Abstract
In this report, the substitution of the oxygen group (=O) of Tetraphenylcyclopentadienone with =CR2 group (R = methyl ester or nitrile) was found to have tuned the electro-optical properties of the molecule. Although both groups are electrons withdrawing in nature, their absorption from UV-vis spectra analysis was observed to have been blue-shifted by methyl ester substitution and red-shifted by nitrile substitution. Interestingly, these substitutions helped to enhance the overall intensity of emission, especially in the context of methyl ester substitution whereby the emission was significantly boosted at higher concentrations due to hypothesized restrictions of intramolecular motions. These observations were explained through detailed descriptions of the electron withdrawing capability and steric properties of the substituents on the basis of density functional theory calculations.
Similar content being viewed by others
Introduction
Small or medium-sized organic molecules with an extended π-conjugation had been studied as photonic materials for light-emitting diodes, bioanalysis, thin film transistors, and photovoltaic devices1,2,3,4,5,6,7,8,9,10,11,12,13. This was due to high electron mobility empowering these molecules with ‘metallic-like’ characteristics as well as a highly accessible HOMO-LUMO energy gap that enabled absorption of UV-visible light. The overall shape and the dynamics of the π-conjugated skeleton arising from electron-withdrawing or donor functional groups is highly crucial in the determining electro-optical properties of the materials. This in turn also suggested that well designed organic synthesis can fine tune electro-optical properties. Furthermore, organic compounds are highly soluble and thus be easily applied for fabricating devices. Consequently, it is this unique ability to customize organic conjugated molecules as potential replacement of the inorganic semiconductors that provided the necessary impetus for detailed studies into π-conjugation systems14.
Conventional π-conjugated compounds are essentially planar D-π-A molecules (D for electron donating group and A for electron accepting group) where the excited state can exhibit charge separation. In recent years, a major breakthrough in the field of organic emitters was the synthesis and functionalization of the helical shaped Hexa-phenylsilole (HPS) and Tetraphenyl-ethylene (TPE) that are both π-conjugated molecules but not of the nominal D-π-A15,16,17,18,19,20,21,22,23. Interestingly, these compounds have turned out to possess many practical properties. Unlike traditional D-π-A emitters, they have exhibited an increased level of emission under higher concentration and condensed phase. This phenomenon are often described through mechanisms involving restricted intramolecular motions. Consequently, D-π-A molecules without exhibiting any planar structures are widely investigated due to this increased emission in concentrated solutions24,25,26,27, and such increment are often rationalized through the formation of J-aggregates that in turn increases and redshift the emission28.
In photovoltaics, helically shaped compounds have been frequently examined as effective replacement for fullerene in Bulk Heterojunction Solar Cells29. The helical shape allows for smaller domain sizes while still providing sufficient electron mobility at the same time. Moreover, these compounds are typically highly soluble in organic solvents even without long aliphatic chains, which is very useful during the device fabrication process. Some of the advantages of these molecules are the similarity in properties akin to that of fullerenes with smaller molecular spatial volumes as well as the reduced costs in terms of production and purification. Tetraphenylcyclopentadienone is one such helical shaped π-conjugated molecule that features unidirectional electron mobility due to the presence of the polar -C=O group (Fig. 1). Its range of UV-visible light absorption falls within the region 250–600 nm that is broader compared with other π-conjugated full organic molecules. As shown in Fig. 1, the molecular structure comprises of a cyclopentadienone linked with four phenyl groups.
The electronic properties of the Tetraphenylcyclopentadienone and its derivatives obtained from the deliberate modification on the phenyl rings were previously reported30,31,32,33,34. These derivatives are subsequently utilized as synthetic intermediates for the production of polyphenylene dendrimers as well as building blocks for gelators that absorb and emit within the UV-visible frequencies35,36,37,38,39,40,41,42,43. To provide further insight toward the synthesis of new helical shaped π-conjugated compounds for electrooptical applications, herein, the effects from the substitution of the oxygen group with =CR2 moeities (where R is –COOMe and –CN) were investigated. The compounds examined in this study were 2,3,4,5-tetraphenylfulvenes where the carbon at position 6 is bonded to two electron withdrawing groups. Pentafulvene is a molecular module that through chemical modification of the carbon at position 6 would switch from aromatic to antiaromatic electronic configuration with substitution at pentene ring, thus enabling for the fine-tuning of the HOMO-LUMO gap44,45,46,47,48. We have shown that the conversion of tetraphenylcyclopentadienone to tetraphenyl pentafulvene with different substituents at the carbon 6 position can fine-tune electro-optical properties in wide range. The absorption and emission spectra, in conjunction with density functional theory (DFT) calculations and femtosecond pump-probe measurements, were corroborated to produce an overall picture regarding to the electronic distribution and the interaction of these compounds with light.
Results and Discussion
Synthesis of compounds 1a and 1b
The synthesis of the compounds 1a and 1b was as shown in Scheme 1. The treatment of Tetraphenylcyclopentadienone 3 and compound 2a (Dimethyl malonate) or 2b (Malononitrile) with TiCl4 and Pyridine allowed for the recovery of compounds 1a or 1b respectively. The compound 1b is known in literature and two methods had been reported for the preparation. The procedure adopted in this work is based on the report by Andrew et al. and has been also utilized for the synthesis of 1a with high yields obtained49,50,51.
