0000000001268218

AUTHOR

Kari T. Rissanen

showing 6 related works from this author

The Effect of the Side Chain on Gelation Properties of Bile Acid Alkyl Amides

2021

Abstract Six bile acid alkyl amide derivatives were studied with respect to their gelation properties. The derivatives were composed of three different bile acids with hexyl or cyclohexyl side chains. The gelation behaviour of all six compounds were studied for 36 solvents with varying polarities. Gelation was observed mainly in aromatic solvents, which is characteristic for bile‐acid‐based low molecular weight gelators. Out of 108 bile acid‐solvent combinations, a total of 44 gel systems were formed, 28 of which from lithocholic acid derivatives, only two from deoxycholic acid derivatives, and 14 from cholic acid derivatives. The majority of the gel systems were formed from bile acids with…

geelitintermolecular interactionssupramolecular gelssolvent influenceCholic AcidAmidesBile Acids and Saltssappihapotamiditbile acid amidessupramolekulaarinen kemiaLithocholic AcidGelsResearch ArticlesröntgenkristallografiaResearch ArticleX-ray crystallography
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CCDC 2194827: Experimental Crystal Structure Determination

2022

Related Article: Johanna M. Alaranta, Khai-Nghi Truong, María Francisca Matus, Sami A. Malola, Kari T. Rissanen, Sailee S. Shroff, Varpu S. Marjomäki, Hannu J. Häkkinen, Tanja M. Lahtinen|2022|Dyes Pigm.|208|110844|doi:10.1016/j.dyepig.2022.110844

4-[2-(dimethylamino)ethenyl]-2-(methylsulfanyl)-1-phenylquinolin-1-ium iodide monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2194825: Experimental Crystal Structure Determination

2022

Related Article: Johanna M. Alaranta, Khai-Nghi Truong, María Francisca Matus, Sami A. Malola, Kari T. Rissanen, Sailee S. Shroff, Varpu S. Marjomäki, Hannu J. Häkkinen, Tanja M. Lahtinen|2022|Dyes Pigm.|208|110844|doi:10.1016/j.dyepig.2022.110844

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters2-{[2-(dimethylamino)-1-phenylquinolin-4(1H)-ylidene]methyl}-3-methyl-13-benzoxazol-3-ium chloride methanol unknown solvate hemihydrateExperimental 3D Coordinates
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CCDC 2194823: Experimental Crystal Structure Determination

2022

Related Article: Johanna M. Alaranta, Khai-Nghi Truong, María Francisca Matus, Sami A. Malola, Kari T. Rissanen, Sailee S. Shroff, Varpu S. Marjomäki, Hannu J. Häkkinen, Tanja M. Lahtinen|2022|Dyes Pigm.|208|110844|doi:10.1016/j.dyepig.2022.110844

2-{[2-(dimethylamino)-1-phenylpyridin-4(1H)-ylidene]methyl}-3-methyl-13-benzoxazol-3-ium chloride dihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2194826: Experimental Crystal Structure Determination

2022

Related Article: Johanna M. Alaranta, Khai-Nghi Truong, María Francisca Matus, Sami A. Malola, Kari T. Rissanen, Sailee S. Shroff, Varpu S. Marjomäki, Hannu J. Häkkinen, Tanja M. Lahtinen|2022|Dyes Pigm.|208|110844|doi:10.1016/j.dyepig.2022.110844

2-{[2-(dimethylamino)-1-phenylquinolin-4(1H)-ylidene]methyl}-3-methyl-13-benzothiazol-3-ium tetrafluoroborateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2194824: Experimental Crystal Structure Determination

2022

Related Article: Johanna M. Alaranta, Khai-Nghi Truong, María Francisca Matus, Sami A. Malola, Kari T. Rissanen, Sailee S. Shroff, Varpu S. Marjomäki, Hannu J. Häkkinen, Tanja M. Lahtinen|2022|Dyes Pigm.|208|110844|doi:10.1016/j.dyepig.2022.110844

Space GroupCrystallographyCrystal System2-{[2-(dimethylamino)-1-phenylpyridin-4(1H)-ylidene]methyl}-3-methyl-13-benzothiazol-3-ium chloride methanol solvate dihydrateCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct