Dynamic Dance of Chirality and Morphology: Interplay of Solvent-Sensitive Self-Assembly in Topological Evolution and Chirality Amplification DOI

Gaurav Kumar,

Manoj Kumar, Vandana Bhalla

и другие.

ACS Applied Materials & Interfaces, Год журнала: 2024, Номер 16(45), С. 62988 - 62998

Опубликована: Окт. 31, 2024

The building block Pyra-Chol has been designed and synthesized, which exhibits different achiral morphologies in good solvents, forming nanospheres THF nanoflowers 1,4-dioxane. In the presence of water as a poor cosolvent, demonstrates an agnostic behavior, generating left-handed superhelices water:THF (80:20) solvent system. However, when is switched to 1,4-dioxane, change chirality observed water:1,4-dioxane (30:70) system, resulting formation fused nanospheres. Interestingly, cosolvent changed from MCH THF, chiral pattern remains unchanged, but morphology changes completely. Supported by collective spectroscopic microscopic analysis, present study efficaciously remarkable control hydrophobic over sense also highlights fascinating influence well supporting distinct molecular packing.

Язык: Английский

Binaphthyl‐Aniline‐Based Chiral Magnetic Polymer DOI Creative Commons
Ryo Miyashita, Kunio Kimura, Reiji Kumai

и другие.

Journal of Polymer Science, Год журнала: 2025, Номер unknown

Опубликована: Март 18, 2025

ABSTRACT Magnetoactive polymers based on 1,1′‐binaphthyl‐2,2′‐diamine with axial chirality were synthesized through cross‐coupling polycondensation of the Buchwald–Hartwig reaction and subsequent oxidation m ‐chloroperoxybenzoic acid. The characterized optical spectroscopy, electron spin resonance, superconducting quantum interference device, synchrotron X‐ray diffraction. Circular dichroism measurements revealed that exhibited activity. Magnetic further showed are organic chiral materials weak antiferromagnetism owing to presence solid oxygen low‐dimensional ordering.

Язык: Английский

Процитировано

0

Chiral Amplification and Regulation: Design and Applications of Circularly Polarized Luminescence‐Active Materials Derived From Macrocyclic Compounds DOI Creative Commons
Wei Zhang,

Mao‐Qin Liu,

Yang Luo

и другие.

Aggregate, Год журнала: 2025, Номер unknown

Опубликована: Май 9, 2025

ABSTRACT Chirality is a fundamental property in molecules and biological systems, characterized by asymmetric configurational features. Circularly polarized luminescence (CPL) materials have gained significant attention due to their unique optical activities, with applications 3D displays, chiral sensors, catalysis, more. Chiral transfer amplification typically involve the generation of chirality excited state, facilitated interactions like energy transfer, electron or induction. Supramolecular self‐assembly strategies, particularly macrocyclic compounds, enable linking achiral luminescent units through intermolecular interactions. Macrocyclic hosts—cyclodextrins, calix[ n ]arenes, pillar[ cyclophanes, cucurbit[ ]urils—are especially promising stable structures adjustable cavities for guest encapsulation. These compounds induce photophysical properties host–guest complexation, making them ideal constructing amplification, CPL‐active materials. This review summarizes advancements multicolor CPL materials, sensing, induction, separation, highlighting potential supramolecular material design. The challenges future directions this field are also discussed, aiming guide further research application systems.

Язык: Английский

Процитировано

0

Dynamic Dance of Chirality and Morphology: Interplay of Solvent-Sensitive Self-Assembly in Topological Evolution and Chirality Amplification DOI

Gaurav Kumar,

Manoj Kumar, Vandana Bhalla

и другие.

ACS Applied Materials & Interfaces, Год журнала: 2024, Номер 16(45), С. 62988 - 62998

Опубликована: Окт. 31, 2024

The building block Pyra-Chol has been designed and synthesized, which exhibits different achiral morphologies in good solvents, forming nanospheres THF nanoflowers 1,4-dioxane. In the presence of water as a poor cosolvent, demonstrates an agnostic behavior, generating left-handed superhelices water:THF (80:20) solvent system. However, when is switched to 1,4-dioxane, change chirality observed water:1,4-dioxane (30:70) system, resulting formation fused nanospheres. Interestingly, cosolvent changed from MCH THF, chiral pattern remains unchanged, but morphology changes completely. Supported by collective spectroscopic microscopic analysis, present study efficaciously remarkable control hydrophobic over sense also highlights fascinating influence well supporting distinct molecular packing.

Язык: Английский

Процитировано

0