Crystal structure of a hydrate of 1,3,5-substituted 2,4,6-tri­alkyl­benzene bearing hy­droxy­methyl and pyridinyl­amino groups

Manuel Stapf; Wilhelm Seichter; Monika Mazik

doi:10.1107/S2056989026008856

. 2026 Sep 8;82(Pt 10):1149–1153. doi: 10.1107/S2056989026008856

Crystal structure of a hydrate of 1,3,5-substituted 2,4,6-trialkylbenzene bearing hydroxymethyl and pyridinylamino groups

Manuel Stapf ^a, Wilhelm Seichter ^a, Monika Mazik ^a,^*

Editor: T Akitsu^b

PMCID: PMC13637998 PMID: 42836246

In the asymmetric unit, two molecules of the 1,3,5-substituted 2,4,6-trialkylbenzene and three water molecules are connected by hydrogen bonds, forming well-defined complexes that constitute the smallest supramolecular entities.

Keywords: crystal structure, hydrogen bonding, hydroxymethyl group, hydrate, water cluster, supramolecular synthons

Abstract

The asymmetric unit of the title compound, (3,5-bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate, C₂₉H₄₀N₄O·1.5H₂O, 1·1.5H₂O, contains two crystallographically independent molecules (I and II) and three water molecules [(1)₂(H₂O)₃]. These components are connected by O—H⋯O and N—H⋯O hydrogen bonds to form a 2:3 complex. Within this structural unit, the three water molecules and one of the hydroxymethyl O atoms create a strongly distorted eight-membered R₄³(8) supramolecular synthon. In addition, the three water molecules form a structure unit that can be defined as a D3 water cluster. In the crystal, neighbouring 2:3 complexes are linked by N—H⋯O and O—H⋯N hydrogen bonds into infinite strand-like aggregates extending along the a-axis direction. The pattern of non-covalent intermolecular bonding is completed by numerous C—H⋯π arene interactions. The crystal contains highly disordered solvent molecules that could not be refined to an acceptable level. Their contribution to the diffraction intensities was therefore removed using the BYPASS routine in OLEX2, and these solvent molecules were excluded from the reported molecular weight and crystal density.

1. Chemical context

Carbohydrate-binding proteins employ a variety of functional groups to achieve the selective recognition of carbohydrate substrates. Among these, the hydroxyl side chains of serine and threonine residues frequently contribute to binding interactions, as revealed by crystal structures of protein–carbohydrate complexes (Sauter et al., 1992 ▸; Naismith & Field, 1996 ▸; Sharon & Lis, 2007 ▸). The molecular recognition strategies adopted by such proteins have provided valuable inspiration for the design of artificial carbohydrate receptors (Davis & Wareham, 1999 ▸; Mazik, 2012 ▸; Manick et al., 2023 ▸). In this context, hydroxy groups have also been incorporated as structural elements for carbohydrate recognition in both acyclic (Mazik & Buthe, 2008 ▸; Mazik & Kuschel, 2008 ▸; Carrero et al., 2013 ▸; Stapf et al., 2023 ▸; Stapf & Mazik, 2026 ▸) and macrocyclic (Amrhein et al., 2016 ▸; Amrhein & Mazik, 2021 ▸) receptor architectures. Furthermore, representatives of the acyclic receptors bearing hydroxy groups have demonstrated the ability to participate in the molecular recognition of substrates beyond carbohydrates, such as hydronium and hydroxide ions (Stapf et al., 2015 ▸). This highlights their broader applicability in artificial receptor design.

The hydroxymethyl-containing compound described here belongs to the class of 1,3,5-substituted 2,4,6-trialkylbenzene derivatives and was synthesized as part of our investigations into the relationship between structure and binding affinity in carbohydrate recognition.

2. Structural Commentary

Compound 1 crystallizes from acetonitrile in the form of colourless platelets in the monoclinic space group P2₁/n. The asymmetric unit comprises two crystallographically independent organic molecules of 1 (labelled I and II) and three water molecules, which are interconnected through O—H⋯O and N—H⋯O hydrogen bonds in the manner shown in Fig. 1 ▸. Additionally, the crystal contains disordered solvent molecules (acetonitrile) that could not be refined satisfactorily. Therefore, a modified data set was generated using the BYPASS routine (van der Sluis & Spek, 1990 ▸) of the OLEX2 program, in which the contribution of the disordered molecular species to the structure factors has been eliminated.

(a) Perspective view of the content of the asymmetric unit of the title compound including labelling of non-hydrogen atoms and ring specification (A–C, A′–C′). The displacement ellipsoids are drawn at the 50% probability level. (b) Ball-and-stick representation of the 2:3 complex of compound 1 and water molecules. Broken lines represent hydrogen-bond interactions.

In the crystal, both molecules I and II adopt a geometry in which the pyridinyl-containing side arms and the hydroxymethyl OH group are located on one side of the central aromatic ring, while the ethyl substituents are directed towards the opposite side, resulting in an alternating ababab arrangement (a = above, b = below; Das & Barbour, 2009 ▸; Koch et al., 2017 ▸; Schulze et al., 2017 ▸). Despite their overall structural similarity, the two independent molecules differ slightly in their conformations. In the case of molecule I, the inclination angles of the pyridine rings with respect to the plane of the benzene ring are 82.2 (1) and 87.6 (1)°, whereas the corresponding angles for molecule II are 76.1 (1) and 82.8 (1)°. The dihedral angles between the pyridinyl units are 39.4 (1) and 48.2 (1)°, respectively. Although the functionalized side arms of the molecules adopt an extended conformation, they exhibit different degrees of torsion. This is evident from the values for the torsion angles along the atomic sequences C_benz—C—N—C_pyr, which are 170.5 (1) and −162.3 (1)° for molecule I and 176.3 (1) and 173.0 (1)° for molecule II.

3. Supramolecular features

The 2:3 complex of compound 1 and water molecules, shown in Fig. 1 ▸, represents the basic supramolecular unit of the crystal structure. Within this unit, the water molecules form a type D3 cluster (Infantes & Motherwell, 2002 ▸; Infantes et al., 2003 ▸). Hydrogen-bond formation between terminal hydrogen atoms of this cluster and the hydroxymethyl atom O2 of molecule II results in formation of a cyclic synthon of O—H⋯O bonds [d(H⋯O) = 1.89 (2)–1.98 (2) Å; Table 1 ▸], the structure of which can be described by the graph set Inline graphic (8) (Etter, 1991 ▸; Bernstein et al., 1995 ▸). Furthermore, the OH groups of the non-equivalent molecules form an O—H⋯O bond with one another [d(H⋯O) = 1.78 (2) Å], while the amino hydrogen atoms of molecule I are involved in the formation of N—H⋯O bonds [d(H⋯O) = 2.09 (1), 2.03 (2) Å] with the water oxygen atoms O4 and O5. Fig. 2 ▸ illustrates the linking of the complexes via hydrogen bonding resulting in the formation of an infinite strand-like molecular aggregate that extends in direction of the crystallographic a axis. Its structure reveals that, in addition to the aforementioned eight-membered motif (light pink), other cyclic and chain-like synthons are present in the pattern formed by hydrogen bonds.

Table 1. Hydrogen-bond geometry (Å, °).

Cg(A) represents the centroid of the C1–C6 ring; Cg(B) represents the centroid of the C11–C15/N2 ring; Cg(C) represents the centroid of the C21–C25/N4 ring; Cg(A′) represents the centroid of the C30–C35 ring; Cg(B′) represents the centroid of the C40–C44/N6 ring; Cg(C′) represents the centroid of the C50–C54/N8 ring.

