Synthesis, FTIR, 13C-NMR and Temperature-Dependent 1HNMR Characteristics of Bis-naphthalimide Derivatives

Chemotherapy is still the most important method of cancer treatment. To make this method more effective and safe, new drugs to destroy cancer cells are needed. Some bis-naphthalimide derivatives show potential anticancer activity via an intercalation mechanism. A higher degree of DNA intercalation corresponds to better therapeutic effects. The degree of intercalation of naphthalimides depends on their structure, molecular dynamics and intermolecular interactions with DNA. In order to apply any active substance as a drug, its molecular dynamics as well as possible interactions with target molecules have to be examined in exhaustive details. This paper describes a practical preparation of some novel bis-naphthalimide derivatives with different functional groups and their FTIR and 1H- and 13C-NMR spectral characteristics. To determine the molecular dynamics of the obtained compounds the temperature, their 1H-NMR spectra were measured. It has been clearly proven in this paper that the unusual temperature-dependent 1H-NMR behavior of the aromatic protons of phthalimide derivatives, previously described in the literature as “hypersensitivity” and explained by n-π interactions and molecular motions of aromatic amide rings, is a result of temperature driven changes of the geometry of carbonyl groups.


Introduction
1,8-Naphthalimide derivatives are a very important class of compounds. Their photophysical properties are useful in many applications as organic light-emitting diodes, [1] fluorescent dyes for solar energy collectors, [2] laser active media, [3] potential photosensitive biologically active units, [4] liquid-crystal additives, [5] effective, non-oxygen based photochemical inactivators of enveloped viruses, including herpes simplex virus and HIV [6], and as fluorescent dyes for synthetic polymers and textile materials [7,8].
The biological activity of N-substituted naphthalimides has been studied since the early 1940s. The activity of simple analogues includes antiviral [9], antibacterial [10] and antitrypanosomal properties [11]. Special attention has been devoted to the high anticancer activity of naphthalimides , which is due to their interactions with DNA by intercalation. Intercalators are molecules which consist of flat π-deficient aromatic or heteroaromatic systems that bind reversibly to double-helical DNA distorting the DNA backbone conformation and interfering with DNA-protein interactions [12][13][14]. The complex molecular structure of DNA can be influenced by intercalators through π-π, electrostatic, hydrogen bonding, dipole-dipole and hydrophobic interactions. In general the stronger the interactions of the intercalator with DNA, the higher the antitumor activity of the drug will be. In order to use any active substance as a drug, the recognition of all possible interactions with target molecules is essential. Neglecting this can lead to tragic results as in case of thalidomide. Because bis-naphthalimides act as DNA intercalators, therefore knowledge about the molecular dynamics of naphthalimide rings is absolutely necessary. In the case of bis-naphthalimide derivatives the problem remains unsolved to date. Some years ago Barrett et al. [35] and Howell et al. [36] observed an unusual temperature behavior of the aromatic protons of phthalimide derivatives in 1 H-NMR. In certain temperature ranges only one peak was observed for four different aromatic protons. Authors explained it as "hypersensitivity" caused by n-π interactions of the n-electrons of substituents with the π-electrons of aromatic rings together with the molecular dynamics of these phthalimide systems. They also calculated some thermodynamic parameters of these interactions.
Because this type of effect observed by Barrett [35] and Howell [36] could be very important for the interactions of bis-naphthalimides with DNA, we have also checked for it in synthesized bis-naphthalimides. We observed a similar temperature behavior for all studied bis-naphthalimides. However, the explanation is quite different from that given by Barrett. In our paper we have very proven precisely, without any doubts, that no n-π interactions are present in these systems and that the unusual behavior of protons in 1 H-NMR spectra is caused by temperature-driven changes in the carbonyl group geometry.

