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Article

AIE/ACQ Effects in Two DR/NIR Emitters: A Structural and DFT Comparative Analysis

by
Ugo Caruso
1,
Barbara Panunzi
2,
Rosita Diana
1,*,
Simona Concilio
3,*,
Lucia Sessa
4,
Rafi Shikler
5,
Shiran Nabha
5,
Angela Tuzi
1 and
Stefano Piotto
4
1
Department of Chemical Sciences, University of Napoli Federico II, 80126 Napoli, Italy
2
Department of Agriculture, University of Napoli Federico II, Portici 80055 Portici NA, Italy
3
Department of Industrial Engineering, University of Salerno, Fisciano 84084 SA, Italy
4
Department of Pharmacy, University of Salerno, Fisciano 84084 SA, Italy
5
Department of Electrical and Computer Engineering, Ben-Gurion University of the Negev, POB 653, Beer-Sheva 84105, Israel
*
Authors to whom correspondence should be addressed.
Molecules 2018, 23(8), 1947; https://doi.org/10.3390/molecules23081947
Submission received: 12 July 2018 / Revised: 1 August 2018 / Accepted: 2 August 2018 / Published: 4 August 2018
(This article belongs to the Special Issue Lumino and Fluorophores—Illuminating Science and Technology)
Browse Figures
Versions Notes

Abstract

:
The effects of aggregation-induced emission (AIE) and of aggregation caused quenching (ACQ) were observed and discussed on two solid materials based on a phenylenevinylene (PV) and a dicyano-PV structure. The brightest emitter in solid films shows a high fluorescence quantum yield in the deep red/near IR (DR/NIR) region (75%). The spectroscopic properties of the two crystalline solids have been described and compared in terms of crystallographic data and time dependent DFT analysis. The influence of the cyano-substituents on AIE/ACQ mechanism activation was discussed.

Graphical Abstract

1. Introduction

The demand for optic [1,2,3,4,5] and electro-optic [6,7,8] active layers has been driven by the desire for novel technologies capable of high-yield low-cost manufacturing based on integrated optics. Fluorescent materials often represent highly required doping molecules for the active layers [9,10,11,12,13,14,15]. Organic red fluorescent dyes are typically extended π-electrons frameworks with planar conformation or a donor–acceptor type π-conjugated structure with strong intramolecular charge transfer. The development of fluorogens with deep red and/or near-IR (DR/NIR) emission is nowadays one of the hottest topics of investigation for a series of advanced technologies, i.e., in the fields of optics and electronics, bio/chemo-sensors, and bioimaging [16].
In order to emit with high quantum yields, traditional fluorescent materials are generally used as dopants. Isolated from each other (either in matrices/solutions at very low concentrations or in nanostructured guest–host systems) the well-known aggregation-caused emission quenching (ACQ), associated with the formation of less emissive species such as exciplexes and excimers, can be avoided and fluorescence maximized.
A still limited number of organic chromophores have been recently found to emit more efficiently in the aggregated state than in solution. In 2001, Tang and coworkers synthesized the first derivative almost non-emissive in solution but strongly emissive in the aggregated solid state [17]. This phenomenon was termed as aggregation-induced emission (AIE) effect. The restriction of intramolecular rotation (RIR) is by far the most frequently assumed mechanism to explain this behavior [18]. The free intramolecular rotation in solution introduces a non-radiative relaxation channel for the excited state to decay. By slowing/stopping the rotation, molecular luminescence can be restored. AIE fluorogens have recently received much research attention for their unique optical properties and extensive applications, because they are highly required for the development of efficient solid-state devices [19,20].
Many probes often show AIE effect depending on twisted structures that greatly reduce non-radiative decay channels in the solid state. Most of the AIE-active molecules reported emit blue and green lights, while the derivatives with efficient red emission in the solid state are rare. DR/NIR solid-state emitters are intrinsically narrow band gap materials typically with π-conjugated planar molecules especially vulnerable to solid-state emission quenching due to the strong π-π overlap favoring aggregation [21]. As an alternative, π-conjugated backbones such as phenylenevinylene (PV) skeleton, with strong donor (D) and acceptor (A) functionalities can show interesting DR/NIR emission in the solid state [22,23,24]. In most cases, the efficient red emission arises from an intramolecular charge-transfer (ICT) state and bulky side groups, such as cyano, can impede excessive excitonic and electronic coupling.
Herein we focus on the properties of two DR/NIR emitters based on symmetrically dinitro-substituted PV scaffolds with or without cyano-substituents in the para-position of the terminal rings, with a general acceptor-donor-acceptor (A-D-A) pattern. Their absorption/emission properties were analyzed and quantitatively evaluated recording PL quantum yield in solution and correlating PLQY measured on solid samples with X-ray diffraction analysis data and computational study results. The influence of the cyano-substituents on AIE/ACQ mechanism activation was discussed.