NMR Characterization
The aromatic 1H NMR signals of the compound 1a were shifted at lower ppm to the respect 1b (the protons 1, 2, 3 of 1a are at 6.73, 7.02, 7.09 ppm, the protons 1, 2, 3 of 1b are at 6.87, 7.07, 7.16 ppm, as displayed in Fig. 2) due to the highest electron-withdrawing character of the -CN group compared to -COOMe, as deduced from the values of the Hammet substituent constants σp and σm of the two functional groups (σm and σp are 0.56 and 0.66 for –CN, 0.37 and 0.45 for –COOMe)52. The proton signals of the phenyl rings closer to the electron-withdrawing groups were distinguishable (protons 1, 2, 3 in Fig. 2). The signals of the other phenyl groups were found to have overlapped (protons 1′, 2′, 3′ in Fig. 2). In compound 3, the 1H NMR signals of protons 1, 2, 3, as reported previously, were observed to exhibit highest chemical shifts with respect 1a and 1b (the protons 1 are at 6.90–6.94 ppm, the protons 2 are at 7.15–7.19 ppm and the protons 3 are at 7.23–7.26 ppm together with the protons 1′, 2′ and 3′)53.
Optical property analysis of compounds 1a, 1b and 3
Absorption profile
The UV spectra of 1a, 1b and 3 in CH3CN are as shown in Fig. 3 while the spectra taken in other solvents (Toluene, DMF and MeOH) are provided in Fig. S5. All absorption peaks as observed were binned into three separate regions: 250–260 nm, 320–380 nm, 500–510 nm and their λmax were labeled as λ1, λ2, λ3 respectively (Table 1). The λ1 was not detectable in all solvent due to the cut-off point of the solvent. Compound 3 exhibited signals at 330–340 nm (λ2) and 500–510 nm (λ3) while the variation was highly dependent on the solvent type. Dependence on compounds was found to be as follows. Compound 3’s λ3 was clearly discernible in all solvents although it displayed a low molar absorption coefficient compared to the other compounds’ signals at λ2. The absorption spectrum of 1a at 320–330 nm (λ2) and 460 nm (λ3) were observed at shorter wavelengths with respect to compound 3. 1b exhibited absorption bands at longer wavelengths compared to the other two compounds at 370–380 nm (λ2) and 500–545 nm (λ3). The molar absorption coefficient at λ3 for both compounds 1a and 1b has been lower than that at λ2 with partially overlapping signals in Toluene, CH3CN and CH2Cl2. On the other hand, in polar solvents such as DMF and MeOH, the peak was observed to be broadened and it was not easily discernable. The molar absorption constants at λ2 have been highest for 1a and 1b while highest for 3 at λ3.
Emission spectra
The excitation wavelength of fluorescence was set at λ2 for all solvents types and all compounds. All compounds of 1a, 1b and 3 had exhibited fluorescence at 430–435 nm in Toluene, CH3CN, MeOH, CH2Cl2. Compound 3 displayed the weakest fluorescence signal among all three compounds for all solvents. Interestingly, in DMF (the solvent with the highest dipolar moment), no fluorescence was observable for all compounds. The intensity of fluorescence of all compounds decreased with increasing polarity of the solvents. The quenching of fluorescence in DMF may be due to the high dipolar moment of the solvent as well as other reasons as previously reported in the literature, i.e. the interactions of the energetically excited molecules of emitter with the molecules of solvent or the presence of impurities in the solvent (even in the commercially available high purity DMF) that could result in the quenching of emission of the solute54. Table 1 listed all the respective optical properties of the compounds 1a, 1b, and 3. The values of the dipolar moments (μ) and orientational polarizability (Δf) of the solvents are as reported from literature55.
All emission spectra of the compounds, in different solvents, and at different concentrations are shown in the Fig. S6 of SI. Compound 3 exhibited fluorescence enhancement with concentration in Toluene and CH2Cl2, while in MeOH and CH3N the discerning of the precise peak maxima is technically challenging because of low fluorescence intensity The compound 1a exhibits highest fluorescence intensity when the concentration increased from 30–60 × 10−7 M to 30–60 × 10−6 M in all solvents with CH2Cl2 being the exception. The fluorescence spectra at six different concentrations of the compound 1a in Toluene is as displayed in Fig. 4. There was a direct correlation between intensity of the fluorescence and the concentration which was more intense at highest concentration. The plot of the fluorescence maxima at different concentration shown as inset of Fig. 4, could be fitted with a Hill equation. It was possible to examine the emission of compound 1a in Toluene with the same modality of other phenomena where physical measurement depends on the supramolecular aggregation between molecules25,57,58. The intermolecular aggregation increased the intensity of emission and the Eq. (1) can be used to correlate with the observed graph as shown in Fig. 4b:
Where ΔEm is the variation of the intensity of emission, [x] is the concentration of the free molecule in solution, \({K}_{a}\)is the value of the constant of formation of aggregate. The Hill coefficient for the curve of Fig. 4b is n = 0.85. The value n < 1 indicates not-cooperative interaction and this suggested that the aggregates are oligomers. Compound 1b was found to demonstrate the quenching of the fluorescence when the concentration was increased in all solvents, with CH2Cl2 being the exception.
Femtosecond time resolved spectroscopy analysis
In order to study the dynamics under photoexcitation and to gain better insights into the mechanism of emission of compounds 1a and 1b, the degenerate femtosecond pump-probe measurements59 were performed in DMF and Toluene. The solutions were taken in a quartz cuvette of 1mm thickness. The sample solutions were excited using the pump pulse (the spectral and temporal profile are given in Fig. S8) and difference in the probe transmittance (ΔΤ) with and without the presence of pump, were collected at each delays of pump with respect to probe pulse. The differential absorbance were calculated using the equation: ΔA = − log (1 + ΔT/T) where T is the sample transmittance in the absence of pump. The differential absorbance (ΔA) for selected probe wavelengths were plotted at each delays and time constants were extracted by fitting the data using exponential functions.
In DMF, there was a strong negative signal (ΔA < 0) in the UV range (<450 nm). Since this wavelength range overlap with resonance absorption of the respective compounds, the signal could be assigned to a ground state bleaching60. The temporal dynamics at probe wavelength of ~440 nm for compounds 1a and 1b in DMF are displayed in Fig. 5. The recovery lifetimes of the ground state population were estimated by the fitted time constants. The time constants were found to be in the range of 0.16–0.28 ps for 1a and 0.60–1.08 ps for 1b in DMF solvent. In DMF, both compounds had shown no photoluminescence and the excited population possibly decayed non-radiatively.