Synthesis
In this paper we report the synthesis of bis-naphthalimide derivatives, their FTIR and 13 C-NMR spectra and the unusual temperature behavior of their protons in 1 H-NMR. The substrate used to obtain the reported bis-naphthalimide derivatives (Scheme 1) is 1,8-naphthalenedicarboxylic anhydride (NP1). Reactions of anhydride NP1 with bis-N,N-(3-aminopropyl)amine and p-phenylenediamine led to N,N-bis- [3-(1,8-naphthalimide)propyl]amine (NP3) and N,N′-(1,4-phenylene)-bis (1,8-naphthalimide) (NP2), respectively. Compound NP2 has six π-electrons more in comparison to the other naphthalimides. Thus, its π-π interaction potency with the heteroaromatic bases in DNA is significantly enhanced. The functionalization of the spacer by nitrogen atom gives the product NP3, which can additionally interact with DNA by hydrogen bonding. To obtain N,N-bis- [3-(1,8naphthalimido)-propyl]-N-propylamine (NP5) and N,N-bis- [3-(1,8-naphthalimido)propyl]-Ndodecylamine (NP4) the alkylations with alkyl chlorides, bromides or iodides in the presence of inorganic carbonates in chloroform, dichloromethane or aliphatic alcohols were carried out. The yields of these reactions were below 10%, due to the low boiling points of the solvents used. The use of high boiling solvents like dimethylformamide or dimethylacetamide leads to N,N-bis- [3-(1,8-naphthalimido)propyl]-N-propylamine (NP5) and N,N-bis- [3-(1,8-naphthalimido)-propyl]-Ndodecylamine (NP4) in yields over 75%. Moreover, the products can be easily isolated from these solvents. Compounds NP4 and NP5 can mainly interact with DNA by π-π interactions and hydrogen bonding. Due to the presence of hydrocarbon chains these compounds can also interact with DNA by hydrophobic interactions. The naphthalimide derivatives NP5 and NP4 are barely soluble in water and alcohols. To improve their solubilities in water, hydrochlorides NP6 and NP7 were obtained by addition of hydrochloric acid to acetonitrile solutions of NP5 and NP4, respectively. The nitrogen atom in the hydrochlorides of bis-naphthalimide derivatives NP6 and NP7 possesses a positive charge, so additional electrostatic interactions can influence DNA structure. The quaternization of N,N-bis- [3- quaternized compounds NP8 and NP9 have positively charged nitrogen atoms and electrostatic interactions with DNA can play important role in the intercalation mechanisms. Solubility in water of the synthesized bis-naphthalimide intercalators is poor; however, using gemini surfactants with high HLB values as solubilizers, satisfactory results were obtained. The synthesized bis-naphthalimide intercalators will be tested as anticancer agents.

FTIR Spectra Study
FTIR spectra of naphthalimide derivatives NP2-NP9 were recorded in KBr pellets at 298 K. The basic FTIR features of the naphthalimide structure are C-C, C-N and C=O bands. The C-C stretching vibration bands of naphthalimide ring appear in the 1630-1400 cm −1 range, while the C-N stretching vibration bands in the dicarboximide ring are present between 1100 and 1050 cm −1 . In the 3100-3000 cm −1 region typical C-H stretching vibration bands of aromatic rings are observed, while the C-H asymmetric and symmetric stretching vibration bands of the methylene and methyl groups of N-substituents lie in 2960-2850 cm −1 the region ( Figure 1). The most characteristic bands in the FTIR spectra are the carbonyl bands. Asymmetric stretching vibration bands of the carbonyl groups of the investigated naphthalimide derivatives, ν as C=O, appear in the 1702-1695 cm −1 range, while the symmetric stretching vibration bands of carbonyl groups, ν s C=O, are observed between 1659-1653 cm −1 (Table 1).
The symmetric stretching vibration bands are very intense, whereas the asymmetric stretching vibration bands are much less intense. The difference of intensities is related to the symmetry of the molecule. When both carbonyl groups of dicarboximide ring are not planar, then the intensity of asymmetric vibrations is lower in comparison to the intensity of symmetric stretching vibration bands [37][38][39] (Table 1). Moreover, the symmetric stretching vibration of the carbonyl group in this compound is split, and two bands are observed at 1681 and 1667 cm −1 ( Figure 2).  Additionally, the splitting of the symmetric stretching vibration band of carbonyl group of NP2 is a result of nonequivalence of the carbonyl bonds which is caused by the slight deviation from planarity of the dicarboximide ring and compact packaging and interactions in the crystal state [37][38][39].