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1⋯O5	0.87 (2)	2.03 (2)	2.878 (2)	165 (2)
N3—H3⋯O4	0.86 (1)	2.09 (1)	2.9326 (19)	165 (2)
O1—H1A⋯O3ⁱ	0.84 (1)	1.82 (1)	2.6631 (17)	174 (2)
N5—H5⋯O4ⁱ	0.87 (1)	2.44 (2)	3.1926 (18)	145 (2)
O2—H2⋯O1	0.84 (1)	1.78 (2)	2.6169 (15)	171 (2)
O3—H3A⋯O4	0.86 (1)	1.95 (2)	2.7938 (19)	166 (2)
O3—H3B⋯O5	0.85 (1)	1.89 (2)	2.7167 (19)	165 (3)
O4—H4A⋯N6ⁱⁱ	0.85 (1)	1.94 (1)	2.7718 (17)	167 (2)
O4—H4B⋯O2	0.85 (1)	1.93 (2)	2.7426 (15)	161 (2)
O5—H5A⋯N8ⁱⁱ	0.85 (1)	1.93 (2)	2.7681 (19)	170 (2)
O5—H5B⋯O2	0.84 (1)	1.98 (2)	2.7946 (16)	163 (2)
C9—H9C⋯Cg(B)ⁱ	0.98	2.84	3.637 (2)	139
C19—H19A⋯Cg(A’)ⁱⁱⁱ	0.98	2.71	3.512 (2)	139
C38—H38A⋯Cg(B’)ⁱⁱ	0.98	2.73	3.612 (2)	150
C45—H45C⋯Cg(C)ⁱ	0.98	2.98	3.916 (2)	161
C48—H48B⋯Cg(A)^iv	0.98	2.83	3.563 (2)	133
C58—H58A⋯Cg(C’)ⁱⁱ	0.98	2.74	3.613 (2)	149

Open in a new tab

Symmetry codes: (i) Inline graphic ; (ii) ; (iii) ; (iv) .

(a) Excerpt of the strand-like supramolecular aggregates in the crystal structure of the title compound including the labelling of the acceptor atoms involved in hydrogen bonding. The supramolecular synthons (rings, chains) are marked by colour highlighting. (b) Schematic illustration of the ring synthons. All of the hydroxymethyl and pyridinylamino groups shown here are part of molecule II.

In the case of the ring synthon of the structure Inline graphic (8) (yellow), the amino hydrogen atom H7 and the ring nitrogen atom N8 of a pyridinylamino group in molecule II act as binding sites, so that this synthon contains an O—H⋯O [d(H⋯O) = 1.89 (2) Å], N—H⋯O [d(H⋯O) = 2.54 (2) Å] and an O—H⋯N hydrogen bond [d(H⋯N) = 1.93 (2) Å].

Another ring synthon [ Inline graphic (6) (purple)] is formed by the second pyridinylamino group of this molecule and comprises N—H⋯O [d(H⋯O) = 2.44 (2) Å] and O—H⋯N hydrogen bonds [d(H⋯N) = 1.94 (1) Å]. The chain-like paths of the hydrogen bonds marked in green and orange, can both be described by the graph set Inline graphic (8). In addition to the hydrogen bonds involving OH and NH groups, a large number of C—H⋯π interactions [d(H⋯Cg) = 2.71–2.98 Å; Nishio et al., 1995 ▸], in which all arene units act as acceptors, contribute to the consolidation of the crystal structure.

The packing diagram shown in Fig. 3 ▸ indicates that the structure formed by the molecules features channel-like voids extending along the crystallographic a axis, with an approximately elliptical cross-section profile. The walls of these voids are essentially defined by the less polar parts of the molecules of 1. These cavities accommodate the disordered solvent molecules. The volume of the potentially solvent-accessible voids is 566 Å³ (9.3%) per unit cell, to which 122 electrons can be assigned. Fig. 4 ▸ shows the surface profile of the crystal voids.

Packing diagram of the title compound viewed down the crystallographic a axis. Broken lines represent hydrogen-bond interactions. The channel-like voids are marked in grey.

Representation of the surface profile (green mesh) of the crystal voids.

Regarding the D3 water cluster mentioned above, it should be noted that such a discrete chain of three water molecules has also been observed in the cavity of another 1,3,5-substituted 2,4,6-trialkylbenzene containing pyridinyl and phenanthrolinyl groups (Mazik & Hartmann, 2008 ▸; Mazik et al., 2009 ▸).

4. Database survey

The Cambridge Structural Database (CSD, Version 6.01, update February 2026; Groom et al., 2016 ▸) was searched for fully alkyl-substituted benzene derivatives bearing at least one hydroxymethyl substituent. This search yielded eight hits, which were reduced to five relevant structures after excluding compounds containing metal ions.

Crystallization of 1,3,5-tris(hydroxymethyl)-2,4,6-triethylbenzene from wet tetrahydrofuran (THF) affords an inclusion complex with a hydronium-hydroxide ion pair (CSD refcode BUGMAT; Stapf et al., 2015 ▸). The hydroxyl groups of the host molecule bind the ions through O—H⋯O hydrogen bonds, thereby generating a coordination environment comparable to the hydration sphere of water molecules. Under modified crystallization conditions, however, the THF solvate of the same compound is obtained (BUGMEX; Stapf et al., 2015 ▸). In contrast, the methyl-substituted analogue, 1,3,5-tris(hydroxymethyl)-2,4,6-trimethylbenzene (BUGLUM; Stapf et al., 2015 ▸), exhibits a lower degree of preorganization and crystallizes as a solvent-free structure. Hexakis(hydroxymethyl)benzene (YICFIA; Rothenberger & Ponikiewski, 2007 ▸) adopts a crystal conformation in which three adjacent hydroxymethyl groups are oriented above and the remaining three below the plane of the benzene ring. This arrangement facilitates the formation of both intra- and, in particular, intermolecular O—H⋯O hydrogen bonds. Likewise, the molecules of 1,4-bis(hydroxymethyl)-2,3,5,6-tetramethylbenzene (OJEZUY; Britton, 2003 ▸) are interconnected by O—H⋯O hydrogen bonds to form a three-dimensional network.

5. Synthesis and crystallization

The synthesis of compound 1 was performed according to the literature (Mazik & Kuschel, 2008 ▸). Crystals suitable for single crystal X-ray diffraction were obtained by slow evaporation of acetonitrile from a solution of this compound at ambient temperature. The acetonitrile was used without prior drying, and the water molecules observed in the crystal structure can be attributed to residual water in the solvent. Analysis data: ¹H NMR (500 MHz, CDCl₃, ppm): δ = 1.22 (t, 3H, ³J = 7.5 Hz, CH₂CH₃), 1.24 (t, 6H, ³J = 7.5 Hz, CH₂CH₃), 2.23 (s, 6H, ArCH₃), 2.35 (s, 6H, ArCH₃), 2.74 (q, 2H, ³J = 7.5 Hz, CH₂CH₃), 2.84 (q, 4H, ³J = 7.5 Hz, CH₂CH₃), 4.20 (br, 2H, CH₂NH), 4.37 (d, 4H, ³J = 4.2 Hz, CH₂NH), 4.76 (s, 2H, CH₂OH), 6.08 (s, 2H, ArH), 6.34 (s, 2H, ArH); ¹³C NMR (125 MHz, CDCl₃, ppm): δ = 16.8 (CH₂CH₃), 17.0 (CH₂CH₃), 21.1 (ArCH₃), 22.8 (CH₂CH₃), 23.0 (CH₂CH₃), 24.2 (ArCH₃), 40.6 (CH₂NH), 58.9 (CH₂OH), 103.6 (ArC), 113.9 (ArC), 133.1 (ArC), 134.8 (ArC), 143.7 (ArC), 144.1 (ArC), 148.9 (ArC), 156.6 (ArC), 158.2 (ArC); IR (ATR, cm⁻¹): 3318, 2961, 2918, 2866, 1609, 1568, 1494, 1452, 1372, 1320, 1229, 1207, 1163, 1010, 981, 813, 751, 535.

6. Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸. The non-hydrogen atoms were refined anisotropically. The positions of the hydrogen atoms bound to O and N were found in difference-Fourier maps and the O—H and N—H distances refined to a target value of 0.84 (1) and 0.89 (1) Å, respectively. All other hydrogen atoms were positioned geometrically and allowed to ride on their parent atoms: C—H = 0.95 Å for aryl H atoms, C—H = 0.99 Å for methylene groups and C—H = 0.98 Å for methyl groups with U_iso(H) = 1.5U_eq(C) for methyl groups and U_iso(H) = 1.2U_eq(C) for other hydrogen atoms.

Table 2. Experimental details.

Crystal data
Chemical formula	2C₂₉H₄₀N₄O·3H₂O
M _r	975.34
Crystal system, space group	Monoclinic, P2₁/n
Temperature (K)	123
a, b, c (Å)	8.2668 (1), 30.7552 (7), 23.8216 (4)
β (°)	91.142 (1)
V (Å³)	6055.37 (19)
Z	4
Radiation type	Mo Kα
μ (mm⁻¹)	0.07
Crystal size (mm)	0.32 × 0.14 × 0.11 × 0.09 (radius)

Data collection
Diffractometer	Stoe Stadivari
Absorption correction	Integration (X-RED32, Stoe, 2024 ▸)
T_min, T_max	0.982, 0.995
No. of measured, independent and observed [I > 2σ(I)] reflections	68973, 13195, 10231
R _int	0.028
(sin θ/λ)_max (Å⁻¹)	0.639

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.048, 0.122, 1.02
No. of reflections	13195
No. of parameters	691
No. of restraints	12
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.32, −0.23

Open in a new tab

Computer programs: X-AREAPilatus3_SV, Recipe and Integrate and X-RED (Stoe, 2024 ▸), SHELXT2018/2 (Sheldrick, 2015a ▸), SHELXL2019/3 (Sheldrick, 2015b ▸) and OLEX2 (Dolomanov et al., 2009 ▸).

