Effects of extending the π-conjugation of the acetylide ligand on the photophysics and reverse saturable absorption of Pt(ii) bipyridine bisacetylide complexes. Issue 41 (7th October 2016)

• Record Type: Journal Article
• Authors: Lu, Taotao; Wang, Chengzhe; Lystrom, Levi; Pei, Chengkui; Kilina, Svetlana; Sun, Wenfang
• Is Part Of: Physical chemistry chemical physics. Volume 18:Issue 41(2016)
• Page Start: 28674
• Page End: 28687
• Publication Date: 2016-10-07
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c6cp02628a
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Extending the acetylide ligand π-conjugation diminishes the terminal substituent effect on the lowest excited states, but expands the triplet excited-state absorption to the near-IR region. Abstract : The synthesis and photophysics of four platinum(ii ) bipyridine (bpy) bisacetylide complexes with different degrees of π-conjugation and an electron-donating diphenylamino (NPh2 ) or electron-withdrawing benzothiazolyl (BTZ) terminal substituent on the acetylide ligands are reported. The UV-vis absorption spectra of these complexes are composed of intense ligand-localized 1 π, π* transitions at 330–430 nm and broad, moderately strong ligand-to-ligand charge transfer/metal-to-ligand charge transfer ( 1 LLCT/ 1 MLCT) transitions at 430–530 nm. All complexes are phosphorescent in solutions at room temperature and exhibit very broad and moderately strong triplet excited-state absorption in the visible to the NIR spectral region (425–800 nm). It is found that extending the π-conjugation of the acetylide ligands via adding one or two more ethynylfluorenyl unit(s) to the acetylide ligand does not change the energies of the 1 π, π* and 1 LLCT/ 1 MLCT transitions pronouncedly except for increasing the molar extinction coefficients of the 1 π, π* transitions. The emitting triplet excited states of the four complexes are the 3 MLCT/ 3 LLCT states and have the same energy. However, the complex that contains the tris(ethynylfluorenyl) units and the terminal NPh2 substituent on the acetylide ligand exhibits longer triplet lifetimes than the corresponding complex that has the bis(ethynylfluorenyl) units. The transient absorption band maxima of the complexes with tris(ethynylfluorenyl) units are slightly red-shifted in comparison to those of their respective counterparts with bis(ethynylfluorenyl) units. The nature of the terminal substituent does not influence the parentage and energies of the lowest singlet and triplet excited states. However, the triplet excited-state lifetimes of the complexes with the NPh2 terminal substituent on the bis(ethynylfluorenyl) or tris(ethynylfluorenyl) ligands are much longer than that of their counterpart with monofluorenylacetylide ligands; while the triplet lifetimes of the complexes containing the BTZ terminal substituent are similar to their counterpart with monofluorenylacetylide ligands. All complexes exhibit strong reverse saturable absorption (RSA) at 532 nm for nanosecond laser pulses.