On the other hand, the temporal dynamics in the range of 380–460 nm in Toluene for both compounds (1a and 1b) had shown existence of much faster decay lifetime (0.07–0.25 ps) which was not found in DMF. The negative signal (ΔA < 0) in the region 380–460 nm for compound 1a and 425–460 nm for compound 1b could be assigned to the stimulated emission from the excited state. However, there is an overlap of absorption band leads to a ground state bleaching in the pump probe signal (ΔA) at lower wavelengths. The temporal dynamics of the compounds 1a and 1b in Toluene at probe wavelength of 434 nm were displayed in Fig. 6. The decay was fitted by a bi-exponential function giving two time constants. The first time constant was comparable with the pulse duration (~ 8.1 fs as shown in Fig. S8). The second time constants were assigned to the decay of excited state population. These decay time constants were found to be 0.1–0.2 ps for 1a and 0.07–0.17 ps for 1b in Toluene as shown in Fig. 7. However in the lower wavelength region (<410 nm for 1a and <430 nm for 1b), due to the overlap of resonance absorption, there would be a contribution of ground state bleach signal in addition to the stimulated emission and hence the time constants from the aforementioned region can not be considered to discuss about the excited state population recovery. The pump probe measurements were, further carried out and analyzed at different concentrations to observe the effect of aggregation to the decay time constants in Toluene solvent.
The time constants at selected probe wavelength for three different concentrations for Toluene solution of compound 1a (6.5 × 10−3 M, 4 × 10−3 M and 1 × 10−3 M) and 1b (3.2 × 10−3 M, 6.5 × 10−5 M, 2 × 10−6 M) were displayed in Fig. 7a,b respectively. It was observed that when the concentration of 1a was increased, the time constants were also increasing gradually at the probe wave lengths which were overlapping with the emission band (420–440 nm) of 1a. However, for compound 1b, the time constants remained almost constant and with the highest concentration (3.2 × 10−3 M) of 1b we were unable to observe any pump-probe signal as the quenching of emission might have occurred at this concentration. The observations showed that the radiative decay takes longer time in the aggregation phase (i.e at higher concentration in Toluene) of 1a through RIM (restricted intramolecular motions) process and hence the enhancement of emission due to the longer time of the excited state.
Fluorescence analysis in solvents with different viscosity
The fluorescence of the compounds 1a and 1b has been analyzed in solutions at different viscosity, as showed in Fig. 8, in order to study the emission in environments with different rigidity. It is expected that the increased viscosity of solutions (increased rigidity of environment), restrict the intramolecular motions. A diluted solution of 1a in mixtures Methanol/Glycerol has resulted in more emission when the viscosity was increased with higher the glycerol percentage. The increasing of emission is not detected when the percentage of glycerol has been increased from 0 to 20%, but increasing at 40% and 60% enhanced the emission. The solutions of 1b (Fig. S15) display a light increasing of emission when the percentage of glycerol was 40% and 60% but the effect is less clear respect compound 1a. The experiments show that in compound 1a, the RIM increases the emission.
Electronic structure analysis
Frontier molecular orbitals
In this computational section, we aim to qualitatively gain insight into the correlation between the substitution effects on molecular structure and maximum wavelength observed in adsorption spectrum through computing their geometry properties, the shapes and the energies of the frontier molecular orbitals (MOs) among compounds 1a, 1b and 3. Based on Potters’s and Hughes’s study on the good correlation of the DFT calculated HOMO-LUMO gap with the experimental absorptions of compound 333, instead of using the time-dependent (TD) DFT approach, we connected the gaps of HOMO/LUMO, HOMO/LUMO+1, HOMO-1/LUMO with the major contribution of the peaks near visible region; such a descriptor with lower computational cost will be beneficial to the future molecular design for optical-electron properties. In this study, the MOs of the compounds 1a, 1b and 3 can be considered as perturbations of the fulvene core (1a and 1b) and cyclopentadienone core (3) due to replacing hydrogens with phenyl rings at positions C2, C3, C4, and C5 in Fig. 9 and replacing =CH2 with =CR2 and =O at position 1. Before analyzing the MOs of the compounds with phenyl rings, we firstly describe the MOs of fulvene as previously reported by R. E. Duke’s group and was schematically represented in Fig. 9 61. In Fig. 9, the six MOs of the fulvene are provided by the combination of the five p orbitals of the cyclopentene carbons and one p orbital of the exocyclic carbon; in the case of the cyclopentadienone, the exocyclic p orbital is provided by the oxygen. The six π-electrons of the fulvene occupy the three highest occupiedMOs.
The MOs of compounds 1a, 1b and 3 and their energies are represented in Fig. 10. The strongest perturbation of the phenyl rings on the orbitals of the fulvene is expected when the reciprocal disposition is coplanar.
The optimized geometries depicted in Fig. S16 show that the dihedral angle between the phenyl rings in position 2 and 5 of the cyclopentene ring and the fulvene group are 39° for compound 3, 80° for compound 1b, 63° for compound 1a. The geometries can be explained with the steric hindrance of the groups in position 6. The size of the oxygen in compound 3 (=O) is smaller than the =CR2 groups of the other two compounds and, as consequence, the phenyl groups in position 2 and 5 of the cyclopentene ring are more free to adopt coplanar disposition respect to the fulvene. The =C(CN)2 group of compound 1b exhibit stronger interaction with phenyl rings than the =C(COOMe)2 of 1a because the –CN groups are coplanar with the cyclopentadiene and in the proximity of the phenyl groups in position 2 and 5. In compound 1a the rotation of the –COOMe group place the –C=O and the –OMe out of the plane of the cyclopentadiene. The electron density of orbital HOMO Aπ is the highest on the carbons of cyclopentadiene and is the most destabilized by the perturbation of the phenyl rings. As a consequence, the HOMO Aπ orbitals of compound 3 and 1b are respectively the most and the less destabilized. These outcomes demonstrate that importance of the steric hindrance of the R group in determining the electronic distribution along the molecular structure and as consequence in tuning the electro-optical properties of the compounds.
