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Optical limiting behaviors of penta-azadentate metal complexes for nanosecond laser

机译:纳秒激光五氮杂化金属配合物的光学限制性

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Pentaazadentate metal complexes are a macrocyclic ligand containing 22 $pi@-electrons, which coordinate with numerous metal ions to form near coplanar configurations with excellent thermal and light stabilities. A more extended optical window between Soret (420 nm) and Q (760 nm) band in visible region provides a condition for requiring high transmittances at low incident light intensity and they are of also large third- order nonlinear optical susceptibilities comparing with porphyrin's and phthalocyanine's metal complexes. The third- order optical susceptibilities $chi$+(3)$/$-1111$/ are determined at 647 nm in methanol by pump-probed procedure and the molecular second hyperpolarizabilities $gamma$-1111$/ which are of approximately 10$+$MIN@31$/ esu are also obtained. Optical limiting based on reverse saturable absorption are observed for ns pulses laser. The optical limiting behaviors may be alternated by introduce different substituents onto the benzene ring or/and different metal ion into the center of macrocylic ligands The limiting threshold at T/T$-0$/ equals 0.5 is 131 mJ/cm$+2$/ for complex $LB@(PL-NO$-2$/)Cd$RB@Cl, the corresponding clamped energy is 34 mJ/cm$+2$/. The optical limiting performance may be influenced by solution concentrations.
机译:五氮齿金属配合物是含有22 $ PI @π电子,这与许多金属离子配位形成具有优良的热和光的稳定性接近共面结构的大环配位体。在可见区域中的SORET(420nm)和Q(760nm)带之间的更加扩展的光学窗口提供了在低入射光强度下需要高透射率的条件,并且它们也是与卟啉和酞菁相比较的大三阶非线性光学敏感性金属配合物。所述三阶光学系数$ $智+(3)/ $ - 1111 $ /在甲醇中647纳米通过泵探测过程和分子超极化第二$ $伽马-1111 $ /它们是约10 $确定+ $ MIN @ 31 $ / esu也获得。对于NS脉冲激光,观察到基于反向可饱和吸收的光学限制。光学限制性行为可以通过将不同的取代基引入苯环或/且不同的金属离子中来交替,将不同的金属离子进入宏观的配体中心,限制阈值在T / T $ -0 $ /等于0.5是131 MJ / cm $ + 2 $ /对于复杂$ lb @(pl-no $ -2 $ /)cd $ rb @ cl,相应的夹紧能量为34 mj / cm $ + 2 $ /。光学限制性性能可能受溶液浓度的影响。

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