2. Results and Discussion

2.1. Photophysical Properties of the Fluorophores

The structures of the two fluorophores C1 and C2 are reported in Scheme 1.
Both the fluorophores show a solvatochromic effect (Table 1), going from the green-yellow emission in dioxane (520–550 nm), yellow-orange in acetone (565–618 nm), to the red emission in DMF (578–620 nm). In Figure 1, the absorption and emission spectra of C1 and C2 can be compared in the two solvents with the higher polarity difference: dioxane and DMF. An image of the same samples observable with naked eye is shown in Figure 2. In dioxane solution, the absorption spectra show two bands separated by about 100 nm (around 350 nm and after 440 nm). The intensity of the bands are comparable for C2, while the second band is weaker than that of C1. In DMF, the two absorption bands show more similar intensity. The emission maxima are found after 520 nm for both compounds in dioxane (Figure 1).
Figure 1 (bottom right) evidences the presence of two fluorescence bands. Compound C1, in particular, shows a NIR band peaked at 712 nm in DMF (Figure 1). As already observed [22], this is consistent with the existence of a polar excited state stabilized in a polar environment with increased probability of decaying to the ground state by non-radiative paths. The presence of a second emission band in more polar solvent is a well-known phenomenon described by Lippert [26], and it is due to an intramolecular charge transfer state stabilized by the solvent. In this case, the orientational relaxation of the solvent leads to an avoided level crossing. After relaxation, the more polar state becomes the lowest excited singlet (fluorescent) state. PL quantum yields were measured in solution by relative methods using zinc phtalocyanine as the standard [27]. PLQY for the simple PV skeleton C1 is about twice the CN substituted derivative C2 (see Table 1). In both cases, quantum efficiency in dioxane does not reach 35%, and considerably decreases in DMF. Optical properties were also studied in acetone/water mixture and, as already observed for similar compounds [28], the fluorescent emission is strongly quenched when small percentages of water are added (see Figure S4 of Supplementary Materials). An exhaustive quantitative analysis of the emission properties was carried out in the solid phase. From the crystalline samples, three kinds of film were prepared by spin coating. In order to test the behavior of C1 and C2 as dopants in solid films, we made a microdispersion of the two crystalline fluorophores in polystyrene. The samples were obtained from shattered crystals dispersed in a polystyrene (PS) matrix at 97%, 50%, or 10% by weight (Table 2). All solid compounds are light red under both natural and UV light (Figure 3). The fluorophores show broad absorption/emission bands in the solid state, sometimes resolved in separate peaks (see Table 2 and Figure S5). The samples are DR/NIR emitters, with emissions up to 620 nm for C2, or to 700 nm for compound C1. The 97% powder crystalline sample of C1 show a second PL maximum greatly red-shifted respect to the first absorption maximum, with a remarkable Stokes Shift from 160 to 250 nm (Table 2). The measurements of PL quantum yields were performed using a 376 nm laser whose emission does not overlap with the emitted photoluminescence spectrum. The use of the crystalline fluorophores micro-dispersed in a polymer matrix usually represents a suitable way to prevent ACQ effect in the solid state [19,23]. In our case, the three polystyrene-doped films show similar PLQY values and the best result is obtained for 50% doped PS film, which is a medium level of fluorophores. For C1, aggregation between π-conjugated planar extended frameworks produces an ACQ effect in the solid film. In C2, the incorporation of the cyano substituents into the phenylenevinylene backbone suppresses the parallel stacking of aromatic rings in the solid state (see discussion below) and results to guarantee excellent PL response in the solid state of C2 respect to C1. These values are among the highest values reported in literature for red emitters with similar [19,29] and not similar structure [30,31]. Fluorophore C2 seems to be the perfect candidate to prove the AIE effect compared with the analogous non-substituted stilbene skeleton. Another easy naked eye qualitative analysis [32] was carried out in dioxane/water providing data consistent with the expected ACQ/AIE behavior of the two chromophores. The progressive addition of water (over 20%) to dioxane solutions of C1 and of C2 caused the precipitation and aggregation of the molecules leading to a fluorescence decrease for C1. On the contrary, when C2 precipitates fluorescence increases turning to reddish color (Figure S6, Supplementary Materials).

