Simple substituents make big differences in photophysical performances of 2,1,3-benzothiadizole-conjugated spiropyrans

Developing multifunctional spiropyran dyes is of particular importance in diverse applications.In the present study,we synthesized two 2,1,3-benzothiadiazole-conjugated spiropyrans(BT-SP-NO2and BTSP-NMe2)with distinct substituents.These donor-acceptor-structured spiropyrans exhibited typical twisted intramolecular charge transfer features and strong emissions in low-polarity solvents with fluorescence quantum yields(QYs)of up to 90.7%.Like traditional spiropyrans,the electron-acceptor-substituted BT-SP-NO2exhibited excellent photochromic behavior under multiple alternating UV—Vis irradiation,while the electron-donor-substituted BT-SP-NMe2was an acidochromic dye.In addition,the substituent groups distinctly affected the packing modes of these spiropyrans in the solid state.BTSP-NMe2showed a much stronger solid-state emission(QY of 59.0%)than BT-SP-NO2.Moreover,these two dyes were utilized as biocompatible probes for the specific light-up imaging of lipid droplets.

Spectral Properties and Photochromic Characteristics of Spiropyran Dyes

A bis-benzospiropyran（BBSP） and nitro-substituted indoline spirobenzopyrans（SBP） were prepared by following a simple procedure. The reaction mechanism of synthesizing bis-benzospiropyran is discussed. A comparative analysis of the spectral and photochromic properties between SBP and BBSP was carried out with the aid of a PMMA film. The results indicate that chemical structures and UV irradiation played an important role in the spectral and photochromic properties of SBP and BBSP, which would readily affect λmax of the colored forms and the reversibility. The IR spectra and ^1H NMR spectra of these compounds are used to interpret the photochromic phenomena under different UV irradiation and determine the configurations of SBP and BBSP.

Study on the Tautomerism of an Indoline Spiropyran in Compressed CO_2 and Ethanol Mixture

Thermodynamic and kinetic properties of the tautomerism of an indoline spiropyran in compressed CO2-ethanol mixture were studied by UV-Vis spectroscopy at 298.15 K, 303. 15 K, and 308.15 K. It was found that the composition of the mixture affects the equilibrium constant and the rate constant significantly.

Preparation of Photochromic Waterborne Polyurethane Films:Effect of Spiropyran Concentration on Photochromic Properties

Incorporation of photochromic compounds to the polymer through chemical bonding will result in an enhancement of photoactivity and stabilization of optical properties.Here,spiropyran(SP)was introduced into polyurethane(PU)through semi-continuous emulsion copolymerization to get waterborne polyurethane dispersion(SPU).Studies on photochromic properties by UV-vis technique demonstrated the absorption intensity increased with the increasing of SP concentration and the colorless film turned to purple under UV irradiation.The kinetics for ring-opening and ring-closing reaction against SP were both first order,but the rate constants decreased with the increasing of SP concentration.The prepared SPU films showed reasonable photostability and photoreversibility according to the convenient test methods under UV-vis irradiation.Temperature dependence studies demonstrated that the photobleaching rate increased at higher temperatures with the same SP concentration.The chemical combination between SP and isocyanate(NCO)end group of polyurethane was confirmed through swelling experiments.Morphology studies were conducted by scanning electron microscope(SEM)micrographs and showed good compatibility between SP and PU.

Synthesis and Crystal Structure of 4-(2-Methylene-1-ethyl-3,3-dimethylindoline-2'-yl)-6,8-dibromo-1'-ethyl-3',3'-dimethylspiro-[3,4-dihydro-2H-1-benzopyran-2,2'-indoline]

The title compound of 4-（2-methylene-1-ethyl-3,3-dimethylindoline-2＇-yl）-6,8-dibro-mo-1＇-ethyl-3＇,3＇-dimethylspiro[3,4-dihydro-2H-1-benzopyran-2,2＇-indoline],C33H36Br2N2O,as a dicondensed spiropyran（DC） has been synthesized by indoline in ethanol with 3,5-dibromo-salicyaldehyde.The compound was characterized by elemental analysis and IR spectra.Meanwhile,the crystal of the compound was obtained and determined by X-ray single-crystal diffraction.Crystal data：monoclinic system,space group P21/n,a=12.9699（15）,b=12.5196（13）,c=19.327（2）,β=106.493（3）°,Mr=636.46,V=3009.1（6） 3,Z=4,F（000）=1304,Dc=1.405 g/cm3,μ=2.722 mm-1,R=0.0554 and wR=0.1176 for 6892 independent reflections（Rint=0.0354） and 5699 observed reflections（Ⅰ〉 2σ（Ⅰ））.

