Patent Application
20250011321
Nonlinear optical (NLO) chromophores provide the electro-optic (EO) activity in poled, electro-optic polymer devices. Electro-optic polymers have been investigated for many years as an alternative to inorganic materials such as lithium niobate in electro-optic devices. Electro-optic devices may include, for example, external modulators for telecom, datacom, RF photonics, and optical interconnects and so forth. Polymeric electro-optic materials have demonstrated enormous potential for core application in a broad range of next-generation systems and devices, including electro-optic modulators, optical switches, phased array radar, satellite and fiber telecommunications, cable television (CATV), optical gyroscopes for application in aerial and missile guidance, electronic counter measure (ECM) systems, backplane interconnects for high-speed computation, ultraquick analog-to-digital conversion, land mine detection, radio frequency photonics, spatial light modulation and all-optical (light-switching-light) signal processing.
Many NLO molecules (chromophores) have been synthesized that exhibit high molecular electro-optic properties. The product of the molecular dipole moment (μ) and hyperpolarizability (β) is often used as a measure of molecular electro-optic performance due to the dipole's involvement in material processing. See Dalton et al., “New Class of High Hyperpolarizability Organic Chromophores and Process for Synthesizing the Same”, WO 00/09613.
Nevertheless, extreme difficulties have been encountered translating microscopic molecular hyperpolarizabilities (β) into macroscopic material hyperpolarizabilities (χ2). Molecular subcomponents (chromophores) must be integrated into NLO materials that exhibit (i) a high degree of macroscopic nonlinearity and (ii) sufficient temporal, thermal, chemical and photochemical stability. High electro-optic activity and the stability of electro-optic activity, which is also referred to as “temporal stability,” are important for commercially viable devices. Electro-optic activity may be increased in electro-optic polymers by increasing the concentration of nonlinear optical chromophores in a host polymer and by increasing of the electro-optic property of chromophores. However, some techniques for increasing chromophore concentration may decrease poling efficiency and temporal stability. Simultaneous solution of these dual issues is regarded as the final impediment in the broad commercialization of EO polymers in numerous devices and systems.
The production of high material hyperpolarizabilities (χ2) is limited by the poor social character of NLO chromophores. Commercially viable materials must incorporate chromophores at large molecular densities with the requisite molecular moment statistically oriented along a single material axis. In order to achieve such an organization, the charge transfer (dipole) character of NLO chromophores is commonly exploited through the application of an external electric field during material processing that creates a localized lower-energy condition favoring noncentrosymmetric order. Unfortunately, even at moderate chromophore densities, molecules form multi-molecular dipolarly-bound (centrosymmetric) aggregates that cannot be dismantled via realistic field energies. To overcome this difficulty, integration of anti-social dipolar chromophores into a cooperative material architecture is commonly achieved through the construction of physical barriers (e.g., anti-packing steric groups) that limit proximal intermolecular relations.
Thus, it has often been considered advantageous in the art to produce nonlinear optical chromophore containing materials that exhibit a high glass transition temperature (Tg). Materials with a high glass transition temperature exhibit improved thermal stability and maintain their macroscopic electro-optic properties to a greater degree than materials with lower glass transition temperatures. It can also be advantageous to produce nonlinear optical chromophores which exhibit desirable macroscopic optical properties, thermal stability and have lower wavelength maximum absorption, i.e., λmax.
The present invention is directed, in general, to nonlinear optical chromophores having an indolizine donor group. Various embodiments of the present invention include nonlinear optical chromophores with indolizine donor group having an indolizine donor connected to a II-bridge group. In various embodiments of the present invention, the indolizine donor groups may be substituted or unsubstituted, including hydro and alkyl substituents, aryl substituents and combination thereof. In certain embodiments of the present invention, the substituent moieties in the indolizine donor groups may be important for isolation. The isolation may reduce chromophore-chromophore interaction. The isolation may reduce charge transfer between molecules. The isolation may increase maximum applied voltage, which may contribute to more optimal poling and higher r33.
