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761.
Mattias Jonsson Brendan Weickert 《Proceedings of the American Mathematical Society》2000,128(10):2999-3002
We construct a nonalgebraic attractor for a holomorphic mapping on . The construction uses ideas from one-dimensional complex dynamics.
762.
Yue Lu Dr. Niamh McGoldrick Dr. Frances Murphy Dr. Brendan Twamley Xiaoneng Cui Dr. Colm Delaney Dr. Gearóid M. Ó Máille Junsi Wang Prof. Dr. Jianzhang Zhao Prof. Dr. Sylvia M. Draper 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(32):11349-11356
A series of IrIII complexes, based on 1,10‐phenanthroline featuring aryl acetylene chromophores, were prepared and investigated as triplet photosensitizers. The complexes were synthesized by Sonogashira cross‐coupling reactions using a “chemistry‐on‐the‐complex” method. The absorption properties and luminescence lifetimes were successfully tuned by controlling the number and type of light‐harvesting group. Intense UV/Vis absorption was observed for the IrIII complexes with two light‐harvesting groups at the 3‐ and 8‐positions of the phenanthroline. The asymmetric IrIII complex (with a triphenylamine (TPA) and a pyrene moiety attached) exhibited the longest lifetime. Red emission was observed for all the complexes in deaerated solutions at room temperature. Their emission at low temperature (77 K) and nanosecond time‐resolved transient difference absorption spectra revealed the origin of their triplet excited states. The singlet‐oxygen (1O2) sensitization and triplet‐triplet annihilation (TTA)‐based upconversion were explored. Highly efficient TTA upconversion (ΦUC=28.1 %) and 1O2 sensitization (ΦΔ=97.0 %) were achieved for the asymmetric IrIII complex, which showed intense absorption in the visible region (λabs=482 nm, ?=50900 m ?1 cm?1) and had a long‐lived triplet excited state (53.3 μs at RT). 相似文献
763.
764.
Chen Cao Xin-Ran Xue Qiu-Yi Li Min-Jie Zhang Prof. Brendan F. Abrahams Prof. Jian-Ping Lang 《Angewandte Chemie (International ed. in English)》2023,62(41):e202306048
Molecular crystals with the ability to transform light energy into macroscopic mechanical motions are a promising class of materials with potential applications in actuating and photonic devices. In regard to such materials, coordination polymers that exhibit dynamic photomechanical motion, associated with a phase transition, are unknown. Herein, we report an intriguing photoactive, one-dimensional ZnII coordination polymer, 1 , derived from 1,3,5-tri-4-pyridyl-1,2-ethenylbenzene and 3,5-difluorobenzoate. Single crystals of 1 under UV light irradiation exhibit rapid shrinking and bending, violent bursting-jumping, splitting, and cracking behavior. Single-crystal X-ray diffraction analysis and 1H NMR spectroscopy reveal an unusual photoinduced phase transition involving a single-crystal-to-single-crystal [2+2] cycloaddition reaction that results in photomechanical responses. Interestingly, crystals of 1 , which are triclinic with space group , are transformed into a higher symmetry, monoclinic cell with space group C2/c. This process represents a rare example of symmetry enhancement upon photoirradiation. The photomechanical activity is likely due to the sudden release of stress associated with strained molecular geometries and significant solid-state molecular movement arising from cleavage and formation of chemical bonds. A composite membrane fabricated from 1 and polyvinyl alcohol (PVA) also displays interesting photomechanical behavior under UV light illumination, indicating the material's potential as a photoactuator. 相似文献
765.