In general, the asymmetric and symmetric stretching vibration bands of the carbonyl groups of naphthalimide derivatives are shifted more than 50 cm −1 to lower frequencies in comparison to the phthalimide analogs [37][38][39]. For N,N-bis-(phthalimidopropyl)-N-propylamine the asymmetric stretching vibrations of carbonyl groups are split and lay at 1771 and 1764 cm −1 , whereas the symmetric stretching vibrations of carbonyl groups appear at 1710 cm −1 [37]. Similarly, for N,N-bis-(phthalimidopropyl)-N-octylamine, where both the asymmetric and symmetric stretching vibration bands of the carbonyl groups are split, ν as C=O is observed at 1771 and 1764 cm −1 , whereas ν s C=O lays at 1721 cm −1 and 1710 cm −1 [38]. The carbonyl bond and C-N bond lengths are 1.212 Ǻ and 1.394 Ǻ for N,N-bis-(phthalimidopropyl)-N-propylamine [37], and 1.210 Ǻ and 1.390 Ǻ for N,N-bis(phthalimidopropyl)-Noctylamine, respectively [38]. In the naphthalimide series, for N,N-bis- [3-(1,8-naphthalimido)propyl]-N-propylamine (NP5), asymmetric and symmetric stretching vibration bands of the carbonyl groups are observed at 1701 cm −1 and 1656 cm −1 (Table 1) and the carbonyl bond and C-N bond lengths are 1.223 Ǻ and 1.400 Ǻ, respectively [39]. These significant shifts of frequencies of the carbonyl groups are due to the increasing interaction between the carbonyl group and the nitrogen atom in naphthalimide derivatives in comparison to phthalimide derivatives, which reflects changes in the bond lengths of C=O and C-N, and as a consequence of this, increasing imide bond character [37].

13 C-NMR Spectra
The remaining naphthalimide derivatives, NP3-NP7, were measured in CDCl 3 . The average value of the chemical shifts for C-2 of the naphthalimide derivatives NP3-NP7 is 131.2 ppm, whereas the chemical shifts for C-3 and C-4 are 126.8 and 133.9 ppm, respectively. Chemical shifts of the carbonyl carbon atoms for naphthalimide derivatives NP3-NP7 are observed at 164.1 ppm. Significant shifts towards higher values of ppm are encountered as expected for the 13 C resonance frequencies of carbons C-2, C-3, C-4 and carbonyl carbon atoms for naphthalimide derivatives which were measured in TFA-d ( Table 2). Kubo et al. showed that trifluoroacetic acid form strong hydrogen bonds O…H-O with N-substitued naphthalimide derivatives [40], changing the electron density in the naphthalimide ring. As a consequence of the lower electron density, 13 C resonance frequencies shift toward higher chemical shifts. The very similar chemical shifts for naphthalimides with different N-substituents suggests that electronic effects of substituents on the electron distribution in the naphthalimide ring can be neglected.

1 H-NMR Spectra
The ABM pattern of protons in N-substituted naphthalimide rings is expressed by one triplet and two doublets in the aromatic region of the 1 H-NMR spectrum as for N-hydroxyethyl-1,8-naphthalimide, where the following signals are observed: 8.6 ppm (d, J = 6Hz, 2H), 8.22 ppm (d, J = 6Hz, 2H) and 7.8 ppm (t, J = 6 Hz, 2H) [41]. In the series of investigated bis-naphthalimides, N,N-bis [3-(1,8naphthalimido)propyl]-N-propylamine (NP5) is characterized by the same ABM pattern, however only below 256 K or at temperatures higher than 300 K one triplet (H-3) and two doublets (H-2 and H-4) with J = 8 Hz are observed ( Figure 5). In a wide range of temperature (253 K-333 K) the H-3 triplet shows practically no changes, whereas signals of H-2 and H-4 undergo an evolution from two doublets at 253 K, through two signals at 283 K, up to a double doublet at 333 K ( Figure 5). A similar temperature behavior of the aromatic protons in 1 H-NMR spectra was observed by Barrett for N,N′,N′′(nitrilotriethylene)trisphthalimide [35] (Figure 6). The proton NMR spectra of this compound in CDCl 3 exhibited a spectacular temperature evolution from a sharp doublet of quartets at high temperature (323 K) to a complex second order behavior and then a singlet at 283 K. As the temperature was further lowered, a complex second order spectrum reappeared, followed by doublet of quartets at 213 K [35]. The unusual proton NMR characteristics of N,N′,N′′-(nitrilotriethylene)trisphthalimide have been explained by n-π interactions and rapid equilibration in solution of four assumed isomers. Using temperature dependency of chemical shifts, the enthalpy of interactions between π-electrons of phthalimide ring and n-electrons of amine was estimated to be ΔH ‡ = 20 kJ/mol [35]. Some years ago Kahwa et al. carried out a very detailed study of crystal structures and 1 H-NMR characteristics of some alkylaminephthalimides (Figure 7), including dendritic polyphthalimides [36]. They also observed a spectacular temperature evolution for the aromatic protons of compounds 1 and 2 in the 1 H-NMR and claimed that the line profiles are attributable to n-π interactions. Like Barrett, those authors also calculated phthalimide-amine interaction enthalpy ΔH ‡ for compound 2 to be 23 ± 1 kJ/mol in CD 3 CN, 17 ± 3 kJ/mol in CD 3 OD and 19 ± 5 kJ/mol in CDCl 3 .