Various embodiments of the present invention include nonlinear optical chromophores having a C8-C20 bridging group between donor and acceptor. Various embodiments of the present invention include nonlinear optical chromophores having a C4-C6 bridging group between donor and acceptor, which chromophores exhibit lowered λmax values. In certain embodiments, nonlinear optical chromophores have a C4-C6 bridging group between donor and acceptor, an R1 moiety which can represent any alkyl group, and a R2 moiety which can represent any aryl group. These nonlinear chromophores having a C4-C6 bridging group between donor and acceptor exhibit lowered λmax values, can have narrow absorption bands. In certain other embodiments nonlinear optical chromophores are characterized by a Δλmax based λmax of chromophore analogs in a nonpolar solvent.
Amax values of the embodiments described herein create a larger transparency range among large wavelengths than do λmax values outside of the ranges described herein. For example, various nonlinear optical chromophore embodiments provide transparency over 800 nm, which have applications in 1) short-distance local area networks, 2) free-space optical fiber communications and optical interconnection in conjunction with LED or semiconductor lasers, and 3) active materials for terahertz (THz) applications. Various embodiments of the present invention include nonlinear optical chromophores having a short chain bridging group between donor and acceptor, which chromophores exhibit decreased optical loss and can provide higher degree of transparency at various wavelengths. In addition, various embodiments of the present invention have optimized characteristics of (1) higher r33 (electro-optic coefficients) at various wavelengths, (2) higher Tg (glass transition temperature), (3) exceptionally high thermal stability, and (4) high photostability.
Various embodiments of the present invention include a nonlinear optical chromophore of the general formula (I):
D-II-A (I)
wherein D represents an organic electron-donating group; A represents an organic electron-accepting group having an electron affinity greater than the electron affinity of D; and II represents a II-bridge between A and D; wherein the II-bridge comprises a carbon chain covalently bound to and separating A and D, wherein the carbon chain length between A and D is 2 to 4 carbon atoms, and wherein the 2 to 4 carbon atom chain comprises up to 2 carbon-carbon double bonds and up to 4 pendant substituents, wherein two or more of the pendant substituents can form a ring structure with the 2 to 4 carbon atom chain.
In various embodiments of the present invention, nonlinear optical chromophores of the general formula (I) have an indolizine donor group. In various embodiments of the present invention, nonlinear optical chromophores of the general formula (I) have an indolizine donor group connected to a II-bridge group.
Other aspects, features and advantages will be apparent from the following disclosure, including the detailed description, preferred embodiments, and the appended claims.
The foregoing summary, as well as the following detailed description of preferred embodiments of the invention, will be better understood when read in conjunction with the appended drawings. For purposes of illustration the invention, there are shown in the drawings embodiments which are presently preferred. It should be understood, however, that the invention is not limited to the precise arrangements and instrumentalities shown.
In the drawings:
Spectrograph 100 of
Spectrograph 200 of
Spectrograph 300 of
Spectrograph 400 of
Spectrograph 500 of
As used herein, the singular terms “a” and “the” are synonymous and used interchangeably with “one or more” and “at least one,” unless the language and/or context clearly indicates otherwise. Accordingly, for example, reference to “a polymer” or “the polymer” herein or in the appended claims can refer to a single polymer or more than one polymer. As a further example, reference to “a solvent” or “the solvent” herein or in the appended claims can refer to a single solvent or a mixture of more than one solvent. Additionally, all numerical values, unless otherwise specifically noted, are understood to be modified by the word “about.”
As used herein, the term “nonlinear optic chromophore” (NLOC) refers to molecules or portions of a molecule that create a nonlinear optic effect when irradiated with light. The chromophores are any molecular unit whose interaction with light gives rise to the nonlinear optical effect. The desired effect may occur at resonant or nonresonant wavelengths. The activity of a specific chromophore in a nonlinear optic material is stated as its hyper-polarizability, which is directly related to the molecular dipole moment of the chromophore. The various embodiments of NLO chromophores of the present invention are useful structures for the production of NLO effects.
The first-order hyperpolarizability (B) is one of the most common and useful NLO properties. Higher-order hyperpolarizabilities are useful in other applications such as all-optical (light-switching-light) applications. To determine if a material, such as a compound or polymer, includes a nonlinear optic chromophore with first-order hyperpolar character and a sufficient electro-optic coefficient (r33), which is a function of β, the following test may be performed. First, the material in the form of a thin film is placed in an electric field to align the dipoles. This may be performed by sandwiching a film of the material between electrodes, such as indium tin oxide (ITO) substrates, gold films, or silver films, for example.