Supplementary Material

Crystal structure: contains datablock(s) I. DOI: 10.1107/S2056989026008856/jp2032sup1.cif

e-82-01149-sup1.cif^{(2.3MB, cif)}

Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989026008856/jp2032Isup2.hkl

e-82-01149-Isup2.hkl^{(1MB, hkl)}

e-82-01149-Isup3.cml^{(10.9KB, cml)}

Supporting information file. DOI: 10.1107/S2056989026008856/jp2032Isup3.cml

CCDC reference: 2583267

Additional supporting information: crystallographic information; 3D view; checkCIF report

Acknowledgments

Open Access Funding by the Publication Fund of the Technische Universität Bergakademie Freiberg is gratefully acknowledged.

supplementary crystallographic information

(3,5-Bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate. Crystal data

2C₂₉H₄₀N₄O·3H₂O	F(000) = 2120
M_r = 975.34	D_x = 1.070 Mg m⁻³
Monoclinic, P2₁/n	Mo Kα radiation, λ = 0.71073 Å
a = 8.2668 (1) Å	Cell parameters from 61413 reflections
b = 30.7552 (7) Å	θ = 1.8–29.8°
c = 23.8216 (4) Å	µ = 0.07 mm⁻¹
β = 91.142 (1)°	T = 123 K
V = 6055.37 (19) Å³	Plate, colourless
Z = 4	0.32 × 0.14 × 0.11 × 0.09 (radius) mm

Open in a new tab

(3,5-Bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate. Data collection

Stoe Stadivari diffractometer	13195 independent reflections
Radiation source: Primux 50 Mo	10231 reflections with I > 2σ(I)
Graded multilayer mirror monochromator	R_int = 0.028
Detector resolution: 5.81 pixels mm^-1	θ_max = 27.0°, θ_min = 1.8°
rotation method, ω scans	h = −10→10
Absorption correction: integration (XRED32, Stoe, 2024)	k = −39→39
T_min = 0.982, T_max = 0.995	l = −30→30
68973 measured reflections

Open in a new tab

(3,5-Bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate. Refinement

Refinement on F²	Primary atom site location: dual
Least-squares matrix: full	Hydrogen site location: mixed
R[F² > 2σ(F²)] = 0.048	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.122	w = 1/[σ²(F_o²) + (0.0499P)² + 2.6826P] where P = (F_o² + 2F_c²)/3
S = 1.02	(Δ/σ)_max = 0.001
13195 reflections	Δρ_max = 0.32 e Å⁻³
691 parameters	Δρ_min = −0.23 e Å⁻³
12 restraints

Open in a new tab

(3,5-Bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate. Special details

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Open in a new tab

(3,5-Bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate. Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²)

