A Hexahomotrioxacalix[3]arene-Based Ditopic Receptor for Alkylammonium Ions Controlled by Ag⁺ Ions.

A receptor cone-1 based on a hexahomotrioxacalix[3]arene bearing three pyridyl groups was successfully synthesized, which has a C₃-symmetric conformation and is capable of binding alkylammonium and metal ions simultaneously in a cooperative fashion. It can bind alkylammonium ions through the -cavity formed by three aryl rings. This behaviour is consistent with the cone-in/cone-out conformational rearrangement needed to reorganize the cavity for endo-complexation. As a C₃-symmetrical pyridyl-substituted calixarene, receptor cone-1 can also bind an Ag⁺ ion, and the nitrogen atoms are turned towards the inside of the cavity and interact with Ag⁺. After complexation of tris(2-pyridylamide) derivative receptor cone-1 with Ag⁺, the original C₃-symmetry was retained and higher complexation selectivity for n-BuNH₃⁺ versus t-BuNH₃⁺ was observed. Thus, it is believed that this receptor will have a role to play in the sensing, detection, and recognition of Ag⁺ and n-BuNH₃+ ions.

1. Introduction

Over the past few decades, the development of artificial receptors for ion recognition, complexation, and transportation has proven to be an important topic in both environmental and supramolecular chemistry [1,2,3,4]. Given their ready availability, and their unique conformational and cavity-containing structures, together with their versatile molecular recognition properties, calixarenes have attracted a great deal of attention during the past several decades, and, indeed, calixarene chemistry has become an indispensable part of supramolecular science [5,6,7,8,9]. Calix[n]arenes can provide useful building blocks for host-guest type receptors by appropriate modification. For example, calix[4]arene derivatives incorporating crown ethers, amides, esters, and carboxylic acid groups have been shown to selectively extract metal ions [10]. Hexahomotrioxacalix[3]arenes, which are structurally related to both calixarenes and to crown ethers, have a three dimensional cavity with a potentially C3-symmetric structure, and have been shown to be useful ligands for metal cations [3]arenes: A review. Beilstein J. Org. Chem.. 2012 ">11,3]arene. J. Incl. Phenom. Macrocycl. Chem.. 2011 ">12,3]arene as a fluorescent chemosensor for Zn. Sens. Actuators B.. 2016 ">13,3]arene: A turn-on fluorescence chemosensor for Fe. Sens. Actuators B.. 2018 ">14], ammonium cations [3]arenes and Complexation between a Nitrohomooxacalix[3]arene Derivative and . J. Org. Chem.. 2002 ">15,16], and fullerene derivatives [3]arene Inclusion Complex and Anionic Porphyrin Polymer. J. Am. Chem. Soc.. 2001 ">17,3]arene-Based Dimeric Capsule Cross-Linked by a Pd. J. Am. Chem. Soc.. 1999 ">18].

Cation recognition by artificial receptors has attracted increasing attention due to the important roles played by ions in both environmental and biological systems [19,20]. All the known modes of cation binding by native and functionalized calixarenes exploit cation-π induced dipoles, or electrostatic interactions [21]. The most important calixarene-based cation receptors are obtained by the introduction of chelating units at the lower rather than at the upper rim. For example, calixarenes fully functionalized at the lower rim with ether groups show an affinity for alkali metal ions [22,23,24,25]. Shinkai et al. reported a series of calix[4]arene-crown-4 derivatives, among which a partial-cone derivative exhibits an exceptional Na+/K+ selectivity, as determined by ion-selective electrodes (ISEs) [23]. We also have developed a series of triazole-derived chemosensors for selective binding of heavy metal ions based on hexahomotrioxacalix[3]arene and thiacalix[4]arene scaffolds [3]arene: A Unique
C. Org. Lett.. 2011 ">26,27,3]arene for Zn. Tetrahedron. 2016 ">28]. For example, chemosensors derived from hexahomotrioxacalix[3]arene appended at the lower rim with pyrenyl groups via triazole linkers exhibited a highly selective affinity for the Pb2+ cation through enhancement of the monomer emission of the pyrene moiety in both organic and organic-aqueous solution [3]arene: A Unique
C. Org. Lett.. 2011 ">26].