The electrons of the group that is of linked to the carbon 1 of the cyclopentadiene destabilize the orbital LUMO Bπ* which electron density is highest on position 6. The =C(COOMe)2 group in compound 1a contain four oxygen atoms and eight electron lone pairs, =O of compound 3 contains two lone pairs, the =C(CN)2 of compound 1b contains two nitrogen atoms and two electron lone pairs. As a consequence, the compound 1a exhibits the highest electron density and the highest destabilization of the orbital LUMO Bπ*. The lowest destabilization in compound 1b respect compound 3 is due to the higher extension of the group where the electron lone pairs are placed.
Correlation between calculated wavelength and observed absorption maxima
In this section, the correlation between calculated frontier MO energy differences and their corresponding wavelengths is illustrated in Fig. 11. The calculated λ1 (243 nm for 1a, 232 nm for 1b, 251 nm for 3), λ2 (330 nm for 1a, 389 nm for 1b and 338 nm for 3) and λ3 (391 nm for 1a, 451 nm for 1b, 433 nm for 3) correlated well with the average absorption maxima in different solvents, λ1 (250 nm for 1a, 260 nm for 1b, 260 nm for 3), λ2 (325 nm for 1a, 375 nm for 1b, 330 nm for 3) and λ3 (460 nm for 1a, 500 nm for 1b, 505 nm for 3) and are as shown in Table 2. A minor disparity between our calculated transitions HOMO Aπ - LUMO Bπ* with the observed experimental λ3 may be due to the effects of the solvent on the energy of the orbital HOMO Aπ that was not considered during our DFT calculations. The λ3 may have been influenced by the polarity of the solvent because the HOMO Aπ orbital is polar as previously described by Diedrich et al.44, and is stabilized by solvents with highest orientational polarizability and dipolar moment. In CH3CN the λ3 of compounds 1a, 1b and 3 were blue-shifted as compared to in Toluene and CH2Cl2 while broaden in DMF and MeOH. The calculated values of the transitions had also revealed that compound 1a’s and 1b’s λ2 and λ3 are partially overlapped (the calculated difference λ3-λ2 is only 60 nm) while in compound 3, these are separated (the calculated difference λ3-λ2 is 100 nm) due to the strong destabilization of the HOMO Aπ that may have red-shifted the λ3.
In short, this consistent relationship between the three calculated wavelengths and absorption spectral peaks implies each of the three transitions identified associates with one predominant single electron excitation. Thus, it is reasonable to expect that there would be a correlation between the difference of corresponding molecular orbital energies by DFT and the observed transitions from experimental spectrum thought more complete contributions of MO to each excited state can be carried out by sophisticated TDDFT calculations62.
Conclusions
In this work, we substituted the oxygen (=O) moiety of the cyclopentadienone with two different =CR2 groups bearing different steric hindrance. The substitution was shown to be an effective method for the tuning of the optical and the electronic properties of the molecule. Although the groups R of compounds 1a and 1b are both electrons withdrawing, the absorption peak shift with respect to compound 3 has been reversed between the two compounds (blue and a red-shifted accordingly). The compounds 1a and 1b have displayed an increased fluorescence when compared to the compound 3 due to having the most strained molecular arrangement. As confirmed with femtosecond time-resolved spectroscopy, the compound 1a has exhibited increased fluorescence in more concentrated solutions. The fluorescence spectra of 1a in solvent with different viscosity had revealed that the restricted intramolecular rotations may have contributed to the increase the fluorescence. The computational outcomes confirmed that the MOs states of –COOMe and –CN had also helped fine-tuning the electronic mobility along the molecular backbone due to the different steric interaction with the phenyl rings bonded to the carbons C2 and C5. In compound 3 the MOs of the cyclopentadienone are strongly extended on the phenyl rings that are bonded to the carbons C2 and C5. In compound 1a the MOs of the fulvene unit are extended along the four phenyl rings and the =C(COOMe)2 group. In compound 1b, the MOs of the fulvene core is extended on the =C(CN)2 group and on the phenyl rings bonded to the carbons C3 and C4. The straightforward DFT description allowed identifying the two excited states S1 (HOMO → LUMO) and S2 (HOMO-1 → LUMO) that have been found in other fulvene derivatives like diphenyl dibenzofulvene which absorption band lies in the wavelength range of 320–510 nm63. Fulvene unit displays a conical intersection seam between the fundamental state S0 and the excited state S1 that is accessed by twisting around the exocyclic bond C1-C6 of Fig. 9 64,65. Blancafort’s group found that the emission of diphenyl dibenzofulvene depends on the accessibility to the conical intersection seam between the states S1 and S066,67. In the solution, the conical intersection seam is more accessible than in solid state because the twisting trough the exocyclic bond C1-C6 is less hindered, and as consequence the emission is quenched more. Compounds 1a, 1b display that absorption and emission spectra are similar to diphenyl dibenzofulvene, indicating that the optical properties are determined by fulvene moiety. The lowest polarity (lowest solubilizing capability), the highest viscosity of solvent and the highest concentration of the solutions are the conditions that restrict the intramolecular motions and thus increase more clearly the emission of 1a and less clearly the emission of 1b. This evidence is coherent with the fact that the molecule 1b is more hindered than 1a. The intrinsic hindrance in 1b (and restricted intramolecular conformational freedom) implies that the external conditions have lesser influence on intramolecular motions. The similarities with the diphenyl dibenzofulvene have demonstrated that the fluorescence depends on the conical intersection seam between the S1-S0 states and the C1-C6 twisting. The exact mechanisms could be analyzed with rigorous computational analyses that is not within the scope of this manuscript.
