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Journal articles on the topic 'Melting points'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Carter, Kenneth Nolon, and Kenneth Nolan Carter. "Meaningful Melting Points." Journal of Chemical Education 72, no. 7 (1995): 647. http://dx.doi.org/10.1021/ed072p647.

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2

Reeves, Roy R., and Richard O. Pendarvis. "Mothball melting points." Annals of Emergency Medicine 15, no. 11 (1986): 1377. http://dx.doi.org/10.1016/s0196-0644(86)80652-7.

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3

Wei, James. "Boiling Points and Melting Points of Chlorofluorocarbons." Industrial & Engineering Chemistry Research 39, no. 8 (2000): 3116–19. http://dx.doi.org/10.1021/ie9909439.

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4

Prahlada Rao, S., and Shravan Sunkada. "Making sense of boiling points and melting points." Resonance 12, no. 6 (2007): 43–57. http://dx.doi.org/10.1007/s12045-007-0059-5.

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5

Grier, David G. "On the points of melting." Nature 379, no. 6568 (1996): 773–75. http://dx.doi.org/10.1038/379773a0.

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6

Seifert, H. J. "Melting points of lanthanide trichlorides." Journal of Thermal Analysis and Calorimetry 82, no. 3 (2005): 575–80. http://dx.doi.org/10.1007/s10973-005-0936-7.

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7

Tan, Ton That Minh, and Bernd Michael Rode. "The melting points of oligomethylenes." Journal of Polymer Science Part B: Polymer Physics 34, no. 13 (1996): 2139–43. http://dx.doi.org/10.1002/(sici)1099-0488(19960930)34:13<2139::aid-polb2>3.0.co;2-r.

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8

Alexander, Steven A. "Generating Molecules with Specific Boiling Points and Melting Points." Match Communications in Mathematical and in Computer Chemistry 94, no. 1 (2025): 77–93. https://doi.org/10.46793/match.94-1.077a.

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We examine a simple algorithm that uses simulated annealing to find molecules with a specific boiling point and melting point. For testing purposes, we consider molecules that contain only carbon, oxygen, nitrogen and hydrogen atoms. We represent these molecules as SMILES strings and use seven distinct operators to modify these strings.

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9

Savchenko, A. M., Yu V. Konovalov, A. V. Laushkin, and G. V. Kulakov. "Zirconium alloys with low melting points." Voprosy Materialovedeniya, no. 2(94) (January 10, 2019): 209–16. http://dx.doi.org/10.22349/1994-6716-2018-93-1-209-216.

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A novel class of low-melting Zr-based alloys has been developed. They are deep triple and quadruple eutectics with very low melting points from 690 to860°C. Low-melting Zr-based alloys proposed as a matrix material for fuel elements with dispersed high-U fuel. Proposed fuel compositions have been developed with high thermal conductivity and U content (25–50% higher than in case of VVER and PWR fuel rods). As applied to PWR and BWR reactors, they have some advantages compared to conventional uranium dioxide fuel pellets. The use of new dispersion fuel can improve neutron-physical characteristic

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10

Savchenko, A. M., Y. V. Konovalov, A. V. Laushkin, and G. V. Kulakov. "Zirconium Alloys with Low Melting Points." Inorganic Materials: Applied Research 10, no. 6 (2019): 1471–76. http://dx.doi.org/10.1134/s2075113319060212.

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11

Yalkowsky, Samuel H., and Doaa Alantary. "Estimation of Melting Points of Organics." Journal of Pharmaceutical Sciences 107, no. 5 (2018): 1211–27. http://dx.doi.org/10.1016/j.xphs.2017.12.013.

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12

Nurgaliev, I. N., A. A. Toropov, V. O. Kudyshkin, I. N. Ruban, N. L. Voropaeva, and S. Sh Rashidova. "QSPR-modeling of oligophenylene melting points." Journal of Structural Chemistry 47, no. 2 (2006): 362–66. http://dx.doi.org/10.1007/s10947-006-0307-7.

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13

Chelikowsky, J. R., and K. E. Anderson. "The melting points of intermetallic compounds." Physics Letters A 114, no. 8-9 (1986): 482–84. http://dx.doi.org/10.1016/0375-9601(86)90699-7.