Nonlinear optical chromophores of embodiments herein have an indolizine electron-donating group and a C6-C8 chain bridging group between donor and acceptor, which chromophores have optimal Amax values and exhibit good electro-optic characters. The λmax has to be in an optimal region for achieving good optimal electro-optic affect. For example, nonlinear optical chromophores having a bridging group between indolizine donor and acceptor can have a λmax in DCM between 725 nm and 900 nm.
The Δλmax is measured by calculating the λmax of the nonlinear optic chromophore in a standard polar solvent (e.g., DCM) versus the λmax an analog in a nonpolar solvent (e.g., 1,4-dioxane). The less-polar (1,4-dioxane) solvent will stabilize the neutral ground-state chromophore, while the more-polar solvent (DCM) will stabilize the charge-transfer state of the chromophore. The more easily the charge-transfer can happen, the more “polarizable”, and hence the more active the chromophore. Here, it has been found that higher wavelengths are directly proportional to lower energy. So, the higher Δλmax between two solvents, the less energy is required to achieve the charge-transfer state. In addition, the r33, which is measured experimentally and equates to the responsiveness of the light passing through to the electric field being applied, has a general correlation with the Δλmax, wherein the larger Δλmax generally correlates to a larger r33. In that manner, the Δλmax is characteristic of the “strength” of the chromophore's electro-optic activity.
Referring to
Referring to
Referring to
Referring to
Referring to
λmax and Δλmax data of short chain bridge chromophores of
To generate a poling electric field, an electric potential is then applied to the electrodes while the material is heated to near its glass transition (Tg) temperature. After a suitable period of time, the temperature is gradually lowered while maintaining the poling electric field. Alternatively, the material can be poled by corona poling method, where an electrically charged needle at a suitable distance from the material film provides the poling electric field. In either instance, the dipoles in the material tend to align with the field. Various embodiments according to the present invention can include or can also include electro-optic materials having a material glass transition temperature greater than or equal to 100° C., greater than or equal to 125° C., or greater than or equal to 150° C., or even higher.
The nonlinear optical property of the poled material is then tested as follows. Polarized light, often from a laser, is passed through the poled material, then through a polarizing filter, and to a light intensity detector. If the intensity of light received at the detector changes as the electric potential applied to the electrodes varies, the material incorporates a nonlinear optic chromophore having an electro-optically variable refractive index. A more detailed discussion of techniques to measure the electro-optic constants of a poled film that incorporates nonlinear optic chromophores may be found in Chia-Chi Teng, Measuring Electro-Optic Constants of a Poled Film, in Nonlinear Optics of Organic Molecules and Polymers, Chp. 7, 447-49 (Hari Singh Nalwa & Seizo Miyata eds., 1997), incorporated by reference in its entirety, except that in the event of any inconsistent disclosure or definition from the present application, the disclosure or definition herein shall be deemed to prevail.
The relationship between the change in applied electric potential versus the change in the refractive index of the material may be represented as its electro-optical (OE) coefficient (r33). This effect is commonly referred to as an electro-optic, or EO, effect. Devices that include materials that change their refractive index in response to changes in an applied electric potential are called electro-optical (EO) devices. For compositions having short chain bridge chromophores described herein, a high EO coefficient of >30 pm/V (measured, e.g., at 980 nm) or >20 pm/V (measured at, e.g., 1310 nm) can be achieved.
Compositions having short chain bridge chromophores described herein can also exhibit decreased optical loss. Optical loss of various of the described embodiments can be <2 dB/cm. Moreover, compositions described herein may provide higher degree of transparency at wavelengths outside of the absorption bands of the various embodiments herein. In addition, compositions described herein can also exhibit exceptionally high thermal stability, characterized by a decomposition temperature greater than 250 C, as well as high photostability, measured by the degradation of photo-optic materials under broadband light and ambient conditions.