Synthesis,Structure and Properties of a Novel Copolymer with Photochromic and Photoluminescence Functions

Photochromic and photoluminescence materials show bright colors under different excitation conditions,and thus,these functional materials have been applied in many fields.Based on the photochromic and photoluminescence theories,a block copolymer,which could be directly processed into nanofibers by electrospinning,was successfully prepared through atom transfer radical polymerization(ATRP).To synthesize the block copolymer,a vinyl monomer containing a spiropyran unit was employed to prepare the photochromic chain segment,and a polymethyl methacrylate(PMMA)chain segment was introduced to improve the processability of the block copolymer.Acting as the photoluminescence unit,the rare earth complex was linked to the side chain through coordination bonding between the rare earth ions and the ester groups of PMMA.When the photochromic and photoluminescence block copolymer was exposed to different wavelengths of ultraviolet(UV)light and visible(Vis)light,it could show white,red,green,yellow,and blue-purple.These results provide the potential of the as-prepared photochromic and photoluminescence block copolymer for application in fibers and fabrics.

Synthesis and Photochromic Properties of the Derivatives of Spiropyrans Containing a Mesogenic Group

Two series of novel spiropyran derivatives containing a mesogenic group have been prepared. Their photochromic behaviors were first investigated with the aid of absorption spectral measurements.

PHOTOSWITCHABLE NANOFLUOROPHORES FOR INNOVATIVE BIOIMAGING

Photosensitive fluorescent probes have become powerful tools in chemical biology and molecular biophysics,which are used to investigate cellular processes with high temporal and spatial resolution.Accordingly,photosensitive fluorescent probes,including photoactivatable,photoconvertible,and photoswitchable fluorophores,have been extensively developed during the past decade.The photoswitchable fluorophores have received much attention because they highlight cellular events clearly.This minireview summarizes recent advances of using reversibly photoswitchable fluorophores and their applications in innovative bioimaging.Photoswitchable fluorophores include photoswitchable fluorescent proteins,photoswitchable fluorescent organic molecules(dyes),and photoswitchable fluorescent nanoparticles.Several strategies have been developed to synthesize photoswitchable fluorophores,including engineering combination proteins,chemical synthesis,polymerization,and self-assembly.Here we concentrate on polymer nanoparticles with optically switchable emission properties:either fluorescence on/offor dualalternating-color fluorescence photoswitching.The essential mechanisms of fluorescence photoswitching enable different types of photoswitchable fluorophores to change emission intensity or wavelength(color)and thus validating the basis of the fluorescence on/offor dual-color photoswitching design.Generally the possible applications of any fluorophores are to label biological targets,followed by specific imaging.The newly developed photoswitchable fluorophores enable super-resolution fluorescence imaging because of their photosensitive emission.Finally,we summarize the important area regarding future research and development on photoswitchable fluorescent nanoparticles.

Some Hybrid Systems of Chiral Schiff Base Zn(II) Complexes and Photochromic Spiropyrans for Environmental Ion Sensing