2.2. X-ray Crystallography

Molecular structures of C1 and C2 were obtained by X-ray analysis performed on single crystals we got by slow evaporation from acetone solutions at room temperature. While it was not possible to obtain very good quality crystals of C2, high quality crystals of C1 were obtained as very long, rectangular cross-shaped tubular crystals (maximum 2.5 mm elongation and 0.5 mm cross-section, see Figure 4). Such kind of topological structure in organic crystals is not frequent, and have attracted much attention because of the potential applications in optics and electronics [33].
Compounds C1 and C2 crystallize in the monoclinic P21/c and the triclinic P-1 space group respectively, with one molecule contained in the asymmetric unit. In both the structures, all bond lengths and angles fall within the normal range. Details of crystallographic data and refinement parameters are reported in Table S1 (Supplementary Materials). Two perspective views of C1 molecular structure are reported in Figure 5.
The molecule exhibits a completely planar conformation, with a strict coplanarity of the three aromatic rings, the two central –C=C– groups and the two terminal –NO2 groups. Outstanding C1/C6 and C17/C22 mean planes rings are 1.26(10)° and 2.51(10)° tilted with respect to the central C9/C14 mean plane ring. Such geometrical peculiarity is in agreement with extended conjugation in the molecule. The branched alkyl group at O4 is disordered in two positions (refined occupancy factor 0.55/0.45) and disposes in an extended conformation quite perpendicular to the mean plane of the molecule. In the crystal packing, a herringbone pattern of molecules is observed with columns of parallel slipped molecules, stacked at about 3.4 Å across the inversion centers along a axis (Figure 6 and Figure S1, Supplementary Materials).
Two perspective views of C2 molecular structure are reported in Figure 7. The molecule is characterized by a flat extended shape due to a fair coplanarity of the three mutually twisted aromatic rings (C1/C6 and C19/C24 mean planes are 13.3(2)° and 14.7(3)° tilted with respect to the central C10/C15 mean plane). As usually found in similar compounds [34,35], the –NO2 group is coplanar with the bound phenyl ring. Similar to C1, also in C2, the alkyl group attached at O4 is disordered in two positions (refined occupancy factor 0.56/0.44) and disposes approximatively perpendicular to the mean plane of the molecule.
In the crystal packing the –CN and –NO2 groups are involved in weak CH∙∙∙N and CH∙∙∙O intermolecular interactions to form layers of co-planar molecules piled up in the (a–b) direction at a strict π-stacking of 3.3 Å (Figures S2 and S3, Supplementary Materials). In the crystal, the aliphatic and aromatic parts of molecules are separated and alternate each to the other. The examination of intermolecular interactions in the crystal put in evidence some peculiar aspects that could be related to the solid-state luminescent properties. In C2, a small mutual torsional parallelism between adjacent molecules is found, with a slipping in the elongation axis of molecule. In this way, adjacent aromatic parts of the molecules are faced with a moderate slipping and strict π-π aromatic interactions can be undertaken (Figure 8).
This is also confirmed by the Hirshfeld surface analysis [36]. Hirshfeld surface analysis was used to show that despite packing in a nearly identical manner, C1 and C2 are distinctly different in their interactions and that the solid-state interactions in C2 are dominated by the cyano moieties. The Hirshfeld analysis of C1 shows a typical plot of an aromatic and planar molecule. The longest contact is at 4.4 Å and the closest are at around 2.2 Å. The fingerprint plot for C2 covers a great range in both de and di (from 1.0 Å to almost 2.6 Å, in Figure 9, C2), and we attribute this to the presence of several anisotropic interactions, as well as the anisotropic shape of this molecule for the analysis of C2, which also shows the presence of several C–H···π contacts. In particular, there is an extremely short head–head H···H contact near 2.0 Å of lateral chain hydrogens. Worth of notice is the presence of extremely loose contacts at de + di = 5.1 Å on the top right region of the diagram. This is due to a strong distortion from planarity of the molecule. The distortion was induced by the presence of the cyano groups. In the Hirshfeld 2D plot the CN···H interaction is at de + di = 2.5 Å.