On the other hand, hexahomotrioxacalix[3]arene derivatives that have C3 symmetry can also selectively bind ammonium ions, which play an important role in both chemistry and biology. The formation of intra-cavity endo-complexes of the resulting alkylammonium ions have been reported. Tripodal NH+···O interactions with the phenolic oxygen atoms and C–H···π interactions stabilized the complex [1,2,3,4,3]arenes: A review. Beilstein J. Org. Chem.. 2012 ">11]. Recently, our group reported the construction of C3 symmetrically functionalized hexahomotrioxacalix[3]arenes, which selectively recognized primary alkylammonium ions [3]arene Triamide Derivative having the Intramolecular Hydrogen-bonding Group. J. Incl. Phenom. Macrocycl. Chem.. 2005 ">29,30].

It is against this background that we describe herein the design, synthesis, and binding properties of receptor cone-1, based on hexahomotrioxacalix[3]arene, which recognizes alkylammonium cations and Ag+ with high association constants.

2. Results and Discussion

Cone-1, which is based on a hexahomotrioxacalix[3]arene, was synthesized by the method shown in Scheme 1. Cone-3 was prepared by O-alkylation of hexahomotrioxacalix[3]arene 2 with N,N-diethylchloroacetamide in the presence of NaH in refluxing THF according to the reported procedure in 85% yield [3]arene triamide derivatives having hydrogen-bonding groups. J. Incl. Phenom. Macrocycl. Chem.. 2001 ">31,3]arenes. Chem. Lett.. 1994 ">32]. Cone-4 was synthesized in 74% yield by hydrolyzing cone-3 in a refluxing mixture of NaOH/H2O/dioxane solution. The cone-hexahomotrioxacalix[3]arene triamide derivative (cone-1) was prepared in 81% yield by a condensation reaction between cone-4 and 2-aminopyridine in the presence of DCC (dicyclohexylcarbodiimide) and HOBt (1-hydroxybenzotriazole) at room temperature for 15 h in CH2Cl2.

Scheme 1

Synthesis of receptor cone-1.

In agreement with its C3-symmetric cone-in conformation, receptor cone-1 displays the following characteristic 1H and 13C-NMR spectroscopic features: (1) the cone-1 conformation is firmly established by the presence of the bridging methylene protons that have a Δδ separation between Hax and Heq of Δδ 0.41 ppm in the 1H-NMR spectrum (CDCl3). In the calix[4]arenes, the Δδ values of the ArCH2Ar methylene protons have been correlated with the orientation of the adjacent aromatic rings [33,34] and similar findings were previously observed with hexahomotrioxacalix[3]arenes [3]arene. J. Incl. Phenom. Macrocycl. Chem.. 2011 ">12,3]arene as a fluorescent chemosensor for Zn. Sens. Actuators B.. 2016 ">13]. (2) The 13C-NMR spectrum of receptor cone-1 in CDCl3 exhibited two peaks at δ 31 and 34 ppm for the tert-butyl carbons and a single peak at δ 69 ppm for the -OCH2- bridge linker carbons [35]. (3) The 1H-NMR spectrum of receptor cone-1 in CDCl3 revealed a single peak at δ 1.15 ppm for the tert-butyl protons and a single peak at δ 6.99 ppm for the aromatic protons, which was in agreement with a C3v-symmetric structure [36].

Single crystal X-ray diffraction studies of cone-1 shows a rather deformed cone conformation (Figure 1). Cone-1 crystallises as solvates incorporating either three methanol molecules, and one water molecule or with 2½ methanol molecules. Within each calixarene is a single N–H···O H-bond between a secondary amine moiety and a single ether oxygen atom. See experimental section and Table S1 for crystal data.

Figure 1

Side-view (a) and top-view (b) of the X-ray structure of cone-1. H-bonds shown as dashed lines; H(3)···O(8) = 2.29(2) Å, ∠N(3)–H(3)···O(8) = 147(2). Solvent molecules of crystallization and H atoms not involved in H-bonding omitted for clarity.