Herein, we demonstrated that substituted tetraphenylfulvenes can serve as valid starting point for the synthesis of novel D-π-A compounds and new emitting molecules. The compounds displayed tunable electronic properties in conjunction with easy manipulability that is conferred by non-coplanar disposition of the phenyl rings. These enhancements of emission by restricting of the intramolecular motion may also have an important role for biosensors, especially in terms of host-guest chemistry based docking sensors. A further work pertaining to this research that will be on the additional chemical modifications of the compounds 1a and 1b to serve as connections of the phenyl rings with electron-withdrawing or electron donor groups.
Experimental Section
Experimental details
Tetraphenylcyclopentadienone, Dimethyl Malonate, TiCl4, Pyridine (dry), Dichloromethane, were purchased from commercial sources. The Dichloromethane was dried with molecular sieves. 1H and 13C NMR spectra were recorded for solutions in CDCl3 on a Bruker Avance III 500 MHz BBFO Probe with the solvent residual proton signal. Flash column chromatography was performed using Silicycle Silica gel 60 (7–230 Mesh, pH 7).
Synthesis of compound 1a
TiCl4 (2.2 mL, 3.8 g, 20 mmol) was added dropwise to an ice-cooled solution of Tetraphenylcyclopentadienone (1.5 g, 3.9 mmol) and Dimethylmalonate (1.98 g, 15 mmol, 0.85 mL) in Dichloromethane (50 mL), under Argon atmosphere. After the addition was complete, dry Pyridine (7.5 mL) was added dropwise over 10 minutes. The reaction mixture was allowed to warm to room temperature and stir under Argon overnight. The solution was cooled at 0 °C and HCl 10% (20 ml) was slowly dropped. The mixture was extracted with Dichloromethane (50 mL × 3) and the organic phase was collected and dried with Na2SO4. After evaporation of the solvent, the crude was obtained as a red powder. The residue was purified by column chromatography, with Hexane/Ethyl Acetate 10:1 as eluent. The product was isolated as a red powder that was filtered with hexane to remove residual Dimethyl malonate (1.8 g, 3.6 mmol, 92%). 1HNMR, (500MHz, CDCl3) ppm, δ: 7.21 (m, 10H), 7.09 (m, 2H), 7.02 (m, 4H), 6.73 (m, 4H), 3.07 (s, 6H). 13CNMR, (140MHz, CDCl3) ppm, δ: 164.7, 150.4, 148.1, 135.0, 133.9, 132.7, 131.5, 130.6, 129.9, 127.7, 127.3, 127.1, 126.8, 52.3. ESI mass [M+Na+]+ calc. 521.1723, exp. 521.1767, [M+H+]+ calc. 499.1904, exp. 499.1915.
Synthesis of compound 1b
TiCL4 (2.2 mL, 3.8 g, 20 mmol) was added dropwise to an ice-cooled solution of Tetraphenylcyclopentadienone (1.5 g, 3.9 mmol) and Malononitrile (0.5 g, 7.5 mmol) in Dichloromethane (50 mL), under Argon atmosphere. After the addition was complete, dry Pyridine (7.5 mL) was added dropwise over 10 minutes. The reaction mixture was allowed to warm to room temperature and stirred under Argon overnight. The solution was cooled at 0 °C and HCl 10% (20 ml) was slowly dropped. The mixture was extracted with Dichloromethane (50 mL × 3) and the organic phase was collected and dried with Na2SO4. After evaporation of the solvent, the crude was obtained as a green powder. The residue was purified by column chromatography, with Hexane/Dichloromethane 7:3 as eluent. The product was isolated as a green-yellow powder. (1.5 g, 3.5 mmol, 44%). 1HNMR, (500MHz, CDCl3) ppm, δ: 7.36 (m, 10H), 7.16 (t, 2H), 7.07 (t, 4H), 6.87 (d, 4H), 13CNMR, (140 MHz, CDCl3) ppm, δ: 168.48, 151.1, 145.1, 132.4, 131.7, 131.1, 129.7, 129.0, 128.7, 128.6, 127.5, 111.2. ESI mass [M+Na+]+calc. 455.1519, exp. 455.1519, [M+H+]+ calc. 433.1699, exp. 433.1694.
Photophysical measurements
Absorption and photoluminescence spectra were recorded using a Spectra Max M2 spectrometer. The QY were obtained using Phenothiazine in Acetonitrile as a reference, which Φ is 0.0135. The degenerate femtosecond pump-probe measurements were performed to study the ultrafast dynamics in fulvene compounds. The spectrum of 390 nm to 450 nm and a pulse duration of ~8 fs of the light source was used in this study. The spectral and temporal profile in Toluene and DMF for all frequencies and concentrations are shown in the SI. The spikes in the spectral profile appear due to the compression of the light source. An average of 50 scans was measured for each forward and backward scan. Five probe wavelengths (398 nm, 403 nm, 410 nm, 424 nm, 434 nm for compound 1a; 397 nm, 410 nm, 423 nm, 434 nm, 444 nm for compound 1b) were selected which showed better SNR. The backward and forward scans were fitted separately and the mean value of both parameters with an error bar is given in Fig. 8. The kinetics shows negative ΔA which implies ground state photobleaching (PB) or stimulated emission (SE) from the first excited state. The PB occurs when the probe wavelength overlaps with the absorption band and SE occurs when the probe wavelength overlaps with the emission band of the molecule. In both the compounds 1a and 1b, the kinetics at shorter wavelengths is mainly contributed from both PB and SE. However, the major contribution for the pump-probe signal ΔA at longer wavelengths is from the SE.