2.3. Computational Studies

As experimentally demonstrated, the presence of a cyano group affects deeply the electronic properties of the material. The properties change can be due to the effect of the cyano group on the molecule itself, for example modifying the frontier orbitals or the dipole moment, or they can be due to a different packing in the crystals. Obviously, the intramolecular and the intermolecular effects are strongly correlated and, in the scientific literature, are often separated for simplicity. The geometric analysis of the crystals permitted to identify in the deviation from planarity and in the different π stack the basis for the AIE effect. We employ the time-dependent perturbation theory approach (TD-DFT) with the adiabatic local density approximation, to calculate the excitation energies. This approach has high reliability in obtaining accurate predictions for excitation energies and oscillator strengths. This analysis is necessary to clarify the role of cyano group in controlling the electronic transitions. Calculations on C1 and C2 in dioxane showed the localization of HOMO and LUMO orbitals (see Figure 10).
The two molecules have very similar frontier orbitals, with HOMO and LUMO delocalized overall the conjugated backbone, with only a moderate contribution of the cyano groups in C2. The electron withdrawing cyano groups are involved in HOMO and in LUMO. The main transitions, at 449 nm for C1 and 477 nm for C2, are the HOMO → LUMO. The second main strong absorptions are due to the transition HOMO-1 → LUMO. The predicted absorption maximum is in good agreement with the experimental values (see Table 1 and Table 2), the two main absorptions corresponding to the HOMO→LUMO and HOMO-1→LUMO transitions. It is noted that, the insertion of the cyano group decreases the HOMO and the LUMO energy of C2, but the HOMO energy decreases not as much as the LUMO, indicating that the presence of the electro withdrawing group is beneficial to electron injection. The calculated absorption spectra are shown in Figure S7 (Supplementary Materials).
Withdrawal of the electron from a compound in a redox reaction is performed from its HOMO. The presence of the electro withdrawing nitro group in the two molecules is responsible for an oxidation potential higher than similar molecule CN-PV-NHMe [22]. C1 and C2 exhibits hole and electron reorganization energies (HRE and ERE respectively) that are typical for these compounds, but the presence of cyano group in C2 increases the ERE. It is worth to notice that the reorganization energy (RE) is one of the parameters governing the hopping rate. It has long been recognized that HRE and ERE are closely related to the geometries of cation and anion states. In fact, the RE is defined as the energy difference between the charged and neutral systems at the two different geometries. The molecules with small RE possess high carrier mobility and these energies are in proportion to the deformation of the geometries in charge transfer process. In C1 and C2, the HRE are smaller than the ERE indicating a smaller geometrical deformation upon electron injection compared to hole injection. The value of 0.248 eV of C2 is remarkably small. Furthermore, as indicated in Table 3, C1 has a minimum hole extraction potential of 6.404 eV, which demonstrates that the injection of hole into C1 is slightly easier than in C2. On the contrary, C2 has maximum electron extraction potential of 2.435 eV, indicating that the injection of electron into the C2 becomes much easier. The above results show that the substitution of electron-withdrawing cyano group can significantly affect the electron-transporting properties of the system. In Table S2 (Supplementary Materials), a complete list of computed properties is given. In agreement with the Hirshfeld analysis, it can be seen that the presence of cyano groups can change the packing motif and increase the π–π overlap to achieve high charge mobility.