In cone-1∙3 MeOH∙H2O the calixarene molecule adopts a collapsed, or squashed, conformation to facilitate this H-bond and a π···π interaction between the arene rings C(13)–C(18) and C(25)–C(30), at a distance of 3.87 Å. The pyridyl groups C(46)–N(4) and C(53)–N(6) are aligned face-to-face but at a distance of 4.80 Å, which is too far for π···π stacking to be adopted. The structure of cone-1∙2.5 MeOH is very similar and is isomorphous (see Figures S7 and S8).

In order to investigate the ionophoric affinities of the receptor cone-1 for alkylammonium ions, the binding properties of receptor cone-1 as a ditopic receptor were investigated by means of 1H-NMR spectroscopic titration experiments, using n-butylammonium and t-butylammonium picrates as the substrates. Binding studies were carried out by adding increasing amounts of the appropriate salt to a 5.0 mM solution of receptor cone-1 in CDCl3/CD3CN co-solvent, so as to reach a 1:1 host/guest ratio. In the case of n-BuNH3+, the proton signals of receptor cone-1 were observed for both the complex and the free host, as shown in Figure 2. Upon increasing the amount of alkylammonium ions, the signals for receptor cone-1 decreased, and, finally, only signals for the complex were observed. Host-guest complexation/decomplexation was judged to be slow on the NMR time scale on the basis of preliminary titration experiments, which, in the presence of greater host than guest concentrations, revealed broadness for the receptor cone-1 peaks. The peak assigned to the aromatic hydrogen atoms of the hexahomotrioxacalix[3]arene unit underwent a significant down-field complexation-induced shift (CIS) (from δ 6.99 to 7.31 ppm), indicating that the cavity was ‘opening-up’ to make room for the incoming cationic guest.

Figure 2

Partial 1H-NMR spectra of receptor cone-1 (5.0 mM) in CDCl3/CD3CN (10:1, v/v); (a) cone-1; (b) cone-1 ⊃ n-BuNH3+ (0.6 equiv.); (c) cone-1 ⊃ n-BuNH3+ (1.0 equiv.).

This behaviour is consistent with a cone-in-cone-out conformational rearrangement needed to reorganize the cavity upon endo-complexation. On the other hand, there are two modes for receptor cone-1 to bind with n-butylammonium ions, i.e., either at the lower rim through the substituent moieties, or at the upper rim through the π-cavity formed by the three aromatic rings (Figure 3). The presence of the target n-BuNH3+ cation was evident from the appearance of high-field resonances for the included n-butyl chain as presented in Table 1 [37,38]. It suggests that the alkyl protons of the n-BuNH3+ ion reside inside the cavity of receptor cone-1 and are subjected to a shielding effect from the phenyl rings (Figure 3a) [3]arene-based Dimeric Capsule Constructed by a Pd. J. Am. Chem. Soc.. 2001 ">39,40,41,3]arene triacetic acid. J. Incl. Phenom. Macrocycl. Chem.. 2011 ">42]. This evidence suggests the binding occurs through the π-cavity formed by the three aromatic rings of the hexahomotrioxacalix[3]arene unit. This binding is attributed to the π-effect of the aromatic rings and is favoured, since both the host and the guest molecules have C3-symmetric conformations.

Figure 3

Two possible interactions between receptor cone-1 and n-BuNH3+.

Table 1

Selected proton chemical shifts (δ, ppm) (300 MHz, CDCl3:CD3CN, 10:1 v/v, 27 °C) of guest.a

		Chemical Shift of Proton
		CH3	CH3CH2	CH3CH2CH2	CH2
	Free	0.94	1.40	1.67	3.02
n-BuNH3+	Complex	0.88	0.30	−0.33	0.30
	Δδ	−0.06	−1.10	−2.00	−2.72
	Free	1.40
t-BuNH3+	Complex	−0.34
	Δδ	−1.74

a chemical shift (δ): ppm. Δδ = δcomplex − δfree.