This is a review article including our recent results and some previous photo functional hybrid system having potential applications for environmental ion sensing. We have prepared several new and known chiral Schiff base Zn(II) complexes and measured (and also calculated) absorption and fluorescence spectra for sole complexes. After assembling hybrid systems with 1,3,3-trime- thylindolino-6’-nitrobenzopyrylospiran (SP) in methanol solutions, we measured spectral changes before and after alternate irradiation of UV and visible light. Intensity of fluorescence spectra for pale yellow Zn(II) complexes (λem = 450 nm, λex = 270 and 360 nm) was quenched by colorless SP (λem = 533 nm, λex = 612 nm). After UV light irradiation to form purple merocyanine (MC), photoisomerization resulted in changes of the intensity of absorption spectra as well as fluorescence spectra. Thus the hybrid systems could successfully act as molecular logic circuit by input (excitation by light) and output (intensity of fluorescence peaks). Moreover, we investigated concentration dependence of doped Zn(II) and Cu(II) ions to confirm quenching of intensity of fluorescence peaks by Zn(II) and Cu(II) MC complexes for metal ion sensing in solutions.

基于碳点功能化的二氧化硅封装螺吡喃的光响应材料用于动态信息加密

开发刺激响应荧光材料对于解决信息安全的新兴需求至关重要.本文中,我们提出了一种刺激响应双发射荧光材料SP@SiO_(2)-CDs(SP:螺吡喃),该材料是通过将螺吡喃化合物封装到碳点功能化的二氧化硅中得到的.这种复合材料显示碳点在470 nm处发射蓝色光,螺吡喃在620 nm处发射红色光.在连续紫外光(365 nm)照射下,螺吡喃分子经历从闭环到开环的过程,SiO_(2)-CDs和异构部花青之间可以实现显著的荧光能量共振转移.SP@SiO_(2)-CDs复合物粉末不仅可以在紫外光刺激下光致变色从黄色到粉色,而且可以实现从淡蓝色到橙红色的双发射荧光转换.当暴露在白光下时,这种动态荧光行为可以完全恢复到初始状态.基于荧光的时间依赖性,本文成功开发了动态防伪图案和多重编码.此外,通过掺杂聚二甲基硅氧烷,获得了具有高柔韧性和机械强度的薄膜,并展示了其在高级信息加密中的应用.该工作为提高离线便携式信息加密的安全性提供了一种新方法.

Photo-induced grease/oil switched lubricant for friction regulation

Controllable friction regulation has drawn much interest in both scientific and industrial fields.And there have been many researches on friction regulation by many physical fields and chemical factors.Photo-sensitive materials are promising because it is relatively easy to change their properties compared with others.Here,a new kind of photo-induced grease/oil switched lubricant is designed and shows great reversibility under ultraviolet(UV)and visible(Vis)irradiation.Its viscosity can change more than 50 times under different irradiation,and the coefficients of friction(COFs)obviously increase under Vis irradiation and decrease under UV irradiation,which performs better than those of the common grease.According to the experimental results,the phenomena are contributed to the break and reconstruction of the three-dimensional network inside the lubricant.With a switchable grease/oil state under different irradiation,this work provides a new principle for designing a smart lubricant with controllable friction regulation.

Novel elastomeric spiropyran‑doped poly(dimethylsiloxane)optical waveguide for UV sensing

Novel poly(dimethylsiloxane)(PDMS)doped with two diferent spiropyran derivatives(SP)were investigated as potential candidates for the preparation of elastomeric waveguides with UV-dependent optical properties.First,free-standing flms were prepared and evaluated with respect to their photochromic response to UV irradiation.Kinetics,reversibility as well as photofatigue and refractive index of the SP-doped PDMS samples were assessed.Second,SP-doped PDMS waveguides were fabricated and tested as UV sensors by monitoring changes in the transmitted optical power of a visible laser(633 nm).UV sensing was successfully demonstrated by doping PDMS using one spiropyran derivative whose propagation loss was measured as 1.04 dB/cm at 633 nm,and sensitivity estimated at 115%change in transmitted optical power per unit change in UV dose.The decay and recovery time constants were measured at 42 and 107 s,respectively,with an average UV saturation dose of 0.4 J/cm2.The prepared waveguides exhibited a reversible and consistent response even under bending.The sensor parameters can be tailored by varying the waveguide length up to 21 cm,and are afected by white light and temperatures up to 70℃.This work is relevant to elastomeric optics,smart optical materials,and polymer optical waveguide sensors.

