A new class of polymers, which have a double-stranded polybinorbornene skeleton with multilayer planar oligoaryl linkers, defined as polymeric ladderphanes, are synthesized. The structures of these ladderphanes are determined by spectroscopic means. Photophysical studies and time-resolved fluorescence spectroscopic investigations reveal that there is a strong interaction between the chromophore linkers. Thus, Soret band splitting in the absorption spectrum of the polymer with porphyrin linker (12e), significant fluorescence quenching with oligoaryl linkers (12b-d), and excimer emission with a terphenylene-diethynylene linker (12a) are characteristic photophysical properties of these polymers. Scanning tunneling microscopy shows that polymers 12b and d exhibit a ladder-like morphology and form a supramolecular assembly leading to a two-dimensional ordered array on a highly oriented pyrolytic graphite surface.
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http://dx.doi.org/10.1021/ja9035362 | DOI Listing |
Chem Commun (Camb)
March 2022
School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200241, China.
Conjugated polyacetylene-based monocyclic and bicyclic polymers were synthesized by blocking-cyclization metathesis polymerization using short ladderphanes as the initial motif and multi-cyclizing unit, and fully characterized to elucidate the cyclic characteristics and good photoelectric properties. Importantly, the molecular topology of rationally designed cyclic polymers was directly observed without a tedious post-modification treatment.
View Article and Find Full Text PDFChem Asian J
June 2020
Key Laboratory of Organosilicon Chemistry and Material, Technology of Ministry of Eduction,\, Hangzhou Normal University, Hangzhou, Zhejiang, 311121, China.
Bis-norbornene and bis-cyclobutene with different kinds of linkers have been extensively used for the synthesis of double stranded ladderphanes under ruthenium- or molybdenum-catalyzed ring opening metathesis polymerization (ROMP) conditions. The key to the success relies on the selective formation of comb-like polynorbornenes or polycycloubtenes, where pendants are all aligned towards similar direction. This minireview summarizes various methods (chemical methods, spectroscopic means, and nonlinear optical measurements) for determining the comb-like conformations of pendants on these rigid-rod polymers.
View Article and Find Full Text PDFChemistry
January 2015
Department of Chemistry, National Taiwan University, Taipei, 106 (Taiwan); Department of Chemical Engineering, Feng Chia University, Taichung, 407 (Taiwan).
Communication between chromophores is vital for both natural and non-natural photophysical processes. Spatial confinements offer unique conditions to scrutinize such interactions. Polynorbornene- and polycyclobutene-based ladderphanes are ideal model compounds in which all tetraarylethylene (TAE) linkers are aligned coherently.
View Article and Find Full Text PDFAcc Chem Res
February 2013
Department of Chemistry, National Taiwan University, Taipei 106, Taiwan.
A polymeric ladderphane is a step-like structure comprising multiple layers of linkers covalently connected to two or more polymeric backbones. The linkers can be planar aromatic, macrocyclic metal complexes, or three-dimensional organic or organometallic moieties. Structurally, a DNA molecule is a special kind of ladderphane, where the cofacially aligned base-pair pendants are linked through hydrogen bonding.
View Article and Find Full Text PDFOrg Biomol Chem
August 2012
Institute of Polymer Science and Engineering, National Taiwan University, Taipei, Taiwan 106.
Three double stranded polymeric ladderphanes with 16-π-electron antiaromatic metallocycle linkers are synthesised by ring opening metathesis polymerisation of the corresponding bisnorbornene monomers. Scanning tunnelling microscopic (STM) images indicate that these polymers can assemble nicely on a graphite surface to form a highly ordered pattern which has been observed in other ladderphanes with different kinds of aromatic linkers. Little change in (1)H NMR, absorption spectra and electrochemical oxidation potential between these polymers and the corresponding monomers suggest that there would be no interactions between adjacent antiaromatic linkers in these polymeric ladderphanes.
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