Similar 1H-NMR spectroscopic titration experiments were conducted to assess the effect of t-BuNH3+, and the spectral changes upon complexation are shown in Table 1 and Figure S3. The association constants of receptor cone-1 with alkylammonium ions were determined and are presented in Table 2. It can be seen that the association constants were affected by the sizes of the respective alkyl groups. Thus, receptor cone-1 binds more readily to the linear alkyl chain ammonium ion than to the branched chain ammonium ion. These findings might be attributable to the greater ease of entering the cavity for the linear alkyl chain analogs, as well as the slower decomplexation rate of the ammonium ions.

Table 2

Association constants Ka (M−1) of host receptor cone-1 with alkylammonium ions, with and without Ag+ picrate salt. a,b

	Ka (M−1)
n-BuNH3+	2680 ± 155
n-BuNH3+ ⊂ [cone-1 ⊃ Ag+]	3270 ± 190
t-BuNH3+	360 ± 20
t-BuNH3+ ⊂ [cone-1 ⊃ Ag+]	No complexation

a Measured in CDCl3/CD3CN (10:1, v/v) at 27 °C by the 1H-NMR titration method, noting the chemical shift change of the NH proton; host concentration was 5.0 mM. b Alkylammonium cations were used as their picrate salts.

On the other hand, host receptor cone-1 was recently reported by us to also have excellent affinity and high selectivity for Ag+, Cu2+, and Al3+ ions during extraction studies [3]arene triamide derivatives having hydrogen-bonding groups. J. Incl. Phenom. Macrocycl. Chem.. 2001 ">31,3]arene triacetic acid. J. Incl. Phenom. Macrocycl. Chem.. 2011 ">42]. In particular, we reported that receptor cone-1 exhibited higher extractability for Ag+ (76.9%), with the Ag+ being complexed by the three pyridine groups via N–Ag+ interactions. Therefore, in order to determine optimized conditions for recognition and selectivity of the ammonium ions, the effects on 1H-NMR spectroscopic titrations of cone-1·Ag+ toward ammonium ions were studied in CDCl3/CD3CN (10:1, v/v). In the case of n-BuNH3+, partial 1H-NMR spectra (Figure 4) revealed that the proton resonances of the n-butyl chain were shifted upfield and the proton resonances of the aromatic hydrogen atoms of the hexahomotrioxacalix[3]arene units were shifted downfield by 0.11 ppm (from 6.99 to 7.29 ppm). These findings imply that Ag+ was encapsulated into the cavity formed by the pyridine rings, and the receptor cone-1 ‘stands up’ when n-BuNH3+ is included, because n-BuNH3+ enters into the cavity formed by the three aromatic rings.

Figure 4

Partial 1H-NMR spectra of receptor cone-1 (CDCl3/CD3CN (10:1, v/v), 5.0 mM); (a) cone-1; (b) cone-1 ⊃ Ag+ (1.0 equiv.); (c) cone-1 ⊃ Ag+ (1.0 equiv.) ⊃ n-BuNH3+ (0.5 equiv.); (d) cone-1 ⊃ Ag+ (1.0 equiv.) ⊃ n-BuNH3+ (1.0 equiv.).

Receptor cone-1 is capable of binding both Ag+ and n-BuNH3+ simultaneously in a cooperative fashion. Thus, the potential to act as a ditopic receptor to complex with these two cations will be of great interest in coordination chemistry. Interestingly, similar 1H-NMR spectroscopic titration experiments were conducted to assess the effect of t-BuNH3+, but no significant changes in the resulting 1H-NMR spectra were observed. Thus, it is evident that receptor cone-1 has lost the capacity to bind t-BuNH3+ when in the presence of Ag+ ion.