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14

Beacall, T. "The melting-points of benzene derivatives." Recueil des Travaux Chimiques des Pays-Bas 47, no. 1 (2010): 37–44. http://dx.doi.org/10.1002/recl.19280470107.

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15

Bunn, C. W. "The melting points of chain polymers." Journal of Polymer Science Part B: Polymer Physics 34, no. 5 (1996): 799–819. http://dx.doi.org/10.1002/polb.1996.900.

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16

Bekö, Sándor L., Edith Alig, Martin U. Schmidt, and Jacco van de Streek. "On the correlation between hydrogen bonding and melting points in the inositols." IUCrJ 1, no. 1 (2013): 61–73. http://dx.doi.org/10.1107/s2052252513026511.

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Inositol, 1,2,3,4,5,6-hexahydroxycyclohexane, exists in nine stereoisomers with different crystal structures and melting points. In a previous paper on the relationship between the melting points of the inositols and the hydrogen-bonding patterns in their crystal structures [Simperleret al.(2006).CrystEngComm8, 589], it was noted that although all inositol crystal structures known at that time contained 12 hydrogen bonds per molecule, their melting points span a large range of about 170 °C. Our preliminary investigations suggested that the highest melting point must be corrected for the effect

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17

Blazquez, S., and C. Vega. "Melting points of water models: Current situation." Journal of Chemical Physics 156, no. 21 (2022): 216101. http://dx.doi.org/10.1063/5.0093815.

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By using the direct coexistence method, we have calculated the melting points of ice I h at normal pressure for three recently proposed water models, namely, TIP3P-FB, TIP4P-FB, and TIP4P-D. We obtained T m = 216 K for TIP3P-FB, T m = 242 K for TIP4P-FB, and T m = 247 K for TIP4P-D. We revisited the melting point of TIP4P/2005 and TIP5P obtaining T m = 250 and 274 K, respectively. We summarize the current situation of the melting point of ice I h for a number of water models and conclude that no model is yet able to simultaneously reproduce the melting temperature of ice I h and the temperatur

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18

Maruzeni, Shoji. "A mathematical technique for estimating the melting points of triacylglycerols from the component fatty acid melting points." European Journal of Lipid Science and Technology 111, no. 12 (2009): 1240–48. http://dx.doi.org/10.1002/ejlt.200800014.

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19

Haydarov, Gennadiy Gasimovich, and Andrey Gennadyevich Haydarov. "Interconnection between melting, boiling and critical points." Interactive science, no. 3 (May 25, 2016): 113–16. http://dx.doi.org/10.21661/r-79535.

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20

Peterson, I. "Fine Points of Melting in Plasma Crystals." Science News 149, no. 10 (1996): 150. http://dx.doi.org/10.2307/3979654.

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21

Tiers, George V. D. ""Melting points are uncorrected": True or false?" Journal of Chemical Education 67, no. 3 (1990): 258. http://dx.doi.org/10.1021/ed067p258.

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22

Jain, Akash, Gang Yang, and Samuel H. Yalkowsky. "Estimation of Melting Points of Organic Compounds." Industrial & Engineering Chemistry Research 43, no. 23 (2004): 7618–21. http://dx.doi.org/10.1021/ie049378m.

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23

Hoffmann, Albrecht, Jost Engert, and Wolfgang Buck. "The fixed points of the3He melting curve." Physica B: Condensed Matter 194-196 (February 1994): 19–20. http://dx.doi.org/10.1016/0921-4526(94)90339-5.

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24

Chou, T., and David R. Nelson. "Dislocation-mediated melting near isostructural critical points." Physical Review E 53, no. 3 (1996): 2560–70. http://dx.doi.org/10.1103/physreve.53.2560.

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25

Gao, Jiabin, Djamal Djaidi, Christopher E. Marjo, Mohan M. Bhadbhade, Alison T. Ung, and Roger Bishop. "Weak Intermolecular Forces, but High Melting Points." Australian Journal of Chemistry 70, no. 5 (2017): 538. http://dx.doi.org/10.1071/ch16565.