3. Materials and Methods

All starting products were commercially available. 4,4’-((1E,1’E)-(2-((2-ethylhexyl)oxy)-5-methoxy-1,4-phenylene) bis (ethene-2,1-diyl)) bis (nitrobenzene) (C1) and (2Z,2’Z)-3,3’-(2-((2-ethylhexyl)oxy)-5-methoxy-1,4-phenylene) bis (2-(4-nitrophenyl)acrylonitrile) (C2) were obtained respectively as described previously [22,25]. The compounds were characterized by mass spectrometry and NMR. Mass spectrometry measurements were performed using a Q-TOF premier instrument (Waters, Milford, MA, USA) equipped by an electrospray ion source and a hybrid quadrupole-time of flight analyzer. 1H-NMR spectra were recorded in DMSO-d6, with Bruker Avance II 400 MHz apparatus (Bruker, Leiderdorp, The Netherlands). Single crystals of C1 and C2 suitable for X-ray structural analysis were obtained by slow evaporation of acetone solution, at room temperature.
Optical observations were performed by using a Zeiss Axioscop polarizing microscope. UV-Visible and fluorescence spectra were recorded with JASCO F-530 (JASCO, Tokyo, Japan) and FP-750 (JASCO, Tokyo, Japan) spectrometers. Thin films were obtained by the spin coating technique of a dispersion of crystalline powder of the samples and low weight commercially available polystyrene in chloroform/hexane (2:1) by a SCS P6700 spin coater (SCS, Indeanapolis, IN, USA) operating at 600 RPM.

3.1. PLQY Measurements

Photoluminescence efficiency measurements on solid samples were conducted with a setup similar to that previously reported [37]. The setup consists of a 376 nm laser, whose emission does not overlap with the emitted photoluminescence spectrum, an integrating sphere (Stellarnet Inc., Tampa, FL, USA), and a photospectrometer (BLACK Comet Stellarnet Inc., Tampa, FL, USA). The setup takes into account both the exciting laser, the direct photoluminescence spectrum, and the photoluminescence that originates due to the scattering effect of the integrating sphere. The emission was measured at five different points on the sample.

3.2. X-ray Crystallography

Selected crystals of C1 and C2 were mounted in flowing N2 at 173 K on a Bruker Nonius Kappa CCD diffractometer, (Bruker, Karlsruhe, Germany), equipped with Oxford Cryostream apparatus (graphite monochromated MoKα radiation, λ = 0.71073 Å, CCD rotation images, thick slices, ϕ and ω scans to fill asymmetric unit). Semiempirical absorption corrections (SADABS [38]) were applied. The structures were solved by direct methods (SIR97 program [39]) and anisotropically refined by the full matrix least-squares method on F2 against all independent measured reflections using SHELXL-2016 (2016, Sheldrick, Germany) [40] and WinGX software (2016, Farrugia, Glasgow) [41]. All the hydrogen atoms were introduced in calculated positions and refined according to the riding model with C–H distances in the range 0.95–0.99 Å and with Uiso(H) equal to 1.2Ueq or 1.5Ueq(Cmethyl) of the carrier atom. The final refinement converged to R1 = 0.0569, wR2= 0.1480 (C1) and R1 = 0.0987, wR2 = 0.2543 (C2). Both in C1 and C2, the aliphatic group attached at O4 atom is disordered in two positions (refined occupancy factor 0.55/0.45 for C1 and 0.56/0.44 for C2). Evidences of a complex disorder of aliphatic group in C2 was found in difference Fourier maps but it was not possible to model the disorder in more than two positions. Some restraints were introduced on the C-C bond distances using the DFIX, SAME, and SIMU instructions of SHELXL program (2016, Sheldrick, Germany) at the last stage of refinement in C2. Crystal data and structure refinement details are reported in Table S1 (Supplementary Materials). The figures were generated using ORTEP-3 [41,42] and Mercury CSD 3.3 [43] programs (version 3.3, CCDC, England).
All crystal data were deposited at Cambridge Crystallographic Data Centre with assigned number CCDC 1851105 (C1) and 1851106 (C2). These data can be obtained free of charge from https://www.ccdc.cam.ac.uk/structures.

