The effect of solvents on crystal morphology of sucralose: Experiments and molecular dynamics simulation studies

[1]  E. Pluhařová,et al.  Understanding structure and dynamics of organic liquid mixtures by molecular simulations , 2019, Journal of Molecular Liquids.

[2]  M. Ramos,et al.  Investigation on the intermolecular interactions in aliphatic isocyanurate liquids: revealing the importance of dispersion , 2019, Journal of Molecular Liquids.

[3]  H. Hao,et al.  Predicting the crystal habit of photoinitiator XBPO and elucidating the solvent effect on crystal faces , 2019, CrystEngComm.

[4]  Shu-sen Chen,et al.  The effect of solution conditions on the crystal morphology of β-HMX by molecular dynamics simulations , 2019, Journal of Crystal Growth.

[5]  Jianlong Wang,et al.  Habit prediction of 3,4,5-trinitro-1H-pyrazole in four solvent mediums using a molecular dynamics simulation , 2019, Journal of Crystal Growth.

[6]  J. Skelton,et al.  Shining Light on Growth-Dependent Surface Chemistry of Organic Crystals: A Polarized Raman Spectroscopic and Computational Study of Aspirin , 2019, Crystal Growth & Design.

[7]  S. Rodrigues,et al.  Production and stability of probiotic cocoa juice with sucralose as sugar substitute during refrigerated storage , 2019, LWT.

[8]  Cheng Zhou,et al.  Theoretical study on crystal morphologies of 1,1-diamino-2,2-dinitroethene in solvents: Modified attachment energy model and occupancy model. , 2018, Journal of molecular graphics & modelling.

[9]  Zhijie Chen,et al.  Effects of crystal chemistry on sodium oleate adsorption on fluorite surface investigated by molecular dynamics simulation , 2018, Minerals Engineering.

[10]  S. Rohani,et al.  Effects of Additives on the Morphology of Thiamine Nitrate: The Great Difference of Two Kinds of Similar Additives , 2018 .

[11]  J. Gong,et al.  Crystal morphology optimization of thiamine hydrochloride in solvent system: Experimental and molecular dynamics simulation studies , 2018 .

[12]  Q. Yin,et al.  Insight into the Role of Hydrogen Bonding in the Molecular Self-Assembly Process of Sulfamethazine Solvates , 2017 .

[13]  K. Roberts,et al.  Crystal Morphology and Interfacial Stability of RS-Ibuprofen in Relation to Its Molecular and Synthonic Structure , 2017 .

[14]  Q. Yin,et al.  Effects of solvent and supersaturation on crystal morphology of cefaclor dihydrate: a combined experimental and computer simulation study , 2016 .

[15]  Zoltan K. Nagy,et al.  Tuning Crystal Morphology of Succinic Acid Using a Polymer Additive , 2016 .

[16]  R. Tan,et al.  Growth Behaviors of Two Similar Crystals: The Great Difference , 2015 .

[17]  Zubin B. Kuvadia,et al.  Interesting Morphological Behavior of Organic Salt Choline Fenofibrate: Effect of Supersaturation and Polymeric Impurity , 2014 .

[18]  Jianfeng Chen,et al.  Qualitative rationalization of the crystal growth morphology of benzoic acid controlled using solvents , 2014 .

[19]  S. Kamarudin,et al.  Morphology and Associated Surface Chemistry of l-Isoleucine Crystals Modeled under the Influence of l-Leucine Additive Molecules , 2012 .

[20]  P. Gupta,et al.  Simulating vapour growth morphology of crystalline urea using modified attachment energy model , 2012 .

[21]  R. Tan,et al.  Molecular simulation study of the effect of various additives on salbutamol sulfate crystal habit. , 2011, Molecular pharmaceutics.

[22]  Xiaoquan Huang,et al.  Solubility of Sucralose in Different Solvents from (283.15 to 333.15) K , 2010 .

[23]  Dylan Jayatilaka,et al.  Hirshfeld surface analysis , 2009 .

[24]  Y. Kawazoe,et al.  Atomic ordering recognized by convergence characteristics of the radial distribution function , 2008 .

[25]  J. Ulrich,et al.  Effect of Solvent on the Crystal Structure and Habit of Hydrocortisone , 2008 .

[26]  P. Bennema,et al.  Experimental and computational morphology of three polymorphs of the free base of Venlafaxine: a comparison of morphology prediction methods. , 2008, International journal of pharmaceutics.

[27]  M. Spackman,et al.  Towards quantitative analysis of intermolecular interactions with Hirshfeld surfaces. , 2007, Chemical communications.

[28]  M. Spackman,et al.  Fingerprinting intermolecular interactions in molecular crystals , 2002 .

[29]  H. Höltje,et al.  Consistent valence force‐field parameterization of bond lengths and angles with quantum chemical ab initio methods applied to some heterocyclic dopamine D3‐receptor agonists , 1998, J. Comput. Chem..

[30]  K. Roberts,et al.  Application of Bravais-Friedel-Donnay-Harker, attachment energy and Ising models to predicting and understanding the morphology of molecular crystals , 1991 .

[31]  P. Bennema,et al.  The attachment energy as a habit controlling factor: I. Theoretical considerations , 1980 .

[32]  P. Hartman The attachment energy as a habit controlling factor: III. Application to corundum , 1980 .

[33]  S. P. Phadnis,et al.  Enhancement in the sweetness of sucrose , 1976, Nature.

[34]  W. G. Perdok,et al.  On the relations between structure and morphology of crystals. I , 1955 .