The kinetics at three different concentrations was measured for compound 1a (0.0065 M, 0.004 M and 0.001M). The spikes near the zero delay are due to the coherent artifacts caused by the interference and nonlinear interaction between pump and probe pulses near the zero delay. The kinetics was fitted bi-exponentially and the longer time constants were plotted at different concentrations. The value of the faster time constant is comparable or less than that of the pulse duration and hence the major contributions from the coherent artifact are expected. The longer time constants could be assigned to the recovery rate of the population in the excited state. In the SI, the amplitude or weight factor of the longer time constant is shown. It is evident from that the amplitude values at shorter wavelengths will have a contribution from both PB and SE. As it goes to longer wavelengths, the contribution of PB reduces and enhances the amplitude.
The kinetics at three different concentrations of compound 1b (0.0032 M, 0.0065 M, 0.002 M) were also performed. However, the sample with the highest concentration was unable to observe any pump-probe signal as the quenching of emission occurred at this concentration. The lowest concentrations show the negative pump-probe signal ΔA and the kinetics have been fitted bi-exponentially.
Computational details
The density functional theory (DFT) calculations were performed for geometry optimization and eigenvalues of molecular orbitals. The B3LYP exchange-correlation functional68,69,70 and the double numerical basis set with polarization (DNP) implemented in the DMol3 program package71,72 were employed for all numerical calculations.
Supporting Informations
The Supporting Information provides all experimental data that are cited and not showed in the paper like the UV spectra in DMF, Toluene, Methanol, CH2Cl2, the PL spectra of compounds 1a, 1b and 3 in Toluene, CH3CN, Methanol, CH2Cl2, all femtosecond spectroscopy experiments, all UV visible and PL spectra in the mixtures MeOH/Glycerol.
References
Batool, F. A Review Paper on: Organic Light-Emitting Diode (OLED) Technology and Applications. International Journal of Advanced Research in Computer and Communication Engineering 5, 152–156 (2016).
Coropceanu, V. et al. Charge transport in organic semiconductors. Chemical reviews 107, 926–52 (2007).
Eftaiha, A. F., Sun, J.-P., Hill, I. G. & Welch, G. C. Recent advances of non-fullerene, small molecular acceptors for solution processed bulk heterojunction solar cells. J Mater Chem A 2, 1201–1213 (2014).
Forrest, S. R. & Thompson, M. E. Introduction: Organic electronics and optoelectronics. Chemical Reviews 107, 923–925 (2007).
Kang, H. et al. Bulk-Heterojunction Organic Solar Cells: Five Core Technologies for Their Commercialization. Advanced Materials 28, 7821–7861 (2016).
Lo, S. C. & Burn, P. L. Development of dendrimers: Macromolecules for use in organic light-emitting diodes and solar cells. Chemical Reviews 107, 1097–1116 (2007).
Mishra, A., Fischer, M. K. R. & Bäuerle, P. Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationships to design rules. Angewandte Chemie (International ed in English) 48, 2474–99 (2009).
Murphy, A. R. & Fréchet, J. M. J. Organic semiconducting oligomers for use in thin film transistors. Chemical Reviews 107, 1066–1096 (2007).
Ooyama, Y. & Harima, Y. Molecular designs and syntheses of organic dyes for dye-sensitized solar cells. European Journal of Organic Chemistry, 2903–2934 (2009).
Prasad, P. N. Introduction to Biophotonics. (Wiley - Interscience, 2003).
Roncali, J., Leriche, P. & Blanchard, P. Molecular materials for organic photovoltaics: Small is beautiful. Advanced Materials 26, 3821–3838 (2014).
Thejo Kalyani, N. & Dhoble, S. J. Organic light emitting diodes: Energy saving lighting technology - A review. Renewable and Sustainable Energy Reviews 16, 2696–2723 (2012).
Shirota, Y. & Kageyama, H. Charge Carrier Transporting Molecular Materials and Their Applications in Devices. Chemical reviews 107, 953–1010 (2007).
Milián-Medina, B. & Gierschner, J. π-Conjugation. Wiley Interdisciplinary Reviews: Computational Molecular Science 2, 513–524 (2012).
Chen, J. et al. Synthesis, light emission, nanoaggregation, and restricted intramolecular rotation of 1,1-substituted 2,3,4,5-tetraphenylsiloles. Chemistry of Materials 15, 1535–1546 (2003).
Ding, D., Li, K., Liu, B. & Tang, B. Z. Bioprobes Based on AIE Fluorogens. Accounts of Chemical Research 46, 2441–2453 (2013).
Hong, Y., Lam, J. W. Y. & Tang, B. Z. Aggregation-induced emission. Chemical Society Reviews 40, 5361 (2011).
Hong, Y., Lam, J. W. Y. & Tang, B. Z. Aggregation-induced emission: phenomenon, mechanism and applications. Chemical Communications, 4332–4353 (2009).
Liu, B. & Zhang, R. FDEmiss17 Closing Remarks Aggregation-Induced Emission: Concluding Remarks. Faraday Discuss 196, 461–472 (2017).
Luo, J. et al. Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole. Chemical Communications 381, 1740–1741 (2001).
Ren, Y., Dong, Y., Lam, J. W. Y., Tang, B. Z. & Wong, K. S. Studies on the aggregation-induced emission of silole film and crystal by time-resolved fluorescence technique. Chemical Physics Letters 402, 468–473 (2005).
Ren, Y., Lam, J. W. Y., Dong, Y., Tang, B. Z. & Wong, K. S. Enhanced Emission Efficiency and Excited State Lifetime Due to Restricted Intramolecular Motion in Silole Aggregates. The Journal of Physical Chemistry B 109, 1135–1140 (2005).
Tang, B. Z. et al. Efficient blue emission from siloles. Journal of Materials Chemistry 11, 2974–2978 (2001).
Cariati, E. et al. Efficient crystallization induced emissive materials based on a simple push–pull molecular structure. Physical Chemistry Chemical Physics 13, 18005–18014 (2011).
Coluccini, C. et al. Switching of emissive and NLO properties in push-pull chromophores with crescent PPV-like structures. Physical chemistry chemical physics: PCCP 15, 1666–1674 (2013).