Since bis-naphthalimide derivatives are structurally very similar to the compounds studied by Barrett [35] and Kahwa [36], we decided to check their hypothesis that n-π interactions were a responsible factor causing the unusual proton NMR characteristics. For our temperature-dependent 1 H-NMR investigations we used N,N-bis [3-(1,8-naphthalimido)propyl]-N-propylamine hydrochloride (NP6), where no lone electrons pair exist on nitrogen atom.
The 1 H-NMR spectra of NP6 taken in DMF-d 7 in the temperature range 258 K-348 K reveal that the H-3 triplet is temperature independent and lays at 7.86 ppm, whereas the signals of H-2 and H-4 show unusual temperature behavior in the 8.37-8.48 ppm range. Starting as two distinct doublets at 258 K, as the temperature increases the signals evolve into two individual peaks at 315 K and again, as the temperature becomes higher the peaks undergo a transformation into two clear doublets at 348 K ( Figure 8). The same temperature-dependent 1

H-NMR behavior of N,N-bis[3-(1,8-naphthalimido)propyl]-N-propylamine hydrochloride (NP6) and N,N-bis[3-(1,8-naphthalimido)propyl]-N-propyl-
amine (NP5) excludes n-π interactions as a factor responsible for the unusual temperature proton behavior in the 1 H-NMR spectra. N,N-bis [3-(1,8-naphthalimido)propyl]-N-propylamine hydrochloride (NP6) is a typical intermolecular complex with a N + -H…Cl − hydrogen bond, where the proton is quickly moving between chloride anion and nitrogen. To avoid any suspicions that the proton transfer process is slower than the NMR time scale and n-electrons can even partially participate in n-π interactions, we measured the 1 H-NMR spectra of a quaternary ammonium salt-N-ethyl-N,N-bis[3-(1,8-naphthalimido)propyl]-N-propylammonium iodide (NP9) in the 263 K-350 K temperature range in DMF-d 7 (Figure 9).  In NP9, where four substituents are connected to the nitrogen atom, there is no doubt that n-electrons cannot interact with any π-electron system. As can be seen from Figure 9, the temperature-dependent 1 H-NMR spectral feature of NP9 with a quaternary nitrogen atom is very similar to that of NP6 with a protonated nitrogen atom. The H-3 triplet is almost temperature independent, whereas the temperature evolution of the H-2 and H-4 signals is like that seen in NP6. In general, comparing the temperature-dependent 1 H-NMR spectra of the amine NP5, protonated amine NP6 and ammonium salt NP9 one can state that the spectral features are very similar and there is no evidence for any participation of n-π interactions and rapid equilibration of naphthalimide isomers in solution. The only difference is that the "coalescence" temperature increase starts from 283 K for amine NP5, 315 K for protonated amine NP6 and 327 K for the ammonium salt NP9.
An additional proof of the absence of n-π interactions of bis-naphthalimide derivatives in solution is derived from the 1 H-NMR temperature-dependent spectra of N,N′-(1,4-phenylene)-bis(1,8-naphthalimide) (NP2; Figure 10). Because of the extremely low solubility of NP2 in DMF-d 7 the spectra were recorded in DMSO-d 6 in which this derivative is slightly more soluble. The 1 H-NMR temperature-dependent spectral behavior of N,N′-(1,4-phenylene)-bis(1,8-naphthalimide) (NP2), which does not contain a nitrogen atom in the substituent, is very similar to those previously observed. This means that n-π interactions play no fundamental role in the unusual temperature-dependent spectral features of naphthalimide derivatives.