3.3. Computational Studies

The DFT calculations were carried out with the program Jaguar (2013, Schrödinger, LLC, NY, USA) [44] available in the Schrödinger Material Science Suite [45]. Geometry optimizations were performed with the B3LYP functional and the 6-31G** basis set. The energies of the optimized structures were estimated by additional single-point calculations using Dunning’s correlation-consistent triple-ζ basis set42 cc-pVTZ(-f) that includes a double set of polarization functions. In order to confirm proper convergence to local minima, to derive the zero-point-energy (ZPE) and entropy corrections at room temperature, we have used vibrational frequency calculation results based on analytical second derivatives at the B3LYP/6-31G**(LACVP**) level of theory.

4. Conclusions

We have comparatively studied two DR/NIR emitters based on phenylenevinylene PV and dicyano-PV structures (C1 and C2, respectively) exhibiting fluorescent emission in the region ranging from red to NIR both solution and solid states (doped PS films). As we expected, by changing the substituents on the phenylenevinylene skeleton, e.g, by adding cyano groups, the fluorescent emission wavelength increases thanks to an aggregation induced emission (AIE) effect. In particular, while an ACQ effect was evident for C1 in the solid, with a fluorescent quantum yields not more than 18%, a bright red emission was recorded for the fluorophore C2, proving a strong AIE of this fluorophore, reaching a maximum of 75% yield. Structure–property relationships were elucidated by X-ray crystallographic analysis and DFT calculations. The comparative analysis demonstrated that in the solid state, fluorescence of C1 is quenched by the strong π-π interactions, due to the ease of aggregation between π-conjugated planar extended frameworks. In C2, the incorporation of the cyano substituents into the phenylenevinylene backbone suppresses close-packing in the solid state and activates the radiative channel, causing an intense aggregation-induced emission effect. Moreover, with the addition of the electron-accepting CN substituents, the energy gap (HOMO-LUMO) of the fluorophore decreases, indicating that the presence of the electro withdrawing groups is beneficial to electron injection. This analysis shows that the fluorophore C2 can be a good candidate for application in optoelectronics, in which electron injection ability and deep red emission are highly required.

Supplementary Materials

The following are available online https://www.mdpi.com/1420-3049/23/8/1947/s1, Table S1: Crystallographic data and structural refinement details of C1 and C2. Table S2: Calculated electro-optical parameters for C1 and C2. Figure S1: Crystal packing of C1, viewed along a + c direction. Figure S2: Partial packing of C2 with layer of coplanar molecules. Figure S3: View of C2 crystal packing in the (a + 2b) direction showing layers of stacked molecules. Figure S4: Emission spectra of C1 and C2 in acetone/water solutions. Figure S5: Absorption and emission spectra of C1 and C2 in solid state. Figure S6. Fluorophores solutions in dioxane; dioxane/water 50% and dioxane/water 90% (v/v) in natural (up) and under 375 nm UV light (down). Figure S7: Predicted absorption spectra of C1 and C2.

Author Contributions

B.P. and U.C. conceived and designed the experiments; R.D. and S.C. performed the experiments; S.P. and L.S. performed the DFT and the Hirshfeld analysis; A.T performed the crystallographic experiments; R.S. and S.N. performed the optical measurements; B.P. and R.D. analyzed the data; R.D. and S.C. wrote the paper.

Funding

This research was funded by the Italian Ministry of Education, University and Research (MIUR) [grant number: 300395FRB17].

Conflicts of Interest

The authors declare no conflicts of interest.

