首页> 外文期刊>Journal of the American Chemical Society >Supermolecular-Chromophore-Sensitized Near-lnfrared-to-Visible Photon Upconversion
【24h】

Supermolecular-Chromophore-Sensitized Near-lnfrared-to-Visible Photon Upconversion

机译:超分子生色团敏化的近红外到可见光子上转换

获取原文
获取原文并翻译 | 示例
       

摘要

Selective near-IR (NIR) excitation (780 nm) of the conjugated supermolecule ruthenium(ll) [15-(4'-ethynyl-(2,2';6',2"-terpyridinyl))-bis[(5,5',-10,20-di(2',6'-bis(3,3-dimethylbutoxy)phenyl)por-phinato)zinc(ll)]ethyne][4'-pyrrolidin-1-yl-2,2';6',2"-terpyridine] bis(hexafluorophosphate) (Pyr_1RuPZn_2) in solutions containing N,N-bis(ethylpropyl)perylene-3,4,9,10-tetracarboxylicdiimide (PDI) ortetracene gives rise to a substantial anti-Stokes energy gain (PDI, 0.70 eV; tetracene, 0.86 eV). Experimental data clearly demonstrate that this upconverted fluorescence signal is produced via Pyr_1RuPZn_2-sensitized triplet-triplet annihilation (TTA) photochemistry. The TTA process was confirmed by the quadratic dependence of the integrated ~1PDI~* emission centered at 541 nm derived from 780 nm laser excitation. The T_1→ T_n excited state absorption decay of Pyr_1RuPZn_2, monitored at 900 nm as a function of PDI concentration, revealed Stern-Volmer and bimolecular quenching constants of 10 048 M~1 and 5.9 × 10~8 M~1 s~1 respectively, for the PDI triplet sensitization process. The T_1→T~n PDI extinction coefficient at 560 nm (ε_T = 6.6 × 10~4 M~(-1) cm~(-1)) was determined through the triplet energy transfer method utilizing anthracene as the donor chromophore. ~3PDI~* transient triplet absorption dynamics observed as a function of 485 nm incident nanosecond pump laser fluence demonstrate a bimolecular ~3PDI~*-~3PDI~* TTA rate constant (k_(TT) = 1.0 ± 0.2 × 10~9 M~(-1) s~(-1)). The maximum quantum yield of the supermolecule-sensitized PDI upconverted emission (Φ_(uc) = 0.0075 ± 0.0002) was determined relative to [Os(phen)_3][PF_6]_2 at an incident laser power of 22 mW at 780 nm. This study successfully demonstrates NIR-to-visible photon upconversion and achieves a new record anti-Stokes shift of 0.86 eV for sensitized TTA, using the supermolecular Pyr_1RuPZn_2sensitizer. The stability of the Pyr_1RuPZn_2/PDI chromophore combination is readily apparent as continuous irradiation at 780 nm produces 541 nm centered fluorescence with no significant decrease in intensity measured over time domains exceeding several hours. The molecular components of these NIR-to-vis upconverting compositions illustrate that substantial anti-Stokes energy gains via a TTA process can be effortlessly realized.
机译:共轭超分子钌(II)[15-(4'-乙炔基-(2,2'; 6',2“-叔吡啶基))-双[(5, 5',-10,20-二(2',6'-双(3,3-二甲基丁氧基)苯基)苯膦酸酯)锌(II)]乙炔] [4'-吡咯烷-1-基-2,2在含有N,N-双(乙基丙基)per-3,4,9,10-四羧酸二亚胺(PDI)或并四苯的溶液中形成'; 6',2“-吡啶吡啶]双(六氟磷酸盐)(Pyr_1RuPZn_2)斯托克斯能量增益(PDI,0.70 eV;并四苯,0.86 eV)。实验数据清楚地表明,该上转换的荧光信号是通过Pyr_1RuPZn_2敏化的三重态三重态三重态an灭(TTA)光化学产生的。 TTA过程是由源自780 nm激光激发的,以541 nm为中心的〜1PDI〜*积分发射的二次依赖性所证实的。在900 nm处监测的Pyr_1RuPZn_2的T_1→T_n激发态吸收衰减是PDI浓度的函数,显示出Stern-Volmer和双分子淬灭常数分别为10048 M〜1和5.9×10〜8 M〜1 s〜1,用于PDI三重态敏化过程。采用蒽作为供体发色团,通过三重态能量转移法确定了560 nm处的T_1→T〜n PDI消光系数(ε_T= 6.6×10〜4 M〜(-1)cm〜(-1))。 〜3PDI〜*瞬态三重态吸收动力学随485 nm入射纳秒泵浦激光注量的变化而变化,表明双分子〜3PDI〜*-〜3PDI〜* TTA速率常数(k_(TT)= 1.0±0.2×10〜9 M〜 (-1)s〜(-1))。在780 nm的入射激光功率为22 mW时,相对于[Os(phen)_3] [PF_6] _2确定了超分子敏感的PDI上转换发射的最大量子产率(Φ_(uc)= 0.0075±0.0002)。这项研究成功证明了使用超分子Pyr_1RuPZn_2敏化剂可实现近红外至可见光子的上转换,并获得了创纪录的0.86 eV的反斯托克斯位移。 Pyr_1RuPZn_2 / PDI生色团组合的稳定性很明显,因为在780 nm处连续照射会产生541 nm居中的荧光,并且在超过几个小时的时域中测得的强度没有明显降低。这些近红外至上转换组合物的分子成分说明,可以轻松实现通过TTA工艺获得的大量反斯托克斯能量。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2010年第40期|p.14203-14211|共9页
  • 作者单位

    Department of Chemistry and Center for Photochemical Sciences, Bowling Green State University,Bowling Green, Ohio 43403 The Dow Chemical Company, Analytical Sciences,1897 Building, Midland, Michigan 48667, USA;

    rnDepartment of Chemistry, 231 South 34th Street, University of Pennsylvania, Philadelphia, Pennsylvania 19104 Department of Chemistry, French Family Science Center, 124 Science Drive, Duke University, Durham, North Carolina 27708;

    rnDepartment of Chemistry and Center for Photochemical Sciences, Bowling Green State University,Bowling Green, Ohio 43403;

    rnDepartment of Chemistry and Center for Photochemical Sciences, Bowling Green State University,Bowling Green, Ohio 43403 Universite d'Angers, CIMA UMR CNRS 6200-UFR Sciences, 2 Boulevard Lavoisier, 49045, Angers, France;

    rnDepartment of Chemistry, 231 South 34th Street, University of Pennsylvania, Philadelphia, Pennsylvania 19104;

    rnDepartment of Chemistry and Center for Photochemical Sciences, Bowling Green State University,Bowling Green, Ohio 43403;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:15:51

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号