98%
921
2 minutes
20
Alkynylplatinum(II) terpyridine complexes have been increasingly explored since the previous decades, mainly arising from their intriguing photophysical properties and aggregation affinities associated with their extensive Pt(II)···Pt(II) and π-π stacking interactions. Through molecular engineering, one can modulate their fundamental properties and assembly behavior by introduction of various functional groups and structural features. They can therefore serve as ideal candidates to construct metal complex-based molecular architectures to provide an alternative to organic compounds. The metal-based framework can be simultaneously built from predetermined building blocks, giving rise to their well-defined, unique, and discrete natures for molecular recognition. The individual constituents can contribute to molecular architectures with their integrated properties, allowing the manipulation of the various noncovalent intermolecular forces and interactions for selective guest capture. In this Account, our recent progress in the development of these metallomolecular frameworks based on the alkynylplatinum(II) terpyridine system and their recognition properties toward different guest molecules will be presented. Phosphorescent molecular tweezers have been constructed from the alkynylplatinum(II) terpyridine moiety to demonstrate host-guest interactions with cationic, charge-neutral and anionic platinum(II), palladium(II), gold(I), and gold(III) complexes and their binding affinities were found to be perturbed by different metal···metal, π-π and electrostatic interactions. The host-guest assembly process has also resulted in dramatic color changes, together with the turning on of near-IR (NIR) emissions as a result of extensive Pt(II)···Pt(II) interactions. Further work has also been performed to demonstrate that the tweezers can selectively recognize π-surfaces of different planar π-conjugated organic guests. The framework of molecular tweezers has been extended to a double-decker tweezers structure, or a triple-decker structure, which can bind two equivalents of square-planar platinum(II) guests cooperatively to induce a significant color change in solution, representing rare examples of discrete Magnus' green-like salts. By the approaches of structural modifications, we have further modulated the host architecture from molecular tweezers to molecular rectangles. The rectangles have been found to show selective encapsulation of different transition metal complex guests based on the size and steric environment of the host cavity. The molecular rectangles also exhibit reversible host-guest association, in which guest capture and ejection processes can be manipulated by the pH environment, illustrating a potential approach for precise and smart delivery of therapeutic reagents to the slightly more acidic cancer cells.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.accounts.8b00339 | DOI Listing |
Chem Asian J
August 2025
Department of Chemistry, Gyeongsang National University (GNU), 501 Jinju-Daero, Jinju, 52828, S. Korea.
We report the self-assembling behavior of a terpyridine-based alkyne platinum(II) complex (R-L-Pt-BP) under varying composition ratios of DMSO and HO. The resulting self-assemblies exhibited distinct photoluminescence and circular dichroism (CD) properties depending on the solvent conditions. Notably, strong positive CD signals were observed for the self-assembled R-L-Pt-BP in DMSO and HO (2:8 v/v), accompanied by a red-shift in emission wavelength.
View Article and Find Full Text PDFChem Sci
July 2025
Institute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong Pokfulam Road Hong Kong PR China
A series of anionic alkynylplatinum(ii) complexes with terpyridine (tpy) or 2,6-bis(benzimidazol-2'-yl)pyridine (bzimpy) as the tridentate -donor pincer ligand has been synthesized and characterized. These complexes are found to form ensembles with a cationic poly(fluorene--phenylene) derivative (PFP-NMe ) through electrostatic, Pt(ii)⋯Pt(ii) and π-π stacking interactions. Förster resonance energy transfer (FRET) has been found to take place, consequently gave rise to fluorescence quenching of the polymer donor and the emergence of low-energy emission from the platinum(ii) complex assemblies.
View Article and Find Full Text PDFSmall
May 2025
Department of Chemistry and Research Institution of Natural Sciences, Gyeongsang National University (GNU), Jinju, 52828, Republic of Korea.
In the process of supramolecular polymerization, kinetic barriers are pivotal in dictating the polymerization pathway and dynamics, thereby intricately modulating both the binding rate and the mechanism involved in the formation of supramolecular polymers. Here, the multistage activation barriers associated with dynamic pathway complexity are reported in the helical metallosupramolecular polymerization of chiral terpyridine-based alkynylplatinum(II) complexes (R-L-Pt and S-L-Pt) in a DMSO and HO mixture (6:4 v/v). The kinetic experiments reveal the presence of a kinetically favored aggregate (Agg-I) that initially forms and subsequently converts to another, more stable kinetic aggregate (Agg-II), accompanied by helicity inversion.
View Article and Find Full Text PDFNanoscale Adv
March 2024
Department of Chemistry, Research Institute of Natural Sciences, Gyeongsang National University Jinju 52828 Korea
Recently, cooperative supramolecular polymerization has garnered considerable attention due to its significant potential for enabling controlled chain-growth polymerization, which offers a route to achieving a well-defined degree of polymerization and low polydispersity. In this study, we synthesized two distinct alkynylplatinum(ii) complexes, one bearing a saturated long alkyl chain (Pt-Sat-C18) and another containing a diacetylene moiety within a long alkyl chain (Pt-DA-C25). Spectroscopic analyses revealed that Pt-Sat-C18 undergoes supramolecular polymerization an isodesmic pathway, while Pt-DA-C25 assembles cooperatively.
View Article and Find Full Text PDFDalton Trans
February 2023
Department of Chemical Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, West Bengal 741246, India.
In this work, the aggregation-induced photoluminescence emission (AIPE) of three water-soluble heterobimetallic Ir-Pt complexes was reported with insight into their photophysical and electrochemical properties and imaging of bacterial cells. An alkyne appended Schiff's base L, bridges bis-cyclometalated iridium(III) and platinum(II) terpyridine centre. The Schiff's base (N-N fragment) serves as the ancillary ligand to the iridium(III) centre, while the alkynyl end is coordinated to platinum(II).
View Article and Find Full Text PDF