Homochiral layered indium phosphonates: solvent modulation of morphology and chiral discrimination adsorption

Assembling chiral coordination polymers into nano/microflower structures may improve their performance in applications such as chiral recognition and separation. In this study, we chose a chiral metal phosphonate system, <i>i.e.</i>, In(NO<sub>3</sub>)<sub>3</sub>/<i>R</i>-, <i>S</i>-pempH<sub>2</sub> [pempH<sub>2</sub> = (1-phenylethylamino)methylphosphonic acid], and carried out systematic work on the self-assembly of this system in different alcohol/H<sub>2</sub>O mixed solvents under solvothermal conditions. Enantiomeric compounds <i>R</i>-, <i>S</i>-[In<sub>2</sub>(pempH)<sub>2</sub>(μ<sub>2</sub>-OH)<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>](NO<sub>3</sub>)<sub>2</sub> (R-, S-1) were obtained showing dense layered structures, but their morphologies varied with alcohol solvent. We obtained crystals of R-, S-1C in triethylene glycol (TEG)/H<sub>2</sub>O mixed solvent and spiral microflowers of R-, S-1MF in isopropanol (IPA)/H<sub>2</sub>O mixed solvent. Adsorption isotherms using enantiopure <i>R</i>-2-butanol and <i>S</i>-2-butanol as probe molecules revealed that compounds R-1MF and S-1MF had higher adsorption capacity compared to the crystalline sample and displayed enantioselective adsorption behaviour.

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Publication Details

Journal
Dalton Transactions
Published
2025-01-01
DOI
https://doi.org/10.1039/d4dt03227f
Citations
3
Primary Topic
Surface Chemistry and Catalysis
Type
article
Field-Weighted Citation Impact
2.02

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article

Homochiral layered indium phosphonates: solvent modulation of morphology and chiral discrimination adsorption

Song‐Song Bao, Ran Gao, Li‐Min Zheng, Qian Teng
3 citations
Dalton Transactions
Surface Chemistry and Catalysis
2.02
article

Homochiral layered indium phosphonates: solvent modulation of morphology and chiral discrimination adsorption

Song‐Song Bao, Ran Gao, Li‐Min Zheng, Qian Teng
article en
3 citations

Abstract

Assembling chiral coordination polymers into nano/microflower structures may improve their performance in applications such as chiral recognition and separation. In this study, we chose a chiral metal phosphonate system, <i>i.e.</i>, In(NO<sub>3</sub>)<sub>3</sub>/<i>R</i>-, <i>S</i>-pempH<sub>2</sub> [pempH<sub>2</sub> = (1-phenylethylamino)methylphosphonic acid], and carried out systematic work on the self-assembly of this system in different alcohol/H<sub>2</sub>O mixed solvents under solvothermal conditions. Enantiomeric compounds <i>R</i>-, <i>S</i>-[In<sub>2</sub>(pempH)<sub>2</sub>(μ<sub>2</sub>-OH)<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>](NO<sub>3</sub>)<sub>2</sub> (R-, S-1) were obtained showing dense layered structures, but their morphologies varied with alcohol solvent. We obtained crystals of R-, S-1C in triethylene glycol (TEG)/H<sub>2</sub>O mixed solvent and spiral microflowers of R-, S-1MF in isopropanol (IPA)/H<sub>2</sub>O mixed solvent. Adsorption isotherms using enantiopure <i>R</i>-2-butanol and <i>S</i>-2-butanol as probe molecules revealed that compounds R-1MF and S-1MF had higher adsorption capacity compared to the crystalline sample and displayed enantioselective adsorption behaviour.

Dalton TransactionsVol. 54(9)
Nanjing University (CN)
National Natural Science Foundation of China
Reduced inequalities
Openalex Percentile: Top 16%
Surface Chemistry and Catalysis
2.02
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