Another factor which can cause an increase or decrease of proton shielding in naphthalimide rings and in turn could cause this unusual temperature 1 H-NMR behavior is the geometry of 1,8-naphthalenedicarboximide derivatives. As Kovalevsky showed the naphthalenedicarboximide fragment can be formally divided into two 10π-electron naphthalene and the 7π electron dicarboximide fragments [42]. As a result the dicarboximide ring is more sensitive to the steric effects of substituents than to their electronic effects [42]. We have previously shown that both imide rings in N,N-bis [3-(1,8-naphthalimido)propyl]-N-propylamine (NP5) are non-planar [39]. This leads to deviations of the oxygen atoms from the imide average plane. It is very reasonable to suppose that these geometry deviations will vary with temperature and it can be a factor responsible for the unusual 1 H-NMR behavior of the naphthalimide protons. To confirm this assumption we have measured 1 H-NMR spectra of 1,8-naphthalimide over a wide range of temperatures in DMF-d 7 (Figure 11). As can be seen from Figure 11, the measured spectra of 1,8-naphthalimide have the same spectral features as the temperature-dependent spectra of the previously discussed bis-naphthalimide derivatives. The coalescence temperature is around 278 K, which is very close to the coalescence temperature of N,N-bis [3-(1,8-naphthalimido)propyl]-N-propylamine.
To be sure that no electrons from the nitrogen atom are involved in this process we have also measured the temperature-dependent 1 H-NMR spectra of 1,8-naphthalenedicarboxylic anhydride (NP1) under the same conditions. The obtained spectra reveal no significant changes in comparison to spectra of 1,8-naphthalimide, except for the coalescence temperature which is 295 K (Figure 12). The above results clearly indicate that the temperature-driven changes of the geometry of the carbonyl group are the direct cause of the unusual behavior of the aromatic protons in the 1 H-NMR spectra. To prove this suggestion the temperature-dependent 1 H-NMR spectra of acenaphthene and indane were taken in CDCl 3 and CD 3 OD respectively. The above compounds ( Figure 13) are analogs of naphthalimide and phthalimide, but do not contain carbonyl groups.

a b
As can be seen from Figures 14 and 15 for acenaphthene and indane, i.e., compounds which do not contain carbonyl groups in the structure, there is no unusual aromatic proton behavior in the temperature-dependent 1 H-NMR, except for regular temperature shifts of unchanged multiplets.  Bis-naphthalimide derivatives are very sensitive to interactions with protic solvents, especially organic acids. Trifluoroacetic acid strongly interacts with the carbonyl groups of the dicarboximide ring, even at very low concentrations [40]. When the ratio of TFA-d to dicarboximide is very large, like in case where TFA-d is a solvent, the equilibrium constant between TFA-d and dicarboximide is shifted towards formation of a complex with strong intermolecular hydrogen bonds. It means that carbonyl group is caught in a cage of TFA-d and the flexibility of the carbonyl group will be very restricted. In such a case the rigid structure of the dicarboximide-TFA-d complex will be less sensitive to variable temperatures. The 1 H-NMR spectra of N,N′-(1,4-phenylene)-bis (1,8-naphthalimide) (NP2) at different temperatures in TFA-d are shown in Figure 16. Over a wide range of temperatures (288 K-333 K) no changes of the multiplicity of H-2, H-3 and H-4 occurred. This is a very strong additional evidence for the participation of carbonyl groups in the unusual temperature-dependent 1 H-NMR characteristics of the naphthalimide protons. It also allows us to firmly reject the notion of n-π interactions as an explanation for the temperature behavior of the 1 H-NMR of the aromatic protons of phthalimide and naphthalimide derivatives.

