Details

Autor(en) / Beteiligte

• Chen , Chih-Hsien
• Satyanarayana, Kamani
• Liu, Yi-Hung
• Huang, Shou-Ling
• Lim, Tsong-Shin
• Luh, Tien-Yau

Titel

Excimer Formation in a Confined Space: Photophysics of Ladderphanes with Tetraarylethylene Linkers

Ist Teil von

• Chemistry : a European journal, 2015-01, Vol.21 (2), p.800-807

Ort / Verlag

Weinheim: WILEY-VCH Verlag

Erscheinungsjahr

2015

Quelle

Wiley-Blackwell Journals

Beschreibungen/Notizen

• 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. The spans for each of the monomeric units in these ladderphanes are 4.5–5.5 Å. Monomers do not exhibit emission, because bond rotation in TAE can quench the excited‐state energy. However, polymers emit at 493 nm (Φ=0.015) with large Stokes shift under ambient conditions and exhibit dual emission at 450 and 493 nm at 150 K. When the temperature is lowered, the emission intensity at 450 nm increases, whereas that at 493 nm decreases. At 100 K, both monomers and polymers emit only at 450 nm. This shorter‐wavelength emission arises from the intrinsic emission of TAE chromophore, and the emission at 493 nm could be attributed to the excimer emission in the confined space of ladderphanes. The fast kinetics suggest diffusion‐controlled formation of the excimer. In a tight spot: Ladderphanes provide a spatially confined environment to induce excimer emission of tetraarylethylene linkers, whereas the chromophore itself does not emit under ambient conditions (see figure). Low‐ temperature photophysical properties of ladderphanes and the corresponding monomers were investigated, and the barriers for excimer formation in these ladderphanes are 0.8–0.9 kcal−1 mol−1, depending on the nature of the polymeric backbones. ROMP: ring‐opening metathesis polymerization.