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The poorly soluble racemic compound 6,6a,13,13a-tetrahydropentaleno[1,2-b:4,5-b′]diquinoline (4) has an exceptionally high melting point range of 352–354°C despite its low molar mass (308.38) and a structure containing only 40 atoms (38 of which are C and H). Analysis of the X-ray crystal structure and Hirshfeld surface of 4, along with comparison with its isostructural homologue 2, reveals how this occurs in the absence of Pauling-type hydrogen bonding. Excellent complementarity between homochiral molecules of 4 allows formation of enantiomerically pure layers using C–H⋯π, aromatic π⋯π, and C

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26

Trohalaki, Steven, and Ruth Pachter. "Prediction of Melting Points for Ionic Liquids." QSAR & Combinatorial Science 24, no. 4 (2005): 485–90. http://dx.doi.org/10.1002/qsar.200430927.

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27

Yang, Rui, Zhen Dong, and Zhiwen Ye. "Exploration of low-melting energetic compounds: influence of substituents on melting points." New Journal of Chemistry 44, no. 32 (2020): 13576–83. http://dx.doi.org/10.1039/d0nj01166e.

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28

Rengstl, Doris, Veronika Fischer, and Werner Kunz. "Low-melting mixtures based on choline ionic liquids." Phys. Chem. Chem. Phys. 16, no. 41 (2014): 22815–22. http://dx.doi.org/10.1039/c4cp02860k.

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29

Elhi, Fred, Mikhail Gantman, Gunnar Nurk, et al. "Influence of Carboxylate Anions on Phase Behavior of Choline Ionic Liquid Mixtures." Molecules 25, no. 7 (2020): 1691. http://dx.doi.org/10.3390/molecules25071691.

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Mixing ionic liquids is a suitable strategy to tailor properties, e.g., to reduce melting points. The present study aims to widen the application range of low-toxic choline-based ionic liquids by studying eight binary phase diagrams of six different choline carboxylates. Five of them show eutectic points with melting points dropping by 13 to 45 °C. The eutectic mixtures of choline acetate and choline 2-methylbutarate were found to melt at 45 °C, which represents a remarkable melting point depression compared to the pure compounds with melting points of 81 (choline acetate) and 90 °C (choline 2

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30

Joseph, Sumy, and Ranganathan Sathishkumar. "Succinate esters: odd–even effects in melting points." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 70, no. 5 (2014): 839–46. http://dx.doi.org/10.1107/s2052520614013730.

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Dialkyl succinates show a pattern of alternating behavior in their melting points, as the number of C atoms in the alkane side chain increases, unlike in the dialkyl oxalates [Josephet al.(2011).Acta Cryst.B67, 525–534]. Dialkyl succinates with odd numbers of C atoms in the alkyl side chain show higher melting points than the immediately adjacent analogues with even numbers. The crystal structures and their molecular packing have been analyzed for a series of dialkyl succinates with 1−4 C atoms in the alkyl side chain. The energy difference (ΔE) between the optimized and observed molecular con

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31

Nianyi, Chen, Liu Gang, Li Chonghe, Qin Pei, and Liu Honglin. "Regularities of melting points and melting types of simple and complex ionic solids." Journal of Physics and Chemistry of Solids 58, no. 5 (1997): 731–34. http://dx.doi.org/10.1016/s0022-3697(96)00192-8.

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32

Van Hook, W. Alexander. "Thermodynamic Analysis of Isotope Effects on Triple Points and/or Melting Temperatures." Zeitschrift für Naturforschung A 50, no. 4-5 (1995): 337–46. http://dx.doi.org/10.1515/zna-1995-4-504.

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Àbstract Available literature information on triple point or melting point isotope effects (and related physical properties) is subjected to thermodynamic analysis and consistency checks. New values for the melting point isotope effects for C6H6/CgD6 and c-C6H12/c-C6D12 are reported. 6Li/7Li melting point isotope effects reported recently by Hidaka and Lunden (Z. Naturforsch. 49 a, 475 (1994)) for various inorganic salts are questioned

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33

Garkushin, Ivan K., Mariya A. Istomova, Alexey I. Garkushin та Gennadiy E. Egortsev. "CHEMICAL INTERACTION IN MIXTURES МF + NaBr (М – K, Rb, Cs) UNDER THERMAL ACTIVATION". IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 63, № 4 (2020): 55–62. http://dx.doi.org/10.6060/ivkkt.20206304.6159.