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Sample Availability: Samples of the compounds C1 and C2 are available from the authors.
Molecules 23 01947 sch001 550
Scheme 1. Chemical structure of the two fluorophores C1 and C2. The double Knoevenagel condensation between 4-nitrophenylacetic acid or 2-(4-nitrophenyl)acetonitrile respectively and the alkoxy-terephthalaldehyde [22,25] was a convenient symmetric pattern to synthesize the 4,4’-dinitrostilbene skeleton. The identification and purity were assessed by mass spectrometry and 1H-NMR and by comparing melting points with the literature data [22]. The optical properties in solution were analyzed in three solvents with different polarity: dioxane < acetone<DMF (see Table 1).
Scheme 1. Chemical structure of the two fluorophores C1 and C2. The double Knoevenagel condensation between 4-nitrophenylacetic acid or 2-(4-nitrophenyl)acetonitrile respectively and the alkoxy-terephthalaldehyde [22,25] was a convenient symmetric pattern to synthesize the 4,4’-dinitrostilbene skeleton. The identification and purity were assessed by mass spectrometry and 1H-NMR and by comparing melting points with the literature data [22]. The optical properties in solution were analyzed in three solvents with different polarity: dioxane < acetone<DMF (see Table 1).
Molecules 23 01947 sch001
Molecules 23 01947 g001 550
Figure 1. Absorption (up) and emission (down) spectra of C1 (red line) and C2 (black line) in dioxane (left) and DMF (right) solution.
Figure 1. Absorption (up) and emission (down) spectra of C1 (red line) and C2 (black line) in dioxane (left) and DMF (right) solution.
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Molecules 23 01947 g002 550
Figure 2. Fluorophores solutions (10%) in DMF (left) and dioxane (right) in natural (left column) and under 375 nm UV light (right column).
Figure 2. Fluorophores solutions (10%) in DMF (left) and dioxane (right) in natural (left column) and under 375 nm UV light (right column).
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Molecules 23 01947 g003 550
Figure 3. Samples of C1 and C2 deposed on quartz slides at different dopant percentages in natural (left column) and under 375 nm UV light (right column).
Figure 3. Samples of C1 and C2 deposed on quartz slides at different dopant percentages in natural (left column) and under 375 nm UV light (right column).
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Molecules 23 01947 g004 550
Figure 4. (a) Single rectangular cross-shaped tubular crystals of C1 on a glass slide; (b) magnification 4 × of one crystal; (c) view of the crystal mounted on the KappaCCD diffractometer (Bruker-Nonius B.V., The Netherlands) using the KappaCCD video microscope (Bruker-Nonius B.V., The Netherlands); (d) unit cell axis are reported on the crystal: a or a* in red, b or b* in green, c or c* in blue.
Figure 4. (a) Single rectangular cross-shaped tubular crystals of C1 on a glass slide; (b) magnification 4 × of one crystal; (c) view of the crystal mounted on the KappaCCD diffractometer (Bruker-Nonius B.V., The Netherlands) using the KappaCCD video microscope (Bruker-Nonius B.V., The Netherlands); (d) unit cell axis are reported on the crystal: a or a* in red, b or b* in green, c or c* in blue.
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Molecules 23 01947 g005 550
Figure 5. Up: Ortep view of C1 with thermal ellipsoids drawn at 30% probability level. Only major part of the disordered aliphatic group is reported for clarity. Down: perspective view in the edge of C9/C14 ring (H atoms and alkyl groups at O3 and O4 are not shown for clarity).
Figure 5. Up: Ortep view of C1 with thermal ellipsoids drawn at 30% probability level. Only major part of the disordered aliphatic group is reported for clarity. Down: perspective view in the edge of C9/C14 ring (H atoms and alkyl groups at O3 and O4 are not shown for clarity).
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Molecules 23 01947 g006 550
Figure 6. Partial packing showing the slipped stacking of molecules of C1 in the a axis direction. Shortest distances are drawn as green dashed lines.
Figure 6. Partial packing showing the slipped stacking of molecules of C1 in the a axis direction. Shortest distances are drawn as green dashed lines.