When the order of addition of Ag+ and alkylammonium ions was changed, in the case of n-BuNH3+, the resulting 1H-NMR spectrum is identical to that obtained in the previous section (Figure S4). Furthermore, in the case of t-BuNH3+, the resulting final 1H-NMR spectrum is the same as that for the complex cone-1·Ag+. These findings indicate that receptor cone-1 does not selectively recognize alkylammonium ions efficiently in the absence of Ag+ ion. Interestingly, when Ag+ ion was added to the present system, Ag+ provided an excellent pathway of organizing alkylammonium ions binding groups for optimal host-guest interactions by adjusting the size of the cavity of receptor cone-1. The association constants of receptor cone-1 with the alkylammonium ions in the absence of and in the presence of Ag+ as calculated from the chemical shift changes of the NH protons are summarized in Table 2. Interestingly, the association constant Ka for the complexation of receptor cone-1 with n-BuNH3+ (Ka = 2680 ± 155) is much larger than that when using t-BuNH3+ (Ka = 360 ± 20). Thus, in the presence of Ag+, the complexation with n-BuNH3+ increases compared with t-BuNH3+, presumably due to the different cavity size of receptor cone-1.

The geometries of the molecular structures were optimized with the PBE0 functional theory with the LANL2DZ basis set. The DFT level of theory used the hybrid Perdew-Burke-Ernzerhof parameter free-exchange correlation functional PBE0 (PBE1PBE in the Gaussian realization) [43,44] with the Hay and Wadt effective core potential LANL2DZ basis set [45,46,47]. The starting structure was generated using SpartanPro10 with the MMFF94 method [48]. The generated structures were then imported into Gaussian-09 Revision D.01 (Wallingford, CT, USA) [49]. and were geometry-optimized in the gas phase. The calculated binding or interaction energies (IE) for cone-1 ⊃ n-BuNH3+, cone-1 ⊃ t-BuNH3+, cone-1 ⊃ Ag+ , and n-BuNH3+ ⊃ [cone-1 ⊃ Ag+] are −298.8 kJ mol−1; –268.3 kJ·mol−1; –457.1 kJ·mol−1, and –525.8 kJ·mol−1, respectively, and were in agreement with the trend for the observed complexation data obtained by the 1H-NMR spectroscopic titration experiments (Figure 5). A conceptualization of complexation by the receptor cone-1 is shown in Figure 6.

Figure 5

Geometry-optimized (PBE0/LANL2DZ) structures of cone-1 and its complex with Ag+ and n-BuNH3+. Left: The free cone-1, Middle: 1:1 cone-1 ⊃ Ag+ complex, and Right: n-BuNH3+ ⊂ [cone-1 ⊃ Ag+] complex. Colour code: carbon = black grey, oxygen atom = red, nitrogen = blue, nitrogen (n- BuNH3+) = magenta and Ag+ = purple. Hydrogen atoms on the host molecule have been removed for clarity.

Figure 6

A plausible binding model. The green circles represent the -CONH-, and the hexagons (purple color) represent the pyridyl groups.

3. Experimental Section

3.1. General

All melting points were determined using a Yanagimoto MP-S1melting point apparatus (Kyoto, Japan). 1H-NMR spectra were recorded at 300 MHz with a Nippon Denshi JEOL FT-300 NMR spectrometer (Tokyo, Japan) with SiMe4 as an internal reference; J values are given in Hz. IR spectra were measured as KBr pellets on a Nippon Denshi JIR-AQ2OM spectrophotometer. UV-vis. spectra were measured with a Shimadzu 240 spectrophotometer (Tokyo, Japan). Mass spectra were obtained on a Nippon Denshi JMS-01SG-2 mass spectrometer at an ionization energy of 70 eV using a direct inlet system through GLC. Elemental analyses were performed with a Yanaco MT-5 (Kyoto, Japan).

3.2. Materials

Synthesis of cone-7,15,23-tri-tert-butyl-25,26,27-tris[(N,N-diethylaminocarbonyl)methoxy]-2,3,10,11,18,19-hexahomo-3,11,19-trioxacalix[3]arene (cone-3) was carried out according to the previously reported procedure [3]arene triamide derivatives having hydrogen-bonding groups. J. Incl. Phenom. Macrocycl. Chem.. 2001 ">31].

