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For: Svärd M, Ahuja D, Rasmuson ÅC. Calorimetric Determination of Cocrystal Thermodynamic Stability: Sulfamethazine–Salicylic Acid Case Study. Crystal Growth & Design 2020;20:4243-51. [DOI: 10.1021/acs.cgd.9b01253] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Nath J, Baruah JB. Polymorphic solvates, ionic cocrystals and C–N bond formation to form ionic cocrystals in sulfamethoxazole and sulfathiazole-derived urea. CrystEngComm. [DOI: 10.1039/d1ce01731d] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Surov AO, Voronin AP, Drozd KV, Volkova TV, Vasilev N, Batov D, Churakov AV, Perlovich GL. Extending the Range of Nitrofurantoin Solid Forms: Effect of Molecular and Crystal Structure on Formation Thermodynamics and Physicochemical Properties. Crystal Growth & Design 2022;22:2569-86. [DOI: 10.1021/acs.cgd.2c00044] [Reference Citation Analysis]
3 Pal S. Mixing Effects on the Ternary Phase Diagram of Cocrystals and Gibbs Formation Energy Calculation. Crystal Growth & Design 2021;21:249-59. [DOI: 10.1021/acs.cgd.0c01077] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Przybyłek M, Miernicka A, Nowak M, Cysewski P. New Screening Protocol for Effective Green Solvents Selection of Benzamide, Salicylamide and Ethenzamide. Molecules 2022;27:3323. [DOI: 10.3390/molecules27103323] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]