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供体-受体-供体非线性光学发色团在电信相关波长下的大超极化率

Large Hyperpolarizabilities at Telecommunication-Relevant Wavelengths in Donor-Acceptor-Donor Nonlinear Optical Chromophores.

作者信息

Nayak Animesh, Park Jaehong, De Mey Kurt, Hu Xiangqian, Duncan Timothy V, Beratan David N, Clays Koen, Therien Michael J

机构信息

Department of Chemistry, Duke University, French Family Science Center, 124 Science Drive, Durham, North Carolina 27708-0346, United States; Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, United States.

Department of Chemistry, University of Leuven , B-3001 Leuven, Belgium.

出版信息

ACS Cent Sci. 2016 Dec 28;2(12):954-966. doi: 10.1021/acscentsci.6b00291. Epub 2016 Dec 16.

Abstract

Octopolar -symmetric chromophores, based on the MPZnM supermolecular motif in which (porphinato)zinc(II) (PZn) and ruthenium(II) polypyridyl (M) structural units are connected via ethyne linkages, were synthesized. These structures take advantage of electron-rich -arylporphyrin or electron-poor -(perfluoroalkyl)porphyrin macrocycles, unsubstituted terpyridyl and 4'-pyrrolidinyl-2,2';6',2″-terpyridyl ligands, and modulation of metal(II) polypyridyl-to-(porphinato)zinc connectivity, to probe how electronic and geometric factors impact the measured hyperpolarizability. Transient absorption spectra obtained at early time delays ( < 400 fs) demonstrate fast excited-state relaxation, and formation of a highly polarized T excited state; the T states of these chromophores display expansive, intense T → T absorption manifolds that dominate the 800-1200 nm region of the NIR, long (μs) triplet-state lifetimes, and unusually large NIR excited absorptive extinction coefficients [ε(T → T ) ∼ 10 M cm]. Dynamic hyperpolarizability (β) values were determined from hyper-Rayleigh light scattering (HRS) measurements, carried out at multiple incident irradiation wavelengths spanning the 800-1500 nm spectral domain. The measured β value (4600 ± 1200 × 10 esu) for one of these complexes, RuPZnRu, is the largest yet reported for any chromophore at a 1500 nm irradiation wavelength, highlighting that appropriate engineering of strong electronic coupling between multiple charge-transfer oscillators provides a critical design strategy to realize octopolar NLO chromophores exhibiting large β values at telecom-relevant wavelengths. Generalized Thomas-Kuhn sum (TKS) rules were utilized to compute the effective excited-state-to-excited-state transition dipole moments from experimental linear-absorption spectra; these data were then utilized to compute hyperpolarizabilities as a function of frequency, that include two- and three-state contributions for both β and β tensor components to the RuPZnRu hyperpolarizability spectrum. This analysis predicts that the β and β tensor contributions to the RuPZnRu hyperpolarizability spectrum maximize near 1550 nm, in agreement with experimental data. The TKS analysis suggests that relative to analogous dipolar chromophores, octopolar supermolecules will be likely characterized by more intricate dependences of the measured hyperpolarizability upon irradiation wavelength due to the interactions among multiple different β tensor components.

摘要

合成了基于MPZnM超分子基序的八极对称发色团,其中(卟啉基)锌(II)(PZn)和钌(II)多吡啶(M)结构单元通过乙炔键相连。这些结构利用富电子的芳基卟啉或缺电子的(全氟烷基)卟啉大环、未取代的三联吡啶和4'-吡咯烷基-2,2';6',2″-三联吡啶配体,以及金属(II)多吡啶与(卟啉基)锌连接性的调节,来探究电子和几何因素如何影响所测量的超极化率。在早期时间延迟(<400 fs)下获得的瞬态吸收光谱表明存在快速的激发态弛豫,以及形成了高度极化的T激发态;这些发色团的T态显示出宽泛、强烈的T→T吸收谱带,在近红外800 - 1200 nm区域占主导,具有长(微秒级)的三重态寿命,以及异常大的近红外激发吸收消光系数[ε(T→T) ∼ 10 M cm]。动态超极化率(β)值通过超瑞利光散射(HRS)测量确定,测量在800 - 1500 nm光谱域的多个入射辐射波长下进行。这些配合物之一RuPZnRu所测量的β值(4600 ± 1200 × 10 esu)是在1500 nm辐射波长下任何发色团报道过的最大β值,突出表明对多个电荷转移振荡器之间强电子耦合进行适当设计提供了一种关键的设计策略,以实现八极非线性光学发色团在与电信相关波长下展现出大的β值。利用广义托马斯 - 库恩总和(TKS)规则从实验线性吸收光谱计算有效的激发态到激发态跃迁偶极矩;然后利用这些数据计算作为频率函数的超极化率,其中包括对RuPZnRu超极化率光谱中β和β张量分量的二态和三态贡献。该分析预测,RuPZnRu超极化率光谱中β和β张量贡献在1550 nm附近达到最大值,与实验数据一致。TKS分析表明,相对于类似的偶极发色团,由于多个不同β张量分量之间的相互作用,八极超分子所测量的超极化率对辐射波长的依赖性可能更复杂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403b/5200929/d45ea9ff7808/oc-2016-00291q_0005.jpg

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