Photo-controllable antifouling hydrogels embedded with AgNPs coated spiropyran functionalized mesoporous silica for long-term antibacterial activity

Silver nanoparticles(AgNPs)are widely used in antimicrobial applications.However,its easy aggregation and rapid loss hinder the effective antifouling.To address this issue,a novel stimuli-responsive antibacterial nanocomposite(Ag@SP-MSN)was developed based on spiropyran covalently conjugated mesoporous silica nanoparticles(284.6 nm)and AgNPs(27.1 nm)via strong electrostatic attraction.Both transmission electron microscopy(TEM)and atomic force microscopy(AFM)images proved the successful modification of AgNPs onto SP-MSN.The light-induced maximum loading amount towards AgNPs was calculated to be 95.0 wt.%after ultraviolet irradiation,while the amount of AgNPs released from Ag@SP-MSN was 94.4 wt.%under visible light in the aid of ammonia(0.1%,v/v).Upon cycled light irradiation,Ag@SP-MSN could recover 84.5 wt.%of AgNPs even after four cycles.The proposed Ag@SP-MSN exhibited better antibacterial activity against both E.coli and S.aureus than Ag@MSN under visible light illumination,indicating the efficient photo-responsive isomerization of spiropyran.Furthermore,the Ag@SP-MSN embedded gel demonstrated outstanding antifouling ability even after 21 days when compared to AgNPs gel.The long-term photo-controllable antifouling property proved the excellent reversible absorption and release of Ag@SP-MSN towards AgNPs.This work provides new insights into the safe utilization of nanomaterials,offering promising advancements to meet clinical antibacterial requirements.

The guest CH_(3)CN molecule triggers solid-state photochromism in a Cu_(2)I_(2)-based MOF for advanced time-dependent encryption and inkless erasable printing

It remains a big challenge to develop solid-state stimuli-responsive materials for time-dependent information encryption and inkless erasable printing with long retention times.Herein,a 2D Cu_(2)I_(2)-based MOF with photoresponsive spiropyran(SP)groups orderly installed on its skeleton is developed.The structural isomerization from SP to colored merocyanine(MC)form can be triggered by removing the CH_(3)CN guests.Besides,the degree of structural isomerization and the retention time can be adjusted by controlling the amount of CH_(3)CN guests,exhibiting dynamic photochromic behavior with multicolor states and tunable retention time.Based on these advantages,time-dependent information encryption is successfully achieved.Furthermore,the long retention time(>72 h)of the MC form under daylight conditions in the CH_(3)CN-removed Cu_(2)I_(2)-based MOF and good repeatability make it promising in various applications,such as temporary calendars,price-cards,billboards,and reusable identity cards.This work provides a novel design strategy to fabricate multi-functional MOF-based smart materials for challenging applications of time-dependent information encryption and inkless erasable printing.

Multistate circularly polarized luminescence switches based on dual stimuli-responsive chiral[2]rotaxanes

Aiming at the construction of novel multistate circularly polarized luminescence(CPL)switches,dual stimuli-responsive chiral[2]rotaxanes towards anions and light have been designed and constructed.Through the light-controlled on/off F?rster resonance energy transfer(FRET)switching between the emissive stoppers and anion-induced controllable motions of the chiral wheel for the precise regulations of chirality information transfer from the chiral wheel to the emissive stoppers,precisely switching between four CPL emission states with varied emission wavelengths and dissymmetry factors has been successfully realized,making them a promising platform for practical uses such as information storage and encryption.This proof-of-concept study not only provides a novel design strategy for multistate CPL switching but also contributes excellent candidates for the construction of novel smart chiral luminescent materials.

