Desired form of polymorphism of 6-chloro-2,4-dinitroaniline crystals grown by controlled growth temperature in melt growth

Krishnakumar, V.; Rajaboopathi, M.

doi:10.1007/s10973-013-3181-5

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“…2 Recently, we have reported the crystal growth of form II and form III using a melt growth technique. 22 The noncentrosymmetric molecular arrangements of form II show high second harmonic generation conversion efficiency. There is no report of pseudomorphism in CDA.…”

Section: Introductionmentioning

confidence: 99%

Growth and characterization of 6-chloro-2,4-dinitroaniline crystals in anti-solvent precipitation and reprecipitation methods

2014

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Section: Introductionmentioning

confidence: 99%

Growth and characterization of 6-chloro-2,4-dinitroaniline crystals in anti-solvent precipitation and reprecipitation methods

2014

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Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds. Sublimation, Vaporization and Fusion Enthalpies From 1880 to 2015. Part 1. C₁− C₁₀

Acree

Chickos

2016

Journal of Physical and Chemical Reference Data

215

116

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Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds and Ionic Liquids. Sublimation, Vaporization, and Fusion Enthalpies from 1880 to 2015. Part 2. C11–C192

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Chickos

2017

Journal of Physical and Chemical Reference Data

126

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The second part of this compendium concludes with a collection of phase change enthalpies of organic molecules inclusive of C11–C192 reported over the period 1880–2015. Also included are phase change enthalpies including fusion, vaporization, and sublimation enthalpies for organometallic, ionic liquids, and a few inorganic compounds. Paper I of this compendium, published separately, includes organic compounds from C1 to C10 and describes a group additivity method for evaluating solid, liquid, and gas phase heat capacities as well as temperature adjustments of phase changes. Paper II of this compendium also includes an updated version of a group additivity method for evaluating total phase change entropies which together with the fusion temperature can be useful in estimating total phase change enthalpies. Other uses include application in identifying potential substances that either form liquid or plastic crystals or exhibit additional phase changes such as undetected solid–solid transitions or behave anisotropically in the liquid state.

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Desired form of polymorphism of 6-chloro-2,4-dinitroaniline crystals grown by controlled growth temperature in melt growth

Cited by 3 publications

References 42 publications

Growth and characterization of 6-chloro-2,4-dinitroaniline crystals in anti-solvent precipitation and reprecipitation methods

Growth and characterization of 6-chloro-2,4-dinitroaniline crystals in anti-solvent precipitation and reprecipitation methods

Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds. Sublimation, Vaporization and Fusion Enthalpies From 1880 to 2015. Part 1. C₁− C₁₀

Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds and Ionic Liquids. Sublimation, Vaporization, and Fusion Enthalpies from 1880 to 2015. Part 2. C11–C192

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Desired form of polymorphism of 6-chloro-2,4-dinitroaniline crystals grown by controlled growth temperature in melt growth

Cited by 3 publications

References 42 publications

Growth and characterization of 6-chloro-2,4-dinitroaniline crystals in anti-solvent precipitation and reprecipitation methods

Growth and characterization of 6-chloro-2,4-dinitroaniline crystals in anti-solvent precipitation and reprecipitation methods

Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds. Sublimation, Vaporization and Fusion Enthalpies From 1880 to 2015. Part 1. C1− C10

Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds and Ionic Liquids. Sublimation, Vaporization, and Fusion Enthalpies from 1880 to 2015. Part 2. C11–C192

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Phase Transition Enthalpy Measurements of Organic and Organometallic Compounds. Sublimation, Vaporization and Fusion Enthalpies From 1880 to 2015. Part 1. C₁− C₁₀