Kanazawa University Research: Synthesis of Helical Ladder Polymers

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May 16, 2019, 08:10 ET

KANAZAWA, Japan, May 16, 2019 /PRNewswire/ -- Researchers at Kanazawa University synthesized helical ladder polymers with a well-defined cyclic repeating unit and one-handed helical geometry, as they reported in the Journal of the American Chemical Society.

A construction of macro-scale architectures with a helical ladder shape is not even a challenge, but it’s a different story when it comes to a molecular scale (PRNewsfoto/Kanazawa University)

Ladder polymers — molecules made of adjacent rings sharing two or more atoms — are challenging to synthesize, because they require highly selective, quantitative reactions to avoid the formation of branching structures or of interruptions in the ring sequence in the polymer chain. Moreover, most existing strategies for the synthesis of ladder polymers suffer from severe limitations in terms of selectivity and quantitativity. Another important type of molecules are molecules with a helical structure (such as DNA and proteins), which play an important role in molecular recognition and catalysis. Thus, the fabrication of molecules that possess both a ladder and a helical structure could open up new applications of polymeric materials.

Tomoyuki Ikai, Timothy M. Swager and colleagues from an international collaboration started from triptycene, an aromatic hydrocarbon that is an achiral molecule, but from which chiral derivatives can be obtained by introducing substituents in the benzene rings in an asymmetric manner. Optically active triptycenes have practical uses as chiral materials, for example for chiral separation and circularly polarized luminescent materials. The researchers then used the chiral triptycenes as a framework to efficiently form single-handed helical ladder polymers using electrophilic aromatic substitution. Steric repulsion in the system resulted in the formation of one-handed twisted ladder units. The reactions were quantitative and regioselective (that is, there is a preferred direction of chemical bonding), which enabled the synthesis of optically active ladder polymers with well-defined helical geometry. No byproducts were detected.

Several techniques, including spectroscopy and microscopy techniques, were used to characterize the reaction products during synthesis, and molecular dynamics simulations were employed to understand the structure of the resulting molecules, confirming the right-handed helical ladder geometry. The researchers also measured the optical activity of the molecules.

The newly reported synthesis route will open up the synthesis of nanoscale helical ladder architectures and optically active chiral materials. "We believe that these ladder polymers, which can fall into a new category of helical polymers, represent a promising class of advanced materials for use as nanochannels for molecular/ion transport, organic electronics, specific reaction fields, and functional hosts through further modification of the backbone and pendant units," commented the authors in the paper.

Background

Chirality

A chiral system is an asymmetric system that cannot be superimposed on its mirror image (the word comes from the Greek for hands, because hands are a good example of a chiral system). Most biomolecules and molecules used in pharmaceutical compounds are chiral. Two molecules with opposite chirality have the same composition and structure, but mirror shapes, and they have different properties when they interact with other chiral molecules.

Electrophilic aromatic substitution

Electrophilic aromatic substitution is an organic reaction in which one atom attached to an aromatic system is replaced by an atom that is an electron acceptor (an electrophile). It is an important class of reactions, usually involving a benzene ring.

Steric repulsion

Steric repulsion is an effect that results from repulsive forces kicking in when atoms get too close to each other, so that their electron clouds overlap.

Reference

Tomoyuki Ikai, Takumu Yoshida, Ken-ichi Shinohara, Tsuyoshi Taniguchi, Yuya Wada, and Timothy M. Swager, Triptycene-Based Ladder Polymers with One-Handed Helical Geometry. J. Am. Chem. Soc. 2019 141 (11), 4696-4703.

DOI: 10.1021/jacs.8b13865

About Kanazawa University

As the leading comprehensive university on the Sea of Japan coast, Kanazawa University has contributed greatly to higher education and academic research in Japan since it was founded in 1949. The University has three colleges and 17 schools offering courses in subjects that include medicine, computer engineering, and humanities.

The University is located on the coast of the Sea of Japan in Kanazawa – a city rich in history and culture. The city of Kanazawa has a highly respected intellectual profile since the time of the fiefdom (1598-1867). Kanazawa University is divided into two main campuses: Kakuma and Takaramachi for its approximately 10,200 students including 600 from overseas.

Kanazawa University website: http://www.kanazawa-u.ac.jp/e/

Further information

Kanazawa University
Kakuma, Kanazawa, Ishikawa 920-1192, JAPAN
E-mail: [email protected]
Tel: +81-(76)-264-5963

SOURCE Kanazawa University