A Multiresponsive Hydrophobic Associating Hydrogel Based on Azobenzene and Spiropyran

Summary of main observation and conclusion Stimuli-responsive hydrogels crosslinked by weak noncovalent bonds such as hydrogen bonds,ionic interactions,host-guest interactions and hydrophobic interactions have been extensively investigated.Herein,azobenzene and spiropyran acting as two hydrophobic pendant groups were introduced into a hydrophilic polyacrylamide (PAM) via free radical copolymerization to construct a hydrophobic interaction based thermo-,light-responsive polymer hydrogel.Its viscosity and color could be reversibly regulated by heating and cooling.Meanwhile,its color could be specifically switched by light without obvious viscosity change.The gel was also capable of being transited to sol by addition of β-cyclodextrin (β-CD),which encaged the hydrophobic groups and then increased the solubility of polymer in water.The hydrogel could be regained after UV irradiation at λ=365 nm,and after irradiation at λ=440 nm,the hydrogel changed into a clear sol again.

Synthesis of novel chalcone derivatives and their stabilization effect of spiropyran in PMMA films

Three novel bis-chalcone derivatives with different alkyldioxy spacers were synthesized and dispersed into polymethyl methacrylate （PMMA） chloroform solution with 6-nitro-1＇-ethyl-3＇,3＇-dimethylspiro-2H-1-benzopyran-2,U-indoline （ESP） to prepare photochromic PMMA films in a facile way. After irradiation with 365 nm UV light, the photocrosslinking reaction between chalcone units was proved to retard the decolorization of merocyanine form of the photochromic spiropyran effectively, as results of the steric hindrance produced by photocycloaddition of chalcone groups. It has been found that the bis-chalcone molecule with the shortest spacer has the most effective stabilizing effect on retardation of decoloration of spiropyran. reserved.

A fluorescent probe based on a spiropyran for sensitive detection of Ce^3+ ion

A spiropyran-based probe was developed.It serves as a fluorescence turn-on probe for selective detection of Ce^3+in both ethanol and aqueous(water/ethanol,1:9 or 9:1,v/v)media.Ce3+can induce photochromism of the probe though the probe exhibits negligible photochromic property by itself.The probe is sensitive to Ce3+and the detection limit reaches 1.7μmol/L.It exhibits a high selectivity for Ce^3+ion over other common metal cations including Li^+,Na^+,Ag^+,Sr^2+,Ni^2+,Co^2+,Hg^2+,Zn^2+,Cr^3+,Al^3+,Fe^3+and Bi^3+and lanthanide ions Nd^3+,Yb^3+and La^3+.The probe may be used for quantitative determination of the concentration of Ce3+ion in a range of 1-10μmol/L and for application to environmental water samples.Sensing mechanism of the probe towards Ce3+ion is proposed.

Dual sensitivity of spiropyran-functionalized carbon dots for full color conversions

Multicolor phosphors that respond rapidly to external stimuli are highly desirable for many applications, including lighting,optical displays and sensors. Herein, spiropyran(SP)-functionalized carbon dots(CDs) were synthesized with a broad-spectrum output that were responsive to both ultraviolet(UV)/visible light and pH. The SP-CDs possessed strong ester linkages between the UV-absorbing/blue-emitting CDs and blue-absorbing/red-emitting surface SP groups, allowing efficient F?rster resonance energy transfer(FRET) between the donor and acceptor. UV irradiation or acid addition cause the SP ring opening to merocyanine(MC) or protonated MCH+forms, respectively, together with the formation of sheet-like aggregates. These processes enhanced the red emissions by the SP groups and attenuated blue emissions from the CDs. These changes were fully reversible under visible light or basic conditions, respectively, allowing dynamic regulation of the fluorescence properties(emission colors from blue to red, photoluminescence(PL) intensity) under photoirradiation on the timescale of minutes. As proof-of concept, we demonstrate that the emission properties of the SP-CDs can be used to construct UV and pH sensing materials as well as light emitting diode(LED) with different colors.

Synthesis of New Spiropyrans With a Polyaromatic or Heteroaromatic Pendant and Their Photochromic Behaviors

A series of spiropyrans with a polyaromatic or heteroaromatic pendant was synthesized conveniently. Their photochromic behaviors were investigated with the aid of absorption spectral measurements. The results indicated that the compounds with the same parent spiropyran but different aromatic pendant show significantly different photochromic properties. This may be due to the π-π orbital interaction between the polyaromatic pendant and the open photomerocyanine form of spiropyran. The results obtained are very useful in the molecule design area.