The second-order hyperpolarizability (γ) or third-order susceptibility (χ(3)), are the normal measures of third-order NLO activity. While there are several methods used to measure these properties, degenerate four-wave mixing (DFWM) is very common. See C. W. Thiel, “Four-wave Mixing and Its Applications,” www.physics.montana.edu.students.thiel.docs/FWMixing.pdf, the entire contents of which are hereby incorporated herein by reference. Referring to Published U.S. Patent Application No. US 2012/0267583A1, the entire contents of which are incorporated herein by reference, a method of evaluating third-order NLO properties of thin films, known in the art as Degenerate Four Wave Mixing (DFWM), can be used. In
Nonlinear optical chromophores suitable for use in accordance with the various embodiments of the invention include those having the general formula (I):
D-II-A (I)
wherein D represents an organic electron-donating group; A represents an organic electron-accepting group having an electron affinity greater than the electron affinity of D; and II represents a II-bridge between A and D. The terms electron-donating group (donor or “D”), II-bridge (bridging group or “II”), and electron-accepting group (acceptor or “A”), and general synthetic methods for forming D-II-A chromophores in accordance with the various embodiments described herein are known in the art, for example as described in U.S. Pat. Nos. 5,670,091, 5,679,763, 6,090,332, and 6,716,995, and U.S. patent application Ser. No. 17/358,960, filed on Jun. 25, 2021, the entire contents of each of which is incorporated herein by reference.
An acceptor is an atom or group of atoms that has a low reduction potential, wherein the atom or group of atoms can accept electrons from a donor through a II-bridge. The acceptor (A) has a higher electron affinity than does the donor (D), so that, at least in the absence of an external electric field, the chromophore is generally polarized in the ground state, with relatively more electron density on the acceptor (D). Typically, an acceptor group contains at least one electronegative heteroatom that is part of a pi bond (a double or triple bond) such that a resonance structure can be drawn that moves the electron pair of the pi bond to the heteroatom and concomitantly decreases the multiplicity of the pi bond (i.e., a double bond is formally converted to single bond or a triple bond is formally converted to a double bond) so that the heteroatom gains formal negative charge. The heteroatom may be part of a heterocyclic ring. Exemplary acceptor groups include but are not limited to —NO2, —CN, —CHO, COR, CO2R, —PO(OR)3, —SOR, —SO2R, and —SO3R where R is alkyl, aryl, or heteroaryl. The total number of heteroatoms and carbons in an acceptor group is about 30, and the acceptor group may be substituted further with alkyl, aryl, and/or heteroaryl.
Suitable electron-accepting groups “A” (also referred to in the literature as electron-withdrawing groups) for nonlinear optical chromophores that can be used in accordance with the various embodiments of the present invention include those described in published U.S. Patent Applications: US 2007/0260062; US 2007/0260063; US 2008/0009620; US 2008/0139812; US 2009/0005561; US 2012/0267583A1 (collectively referred to as “the prior publications”), each of which is incorporated herein by reference in its entirety; and in U.S. Pat. Nos. 6,584,266; 6,393,190; 6,448,416; 6,44,830; 6,514,434; 5,044,725; 4,795,664; 5,247,042; 5,196,509; 4,810,338; 4,936,645; 4,767,169; 5,326,661; 5,187,234; 5,170,461; 5,133,037; 5,106,211; and 5,006,285; each of which is also incorporated herein by reference in its entirety.
In nonlinear optical chromophores suitable for use in accordance with various embodiments of the present invention, suitable electron-accepting groups can include those according to general formula (Aa):
wherein R4 and R5 each independently represents a moiety selected from the group consisting of H, substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C2-C10 alkenyl, substituted or unsubstituted C2-C10 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted alkylaryl, substituted or unsubstituted carbocyclic, substituted or unsubstituted heterocyclic, substituted or unsubstituted cyclohexyl, and (CH2)n—O—(CH2)n where n is 1-10. As used herein,
represents a point of bonding to another portion of a larger molecular structure. In various preferred embodiments, one or both of R4 and R5 represent a halogen-substituted moiety. Halogen-substituted may refer to mono-, di-, tri- and higher degrees of substitution. In various embodiments, one of R4 and R5 represent a halogen-substituted alkyl moiety and the other represents an aromatic moiety. In various embodiments, one of R4 and R5 represent a halogen-substituted aromatic moiety and the other represents an alkyl moiety. In various embodiments, the electron-accepting group can be:
In various embodiments, the electron-accepting group can be:
In various embodiments, the electron-accepting group can be:
In general, the choice of electron-accepting group may match the strength of electron-donating group. The overall strength between electron-donating group and electron-accepting group may not be too weak or too strong. If the overall strength is too weak, the λmax may be blue shifted with a lower r33. If the overall strength is too strong, the λmax may be red shifted with a lower r33 and more lossy. The choice of R4 and R5 groups in the electron-accepting group may also depend on the volume of the acceptor moiety to isolate. A better isolation for the acceptor moiety may bring better electro-optics property.
