioxanonane, + 3,6,9-trioxaundecane, + 5,8,11-trioxapentadecane, + 2,5,8,11-tetraoxadodecane, and + 2,5,8,11,14-pentaoxapentadecane have been obtained from densities measured with an Anton-Paar DMA 602 vibrating-tube densimeter. All the excess volumes are negative over the whole mole fraction range.The VmE curves are shifted to the region rich in the alkanol, increasing their asymmetry with the number of oxygen groups in the polyethers. Results seem to remark th

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29

Panayiotou, Constantinos G. "Thermodynamics of alkanol-alkane mixtures." Journal of Physical Chemistry 92, no. 10 (1988): 2960–69. http://dx.doi.org/10.1021/j100321a048.

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30

Heldebrant, David J., Phillip K. Koech, M. Trisha C. Ang, et al. "Reversible zwitterionic liquids, the reaction of alkanol guanidines, alkanol amidines, and diamines with CO2." Green Chemistry 12, no. 4 (2010): 713. http://dx.doi.org/10.1039/b924790d.

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31

Romagnoli, Carlo, Bora Sieng, and Mohamed Amedjkouh. "Kinetic relationship in parallel autocatalytic amplifications of pyridyl alkanol and chiral trigger pyrimidyl alkanol." Chirality 32, no. 9 (2020): 1143–51. http://dx.doi.org/10.1002/chir.23256.

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32

Gürbüz, Elif I., David D. Hibbitts, and Enrique Iglesia. "Kinetic and Mechanistic Assessment of Alkanol/Alkanal Decarbonylation and Deoxygenation Pathways on Metal Catalysts." Journal of the American Chemical Society 137, no. 37 (2015): 11984–95. http://dx.doi.org/10.1021/jacs.5b05361.

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33

González, Juan Antonio. "Thermodynamics of mixtures containing the CO and OH groups. I. Estimation of the DISQUAC interchange coefficients for 1-alkanol + n-alkanone systems." Canadian Journal of Chemistry 75, no. 10 (1997): 1412–23. http://dx.doi.org/10.1139/v97-170.

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1-Alkanol + n-alkanone mixtures are treated in terms of the DISQUAC group contribution model, reporting the interaction parameters for hydroxyl–carbonyl contacts. The quasichemical interchange coefficients are independent of the compounds in the mixture; the dispersive interchange coefficients depend on the intramolecular environment of the hydroxyl and (or) carbonyl groups. Mixtures of a given 1-alkanol with isomeric ketones are characterized by the same first dispersive interaction parameter, which is constant from 2-pentanone. This type of system, when including an alcohol up to 1-pentanol,

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34

Doğruer Akan, Bürge, and Ümide Demir Özkay. "Bazı piperazin alkanol türevlerinin antinosiseptif etkinlikleri." Cukurova Medical Journal 44, no. 3 (2019): 729–44. http://dx.doi.org/10.17826/cumj.490690.

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35

Alcalde, Rafael, Mert Atilhan, José Luis Trenzado, and Santiago Aparicio. "Physicochemical Insights on Alkylcarbonate–Alkanol Solutions." Journal of Physical Chemistry B 120, no. 22 (2016): 5015–28. http://dx.doi.org/10.1021/acs.jpcb.6b02961.

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36

Dewan, R. K., and S. K. Mehta. "Excess volumes of (ethylbenzene + an alkanol)." Journal of Chemical Thermodynamics 19, no. 8 (1987): 819–22. http://dx.doi.org/10.1016/0021-9614(87)90028-0.

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37

Endler, Ingolf, Gerd Hradetzky, and Hans-Joachim Bittrich. "Grenzaktivitätskoeffizienten in binären Systemen Benzen-Alkanol." Journal für Praktische Chemie 327, no. 4 (1985): 693–97. http://dx.doi.org/10.1002/prac.19853270422.

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38

Vale, V., B. Rathke, S. Will, and W. Schröer. "Eigenschaften von CnmimNTf2/n-Alkanol Mischungen." Chemie Ingenieur Technik 81, no. 8 (2009): 1051. http://dx.doi.org/10.1002/cite.200950455.

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39

Dewan, Raj K., Surinder K. Mehta, Ravi Parashar, and Kiran Bala. "Topological investigations on the association of alkanols: excess volume of pyridine–alkanol (C1–C10) mixtures." J. Chem. Soc., Faraday Trans. 87, no. 10 (1991): 1561–68. http://dx.doi.org/10.1039/ft9918701561.

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40

Jaradat, Adnan, Rakan Al-Salman, and Abdalla Obeidat. "Self-diffusion and shear viscosity of pure 1-alkanol unary system: molecular dynamics simulation and review of experimental data." RSC Advances 14, no. 32 (2024): 22947–61. http://dx.doi.org/10.1039/d4ra03494e.

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41

Cen, Peipei, Weize Yuan, Shuchang Luo, Xiangyu Liu, Gang Xie, and Sanping Chen. "Solvent coligands fine-tuned the structures and magnetic properties of triple-bridged 1D azido-copper(ii) coordination polymers." New Journal of Chemistry 43, no. 2 (2019): 601–8. http://dx.doi.org/10.1039/c8nj04731f.