	x	y	z	U_iso*/U_eq
C1	0.47235 (16)	0.21319 (5)	0.63944 (6)	0.0234 (3)
C2	0.55636 (17)	0.17364 (5)	0.63758 (6)	0.0257 (3)
C3	0.70858 (17)	0.17176 (5)	0.61240 (6)	0.0250 (3)
C4	0.77677 (16)	0.20923 (4)	0.58941 (6)	0.0220 (3)
C5	0.69081 (16)	0.24846 (4)	0.59037 (6)	0.0214 (3)
C6	0.54056 (16)	0.25097 (4)	0.61683 (6)	0.0228 (3)
C7	0.30872 (17)	0.21518 (5)	0.66683 (6)	0.0273 (3)
H7A	0.244636	0.239518	0.650716	0.033*
H7B	0.248771	0.187814	0.659618	0.033*
C8	0.48126 (19)	0.13303 (5)	0.66188 (7)	0.0353 (4)
H8A	0.410659	0.141203	0.693264	0.042*
H8B	0.567864	0.113861	0.677037	0.042*
C9	0.3816 (2)	0.10826 (6)	0.61740 (9)	0.0465 (5)
H9A	0.451639	0.099720	0.586589	0.070*
H9B	0.294535	0.127011	0.602838	0.070*
H9C	0.334719	0.082216	0.634327	0.070*
C10	0.80491 (18)	0.12966 (5)	0.61329 (7)	0.0306 (3)
H10A	0.730775	0.104378	0.612616	0.037*
H10B	0.874540	0.128029	0.580020	0.037*
C11	0.98936 (18)	0.09411 (5)	0.68361 (7)	0.0323 (3)
C12	1.09036 (19)	0.02518 (5)	0.67132 (8)	0.0377 (4)
C13	1.15631 (19)	0.02462 (5)	0.72469 (8)	0.0405 (4)
H13	1.213258	−0.000326	0.737845	0.049*
C14	1.13959 (19)	0.06075 (6)	0.75959 (8)	0.0397 (4)
C15	1.0574 (2)	0.09595 (6)	0.73805 (7)	0.0378 (4)
H15	1.046518	0.121562	0.759954	0.045*
C16	1.1074 (3)	−0.01276 (6)	0.63265 (10)	0.0579 (6)
H16A	1.000601	−0.021030	0.617563	0.087*
H16B	1.154856	−0.037329	0.653355	0.087*
H16C	1.177842	−0.004800	0.601690	0.087*
C17	1.2031 (2)	0.06128 (7)	0.81926 (9)	0.0554 (5)
H17A	1.125943	0.046601	0.843544	0.083*
H17B	1.217435	0.091430	0.831695	0.083*
H17C	1.307400	0.046140	0.821368	0.083*
C18	0.94405 (16)	0.20720 (5)	0.56401 (6)	0.0267 (3)
H18A	1.012420	0.187117	0.586661	0.032*
H18B	0.993993	0.236424	0.566283	0.032*
C19	0.94293 (18)	0.19208 (6)	0.50273 (7)	0.0333 (3)
H19A	0.883362	0.213139	0.479388	0.050*
H19B	0.890302	0.163591	0.499811	0.050*
H19C	1.054405	0.189821	0.489791	0.050*
C20	0.75808 (17)	0.28807 (4)	0.56159 (6)	0.0242 (3)
H20A	0.816365	0.278931	0.527659	0.029*
H20B	0.667814	0.307288	0.549522	0.029*
C21	0.90842 (17)	0.35420 (5)	0.58739 (7)	0.0296 (3)
C22	0.9024 (2)	0.41272 (5)	0.52749 (9)	0.0416 (4)
C23	0.9845 (2)	0.43814 (6)	0.56621 (10)	0.0507 (5)
H23	1.007095	0.467703	0.557851	0.061*
C24	1.0347 (2)	0.42052 (6)	0.61776 (9)	0.0460 (5)
C25	0.99841 (19)	0.37787 (5)	0.62811 (8)	0.0378 (4)
H25	1.033201	0.364406	0.662154	0.045*
C26	0.8561 (2)	0.42926 (6)	0.47003 (10)	0.0563 (6)
H26A	0.875287	0.460672	0.468306	0.084*
H26B	0.741278	0.423309	0.462434	0.084*
H26C	0.921519	0.414585	0.441875	0.084*
C27	1.1256 (3)	0.44733 (7)	0.66109 (11)	0.0669 (7)
H27A	1.212895	0.463292	0.642966	0.100*
H27B	1.171663	0.428111	0.690067	0.100*
H27C	1.051292	0.467987	0.678352	0.100*
C28	0.45255 (18)	0.29408 (5)	0.62098 (7)	0.0296 (3)
H28A	0.533259	0.317859	0.621873	0.036*
H28B	0.393772	0.294919	0.656764	0.036*
C29	0.33193 (19)	0.30222 (6)	0.57234 (8)	0.0382 (4)
H29A	0.389047	0.301467	0.536700	0.057*
H29B	0.281338	0.330777	0.576999	0.057*
H29C	0.248353	0.279622	0.572261	0.057*
N1	0.90393 (18)	0.12930 (5)	0.66457 (6)	0.0382 (3)
H1	0.875 (2)	0.1482 (6)	0.6898 (8)	0.057*
N2	1.00529 (15)	0.05961 (4)	0.65004 (6)	0.0337 (3)
N3	0.86811 (16)	0.31210 (4)	0.59870 (6)	0.0295 (3)
H3	0.867 (2)	0.3052 (6)	0.6337 (6)	0.044*
N4	0.86188 (15)	0.37088 (4)	0.53786 (6)	0.0319 (3)
O1	0.33128 (13)	0.22139 (5)	0.72605 (5)	0.0410 (3)
H1A	0.2406 (13)	0.2282 (7)	0.7389 (9)	0.062*
C30	0.44206 (16)	0.26971 (4)	0.84899 (6)	0.0224 (3)
C31	0.36855 (16)	0.31078 (4)	0.84497 (6)	0.0234 (3)
C32	0.21382 (16)	0.31681 (4)	0.86698 (6)	0.0230 (3)
C33	0.13284 (16)	0.28232 (4)	0.89266 (6)	0.0229 (3)
C34	0.20841 (16)	0.24165 (4)	0.89664 (6)	0.0223 (3)
C35	0.36159 (16)	0.23485 (4)	0.87402 (6)	0.0226 (3)
C36	0.60855 (16)	0.26297 (5)	0.82526 (6)	0.0246 (3)
H36A	0.672931	0.289805	0.830974	0.030*
H36B	0.663575	0.239228	0.846208	0.030*
C37	0.45769 (18)	0.34851 (5)	0.81916 (7)	0.0295 (3)
H37A	0.378703	0.368347	0.800715	0.035*
H37B	0.530995	0.337450	0.790072	0.035*
C38	0.55657 (19)	0.37380 (5)	0.86350 (7)	0.0346 (4)
H38A	0.609616	0.398582	0.845701	0.052*
H38B	0.638725	0.354627	0.880408	0.052*
H38C	0.484514	0.384342	0.892702	0.052*
C39	0.13181 (17)	0.36062 (5)	0.86177 (6)	0.0262 (3)
H39A	0.061572	0.365462	0.894358	0.031*
H39B	0.214330	0.383946	0.861405	0.031*
C40	−0.05989 (17)	0.39695 (5)	0.79592 (6)	0.0258 (3)
C41	−0.26181 (17)	0.42474 (5)	0.73751 (7)	0.0309 (3)
C42	−0.24800 (18)	0.46498 (5)	0.76224 (7)	0.0349 (4)
H42	−0.315120	0.488249	0.749693	0.042*
C43	−0.13555 (19)	0.47163 (5)	0.80569 (8)	0.0340 (4)
C44	−0.04145 (18)	0.43687 (5)	0.82306 (7)	0.0295 (3)
H44	0.034881	0.440113	0.853116	0.035*
C45	−0.3812 (2)	0.41600 (6)	0.69036 (8)	0.0432 (4)
H45A	−0.450415	0.441550	0.684628	0.065*
H45B	−0.448173	0.390876	0.699886	0.065*
H45C	−0.322723	0.409890	0.655854	0.065*
C46	−0.1145 (2)	0.51527 (6)	0.83292 (10)	0.0508 (5)
H46A	−0.055943	0.511878	0.868836	0.076*
H46B	−0.220899	0.528139	0.839469	0.076*
H46C	−0.052805	0.534328	0.808262	0.076*
C47	−0.03573 (16)	0.28947 (5)	0.91572 (6)	0.0262 (3)
H47A	−0.095523	0.261585	0.914568	0.031*
H47B	−0.094797	0.310334	0.891200	0.031*
C48	−0.03339 (18)	0.30681 (6)	0.97602 (7)	0.0336 (3)
H48A	0.029238	0.333842	0.977827	0.050*
H48B	0.016516	0.285183	1.001125	0.050*
H48C	−0.144431	0.312486	0.987674	0.050*
C49	0.12224 (17)	0.20453 (5)	0.92486 (6)	0.0251 (3)
H49A	0.202775	0.184195	0.941466	0.030*
H49B	0.055188	0.215950	0.955516	0.030*
C50	−0.05875 (17)	0.14396 (5)	0.89678 (7)	0.0301 (3)
C51	−0.03800 (19)	0.12342 (5)	0.94899 (7)	0.0342 (4)
H51	0.028731	0.136114	0.977483	0.041*
C52	−0.1160 (2)	0.08447 (6)	0.95837 (9)	0.0440 (4)
C53	−0.2123 (2)	0.06731 (6)	0.91488 (10)	0.0502 (5)
H53	−0.265754	0.040258	0.919734	0.060*
C54	−0.2298 (2)	0.08956 (6)	0.86509 (9)	0.0443 (5)
C55	−0.0965 (3)	0.06219 (7)	1.01440 (10)	0.0623 (6)
H55A	−0.176859	0.073558	1.040285	0.093*
H55B	0.012474	0.067692	1.029743	0.093*
H55C	−0.112362	0.030818	1.009626	0.093*
C56	−0.3334 (3)	0.07343 (7)	0.81680 (11)	0.0637 (6)
H56A	−0.267484	0.070929	0.783201	0.096*
H56B	−0.421998	0.093968	0.809598	0.096*
H56C	−0.378068	0.044874	0.826134	0.096*
C57	0.44155 (18)	0.19044 (5)	0.87741 (7)	0.0287 (3)
H57A	0.506784	0.185902	0.843502	0.034*
H57B	0.356679	0.167737	0.877816	0.034*
C58	0.55071 (19)	0.18539 (5)	0.92963 (7)	0.0354 (4)
H58A	0.601338	0.156577	0.929460	0.053*
H58B	0.485826	0.188527	0.963379	0.053*
H58C	0.634879	0.207825	0.929511	0.053*
N5	0.03485 (16)	0.36201 (4)	0.80992 (6)	0.0301 (3)
H5	0.004 (2)	0.3376 (5)	0.7948 (8)	0.045*
N6	−0.16924 (14)	0.39081 (4)	0.75401 (5)	0.0277 (3)
N7	0.02003 (16)	0.18156 (4)	0.88432 (6)	0.0321 (3)
H7	−0.001 (2)	0.1937 (6)	0.8516 (7)	0.048*
N8	−0.15559 (15)	0.12782 (4)	0.85572 (6)	0.0344 (3)
O2	0.60453 (12)	0.25235 (3)	0.76643 (4)	0.0280 (2)
H2	0.5120 (12)	0.2450 (7)	0.7544 (9)	0.060 (7)*
O3	1.03595 (15)	0.23831 (5)	0.76301 (6)	0.0519 (3)
H3A	0.989 (3)	0.2602 (5)	0.7474 (10)	0.078*
H3B	0.965 (2)	0.2191 (6)	0.7560 (11)	0.078*
O4	0.83665 (14)	0.30448 (4)	0.72071 (5)	0.0374 (3)
H4A	0.819 (2)	0.3308 (3)	0.7297 (9)	0.056*
H4B	0.7527 (15)	0.2899 (6)	0.7280 (9)	0.056*
O5	0.79655 (16)	0.17779 (4)	0.76018 (6)	0.0475 (3)
H5A	0.799 (3)	0.1627 (7)	0.7899 (6)	0.071*
H5B	0.722 (2)	0.1965 (6)	0.7612 (10)	0.071*

Open in a new tab

(3,5-Bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate. Atomic displacement parameters (Å²)