General Procedures
The 1 H-NMR spectra were recorded on a Bruker Avance DRX 600 MHz spectrometer over a wide range of temperatures. Typical conditions for the proton spectra were: pulse width 32°, acquisition time 5 s, FT size 32 K and digital resolution of 0.096 Hz per point. The 13 C-NMR spectra were measured with a Varian Gemini 300VT spectrometer, operating at 75.4614 MHz. Typical conditions for the carbon spectra were: pulse width 60°, FT size 60 K and digital resolution of 0.6 Hz per point, the number of scans varied from 1,200 to 10,000 per spectrum. 2D-NMR spectra taken to correctly assign of the chemical shifts of protons and carbon atoms were recorded at 298 K on a Bruker Avance DRX 600 spectrometer operating at the frequencies of 600.315 MHz ( 1 H) and 150.963 MHz ( 13 C), and equipped with a 5 mm triple-resonance inverse probe head [1H/31P/BB] with a self-shielded z gradient coil (90° 1H pulse width 9.0 μs and 13C pulse width 13.3 μs). Chemical shifts are given in ppm versus TMS as internal standard. Chemical shifts for temperature 1 H-NMR measurements are calculated versus chemical shift of solvent, assumed to be temperature independent. Infrared spectra were recorded in KBr pellets at 2 cm −1 resolution on a FT-IR Bruker IFS 66v/S instrument, evacuated to avoid water and CO 2 absorption. Melting points were determined on a Melt-Temp II capillary melting point apparatus and are uncorrected. The deuterated solvents (>97% D), 1,8-naphthalenedicarboxylic anhydride, 1,8-naphthalimide, acenaphthene, and indane were purchased from Aldrich (Poznań, Poland) and used without any additional purification. Ethyl iodoacetate was obtained by reaction of commercially available ethyl chloroacetate with sodium iodide in acetone as a solvent. N,N-bis- propyl]-N-dodecylamine (NP4). A mixture of N,N-bis- [3-(1,8naphthalimido)propyl]amine (5.0 g, 10.17 mmol), dodecyl bromide (4.0 g, 16.05 mmol), anhydrous Na 2 CO 3 (0.59 g, 5.6 mmol) and dimethylformamide (60 mL) was heated and stirred at 100-120 °C for 12 h. After evaporation of solvent the oily residue was dissolved in chloroform and the precipitated inorganic salts were filtered off. The viscous product which was obtained after evaporation of chloroform, solidified after three months. Yield: 6.3 g (89%), mp 62-65 °C. 1  N,N-bis- propyl]-N-propylamine (NP5). We have reported previously another synthesis of this compound [39]. A mixture of N,N-bis- [3-(1,8-naphthalimido)propyl]amine (NP4, 5.0 g, 10.2 mmol), propyl bromide (1.88 g, 16.1 mmol), anhydrous Na 2 CO 3 (0.59 g, 5.6 mmol) and dimethylformamide (60 mL) was heated and stirred at 100-120 °C for 10 h. Then, the mixture was cooled to 20 °C and solvent was evaporated under reduced pressure. The crude product was dissolved in chloroform and precipitated inorganic salts were filtered off. The solvent was evaporated and the pale-yellow residue was recrystallized twice from acetonitrile. Yield: 4.07 g (75%), mp 141-142 °C. 1 [3-(1,8-naphthalimido)propyl]-N-propylammonium iodide (NP8). A mixture of N,N-bis- [3-(1,8-naphthalimido)propyl]-N-propylamine (2.01 g, 3.77 mmol), an excess of freshly obtained ethyl iodoacetate (1.6 g, 7.50 mmol,) and acetonitrile (130 mL) was refluxed for 50 h.

Conclusions
New bis-naphthalimide derivatives containing functionalized spacers were obtained using 1,8-naphthalenodicarboxylic anhydride as a starting material. Yields of the reactions in most cases were over 75% in high boiling solvents. The obtained bis-naphthalimide derivatives are very stable. Most of the synthesized naphthalimide derivatives are barely soluble in water, however, in the presence of solubilizers, like gemini surfactants with high HLB value, their solubilities are satisfactory. The synthesized bis-naphthalimide derivatives have been studied by FTIR in the solid state and 1 H and 13 C-NMR in solution. The infrared spectra revealed some nonequivalency of the carbonyl groups in the solid state caused by the crystal structure. The carbonyl groups are very sensitive to polar protic organic solvents and formation of intermolecular hydrogen bonds between the carbonyl groups and trifluoroacetic acid has been shown by 13 C-NMR. A detailed 1 H-NMR study of the bis-naphthalimide derivatives at different temperatures demonstrated the unusual behavior of the aromatic protons of the naphthalimide rings. We proved that changing geometry of the carbonyl groups is responsible for this temperature behaviour of the aromatic protons of naphthalimide derivatives and n-π interactions play no role in the unusual temperature features of the 1 H-NMR spectra.