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42

Matsumoto, Arimasa, Ayame Tanaka, Yoshiyasu Kaimori, Natsuki Hara, Yuji Mikata, and Kenso Soai. "Circular dichroism spectroscopy of catalyst preequilibrium in asymmetric autocatalysis of pyrimidyl alkanol." Chemical Communications 57, no. 85 (2021): 11209–12. http://dx.doi.org/10.1039/d1cc04206h.

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43

Akhter, M. Salim, and Sadeq M. Alawi. "Micellar behaviour of cetyltrimethylammonium bromide in N-methyl acetamide—alkanol and N,N-dimethyl acetamide—alkanol mixtures." Colloids and Surfaces A: Physicochemical and Engineering Aspects 196, no. 2-3 (2002): 163–74. http://dx.doi.org/10.1016/s0927-7757(01)00864-0.

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Okada, Shuji, Hiro Matsuda, Masaaki Otsuka та ін. "Synthesis and Solid-State Polymerization ofω-(1,3-Butadiynyl) Substituted 1-Alkanol and Alkanoic Acid". Bulletin of the Chemical Society of Japan 67, № 2 (1994): 455–61. http://dx.doi.org/10.1246/bcsj.67.455.

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Holland, A. R., S. T. Petsch, I. S. Castañeda, K. M. Wilkie, S. J. Burns, and J. Brigham-Grette. "A biomarker record of Lake El'gygytgyn, Far East Russian Arctic: investigating sources of organic matter and carbon cycling during marine isotope stages 1–3." Climate of the Past 9, no. 1 (2013): 243–60. http://dx.doi.org/10.5194/cp-9-243-2013.

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Abstract. Arctic paleoenvironmental archives serve as sensitive recorders of past climate change. Lake El'gygytgyn (Far East Russian Arctic) is a high-latitude crater impact lake that contains a continuous sediment record influenced by neither glaciation nor glacial erosion since the time of impact 3.58 Ma ago. Prior research on sediments collected from Lake El'gygytgyn suggest times of permanent ice cover and anoxia corresponding to global glacial intervals, during which the sediments are laminated and are characterized by the co-occurrence of high total organic carbon, microscopic magnetite

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Holland, A. R., S. T. Petsch, I. S. Castañeda, K. M. Wilkie, S. J. Burns, and J. Brigham-Grette. "A biomarker record of Lake El'gygytgyn, far east Russian Arctic: investigating sources of organic matter and carbon cycling during marine isotope stages 1–3." Climate of the Past Discussions 8, no. 5 (2012): 4625–61. http://dx.doi.org/10.5194/cpd-8-4625-2012.

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Abstract. Paleoenvironmental archives in Arctic regions serve as sensitive recorders of past climate change where summer temperatures hover near freezing and small climate variations may exhibit strong threshold-crossing environment responses. Lake El'gygytgyn (Far East Russian Arctic) is a high-latitude crater impact lake that contains a continuous sediment record influenced by neither glaciation nor glacial erosion since the time of impact at 3.58 Ma. Prior research on sediments collected from Lake El'gygytygyn suggest times of permanent ice cover and anoxia corresponding to global glacial i

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Matsumoto, Arimasa, Kento Yonemitsu, Hanae Ozaki, et al. "Reversal of the sense of enantioselectivity between 1- and 2-aza[6]helicenes used as chiral inducers of asymmetric autocatalysis." Organic & Biomolecular Chemistry 15, no. 6 (2017): 1321–24. http://dx.doi.org/10.1039/c6ob02745h.

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Kawasaki, Tsuneomi, Yuko Araki, Kunihiko Hatase, et al. "Helical mesoporous silica as an inorganic heterogeneous chiral trigger for asymmetric autocatalysis with amplification of enantiomeric excess." Chemical Communications 51, no. 42 (2015): 8742–44. http://dx.doi.org/10.1039/c5cc01750e.

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Soai, Kenso, Tsuneomi Kawasaki, and Arimasa Matsumoto. "Role of Asymmetric Autocatalysis in the Elucidation of Origins of Homochirality of Organic Compounds." Symmetry 11, no. 5 (2019): 694. http://dx.doi.org/10.3390/sym11050694.

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Pyrimidyl alkanol and related compounds were found to be asymmetric autocatalysts in the enantioselective addition of diisopropylzinc to pyrimidine-5-carbaldehyde and related aldehydes. In the asymmetric autocatalysis with amplification of enantiomeric excess (ee), the very low ee (ca. 0.00005%) of 2-alkynyl-5-pyrimidyl alkanol was significantly amplified to >99.5% ee with an increase in the amount. By using asymmetric autocatalysis with amplification of ee, several origins of homochirality have been examined. Circularly polarized light, chiral quartz, and chiral crystals formed from achira

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Ghazipour, H., A. Gutiérrez, D. Mohammad-Aghaie, M. M. Alavianmher, S. M. Hosseini, and S. Aparicio. "Insights on biodiesel blends with alkanol solvents." Journal of Molecular Liquids 332 (June 2021): 115864. http://dx.doi.org/10.1016/j.molliq.2021.115864.

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