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
C1	0.0219 (6)	0.0279 (7)	0.0201 (7)	−0.0037 (5)	−0.0019 (5)	0.0005 (6)
C2	0.0260 (7)	0.0247 (7)	0.0262 (7)	−0.0042 (6)	−0.0016 (6)	0.0047 (6)
C3	0.0252 (7)	0.0231 (7)	0.0266 (7)	0.0000 (6)	−0.0025 (6)	0.0027 (6)
C4	0.0206 (6)	0.0252 (7)	0.0202 (7)	−0.0021 (5)	−0.0030 (5)	0.0008 (5)
C5	0.0223 (6)	0.0219 (7)	0.0199 (7)	−0.0046 (5)	−0.0027 (5)	0.0002 (5)
C6	0.0243 (7)	0.0232 (7)	0.0209 (7)	−0.0012 (5)	−0.0030 (5)	−0.0012 (5)
C7	0.0234 (7)	0.0341 (8)	0.0242 (7)	−0.0035 (6)	−0.0005 (6)	0.0011 (6)
C8	0.0331 (8)	0.0284 (8)	0.0445 (10)	−0.0022 (6)	0.0065 (7)	0.0120 (7)
C9	0.0381 (9)	0.0296 (8)	0.0721 (14)	−0.0112 (7)	0.0057 (9)	0.0022 (9)
C10	0.0310 (8)	0.0247 (7)	0.0361 (9)	0.0019 (6)	0.0002 (6)	0.0054 (6)
C11	0.0268 (7)	0.0307 (8)	0.0395 (9)	0.0070 (6)	0.0070 (6)	0.0092 (7)
C12	0.0275 (7)	0.0253 (8)	0.0605 (12)	0.0000 (6)	0.0028 (8)	0.0075 (7)
C13	0.0288 (8)	0.0316 (8)	0.0612 (12)	0.0058 (7)	−0.0009 (8)	0.0154 (8)
C14	0.0287 (8)	0.0426 (9)	0.0481 (11)	0.0090 (7)	0.0030 (7)	0.0133 (8)
C15	0.0360 (8)	0.0393 (9)	0.0383 (9)	0.0145 (7)	0.0039 (7)	0.0056 (7)
C16	0.0558 (12)	0.0315 (9)	0.0856 (16)	0.0078 (9)	−0.0150 (11)	−0.0047 (10)
C17	0.0512 (11)	0.0611 (13)	0.0535 (12)	0.0236 (10)	−0.0060 (9)	0.0127 (10)
C18	0.0198 (6)	0.0306 (7)	0.0295 (8)	−0.0003 (6)	−0.0020 (6)	0.0028 (6)
C19	0.0275 (7)	0.0434 (9)	0.0291 (8)	0.0041 (7)	0.0033 (6)	0.0025 (7)
C20	0.0255 (7)	0.0217 (7)	0.0254 (7)	−0.0041 (5)	0.0001 (6)	0.0002 (5)
C21	0.0261 (7)	0.0261 (7)	0.0372 (9)	−0.0071 (6)	0.0110 (6)	−0.0065 (6)
C22	0.0334 (8)	0.0266 (8)	0.0654 (12)	−0.0040 (7)	0.0155 (8)	0.0052 (8)
C23	0.0413 (10)	0.0231 (8)	0.0884 (16)	−0.0110 (7)	0.0195 (10)	−0.0050 (9)
C24	0.0388 (9)	0.0366 (9)	0.0632 (13)	−0.0151 (8)	0.0201 (9)	−0.0213 (9)
C25	0.0334 (8)	0.0386 (9)	0.0418 (10)	−0.0135 (7)	0.0129 (7)	−0.0127 (7)
C26	0.0472 (11)	0.0364 (10)	0.0856 (16)	−0.0065 (8)	0.0089 (10)	0.0251 (10)
C27	0.0593 (13)	0.0543 (13)	0.0878 (17)	−0.0304 (10)	0.0193 (12)	−0.0364 (12)
C28	0.0299 (7)	0.0242 (7)	0.0350 (8)	0.0003 (6)	0.0055 (6)	−0.0023 (6)
C29	0.0309 (8)	0.0360 (9)	0.0478 (10)	0.0078 (7)	0.0051 (7)	0.0090 (8)
N1	0.0451 (8)	0.0341 (7)	0.0352 (8)	0.0161 (6)	−0.0022 (6)	0.0032 (6)
N2	0.0259 (6)	0.0279 (7)	0.0474 (8)	0.0018 (5)	0.0046 (6)	0.0069 (6)
N3	0.0327 (7)	0.0273 (6)	0.0283 (7)	−0.0113 (5)	0.0002 (6)	−0.0009 (5)
N4	0.0286 (6)	0.0239 (6)	0.0437 (8)	−0.0052 (5)	0.0093 (6)	0.0020 (6)
O1	0.0248 (5)	0.0730 (9)	0.0253 (6)	−0.0070 (6)	0.0036 (5)	−0.0070 (6)
C30	0.0222 (6)	0.0245 (7)	0.0203 (7)	0.0005 (5)	−0.0017 (5)	−0.0026 (5)
C31	0.0258 (7)	0.0241 (7)	0.0201 (7)	−0.0012 (6)	−0.0025 (5)	−0.0009 (5)
C32	0.0252 (7)	0.0226 (7)	0.0211 (7)	0.0031 (5)	−0.0034 (5)	−0.0014 (5)
C33	0.0208 (6)	0.0256 (7)	0.0220 (7)	0.0006 (5)	−0.0032 (5)	−0.0029 (5)
C34	0.0229 (6)	0.0236 (7)	0.0203 (7)	−0.0016 (5)	−0.0020 (5)	−0.0013 (5)
C35	0.0242 (6)	0.0231 (7)	0.0203 (7)	0.0013 (5)	−0.0026 (5)	−0.0027 (5)
C36	0.0234 (7)	0.0278 (7)	0.0226 (7)	0.0016 (6)	−0.0007 (6)	−0.0022 (6)
C37	0.0316 (7)	0.0259 (7)	0.0312 (8)	0.0003 (6)	0.0054 (6)	0.0036 (6)
C38	0.0338 (8)	0.0270 (8)	0.0431 (10)	−0.0054 (6)	0.0058 (7)	−0.0023 (7)
C39	0.0277 (7)	0.0234 (7)	0.0274 (8)	0.0034 (6)	−0.0033 (6)	−0.0008 (6)
C40	0.0253 (7)	0.0242 (7)	0.0281 (8)	0.0030 (6)	0.0030 (6)	0.0029 (6)
C41	0.0249 (7)	0.0341 (8)	0.0338 (8)	0.0036 (6)	0.0015 (6)	0.0072 (7)
C42	0.0279 (7)	0.0286 (8)	0.0482 (10)	0.0072 (6)	0.0016 (7)	0.0096 (7)
C43	0.0300 (8)	0.0236 (7)	0.0484 (10)	0.0029 (6)	0.0050 (7)	0.0032 (7)
C44	0.0273 (7)	0.0261 (7)	0.0351 (8)	0.0038 (6)	−0.0018 (6)	−0.0004 (6)
C45	0.0358 (9)	0.0503 (10)	0.0432 (10)	0.0066 (8)	−0.0095 (8)	0.0050 (8)
C46	0.0464 (10)	0.0271 (9)	0.0786 (15)	0.0080 (8)	−0.0082 (10)	−0.0086 (9)
C47	0.0196 (6)	0.0297 (7)	0.0291 (8)	0.0026 (6)	−0.0024 (6)	0.0019 (6)
C48	0.0270 (7)	0.0445 (9)	0.0294 (8)	0.0076 (7)	0.0029 (6)	0.0004 (7)
C49	0.0253 (7)	0.0247 (7)	0.0251 (7)	−0.0011 (6)	0.0000 (6)	−0.0004 (6)
C50	0.0248 (7)	0.0255 (7)	0.0404 (9)	−0.0007 (6)	0.0075 (6)	−0.0068 (6)
C51	0.0313 (8)	0.0277 (8)	0.0441 (10)	0.0011 (6)	0.0100 (7)	0.0010 (7)
C52	0.0359 (9)	0.0306 (8)	0.0662 (13)	0.0038 (7)	0.0201 (9)	0.0073 (8)
C53	0.0374 (9)	0.0269 (8)	0.0871 (16)	−0.0081 (7)	0.0186 (10)	−0.0036 (9)
C54	0.0303 (8)	0.0323 (9)	0.0706 (13)	−0.0056 (7)	0.0120 (8)	−0.0161 (9)
C55	0.0562 (12)	0.0464 (11)	0.0853 (17)	0.0032 (10)	0.0259 (12)	0.0269 (11)
C56	0.0486 (11)	0.0504 (12)	0.0921 (18)	−0.0198 (10)	0.0037 (11)	−0.0270 (12)
C57	0.0311 (7)	0.0237 (7)	0.0315 (8)	0.0035 (6)	0.0071 (6)	−0.0008 (6)
C58	0.0342 (8)	0.0362 (9)	0.0361 (9)	0.0136 (7)	0.0067 (7)	0.0090 (7)
N5	0.0377 (7)	0.0222 (6)	0.0299 (7)	0.0076 (5)	−0.0093 (6)	−0.0026 (5)
N6	0.0265 (6)	0.0277 (6)	0.0288 (7)	0.0032 (5)	0.0010 (5)	0.0034 (5)
N7	0.0362 (7)	0.0297 (7)	0.0302 (7)	−0.0102 (6)	−0.0045 (6)	0.0015 (6)
N8	0.0267 (6)	0.0299 (7)	0.0469 (8)	−0.0046 (5)	0.0051 (6)	−0.0120 (6)
O2	0.0237 (5)	0.0361 (6)	0.0242 (5)	−0.0021 (4)	0.0017 (4)	−0.0055 (4)
O3	0.0323 (7)	0.0768 (10)	0.0463 (8)	0.0052 (6)	−0.0018 (6)	−0.0102 (7)
O4	0.0398 (6)	0.0325 (6)	0.0401 (7)	−0.0074 (5)	0.0078 (5)	−0.0037 (5)
O5	0.0470 (7)	0.0441 (8)	0.0517 (8)	0.0182 (6)	0.0086 (6)	−0.0003 (6)

