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论文类型：期刊论文

发表时间：2017-12-01

发表刊物：EUROPEAN JOURNAL OF INORGANIC CHEMISTRY

收录刊物：SCIE

期号：44,SI

页面范围：5196-5204

ISSN号：1434-1948

关键字：Energy transfer; N ligands; Fused-ring systems; Platinum; Upconversion

摘要：Two different chromophores, pyrene (Py) and naphthalimide (NI), were introduced as acetylide ligands in a heteroleptic diimine N<^>N Pt-II bis(acetylide) complex (Pt-NI-Py) to broaden the absorption bands and enable the intramolecular energy-transfer process. Steady-state and transient spectroscopy were used to study the photophysical properties of the complexes. The lowest triplet state of Pt-NI-Py ((T) = 34 mu s) is localized on the pyrene part, although the singlet-state energy level of the naphthalimide unit is lower. Intramolecular energy-transfer processes were observed. Moreover, Pt-NI-Py shows enhanced visible-light harvesting compared with the bis(pyrenylacetylide) complex (Pt-Py) and a lower triplet-state energy level than that of the bis(ethynylnaphthalimide) complex (Pt-NI). The results demonstrate that the relative energy levels of the singlet excited states of the different chromophores do not agree with the relative energy levels of the triplet states of the same chromophores. Efficient triplet-state generation (phi = 0.8) gives Pt-NI-Py a high triplet-triplet annihilation (TTA) upconversion efficiency (34%).