3.3. Preparation of cone-4

A mixture of cone-3 (500 mg, 0.55 mmol) and 15 mL of an aqueous 1.0 M NaOH solution in dioxane (15 mL) was heated at reflux for 72 h under N2. After cooling the reaction mixture to room temperature, the solution was acidified with 1M HCl (pH 1–2) and extracted three times (30 mL × 3) with ethyl acetate. The organic layer was separated, dried (MgSO4), and the solvent was evaporated. The residue was dried to afford cone-4, which was washed with methanol to afford the desired product cone-4 as a white solid (320 mg, 74%), m.p. 227–229 °C (lit. [42], m.p. 227–229 °C).

3.4. Preparation of cone-1

A solution of cone-4 (100 mg, 0.13 mmol), 2-aminopyridine (120 mg, 1.11 mmol), and HOBt (75 mg, 0.49 mmol) in dry CH2Cl2 (15 mL) was cooled in an ice bath. DCC (560 mg, 2.71 mmol) and dry CH2Cl2 (5 mL) were added, and the mixture was stirred for an additional 15 h at r.t., and then the solvent was evaporated. The residue was extracted three times (3 × 30 mL) with ethyl acetate. The organic layer was separated, dried (MgSO4), and the solvent was evaporated. The residue was dried to afford 1 as a colourless oil, which was recrystallized from CHCl3–hexane (1:3 v/v) to afford the desired product cone-1 (85 mg, 81%) as colourless prisms. M.p. 217–218 °C. IR: νmax (KBr)/cm−1 3345, 3015, 2915, 2867, 1758, 1483, 1456, 1363, 1234, 1199, 1094 and 1058. 1H-NMR (300 MHz, CDCl3): δH = 1.15 (s, 27H, t-Bu-H), 4.49 (s, 6H, –CH2), 4.53 (d, J = 11 Hz, 6H, –OCH2), 4.94 (d, J = 11 Hz, 6H, –OCH2), 6.89 (m, 3H, Py–H), 6.99 (s, 6H, Calix-H), 7.47 (m, 3H, Py–H), 7.87 (d, 3H, J = 8.0 Hz, Py–H), 8.17 (d, J = 8.0 Hz, 3H, Py–H) and 9.69 (s, 3H, NH) ppm. 13C-NMR (100 MHz, CDCl3): δC = 31.42, 34.26, 69.65, 73.16, 113.92, 119.65, 126.94, 130.54, 137.58, 147.05, 147.74, 150.74, 152.58 and 167.45 ppm. FABMS: m/z calcd for C57H66N6O9 978.17 [M+]; found 978.45 [M+]. C57H66N6O9 (978.17): calcd C 69.92, H 6.79; found: C 69.74, H 6.93.

3.5. 1H-NMR Spectroscopic Complexation Experiments

To a CDCl3/CD3CN solution (10:1, v/v) of cone-1 (4 × 10−3 M) in an NMR tube was added 1.0 equivalent of related metal perchlorates. The spectrum was recorded after addition, and the temperature of the NMR probe was kept constant at 27 °C.

The 1H-NMR spectroscopic data of the host molecules of the respective complexes only are given below: The 1H-NMR data of the most representative complexes is given below:

Receptor : δH (CDCl3/CD3CN, 10:1): 1.24 (s, 27H, t-Bu–H), 4.36 (bs, 6H, –OCH), 4.94 (bs, 6H, –CH), 5.32 (bs, 6H, –OCH), 6.91 (m, 3H, Py–H), 7.31 (s, 6H, Calix–H), 7.45 (m, 3H, Py–H), 7.91 (m, 3H, Py–H), 8.17 (d, 3H, J = 3.0 Hz, Py–H) and 9.35 (s, 3H, NH) ppm.

Receptor : δH (CDCl3/CD3CN, 10:1): 1.23 (s, 27H, t-Bu–H), 4.49 (bs, 6H, –OCH), 5.11 (bs, 6H, –CH), 5.40 (m, 6H, –OCH), 6.93 (t, J = 6.6 Hz, 3H, Py–H), 7.29 (s, 6H, Calix–H), 7.48 (m, 3H, Py–H), 7.91 (m, 3H, Py–H), 8.17 (d, 3H, J = 3.0 Hz, Py–H) and 9.35 (s, 3H, NH) ppm.