Open in a new tab

(3,5-Bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate. Geometric parameters (Å, º)

C1—C2	1.402 (2)	C31—C32	1.404 (2)
C1—C6	1.4037 (19)	C31—C37	1.512 (2)
C1—C7	1.5147 (19)	C32—C33	1.401 (2)
C2—C3	1.406 (2)	C32—C39	1.5125 (19)
C2—C8	1.5150 (19)	C33—C34	1.4004 (19)
C3—C4	1.3993 (19)	C33—C47	1.5241 (19)
C3—C10	1.520 (2)	C34—C35	1.4017 (19)
C4—C5	1.4006 (19)	C34—C49	1.5107 (19)
C4—C18	1.5217 (19)	C35—C57	1.5189 (19)
C5—C6	1.406 (2)	C36—H36A	0.9900
C5—C20	1.5096 (18)	C36—H36B	0.9900
C6—C28	1.5165 (19)	C36—O2	1.4386 (17)
C7—H7A	0.9900	C37—H37A	0.9900
C7—H7B	0.9900	C37—H37B	0.9900
C7—O1	1.4322 (18)	C37—C38	1.534 (2)
C8—H8A	0.9900	C38—H38A	0.9800
C8—H8B	0.9900	C38—H38B	0.9800
C8—C9	1.532 (3)	C38—H38C	0.9800
C9—H9A	0.9800	C39—H39A	0.9900
C9—H9B	0.9800	C39—H39B	0.9900
C9—H9C	0.9800	C39—N5	1.4594 (18)
C10—H10A	0.9900	C40—C44	1.395 (2)
C10—H10B	0.9900	C40—N5	1.3672 (18)
C10—N1	1.457 (2)	C40—N6	1.3467 (19)
C11—C15	1.404 (2)	C41—C42	1.374 (2)
C11—N1	1.3651 (19)	C41—C45	1.504 (2)
C11—N2	1.337 (2)	C41—N6	1.3482 (19)
C12—C13	1.373 (3)	C42—H42	0.9500
C12—C16	1.495 (3)	C42—C43	1.393 (2)
C12—N2	1.363 (2)	C43—C44	1.381 (2)
C13—H13	0.9500	C43—C46	1.499 (2)
C13—C14	1.396 (3)	C44—H44	0.9500
C14—C15	1.372 (2)	C45—H45A	0.9800
C14—C17	1.506 (3)	C45—H45B	0.9800
C15—H15	0.9500	C45—H45C	0.9800
C16—H16A	0.9800	C46—H46A	0.9800
C16—H16B	0.9800	C46—H46B	0.9800
C16—H16C	0.9800	C46—H46C	0.9800
C17—H17A	0.9800	C47—H47A	0.9900
C17—H17B	0.9800	C47—H47B	0.9900
C17—H17C	0.9800	C47—C48	1.532 (2)
C18—H18A	0.9900	C48—H48A	0.9800
C18—H18B	0.9900	C48—H48B	0.9800
C18—C19	1.532 (2)	C48—H48C	0.9800
C19—H19A	0.9800	C49—H49A	0.9900
C19—H19B	0.9800	C49—H49B	0.9900
C19—H19C	0.9800	C49—N7	1.4536 (19)
C20—H20A	0.9900	C50—C51	1.402 (2)
C20—H20B	0.9900	C50—N7	1.3628 (19)
C20—N3	1.4571 (18)	C50—N8	1.346 (2)
C21—C25	1.413 (2)	C51—H51	0.9500
C21—N3	1.3652 (19)	C51—C52	1.381 (2)
C21—N4	1.336 (2)	C52—C53	1.398 (3)
C22—C23	1.378 (3)	C52—C55	1.506 (3)
C22—C26	1.503 (3)	C53—H53	0.9500
C22—N4	1.354 (2)	C53—C54	1.374 (3)
C23—H23	0.9500	C54—C56	1.504 (3)
C23—C24	1.398 (3)	C54—N8	1.348 (2)
C24—C25	1.369 (2)	C55—H55A	0.9800
C24—C27	1.510 (3)	C55—H55B	0.9800
C25—H25	0.9500	C55—H55C	0.9800
C26—H26A	0.9800	C56—H56A	0.9800
C26—H26B	0.9800	C56—H56B	0.9800
C26—H26C	0.9800	C56—H56C	0.9800
C27—H27A	0.9800	C57—H57A	0.9900
C27—H27B	0.9800	C57—H57B	0.9900
C27—H27C	0.9800	C57—C58	1.530 (2)
C28—H28A	0.9900	C58—H58A	0.9800
C28—H28B	0.9900	C58—H58B	0.9800
C28—C29	1.534 (2)	C58—H58C	0.9800
C29—H29A	0.9800	N5—H5	0.869 (14)
C29—H29B	0.9800	N7—H7	0.878 (15)
C29—H29C	0.9800	O2—H2	0.843 (5)
N1—H1	0.870 (15)	O3—H3A	0.859 (5)
N3—H3	0.860 (14)	O3—H3B	0.849 (5)
O1—H1A	0.842 (5)	O4—H4A	0.849 (5)
C30—C31	1.4042 (19)	O4—H4B	0.847 (5)
C30—C35	1.401 (2)	O5—H5A	0.846 (5)
C30—C36	1.5125 (19)	O5—H5B	0.844 (5)