Nitti, A. et al. Structure-activity relationship for the solid state emission of a new family of ‘push-pull’ π-extended chromophores. Faraday Discussions 196, 143–161 (2017).
Yuan, W. Z. et al. Efficient Solid Emitters with Aggregation-Induced Emission and Intramolecular Charge Transfer Characteristics: Molecular Design, Synthesis, Photophysical Behaviors, and OLED Applications. Chemistry of Materials 24, 1518–1528 (2012).
Würthner, F., Kaiser, T. E. & Saha-Möller, C. R. J-aggregates: From serendipitous discovery to supramolecular engineering of functional dye materials. Angewandte Chemie - International Edition 50, 3376–3410 (2011).
Liu, Y. et al. A tetraphenylethylene core-based 3d structure small molecular acceptor enabling efficient non-fullerene organic solar cells. Advanced Materials 27, 1015–1020 (2015).
Coan, S. B., Trucker, D. E. & Becker, E. I. The Absorption Spectra of Tetracyclones. Journal of the American Chemical Society 75, 900–903 (1953).
Coan, S. B., Trucker, D. E. & Beckerr, E. I. The Absorption Spectra of Tetracyclones. IV 1,2. Journal of the American Chemical Society 77, 60–66 (1955).
Pal, R., Mukherjee, S., Chandrasekhar, S. & Guru Row, T. N. Exploring cyclopentadienone antiaromaticity: Charge density studies of various tetracyclones. Journal of Physical Chemistry A 118, 3479–3489 (2014).
Potter, R. G. & Hughes, T. S. Predicting the UV−Vis Spectra of Tetraarylcyclopentadienones: Using DFT Molecular Orbital Energies to Model Electronic Transitions of Organic Materials. The Journal of Organic Chemistry 73, 2995–3004 (2008).
Shapiro, E. L. & Becker, E. I. Steric Effects and Spectra in the Tetracyclones. Journal of the American Chemical Society 75, 4769–4775 (1953).
Bernhardt, S., Baumgarten, M., Wagner, M. & Müllen, K. Multiple functionalization of benzophenones inside polyphenylene dendrimers - Toward entrapped ions and radicals. Journal of the American Chemical Society 127, 12392–12399 (2005).
Boiani, M. et al. A new tetraarylcyclopentadienone based low molecular weight gelator: Synthesis, self-assembly properties and anion recognition. New Journal of Chemistry 36, 1469–1478 (2012).
Iniesta, J. et al. Electrochemical oxidation of tetracyclones and tetraphenylthiophene-S-oxide. Electrochimica Acta 51, 5682–5690 (2006).
Maly, K. E., Gagnon, E., Maris, T. & Wuest, J. D. Engineering hydrogen-bonded molecular crystals built from derivatives of hexaphenylbenzene and related compounds. Journal of the American Chemical Society 129, 4306–4322 (2007).
Oesterling, I. & Müllen, K. Multichromophoric polyphenylene dendrimers: Toward brilliant light emitters with an increased number of fluorophores. Journal of the American Chemical Society 129, 4595–4605 (2007).
Ren, H. et al. Synthesis and luminescent properties of perylene bisimide-cored dendrimers with carbazole surface groups. Polymer 52, 3639–3646 (2011).
Ren, H. et al. Synthesis and properties of novel perylenebisimide-cored dendrimers. Dyes and Pigments 91, 298–303 (2011).
Ren, H., Tao, Q., Gao, Z. & Liu, D. Synthesis and properties of novel spirobifluorene-cored dendrimers. Dyes and Pigments 94, 136–142 (2012).
Xiang, Q. et al. 2,3,4,5-tetraphenylbiphenyl-containing Cu I/Re I complexes: Synthesis, property analysis and theoretical studies. European Journal of Inorganic Chemistry, 4012–4019 (2012).
Finke, A. D. & Diederich, F. 6,6-Dicyanopentafulvenes: Teaching an old dog new tricks. Chemical Record 15, 19–30 (2015).
Kleinpeter, E. & Fettke, A. Quantification of the (anti)aromaticity of fulvenes subject to ring size. Tetrahedron Letters 49, 2776–2781 (2008).
Krygowski, T. M., Oziminski, W. P., Palusiak, M., Fowler, P. W. & McKenzie, A. D. Aromaticity of substituted fulvene derivatives: Substituent-dependent ring currents. Physical Chemistry Chemical Physics 12, 10740–10745 (2010).
Najafian, K., Schleyer, P. V. R. & Tidwell, T. T. Aromaticity and antiaromaticity in fulvenes, ketocyclopolyenes, fulvenones, and diazocyclopolyenes. Organic and Biomolecular Chemistry 1, 3410–3417 (2003).
Rosenberg, M., Ottosson, H. & Kilså, K. Influence of excited state aromaticity in the lowest excited singlet states of fulvene derivatives. Physical Chemistry Chemical Physics 13, 12912–12919 (2011).
Andrew, T. L., Cox, J. R. & Swager, T. M. Synthesis, reactivity, and electronic properties of 6,6-dicyanofulvenes. Organic letters 12, 5302–5 (2010).
Finke, A. D. et al. 6,6-Dicyanopentafulvenes: electronic structure and regioselectivity in [2 + 2] cycloaddition-retroelectrocyclization reactions. Journal of the American Chemical Society 134, 18139–46 (2012).
King, R. B. & Saran, M. S. Cyclization of dicyanovinylidene with two diphenylacetylene units to form a 6,6-dicyanofulvene derivative. Journal of the Chemical Society, Chemical Communications, 851–852 (1974).
Hansch, C., Leo, A. & Taft, R. W. A survey of Hammett substituent constants and resonance and field parameters. Chemical Reviews 91, 165–195 (1991).