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Molecules 23 01947 g007 550
Figure 7. Up: Ortep view of C2 with thermal ellipsoids drawn at 30% probability level. Only major part of disordered alifatic group attached at O4 is reported for clarity. Down: perspective view in the edge of C10/C15 ring (H atoms and alkyl groups at O3 and O4 are not shown for clarity).
Figure 7. Up: Ortep view of C2 with thermal ellipsoids drawn at 30% probability level. Only major part of disordered alifatic group attached at O4 is reported for clarity. Down: perspective view in the edge of C10/C15 ring (H atoms and alkyl groups at O3 and O4 are not shown for clarity).
Molecules 23 01947 g007
Molecules 23 01947 g008 550
Figure 8. Facing of aromatic rings in C2 packing. Shortest distances involving centroids of aromatic rings are drawn as green lines. Aliphatic groups bonded at O3 and O4 and H atoms are not reported for clarity.
Figure 8. Facing of aromatic rings in C2 packing. Shortest distances involving centroids of aromatic rings are drawn as green lines. Aliphatic groups bonded at O3 and O4 and H atoms are not reported for clarity.
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Molecules 23 01947 g009 550
Figure 9. Hirshfeld fingerprint plots for C1 (left) and C2 (right).
Figure 9. Hirshfeld fingerprint plots for C1 (left) and C2 (right).
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Molecules 23 01947 g010 550
Figure 10. HOMO-1, HOMO, LUMO, and LUMO+1 orbitals for C1 (left) and C2 (right).
Figure 10. HOMO-1, HOMO, LUMO, and LUMO+1 orbitals for C1 (left) and C2 (right).
Molecules 23 01947 g010
Table
Table 1. Optical data recorded in solution.
Table 1. Optical data recorded in solution.
Compoundλabs-sol (nm) aλem-sol (nm) bPLQY% c
C1352; 437 i
357; 439 ii
361; 448 iii		521 i
618; 708 ii
633; 712 iii		33 i
15 ii
≤10 iii
C2354; 444 i
353; 440 ii
358; 446 iii		550 i
565 ii
578 iii		19 i
15 ii
≤10 iii
a UV-Visible absorbance maxima in i dioxane, ii acetone, and iii DMF solution. b Wavelength of emission maxima in i dioxane, ii acetone, and iii DMF solution. c PL quantum yield ±3% in i dioxane, ii acetone, and iii DMF solution.
Table
Table 2. Optical data recorded on solid samples.
Table 2. Optical data recorded on solid samples.
Compound% aλabs-film (nm) bλem-film (nm) cPLQY% dStokes shift (nm) e
C197%353; 400; 505652; 70211 ± 0.1252
50%350; 455; 500651; 71118 ± 0.1196
10%350; 456; 559507; 61812 ± 0.5162
C297%352; 407; 56762166 ± 3214
50%372; 47561675 ± 4141
10%372; 49461167 ± 2117
a Shattered crystals of C1 or C2, dispersed in PS at 97, 50 or 10% w/w. b Wavelength of UV-Visible absorbance maxima on thin film. c Wavelength of emission maxima on thin film. d PL quantum yield on thin film. e Stokes shift measured as difference between the band maxima of the absorption and emission spectra of the main electronic transition.
Table
Table 3. Calculated electro-optical parameters for C1 and C2.
Table 3. Calculated electro-optical parameters for C1 and C2.
Hole Reorganization Energy (eV)Electron Reorganization Energy (eV)λabs Solution (nm)λem Solution (nm)Hole Extraction Potential (eV)Electron Extraction Potential (eV)Scaled HOMO (eV)Scaled LUMO (eV)
C10.2570.3064494856.4041.799−5.877−3.472
C20.2480.3354775226.8612.435−6.169−3.980

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Caruso, U.; Panunzi, B.; Diana, R.; Concilio, S.; Sessa, L.; Shikler, R.; Nabha, S.; Tuzi, A.; Piotto, S. AIE/ACQ Effects in Two DR/NIR Emitters: A Structural and DFT Comparative Analysis. Molecules 2018, 23, 1947. https://doi.org/10.3390/molecules23081947

AMA Style

Caruso U, Panunzi B, Diana R, Concilio S, Sessa L, Shikler R, Nabha S, Tuzi A, Piotto S. AIE/ACQ Effects in Two DR/NIR Emitters: A Structural and DFT Comparative Analysis. Molecules. 2018; 23(8):1947. https://doi.org/10.3390/molecules23081947

Chicago/Turabian Style

Caruso, Ugo, Barbara Panunzi, Rosita Diana, Simona Concilio, Lucia Sessa, Rafi Shikler, Shiran Nabha, Angela Tuzi, and Stefano Piotto. 2018. "AIE/ACQ Effects in Two DR/NIR Emitters: A Structural and DFT Comparative Analysis" Molecules 23, no. 8: 1947. https://doi.org/10.3390/molecules23081947

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