C2—C1—C6	120.20 (13)	C35—C30—C36	119.84 (12)
C2—C1—C7	119.74 (13)	C30—C31—C32	119.31 (13)
C6—C1—C7	120.06 (13)	C30—C31—C37	120.29 (13)
C1—C2—C3	119.83 (13)	C32—C31—C37	120.36 (12)
C1—C2—C8	119.75 (13)	C31—C32—C39	119.80 (13)
C3—C2—C8	120.41 (13)	C33—C32—C31	120.64 (12)
C2—C3—C10	120.15 (13)	C33—C32—C39	119.54 (12)
C4—C3—C2	120.27 (13)	C32—C33—C47	119.75 (12)
C4—C3—C10	119.47 (13)	C34—C33—C32	119.29 (12)
C3—C4—C5	119.64 (12)	C34—C33—C47	120.95 (13)
C3—C4—C18	119.88 (12)	C33—C34—C35	120.83 (13)
C5—C4—C18	120.48 (12)	C33—C34—C49	119.44 (12)
C4—C5—C6	120.51 (12)	C35—C34—C49	119.72 (12)
C4—C5—C20	119.74 (12)	C30—C35—C34	119.32 (12)
C6—C5—C20	119.73 (12)	C30—C35—C57	120.05 (12)
C1—C6—C5	119.46 (13)	C34—C35—C57	120.62 (13)
C1—C6—C28	120.12 (13)	C30—C36—H36A	109.0
C5—C6—C28	120.43 (12)	C30—C36—H36B	109.0
C1—C7—H7A	109.8	H36A—C36—H36B	107.8
C1—C7—H7B	109.8	O2—C36—C30	113.05 (11)
H7A—C7—H7B	108.3	O2—C36—H36A	109.0
O1—C7—C1	109.25 (11)	O2—C36—H36B	109.0
O1—C7—H7A	109.8	C31—C37—H37A	109.3
O1—C7—H7B	109.8	C31—C37—H37B	109.3
C2—C8—H8A	109.4	C31—C37—C38	111.50 (13)
C2—C8—H8B	109.4	H37A—C37—H37B	108.0
C2—C8—C9	111.38 (14)	C38—C37—H37A	109.3
H8A—C8—H8B	108.0	C38—C37—H37B	109.3
C9—C8—H8A	109.4	C37—C38—H38A	109.5
C9—C8—H8B	109.4	C37—C38—H38B	109.5
C8—C9—H9A	109.5	C37—C38—H38C	109.5
C8—C9—H9B	109.5	H38A—C38—H38B	109.5
C8—C9—H9C	109.5	H38A—C38—H38C	109.5
H9A—C9—H9B	109.5	H38B—C38—H38C	109.5
H9A—C9—H9C	109.5	C32—C39—H39A	109.8
H9B—C9—H9C	109.5	C32—C39—H39B	109.8
C3—C10—H10A	110.2	H39A—C39—H39B	108.2
C3—C10—H10B	110.2	N5—C39—C32	109.47 (12)
H10A—C10—H10B	108.5	N5—C39—H39A	109.8
N1—C10—C3	107.68 (13)	N5—C39—H39B	109.8
N1—C10—H10A	110.2	N5—C40—C44	121.47 (13)
N1—C10—H10B	110.2	N6—C40—C44	122.20 (13)
N1—C11—C15	118.02 (15)	N6—C40—N5	116.32 (13)
N2—C11—C15	122.83 (14)	C42—C41—C45	121.91 (14)
N2—C11—N1	119.14 (15)	N6—C41—C42	122.02 (14)
C13—C12—C16	121.34 (16)	N6—C41—C45	116.07 (14)
N2—C12—C13	123.11 (16)	C41—C42—H42	120.0
N2—C12—C16	115.55 (17)	C41—C42—C43	119.95 (14)
C12—C13—H13	120.0	C43—C42—H42	120.0
C12—C13—C14	119.93 (15)	C42—C43—C46	121.54 (15)
C14—C13—H13	120.0	C44—C43—C42	118.23 (15)
C13—C14—C17	122.26 (15)	C44—C43—C46	120.23 (16)
C15—C14—C13	117.35 (17)	C40—C44—H44	120.4
C15—C14—C17	120.35 (17)	C43—C44—C40	119.14 (14)
C11—C15—H15	120.0	C43—C44—H44	120.4
C14—C15—C11	119.97 (17)	C41—C45—H45A	109.5
C14—C15—H15	120.0	C41—C45—H45B	109.5
C12—C16—H16A	109.5	C41—C45—H45C	109.5
C12—C16—H16B	109.5	H45A—C45—H45B	109.5
C12—C16—H16C	109.5	H45A—C45—H45C	109.5
H16A—C16—H16B	109.5	H45B—C45—H45C	109.5
H16A—C16—H16C	109.5	C43—C46—H46A	109.5
H16B—C16—H16C	109.5	C43—C46—H46B	109.5
C14—C17—H17A	109.5	C43—C46—H46C	109.5
C14—C17—H17B	109.5	H46A—C46—H46B	109.5
C14—C17—H17C	109.5	H46A—C46—H46C	109.5
H17A—C17—H17B	109.5	H46B—C46—H46C	109.5
H17A—C17—H17C	109.5	C33—C47—H47A	108.9
H17B—C17—H17C	109.5	C33—C47—H47B	108.9
C4—C18—H18A	108.8	C33—C47—C48	113.19 (12)
C4—C18—H18B	108.8	H47A—C47—H47B	107.8
C4—C18—C19	113.77 (12)	C48—C47—H47A	108.9
H18A—C18—H18B	107.7	C48—C47—H47B	108.9
C19—C18—H18A	108.8	C47—C48—H48A	109.5
C19—C18—H18B	108.8	C47—C48—H48B	109.5
C18—C19—H19A	109.5	C47—C48—H48C	109.5
C18—C19—H19B	109.5	H48A—C48—H48B	109.5
C18—C19—H19C	109.5	H48A—C48—H48C	109.5
H19A—C19—H19B	109.5	H48B—C48—H48C	109.5
H19A—C19—H19C	109.5	C34—C49—H49A	109.6
H19B—C19—H19C	109.5	C34—C49—H49B	109.6
C5—C20—H20A	109.3	H49A—C49—H49B	108.1
C5—C20—H20B	109.3	N7—C49—C34	110.16 (12)
H20A—C20—H20B	108.0	N7—C49—H49A	109.6
N3—C20—C5	111.40 (12)	N7—C49—H49B	109.6
N3—C20—H20A	109.3	N7—C50—C51	121.66 (14)
N3—C20—H20B	109.3	N8—C50—C51	122.59 (14)
N3—C21—C25	118.71 (15)	N8—C50—N7	115.75 (15)
N4—C21—C25	123.16 (14)	C50—C51—H51	120.5
N4—C21—N3	118.13 (13)	C52—C51—C50	119.01 (17)
C23—C22—C26	122.07 (16)	C52—C51—H51	120.5
N4—C22—C23	122.53 (18)	C51—C52—C53	117.95 (18)
N4—C22—C26	115.37 (17)	C51—C52—C55	119.73 (19)
C22—C23—H23	119.9	C53—C52—C55	122.31 (17)
C22—C23—C24	120.12 (16)	C52—C53—H53	120.0
C24—C23—H23	119.9	C54—C53—C52	120.01 (16)
C23—C24—C27	121.60 (18)	C54—C53—H53	120.0
C25—C24—C23	117.87 (17)	C53—C54—C56	122.97 (17)
C25—C24—C27	120.5 (2)	N8—C54—C53	122.50 (17)
C21—C25—H25	120.5	N8—C54—C56	114.53 (19)
C24—C25—C21	118.97 (18)	C52—C55—H55A	109.5
C24—C25—H25	120.5	C52—C55—H55B	109.5
C22—C26—H26A	109.5	C52—C55—H55C	109.5
C22—C26—H26B	109.5	H55A—C55—H55B	109.5
C22—C26—H26C	109.5	H55A—C55—H55C	109.5
H26A—C26—H26B	109.5	H55B—C55—H55C	109.5
H26A—C26—H26C	109.5	C54—C56—H56A	109.5
H26B—C26—H26C	109.5	C54—C56—H56B	109.5
C24—C27—H27A	109.5	C54—C56—H56C	109.5
C24—C27—H27B	109.5	H56A—C56—H56B	109.5
C24—C27—H27C	109.5	H56A—C56—H56C	109.5
H27A—C27—H27B	109.5	H56B—C56—H56C	109.5
H27A—C27—H27C	109.5	C35—C57—H57A	109.1
H27B—C27—H27C	109.5	C35—C57—H57B	109.1
C6—C28—H28A	108.9	C35—C57—C58	112.55 (12)
C6—C28—H28B	108.9	H57A—C57—H57B	107.8
C6—C28—C29	113.52 (13)	C58—C57—H57A	109.1
H28A—C28—H28B	107.7	C58—C57—H57B	109.1
C29—C28—H28A	108.9	C57—C58—H58A	109.5
C29—C28—H28B	108.9	C57—C58—H58B	109.5
C28—C29—H29A	109.5	C57—C58—H58C	109.5
C28—C29—H29B	109.5	H58A—C58—H58B	109.5
C28—C29—H29C	109.5	H58A—C58—H58C	109.5
H29A—C29—H29B	109.5	H58B—C58—H58C	109.5
H29A—C29—H29C	109.5	C39—N5—H5	118.6 (13)
H29B—C29—H29C	109.5	C40—N5—C39	122.12 (12)
C10—N1—H1	114.7 (14)	C40—N5—H5	114.5 (13)
C11—N1—C10	124.27 (14)	C40—N6—C41	118.44 (13)
C11—N1—H1	116.4 (15)	C49—N7—H7	119.0 (13)
C11—N2—C12	116.76 (15)	C50—N7—C49	122.79 (13)
C20—N3—H3	116.5 (13)	C50—N7—H7	117.9 (13)
C21—N3—C20	120.87 (13)	C50—N8—C54	117.87 (16)
C21—N3—H3	115.6 (13)	C36—O2—H2	113.3 (15)
C21—N4—C22	117.27 (15)	H3A—O3—H3B	99 (2)
C7—O1—H1A	107.0 (15)	H4A—O4—H4B	108 (2)
C31—C30—C36	119.58 (12)	H5A—O5—H5B	111 (2)
C35—C30—C31	120.58 (12)

