Modulated conjugation as a means of improving the intrinsic hyperpolarizability.

A new strategy for optimizing the first hyperpolarizability based on the concept of a modulated conjugated path in linear molecules is investigated. A series of seven novel chromophores with different types of conjugated paths were synthesized and characterized. Hyper-Rayleigh scattering experiments confirmed that modulated conjugation paths that include benzene, thiophene, and/or thiazole rings in combination with azo and/or ethenyl linkages between dihydroxyethylamino donor groups and various acceptor groups result in enhanced intrinsic hyperpolarizabilities that exceed the long-standing apparent limit for two of the chromophores. The experimental results are analyzed and interpreted in the context of quantum limits, which show that conjugation modulation of the bridge in donor/acceptor molecules simultaneously optimizes the transition moments and the energy-level spacing.

[1]  Zhang Xinxin,et al.  The second-order nonlinear optical properties of a series of polyesters containing push-pull azobenzene chromophore in their side chain , 1999 .

[2]  O.F.J. Noordman,et al.  Time-resolved hyper-Rayleigh scattering: measuring first hyperpolarizabilities β of fluorescent molecules , 1996 .

[3]  C. C. Teng,et al.  Dispersion of the Nonlinear Second-Order Optical Susceptibility of an Organic System: p-Nitroaniline , 1983 .

[4]  W. Stahel,et al.  Log-normal Distributions across the Sciences: Keys and Clues , 2001 .

[5]  Koen Clays,et al.  INVESTIGATIONS OF THE HYPERPOLARIZABILITY IN ORGANIC MOLECULES FROM DIPOLAR TO OCTOPOLAR SYSTEMS , 1994 .

[6]  Koen Clays,et al.  Why hyperpolarizabilities fall short of the fundamental quantum limits. , 2004, The Journal of chemical physics.

[7]  Mark G. Kuzyk,et al.  Fundamental limits on third-order molecular susceptibilities: erratum , 2003 .

[8]  Brian J. Orr,et al.  Perturbation theory of the non-linear optical polarization of an isolated system , 1971 .

[9]  Mark G Kuzyk,et al.  The effects of geometry on the hyperpolarizability. , 2006, The Journal of chemical physics.

[10]  A. Jen,et al.  Efficient acceptor groups for NLO chromophores: competing inductive and resonance contributions in heterocyclic acceptors derived from 2-dicyanomethylidene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran , 2007 .

[11]  Juefei Zhou,et al.  Pushing the hyperpolarizability to the limit. , 2006, Optics letters.

[12]  M. Kuzyk,et al.  Fundamental limits of all nonlinear-optical phenomena that are representable by a second-order nonlinear susceptibility. , 2006, The Journal of chemical physics.

[13]  A. Jen,et al.  Focused Microwave‐Assisted Synthesis of 2,5‐Dihydrofuran Derivatives as Electron Acceptors for Highly Efficient Nonlinear Optical Chromophores , 2003 .

[14]  C. H. Wang,et al.  HYPER-RAYLEIGH SCATTERING USING 1907 NM LASER EXCITATION , 1999 .

[15]  Koen Clays,et al.  Hyper‐Rayleigh scattering in solution with tunable femtosecond continuous‐wave laser source , 1994 .

[16]  Seth R. Marder,et al.  Experimental investigations of organic molecular nonlinear optical polarizabilities. 1. Methods and results on benzene and stilbene derivatives , 1991 .

[17]  Joseph Zyss,et al.  Nonlinear optics in multipolar media: theory and experiments , 1994 .

[18]  Mark G. Kuzyk,et al.  Nonlinear Optics: Fundamental Limits ofNonlinear Susceptibilities , 2003 .

[19]  Persoons,et al.  Hyper-Rayleigh scattering in solution. , 1991, Physical review letters.

[20]  Robert J. McMahon,et al.  Thiazole and Thiophene Analogues of Donor−Acceptor Stilbenes: Molecular Hyperpolarizabilities and Structure−Property Relationships , 2000 .

[21]  Zhuangqi Cao,et al.  SYNTHESIS OF A NOVEL POLYURETHANE NLO POLYMER AND CHARACTERIZATION IN OPTICAL NONLINEARITY OF ITS DAS-TCF CHROMOPHORE , 2004 .

[22]  Koen Clays,et al.  Reversible switching of the first hyperpolarisability of an NLO-active donor–acceptor molecule based on redox interconversion of the octamethylferrocene donor unit , 2001 .