A donor includes an atom or group of atoms that has a low oxidation potential, wherein the atom or group of atoms can donate electrons to an acceptor “A” through a II-bridge. The donor (D) has a lower electron affinity than does the acceptor (A), so that, at least in the absence of an external electric field, the chromophore is generally polarized, with relatively less electron density on the donor (D). Typically, a donor group contains at least one heteroatom that has a lone pair of electrons capable of being in conjugation with the p-orbitals of an atom directly attached to the heteroatom such that a resonance structure can be drawn that moves the lone pair of electrons into a bond with the p-orbital of the atom directly attached to the heteroatom to formally increase the multiplicity of the bond between the heteroatom and the atom directly attached to the heteroatom (i.e., a single bond is formally converted to double bond, or a double bond is formally converted to a triple bond) so that the heteroatom gains formal positive charge. The p-orbitals of the atom directly attached to the heteroatom may be vacant or part of a multiple bond to another atom other than the heteroatom. The heteroatom may be a substituent of an atom that has pi bonds or may be in a heterocyclic ring. Exemplary donor groups include but are not limited to R2N— and RnX1—, where R is alkyl, aryl or heteroaryl, X1 is O, S, P, Se, or Te, and n is 1 or 2. The total number of heteroatoms and carbons in a donor group may be about 30, and the donor group may be substituted further with alkyl, aryl, or heteroaryl.
In nonlinear optical chromophores suitable for use in accordance with various embodiments of the present invention, suitable electron-donating groups can include the following indolizine donor group (Da):
wherein R1 in the indolizine electron-donating group represents a moiety selected from the group consisting of H, substituted or unsubstituted C2-C10 alkyl, substituted or unsubstituted C2-C10 alkenyl, and substituted or unsubstituted C2-C10 alkynyl, wherein R2 in the indolizine electron-donating group represents a moiety selected from the group consisting of substituted monocyclic or unsubstituted aryl, substituted or unsubstituted polycyclic aryl, substituted or unsubstituted alkylaryl, substituted or unsubstituted carbocyclic, substituted or unsubstituted heterocyclic, and substituted or unsubstituted cyclohexyl. The selection of R1 and R2 groups to isolate the nitrogen in the indolizine donor moiety plays an important role in achieving good characters in the nonlinear optical chromophore. Selected R1 and R2 groups on the indolizine donor group may reduce the chromophore-chromophore interaction, since less chromophore-chromophore interaction contributes to better loading limitations, better conductivity, and better characters against dielectric breakdown. Selected R1 and R2 groups on the indolizine donor group may reduce charge transfer and minimize II-bond stacking, since less charge transfer and minimized II-bond stacking contributes to less counterproductive to poling and better solubility.
In various embodiments, the electron-donating group can be:
In various embodiments, the electron-donating group can include one or more substituents on the six-member ring of the indolizine structure:
wherein R1, R2, R3 and R4 each independently represents a moiety selected from the group consisting of H, heteroatoms, substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C2-C10 alkenyl, substituted or unsubstituted C2-C10 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted alkylaryl, substituted or unsubstituted carbocyclic, substituted or unsubstituted heterocyclic, substituted or unsubstituted cyclohexyl, and/or (CH2)n—O—(CH2)n where n is 1-10, and wherein R5 represents a moiety selected from the group consisting of H and/or substituted or unsubstituted aryl. For example, R5 may represent a phenyl substituent.