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The chemical interaction of equivalent amounts of MF+NaBr (M – K, Rb, Cs) was studied by differential thermal and X-ray phase analysis. A mechanism of interaction during thermal activation is proposed, including the formation of NaF+MBr products at the contact boundaries of the initial substance grains due to the diffusion of Na+ and M+ followed by contact melting of four substances that form a labile liquid phase below or equal to the melting points of low-melting triple eutectics. The labile liquid occurrence in the sample promotes rapid ionic interaction. The heating curves of equivalent am

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34

Lotfi, Shahram, Shahin Ahmadi, and Parvin Kumar. "The Monte Carlo approach to model and predict the melting point of imidazolium ionic liquids using hybrid optimal descriptors." RSC Advances 11, no. 54 (2021): 33849–57. http://dx.doi.org/10.1039/d1ra06861j.

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The melting points of imidazolium ILs are studied employing a quantitative structure–property relationship (QSPR) approach to develop a model for predicting the melting points of a data set of imidazolium ILs.

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35

Xiong, Yeyue, Parviz Seifpanahi Shabane, and Alexey V. Onufriev. "Melting Points of OPC and OPC3 Water Models." ACS Omega 5, no. 39 (2020): 25087–94. http://dx.doi.org/10.1021/acsomega.0c02638.

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36

Coker, Eric N., Timothy J. Boyle, Mark A. Rodriguez, and Todd M. Alam. "Structurally characterized magnesium carboxylates with tuned melting points." Polyhedron 23, no. 10 (2004): 1739–47. http://dx.doi.org/10.1016/j.poly.2004.04.005.

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37

Venkatraman, Vishwesh, Sigvart Evjen, Hanna K. Knuutila, Anne Fiksdahl, and Bjørn Kåre Alsberg. "Predicting ionic liquid melting points using machine learning." Journal of Molecular Liquids 264 (August 2018): 318–26. http://dx.doi.org/10.1016/j.molliq.2018.03.090.

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38

Wei, James. "Molecular Symmetry, Rotational Entropy, and Elevated Melting Points." Industrial & Engineering Chemistry Research 38, no. 12 (1999): 5019–27. http://dx.doi.org/10.1021/ie990588m.

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39

Jensen, William B. "Melting Points and the Characterization of Organic Compounds." Journal of Chemical Education 86, no. 1 (2009): 23. http://dx.doi.org/10.1021/ed086p23.

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40

Petrov, Yu V., and E. V. Sitnikova. "Effect of anomalous melting points upon impact loading." Doklady Physics 50, no. 2 (2005): 88–90. http://dx.doi.org/10.1134/1.1881718.

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41

Greenspan, Donald. "A simple computer approach for determining melting points." Thermochimica Acta 179 (April 1991): 333–36. http://dx.doi.org/10.1016/0040-6031(91)80363-n.

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42

Jain, Akash, and Samuel H. Yalkowsky. "Estimation of Melting Points of Organic Compounds-II." Journal of Pharmaceutical Sciences 95, no. 12 (2006): 2562–618. http://dx.doi.org/10.1002/jps.20634.

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43

Kuduva, Srinivasan S., Jagarlapudi A. R. P. Sarma, Amy K. Katz, H. L. Carrell, and Gautam R. Desiraju. "Melting-points of themeta- andpara-isomers of anisylpinacolone." Journal of Physical Organic Chemistry 13, no. 11 (2000): 719–28. http://dx.doi.org/10.1002/1099-1395(200011)13:11<719::aid-poc308>3.0.co;2-2.

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44

Karu, Karl, Fred Elhi, Kaija Põhako-Esko, and Vladislav Ivaništšev. "Predicting Melting Points of Biofriendly Choline-Based Ionic Liquids with Molecular Dynamics." Applied Sciences 9, no. 24 (2019): 5367. http://dx.doi.org/10.3390/app9245367.

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In this work, we introduce a simulation-based method for predicting the melting point of ionic liquids without prior knowledge of their crystal structure. We run molecular dynamics simulations of biofriendly, choline cation-based ionic liquids and apply the method to predict their melting point. The root-mean-square error of the predicted values is below 24 K. We advocate that such precision is sufficient for designing ionic liquids with relatively low melting points. The workflow for simulations is available for everyone and can be adopted for any species from the wide chemical space of ionic

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45

Perlovich, German. "Melting points of one- and two-component molecular crystals as effective characteristics for rational design of pharmaceutical systems." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, no. 4 (2020): 696–706. http://dx.doi.org/10.1107/s2052520620007362.