Receptor δH (CDCl3/CD3CN, 10:1): 1.01 (s, 27H, t-Bu–H), 4.20 (d, J = 12.0 Hz, 6H, –OCH), 4.28 (s, 6H, –CH), 4.84 (d, 6H, J = 12.0 Hz, –OCH), 6.81 (s, 6H, Calix–H), 7.07 (m, 3H, Py–H), 7.76 (m, 6H, Py–H), 8.17 (d, 3H, J = 3.8 Hz, Py–H) and 9.96 (s, 3H, NH) ppm.

Receptor : δH (CDCl3/CD3CN, 10:1): 1.26 (s, 27H, t-Bu–H), 4.35 (d, 6H, J = 9 Hz, –OCH), 4.99 (d, J = 9 Hz, 6H, –CH), 5.32 (b, 6H, –OCH), 7.05 (b, 3H, Py–H), 7.29 (s, 6H, Calix–H), 7.62 (m, 3H, Py–H), 7.92 (d, 3H, J = 7.5 Py–H), 8.19 (d, 3H, J = 4.5 Hz, Py–H) and 9.80 (s, 3H, NH) ppm.

3.6. Single-Crystal X-Ray Diffraction Measurements for cone-1

A suitable single crystal (size ca. 0.30 × 0.17 × 0.03 mm3) was selected and mounted on a Bruker APEX 2 CCD diffractometer (Billerica, MA, USA) equipped with synchrotron radiation (λ = 0.7805 Å) at ALS Station 11.3.1 [49]. Data were corrected for Lorentz and polarisation effects and for absorption [50]. Crystal data for cone-1·3 (CH4O)·H2O: C57H66N6O9·3(CH4O)·H2O, M = 1093.30, monoclinic, C2/c, a = 26.1641(11), b = 15.4995(6), c = 28.5153(11) Å, β = 94.063(3)°, V = 11534.8(8) Å3, Z = 8, μ = 0.09 mm−1, 113193 reflections measured, 22109 unique, Rint = 0.074, R1[F2 > 2σ(F2)] = 0.067, wR2 (all data) = 0.205 [51]. The o-pyridyl group C(53) > N(6) and the tert-butyl group C(7) > C(10) were modelled as fully disordered over two sets of positions. The solvent molecules of crystallisation were modelled using the Platon Squeeze procedure due to substantial disorder [52]. Crystal data for cone-1·2.5(CH4O): C57H66N6O9·2.5(CH4O, M = 1059.26, monoclinic, C2/c, a = 26.308(2), b = 15.6159(14), c = 28.644(3) Å, β = 94.1811(15)°, V = 11736.3(18) Å3, Z = 8, μ = 0.08 mm−1, 67896 reflections measured, 17827 unique, Rint = 0.053, R1[F2 > 2σ(F2)] = 0.059, wR2 (all data) = 0.178 [50]. The o-pyridyl group C(51) > N(6) and the tert-butyl group C(27) > C(29) were modelled as fully disordered over two sets of positions. The solvent molecules of crystallisation were modelled using the Platon Squeeze procedure due to substantial disorder except for atom O(10) due to its proximity to the disordered ring [52]. Further details of the crystal parameters, data collection conditions, and refinement parameters are summarized in Table S2. CCDC 1500977 & 1817851 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.

4. Conclusions

In conclusion, a novel receptor cone-1 based on hexahomotrioxacalix[3]arene was successfully synthesized, and was found to possess a C3-symmetric conformation. It can bind alkylammonium ions through the π-cavity formed by three aryl rings. As a C3-symmetrical pyridyl-substituted calixarene, ionophore receptor cone-1 can bind an Ag+ ion, and after complexation of the tris(2-pyridylamide) derivative receptor cone-1 with Ag+, the original C3-symmetry has been retained, and the complex showed high selectivity for n-BuNH3+, but not for t-BuNH3+. Thus, it is believed that this receptor will have a role to play in the sensing, detection, and recognition of Ag+ and n-BuNH3+ ions simultaneously.