Luo, Q., Wang, C., Zhang, W.-X. & Xi, Z. CuCl-mediated tandem CO insertion and annulation of 1,4-dilithio-1,3-dienes: formation of multiply substituted cyclopentadienones and/or their head-to-head dimers. Chemical Communications, 1593–1595 (2008).
Chatterjee, S., Basu, S., Ghosh, N. & Chakrabarty, M. Unique behavior of DMF as solvent in fluorescence quenching process. Chemical Physics Letters 388, 79–83 (2004).
Smallwood, I. M. Handbook of Organic Solvent Properties. Handbook of Organic Solvent Properties (Elsevier Ltd, 1996).
Nath, S., Pal, H., Palit, D. K., Sapre, A. V. & Mittal, J. P. Steady-state and time-resolved studies on photoinduced interaction of phenothiazine and 10-methylphenothiazine with chloroalkanes. Journal of Physical Chemistry A 102, 5822–5830 (1998).
Caricato, M., Coluccini, C., Vander Griend, D. A., Forni, A. & Pasini, D. From red to blue shift: Switching the binding affinity from the acceptor to the donor end by increasing the π-bridge in push-pull chromophores with coordinative ends. New Journal of Chemistry 37, 2792–2799 (2013).
Coluccini, C., Pasini, D., Righetti, P. & Vander Griend, D. A. Dynamic switching between binding sites in the complexation of macrocyclic ‘push-pull’ chromophores to lanthanides. Tetrahedron 65, 10436–10440 (2009).
Hashimoto, S., Hamada, K., Iwakura, I., Yabushita, A. & Kobayashi, T. Photochemical reaction mechanisms of 4, 5-dimethoxy-2-nitrobenzyl acetate analysed by a sub-10 fs near-ultraviolet pulse laser. Chemical Physics 524, 70–76 (2019).
Claude, J., R. Ultrashort Laser Pulse phenomena – Fundamentals, Techniques, and Aapplications on a Femtosecond Time Scale, 2nd edition. (Elsevier, USA, 2006).
Houk, K. N., George, J. K. & Duke, R. E. A frontier molecular orbital treatment of fulvene cycloadditions. Tetrahedron 30, 523–533 (1974).
Dreuw, A. & Head-gordon, M. Single-Reference ab Initio Methods for the Calculation of Excited States of Large Molecules. Chemical Reviews 105, 4009–4037 (2005).
Tong, H. et al. Aggregation-Induced Emission: Effects of Molecular Structure, Solid-State Conformation, and Morphological Packing Arrangement on Light-Emitting Behaviors of Diphenyldibenzofulvene Derivatives. The Journal of Physical Chemistry C 111, 2287–2294 (2007).
Deeb, O., Cogan, S. & Zilberg, S. The nature of the S1/S0conical intersection of fulvene. Chemical Physics 325, 251–256 (2006).
Sicilia, F., Bearpark, M. J., Blancafort, L. & Robb, M. A. An analytical second-order description of the S 0/S 1 intersection seam: fulvene revisited, 241–251 (2007).
Crespo-otero, R., Li, Q. & Blancafort, L. Exploring Potential Energy Surfaces for Aggregation-Induced Emission — From Solution to Crystal (2019).
Online, V. A. A conical intersection model to explain aggregation induced emission in diphenyl dibenzofulvene †, 5966–5968 (2013).
Becke, A. D. Density functional thermochemistry. III. The role of exact exchange Density-functional thermochemistry. III. The role of exact exchange. J Chern Phys 98, 5648–5652 (2005).
Lee, C., Yang, W. & Parr, R. G. Into a Functional of the Electron Density F F. Physical Review B 37, 785–789 (1988).
Stephens, P. J., Devlin, F. J., Chabalowski, C. F. & Frisch, M. J. Ab Initio calculation of vibrational absorption and circular dichroism spectra using density functional force fields. Journal of Physical Chemistry® 98, 11623–11627 (1994).
Delley, B. An all-electron numerical method for solving the local density functional for polyatomic molecules. The Journal of Chemical Physics 92, 508–517 (1990).
Delley, B. From molecules to solids with the DMol3 approach. Journal of Chemical Physics 113, 7756–7764 (2000).
Acknowledgements
This work was carried out grant from the Ministry of Science and Technology in Taiwan (MOST 107-221-NU, 107-2113-M-039 -002 -MY2, 107-2119-M-009-010-MY2, 106-2628-M-009-003-MY3) and the Center for Emergent Functional Matter Science of National Chiao Tung University from The Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education (MOE) in Taiwan. The work had also been supported by China Medical University grants CMU107-N-31 and CMU107-N-25.
Author information
Authors and Affiliations
Contributions
C.C. and Y.L.K. had both conceived and design the study for this manuscript while Y.L.K. provided all necessary resources for the synthesis of the compounds. C.C. and Y.M.N. had performed the organic synthesis, NMR analysis and all UV studies. P.T.A., Y.K.K., A.Y. and C.W.L. had undertaken all work on the femtosecond pump-probe examinations while H.Y.T.C. and S.L.L. had performed all DFT measurements. C.C. and Y.L.K. had written the bulk of the manuscript while the rest of the authors had contributed to parts of their respective segments.
Corresponding author
Ethics declarations
Competing Interests
The authors declare no competing interests.
Additional information
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Coluccini, C., Anusha, P.T., Chen, HY.T. et al. Tuning of the Electro-Optical Properties of Tetraphenylcyclopentadienone via Substitution of Oxygen with Sterically-Hindered Electron Withdrawing Groups. Sci Rep 9, 12762 (2019). https://doi.org/10.1038/s41598-019-49303-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-019-49303-w
This article is cited by
-
DFT/TDDFT calculations of geometry optimization, electronic structure and spectral properties of clevudine and telbivudine for treatment of chronic hepatitis B
Scientific Reports (2024)
-
Synthesis and characterization of soluble intrinsic black polyimide with excellent comprehensive properties
Science China Technological Sciences (2023)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.