Newly synthesized two kinds of achiral phenylacetylenes having a free-base- or a zinc-porphyrin ( and , respectively) were polymerized by using a chiral rhodium catalyst system, Rh⁺(nbd)[(⁶-C₆H₅)B(C₆H₅)₃] catalyst and ()-(+)- or ()-(⁻)-1-phenylethylamine (()- or ()-PEA, respectively) cocatalyst. Poly() and poly() in THF showed a Cotton signal at the absorption region of the porphyrin and the main chain in the circular dichroism (CD) spectra. This result suggests that poly() and poly() exist in a conformation with an excess of one-handed helix sense and the porphyrin moiety arranged in chiral helical fashion. The one-handed helical structure of poly() could be sustained in a mixture of THF/HMPA (10/2, /) due to stabilizing by stacking effect of porphyrin moieties along the main chain. This is the first example about helix-sense-selective polymerization by using Rh⁺(nbd)[(⁶-C₆H₅)B(C₆H₅)₃] catalyst. Additionally, poly() showed about 10 times larger CD intensity in comparison with poly(). This result suggests the regularity of arrangement of the porphyrin in poly() is higher compared with poly(). Spatial arrangement of porphyrins was achieved by utilizing a one-handed helical poly(phenylacetylenes) as a template.
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http://dx.doi.org/10.3390/polym11020274 | DOI Listing |
Chemistry
December 2024
Department of Chemistry, Graduate School of Advanced Science and Engineering, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8526, Japan.
Non-covalent interactions offer an alternative way for developing stimulus-responsive materials such as sensors, machines, and drug-delivery systems. We recently reported that a urethane-equipped tetrakis(porphyrin) forms one-handed helical supramolecular polymers in solution in response to chirality of chiral solvents. Conformational changes in helical sense were detected using circular dichroism (CD) spectroscopy, which showed that the tetrakis(porphyrin) can possibly be used as a sensor for determining the enantiomeric excess of a chiral analyte.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2024
Department of Chemistry Graduate School of Advanced Science and Engineering, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8526, Japan.
Tetrakisporphyrin monomers with amino acid side chains at each end form intramolecular antiparallel hydrogen-bonds to adopt chirally twisted pseudo-macrocyclic structures that result in right-handed and left-handed (P)- and (M)-conformations. The pseudo-macrocyclic tetrakisporphyrin monomers self-assembled to form supramolecular helical pseudo-polycatenane polymers via head-to-head complementary dimerization of the bisporphyrin cleft units in an isodesmic manner. The formation of one-handed supramolecular helical pseudo-polycatenane polymers was confirmed by circular dichroism (CD) spectroscopy.
View Article and Find Full Text PDFJ Am Chem Soc
August 2024
Roy & Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
Helical self-organizations are equilibrium structures responsible for the assembly of nonequilibrium and equilibrium living and synthetic systems. Racemic helical columnar systems transform into one-handed systems with the help of enantiomerically rich or pure components. Racemic, enantiomerically rich, and enantiomerically pure helical periodic arrays of columns are analyzed by oriented fiber X-ray diffraction (XRD).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Department of Molecular and Macromolecular Chemistry Graduate School of Engineering, Nagoya University Chikusa-ku, Nagoya, 464-8603, Japan.
We report the helix-sense-selective memory polymerization (HSMP) of achiral biphenylylacetylenes bearing carboxy and amino pendant groups in the presence of basic and acidic chiral guests in water, respectively. The HSMP proceeds in a highly helix-sense-selective manner driven by noncovalent chiral ionic interactions between the monomers and guests under kinetic control, producing the one-handed helical polymers with a static memory of helicity in one-pot during the polymerization in a very short time, accompanied by amplification of asymmetry. The carboxy-bound helicity-memorized polymer self-assembles into a cholesteric liquid crystal in concentrated water, in which a variety of basic achiral fluorophores further co-assembles to form supramolecular helical aggregates that exhibit an induced circularly polarized luminescence in a color tunable manner.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2024
Department of Chemistry and INSTM Research Unit, University of Pavia, Via Taramelli 12, 27100, Pavia, Italy.
In the last decades, chemists have developed methods to synthesize helical molecular architectures using a combination of covalent and non-covalent interactions. Very recently, the new class of completely covalent, one-handed helical ladder polymers has vigorously emerged. Such polymers can be rationally and programmably obtained through an approach guided by the principles of chirality-assisted-synthesis (CAS) and making use synergically of two disciplines that have so far rarely interacted: non-planar chiral π-conjugated synthons and ladder polymer chemistry.
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