[23]  Antao Chen,et al.  The molecular and supramolecular engineering of polymeric electro-optic materials , 1999 .

[24]  Zhang,et al.  Low (Sub-1-volt) halfwave voltage polymeric electro-optic modulators achieved by controlling chromophore shape , 2000, Science.

[25]  Inge Asselberghs,et al.  Unusual frequency dispersion effects of the nonlinear optical response in highly conjugated (polypyridyl)metal-(porphinato)zinc(II) chromophores. , 2002, Journal of the American Chemical Society.

[26]  Mark G. Kuzyk,et al.  Monte Carlo studies of the fundamental limits of the intrinsic hyperpolarizability , 2007, 0708.1219.

[27]  Jean-Michel Nunzi,et al.  Donor-acceptor complexes incorporating ferrocenes: spectroelectrochemical characterisation, quadratic hyperpolarisabilities and the effects of oxidising and reducing agents , 2001 .

[28]  J. Oudar,et al.  Hyperpolarizabilities of the nitroanilines and their relations to the excited state dipole moment , 1977 .

[29]  Rolland Hierle,et al.  Huge enhancement of the quadratic nonlinear optical susceptibility in push–pull chromophores based on bridged dithienylethylene spacers , 2000 .

[30]  Mark G. Kuzyk,et al.  Erratum: “Why hyperpolarizabilities fall short of the fundamental quantum limit” [J. Chem. Phys.121, 7932 (2004)] , 2006 .

[31]  L. Qiu,et al.  Synthesis and Characterization of Photonic Polyesters Containing Azo Chromophore in the Side Chain , 1996 .

[32]  F. Rouessac,et al.  Synthesis of Substituted Dicyanomethylendihydrofurans , 1995 .

[33]  M. G. Kuzyk,et al.  Connecting at the speed of light , 2003 .

[34]  Mark G. Kuzyk Compact sum-over-states expression without dipolar terms for calculating nonlinear susceptibilities , 2005 .

[35]  Kai Song,et al.  Combined molecular and supramolecular bottom-up nanoengineering for enhanced nonlinear optical response: experiments, modeling, and approaching the fundamental limit. , 2007, The Journal of chemical physics.

[36]  B H Robinson,et al.  Influence of isomerization on nonlinear optical properties of molecules. , 2006, The journal of physical chemistry. B.

[37]  Kuzyk Physical limits on electronic nonlinear molecular susceptibilities , 2000, Physical review letters.

[38]  Xiaoguang Meng,et al.  A novel NLO azothiophene-based chromophore: Synthesis, characterization, thermal stability and optical nonlinearity , 2008 .

[39]  Mark G. Kuzyk,et al.  Quantum limits of the hyper-Rayleigh scattering susceptibility , 2001 .

[40]  Seth R. Marder,et al.  Experimental investigations of organic molecular nonlinear optical polarizabilities. 2. A study of conjugation dependences , 1991 .

[41]  M. Kuzyk,et al.  Fundamental limits on third-order molecular susceptibilities. , 2000, Optics letters.

[42]  Koen Clays,et al.  High-frequency demodulation of multi-photon fluorescence in hyper-Rayleigh scattering , 1998 .

[43]  Kenneth D. Singer,et al.  Second-order nonlinear-optical properties of donor- and acceptor-substituted aromatic compounds , 1989 .

[44]  Tapas Kar,et al.  Theoretical study of the nonlinear polarizabilities in H2N and NO2 substituted chromophores containing two hetero aromatic rings , 2003 .

[45]  K. Wostyn,et al.  High-frequency demodulation of multiphoton fluorescence in long-wavelength hyper-Rayleigh scattering. , 1999, Optics letters.

[46]  Yuxia Zhao,et al.  Modulated conjugation as a means for attaining a record high intrinsic hyperpolarizability. , 2007, Optics letters.

[47]  Yuxia Zhao,et al.  Study on novel second-order NLO azo-based chromophores containing strong electron-withdrawing groups and different conjugated bridges , 2004 .

[48]  A. F. Garito,et al.  Dispersion of the nonlinear second-order optical susceptibility of organic systems (A) , 1983 .

[49]  Mark G. Kuzyk,et al.  Erratum: Physical Limits on Electronic Nonlinear Molecular Susceptibilities [Phys. Rev. Lett. 85, 001218 (2000)] , 2003 .

[50]  Larry R. Dalton,et al.  Realization of sub 1 V polymeric EO modulators through systematic definition of material structure/function relationships , 2001 .