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Based on the review of the literature results the database of the fusion temperatures of two-component molecular crystals (1947 co-crystals) and individual components thereof was built up. To improve the design of co-crystals with predictable melting temperatures, the correlation equations connecting co-crystals and individual components melting points were deduced. These correlations were discovered for 18 co-crystals of different stoichiometric compositions. The correlation coefficients were analysed, and the conclusions about the main/determinative and slave components of a co-crystal were

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46

RAJENDRA, S. VARMA, and P. SINGH A. "Addition-Elimination Reactions of lsatins with Arylthiosemicarbazides." Journal of Indian Chemical Society Vol. 68, Aug 1991 (1991): 469–70. https://doi.org/10.5281/zenodo.6196633.

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Department of Chemistry, Lucknow University, Lucknow-226 007 <em>Manuscript received 4 September 1990, revised 23 May 1991, accepted 5 August 1991</em> Addition-Elimination Reactions of lsatins with Arylthiosemicarbazides.

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47

Frank, Craig L. "Adaptations for hibernation in the depot fats of a ground squirrel (Spermophilus beldingi)." Canadian Journal of Zoology 69, no. 11 (1991): 2707–11. http://dx.doi.org/10.1139/z91-382.

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Ground squirrels are small herbivores that hibernate during winter. The ecological–nutritional limitations on hibernation are virtually unknown, but one constraint may be the melting point of stored fat. Lipids must be fluid to be metabolizable, and body temperatures maintained during hibernation are usually 30 °C below the melting point of typical mammalian fats. Fats containing greater amounts of unsaturated fatty acids, however, have correspondingly lower melting points. White adipose tissue was sampled from free-ranging Belding's ground squirrels, Spermophilus beldingi, during both the sum

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48

Popok, Vladimir N., and Vladimir A. Shandakov. "New correlations for the prediction of double-mix phase chart characteristics components of energy materials." Butlerov Communications 59, no. 9 (2019): 18–28. http://dx.doi.org/10.37952/roi-jbc-01/19-59-9-18.

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Special phase diagram points (eutecism, peritectics, co-crystallizates) of double (generally multi-component) mixtures of energy material components characterize the states and properties of mixtures some interest to mixed energy materials. The construction of phase charts in the form of the dependence of melting temperature on the content of components in the mixture is based on experimental data. The Schroeder equation is traditionally used to predict special points (melting and component content at eutecical, peritic, socrystalsitis) and approximation of experimental data. The use of Schroe

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49

FATEMI, MOHAMMAD H., and PARISA IZADIAN. "IN SILICO PREDICTION OF MELTING POINTS OF IONIC LIQUIDS BY USING MULTILAYER PERCEPTRON NEURAL NETWORKS." Journal of Theoretical and Computational Chemistry 11, no. 01 (2012): 127–41. http://dx.doi.org/10.1142/s0219633612500083.

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Quantitative structure–property relationship (QSPR) was used to predict melting points of 62 ionic liquids (ILs), which include ammonium, pyrrolidiniu, imidazolium, pyridiniu, piperidiniu, phosphonium ionic liquid salts. The structures of ionic liquids were optimized by Hyperchem software and MOPAC program, and stepwise multiple linear regression method was applied to select the relevant structural descriptors. The predicting models correlating selected descriptors and melting points were set up using multiple linear regressions (MLR) and multilayer perceptron neural network (MLP NN), separate

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50

Neto, Brenno A. D., Pedro S. Beck, Jenny E. P. Sorto, and Marcos N. Eberlin. "In Melting Points We Trust: A Review on the Misguiding Characterization of Multicomponent Reactions Adducts and Intermediates." Molecules 27, no. 21 (2022): 7552. http://dx.doi.org/10.3390/molecules27217552.

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We discuss herein the problems associated with using melting points to characterize multicomponent reactions’ (MCRs) products and intermediates. Although surprising, it is not rare to find articles in which these MCRs final adducts (or their intermediates) are characterized solely by comparing melting points with those available from other reports. A brief survey among specialized articles highlights serious and obvious problems with this practice since, for instance, cases are found in which as many as 25 quite contrasting melting points have been attributed to the very same MCR adduct. Indee

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