In various examples, the electron-donating group can include a five-member or six-member ring-locked indolizine structure:
wherein R5 represents a moiety selected from the group consisting of H and/or substituted or unsubstituted aryl. For example, R5 may represent a phenyl substituent.
A “II-bridge” includes an atom or group of atoms through which electrons may be delocalized from an electron donor (defined above) to an electron acceptor (defined above) through the orbitals of atoms in the bridge. Typically, the orbitals will be p-orbitals on double (sp2) or triple (sp) bonded carbon atoms such as those found in alkenes, alkynes, neutral or charged aromatic rings, and neutral or charged heteroaromatic ring systems. Additionally, the orbitals may be p-orbitals on atoms such as boron or nitrogen. Additionally, the orbitals may be p, d or f organometallic orbitals or hybrid organometallic orbitals. The atoms of the bridge that contain the orbitals through which the electrons are delocalized are referred to here as the “critical atoms.” The number of critical atoms in a bridge may be a number from 1 to about 30. The critical atoms may be substituted with an organic or inorganic group. The substituent may be selected with a view to improving the solubility of the chromophore in a polymer matrix, to enhance the stability of the chromophore, or for other purposes.
Suitable bridging groups (II) for nonlinear optical chromophores according to general formula (I) can include those described in U.S. Pat. Nos. 6,584,266; 6,393,190; 6,448,416; 6,44,830; 6,514,434; each of which is also incorporated herein by reference in its entirety.
In various embodiments, bridging groups (II) for nonlinear optical chromophores according to general formula (I) can include those of the general formula (IIa):
wherein X represents a substituted or unsubstituted, branched or unbranched C2-C4 diyl moiety; wherein each a and b independently represents an integer of 0 to 3; and z represents an integer of 1 to 3. In various embodiments wherein a or b in general formula (II1) is 1, that carbon-carbon double bond in the formula can be replaced with a carbon-carbon triple bond. Alternatively, in various embodiments, bridging groups (II) for nonlinear optical chromophores according to general formula (I) can include those of the general formula (II2):
wherein X represents a substituted or unsubstituted, branched or unbranched C2-C4 diyl moiety. In various embodiments wherein one or more diamondoid groups is covalently attached to a bridging group according to general formulae II1 or II2, the one or more diamondoid groups may be bound, for example, to the sulfur or oxygen atoms of the thiophene group or to one or more carbon atoms in X through an ether or thioether linkage.
In various embodiments, bridging groups (II) for nonlinear optical chromophores according to general formula (I) can include those of the general formula (II3):
wherein each Y independently represents: a diamondoid-containing group covalently bound to the bridging group through any of the various linkages described herein below including but not limited to ether and thioether linkages; or each Y may represent a hydrogen, an alkyl group, aryl group, sulfur or oxygen linked akyl or aryl group, or a branched or unbranched, optionally heteroatom-containing C1-C4 substituent; wherein each a and b independently represents an integer of 0 to 3; z represents an integer of 1 to 3; and wherein each arc A independently represents a substituted or unsubstituted C2-C4 alkyl group, which together with the carbon bearing the Y substituent and its two adjacent carbon atoms forms a cyclic group. Substituted or unsubstituted C2-C4 alkyl groups which constitute arc A may include 1 to 4 hydrogen substituents each comprising a moiety selected from the group consisting of substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C2-C10 alkenyl, substituted or unsubstituted C2-C10 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted alkylaryl, substituted or unsubstituted carbocyclic, substituted or unsubstituted heterocyclic, substituted or unsubstituted cyclohexyl, and (CH2)n—O—(CH2)n where n is 1-10. In various embodiments, z represents 1. In various embodiments, the electron-donating group or electron-accepting group can include one or more covalently bound diamondoid groups, and Y in general formula II3 may represent any of the above substituents. In various embodiments, a chromophore may include an electron-donating group including one or more covalently linked diamondoid groups, preferably adamantyl, and the bridging group may include an isophorone group in accordance with general formula II3 wherein Y represent an aryl thioether substituent.
In various embodiments, bridging groups (II) for nonlinear optical chromophores according to general formula (I) can include those of the general formula (II4):
wherein each Y independently represents: a diamondoid-containing group covalently bound to the bridging group through any of the various linkages described herein below including but not limited to ether and thioether linkages; or each Y may represent a hydrogen, an alkyl group, aryl group, sulfur or oxygen linked alkyl or aryl group, an aryl group (optionally bearing a diamondoid group) linked directly by a carbon-carbon bond (e.g., adamantly anisole), a halogen, a halogenated alkyl group, a halogenated aryl group, or a branched or unbranched, optionally heteroatom-containing C1-C4 substituent; wherein each a and b independently represents an integer of 0 to 3; and z represents an integer of 1 to 3. In various embodiments, the electron-donating group or electron-accepting group can include one or more covalently bound diamondoid groups, and Y in general formula II4 may represent any of the above substituents. In various embodiments, a chromophore may include an electron-donating group including one or more covalently linked diamondoid groups, preferably adamantyl, and the bridging group may include an isophorone group in accordance with general formula II4 wherein Y represent an aryl thioether substituent. In various embodiments, each of the geminal methyl groups on the isophorone bridge of the general formula II4 can instead independently represent a moiety selected from the group consisting of substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C2-C10 alkenyl, substituted or unsubstituted C2-C10 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted alkylaryl, substituted or unsubstituted carbocyclic, substituted or unsubstituted heterocyclic, substituted or unsubstituted cyclohexyl, halogens, halogenated alkyl groups (e.g., —CF3), halogenated aryls and heteroaryl groups (e.g., pentafluorothiophenol), and (CH2)n—O—(CH2)n where n is 1-10.
In nonlinear optical chromophores suitable for use in accordance with various embodiments of the present invention, suitable bridging groups (II) can include the following structure (IIa):
wherein R3 represents a moiety selected from the group consisting of substituted or unsubstituted aryl, substituted or unsubstituted alkylaryl, substituted or unsubstituted carbocyclic, substituted or unsubstituted heterocyclic, and substituted or unsubstituted cyclohexyl; wherein R6 represents a moiety selected from the group consisting of H, halogen molecule, substituted or unsubstituted C2-C10 alkyl, substituted or unsubstituted C2-C10 alkenyl, and substituted or unsubstituted C2-C10 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted alkylaryl, substituted or unsubstituted carbocyclic, substituted or unsubstituted heterocyclic, and substituted or unsubstituted cyclohexyl; and wherein a is an integer of 1 or 2.
The choice of R3 and R6 groups may rest on the thermal stability and optical stability of the bridging groups. In other words, a bridging group without good thermal and optical stability may not achieve the desired electro-optic effect.
For example, bridging groups (II) for nonlinear optical chromophores according to general formula (I) can include:
For example, bridging groups (II) for nonlinear optical chromophores according to general formula (I) can include:
In various embodiments, the nonlinear optical chromophore with indolizine donor group may include, for example:
Indolizine donor groups suitable for use in the various embodiments of the present invention may be substituted or unsubstituted, including hydro and alkyl substituents, aryl substituents and combination thereof. The substituent moieties in the nonlinear optical chromophores with indolizine donor groups may be important for isolation. The isolation may reduce chromophore-chromophore interaction. The isolation may reduce charge transfer between molecules. The isolation may increase maximum applied voltage, which may contribute to more optimal poling and higher r33.
On one hand, nonlinear optical chromophores with indolizine donor group in accordance with various embodiments of the present invention may be a short chromophore with indolizine donor or a long chromophore with indolizine donor group. The short chromophore with indolizine donor may have three conjugated double bonds as II-bridge between the acceptor and the donor. The short chromophore may only be feasible if there is a strong donor (e.g., indolizine donor) that provides a red shifted maximum absorption (λmax). The short chromophore may therefore provide a narrow λmax and reduce the loss of light in a device. On the other hand, nonlinear optical chromophores with indolizine donor group in accordance with various embodiments of the present invention may be a long chromophore with indolizine donor group. The long chromophore with indolizine donor may have four or more conjugated double bonds as II-bridge between the acceptor and the donor.
This application claims the benefit of U.S. Provisional Application No. 63/524,047 filed on Jun. 29, 2023, the entire contents of which is incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 63524047 | Jun 2023 | US |