C1—C2—C3—C4	0.3 (2)	C30—C31—C32—C33	−0.1 (2)
C1—C2—C3—C10	176.34 (13)	C30—C31—C32—C39	−178.64 (12)
C1—C2—C8—C9	90.87 (18)	C30—C31—C37—C38	−90.02 (16)
C1—C6—C28—C29	−87.45 (17)	C30—C35—C57—C58	86.73 (17)
C2—C1—C6—C5	2.5 (2)	C31—C30—C35—C34	−1.9 (2)
C2—C1—C6—C28	−177.53 (13)	C31—C30—C35—C57	179.19 (13)
C2—C1—C7—O1	84.99 (16)	C31—C30—C36—O2	−85.91 (16)
C2—C3—C4—C5	−1.6 (2)	C31—C32—C33—C34	0.5 (2)
C2—C3—C4—C18	177.93 (13)	C31—C32—C33—C47	−179.37 (13)
C2—C3—C10—N1	−88.80 (16)	C31—C32—C39—N5	90.78 (16)
C3—C2—C8—C9	−88.12 (17)	C32—C31—C37—C38	87.68 (16)
C3—C4—C5—C6	3.3 (2)	C32—C33—C34—C35	−1.7 (2)
C3—C4—C5—C20	−175.19 (12)	C32—C33—C34—C49	179.32 (12)
C3—C4—C18—C19	84.73 (17)	C32—C33—C47—C48	−86.63 (16)
C3—C10—N1—C11	170.47 (14)	C32—C39—N5—C40	176.29 (13)
C4—C3—C10—N1	87.31 (17)	C33—C32—C39—N5	−87.76 (16)
C4—C5—C6—C1	−3.8 (2)	C33—C34—C35—C30	2.3 (2)
C4—C5—C6—C28	176.21 (13)	C33—C34—C35—C57	−178.75 (13)
C4—C5—C20—N3	−86.80 (16)	C33—C34—C49—N7	87.69 (16)
C5—C4—C18—C19	−95.77 (16)	C34—C33—C47—C48	93.46 (16)
C5—C6—C28—C29	92.54 (16)	C34—C35—C57—C58	−92.17 (16)
C5—C20—N3—C21	−162.33 (13)	C34—C49—N7—C50	173.00 (13)
C6—C1—C2—C3	−0.7 (2)	C35—C30—C31—C32	0.8 (2)
C6—C1—C2—C8	−179.73 (13)	C35—C30—C31—C37	178.52 (13)
C6—C1—C7—O1	−94.00 (16)	C35—C30—C36—O2	93.18 (15)
C6—C5—C20—N3	94.65 (15)	C35—C34—C49—N7	−91.33 (15)
C7—C1—C2—C3	−179.73 (13)	C36—C30—C31—C32	179.88 (12)
C7—C1—C2—C8	1.3 (2)	C36—C30—C31—C37	−2.4 (2)
C7—C1—C6—C5	−178.53 (12)	C36—C30—C35—C34	179.02 (12)
C7—C1—C6—C28	1.5 (2)	C36—C30—C35—C57	0.1 (2)
C8—C2—C3—C4	179.26 (14)	C37—C31—C32—C33	−177.83 (13)
C8—C2—C3—C10	−4.7 (2)	C37—C31—C32—C39	3.6 (2)
C10—C3—C4—C5	−177.67 (13)	C39—C32—C33—C34	179.08 (12)
C10—C3—C4—C18	1.8 (2)	C39—C32—C33—C47	−0.84 (19)
C12—C13—C14—C15	−0.6 (2)	C41—C42—C43—C44	−0.6 (2)
C12—C13—C14—C17	177.35 (17)	C41—C42—C43—C46	178.71 (17)
C13—C12—N2—C11	0.8 (2)	C42—C41—N6—C40	−0.2 (2)
C13—C14—C15—C11	2.2 (2)	C42—C43—C44—C40	1.3 (2)
C15—C11—N1—C10	−169.53 (15)	C44—C40—N5—C39	15.1 (2)
C15—C11—N2—C12	0.8 (2)	C44—C40—N6—C41	1.0 (2)
C16—C12—C13—C14	179.39 (17)	C45—C41—C42—C43	−179.87 (16)
C16—C12—N2—C11	−179.49 (15)	C45—C41—N6—C40	179.72 (14)
C17—C14—C15—C11	−175.83 (16)	C46—C43—C44—C40	−178.05 (16)
C18—C4—C5—C6	−176.15 (12)	C47—C33—C34—C35	178.24 (13)
C18—C4—C5—C20	5.32 (19)	C47—C33—C34—C49	−0.8 (2)
C20—C5—C6—C1	174.74 (12)	C49—C34—C35—C30	−178.65 (12)
C20—C5—C6—C28	−5.3 (2)	C49—C34—C35—C57	0.3 (2)
C22—C23—C24—C25	−0.5 (3)	C50—C51—C52—C53	0.1 (2)
C22—C23—C24—C27	179.70 (17)	C50—C51—C52—C55	−179.36 (16)
C23—C22—N4—C21	−1.7 (2)	C51—C50—N7—C49	−4.0 (2)
C23—C24—C25—C21	−1.9 (2)	C51—C50—N8—C54	−2.5 (2)
C25—C21—N3—C20	171.93 (13)	C51—C52—C53—C54	−1.3 (3)
C25—C21—N4—C22	−0.9 (2)	C52—C53—C54—C56	−179.08 (17)
C26—C22—C23—C24	−175.71 (17)	C52—C53—C54—N8	0.7 (3)
C26—C22—N4—C21	176.57 (15)	C53—C54—N8—C50	1.3 (2)
C27—C24—C25—C21	177.87 (16)	C55—C52—C53—C54	178.13 (17)
N1—C11—C15—C14	177.81 (16)	C56—C54—N8—C50	−178.97 (15)
N1—C11—N2—C12	−179.36 (14)	N5—C40—C44—C43	177.27 (15)
N2—C11—C15—C14	−2.4 (2)	N5—C40—N6—C41	−177.88 (13)
N2—C11—N1—C10	10.6 (2)	N6—C40—C44—C43	−1.5 (2)
N2—C12—C13—C14	−0.9 (3)	N6—C40—N5—C39	−166.03 (13)
N3—C21—C25—C24	−177.92 (15)	N6—C41—C42—C43	0.1 (2)
N3—C21—N4—C22	179.76 (14)	N7—C50—C51—C52	−177.41 (14)
N4—C21—C25—C24	2.8 (2)	N7—C50—N8—C54	176.79 (14)
N4—C21—N3—C20	−8.7 (2)	N8—C50—C51—C52	1.9 (2)
N4—C22—C23—C24	2.4 (3)	N8—C50—N7—C49	176.61 (13)

Open in a new tab

(3,5-Bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylphenyl)methanol sesquihydrate. Hydrogen-bond geometry (Å, º)

Cg(A) represents the centroid of the C1–C6 ring; Cg(B) represents the centroid of the C11–C15/N2 ring; Cg(C) represents the centroid of the C21–C25/N4 ring; Cg(A') represents the centroid of the C30–C35 ring; Cg(B') represents the centroid of the C40–C44/N6 ring; Cg(C') represents the centroid of the C50–C54/N8 ring.

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···O5	0.87 (2)	2.03 (2)	2.878 (2)	165 (2)
N3—H3···O4	0.86 (1)	2.09 (1)	2.9326 (19)	165 (2)
O1—H1A···O3ⁱ	0.84 (1)	1.82 (1)	2.6631 (17)	174 (2)
N5—H5···O4ⁱ	0.87 (1)	2.44 (2)	3.1926 (18)	145 (2)
O2—H2···O1	0.84 (1)	1.78 (2)	2.6169 (15)	171 (2)
O3—H3A···O4	0.86 (1)	1.95 (2)	2.7938 (19)	166 (2)
O3—H3B···O5	0.85 (1)	1.89 (2)	2.7167 (19)	165 (3)
O4—H4A···N6ⁱⁱ	0.85 (1)	1.94 (1)	2.7718 (17)	167 (2)
O4—H4B···O2	0.85 (1)	1.93 (2)	2.7426 (15)	161 (2)
O5—H5A···N8ⁱⁱ	0.85 (1)	1.93 (2)	2.7681 (19)	170 (2)
O5—H5B···O2	0.84 (1)	1.98 (2)	2.7946 (16)	163 (2)
C9—H9C···Cg(B)ⁱ	0.98	2.84	3.637 (2)	139
C19—H19A···Cg(A')ⁱⁱⁱ	0.98	2.71	3.512 (2)	139
C38—H38A···Cg(B')ⁱⁱ	0.98	2.73	3.612 (2)	150
C45—H45C···Cg(C)ⁱ	0.98	2.98	3.916 (2)	161
C48—H48B···Cg(A)^iv	0.98	2.83	3.563 (2)	133
C58—H58A···Cg(C')ⁱⁱ	0.98	2.74	3.613 (2)	149

Open in a new tab

Symmetry codes: (i) x−1, y, z; (ii) x+1, y, z; (iii) x+1/2, −y+1/2, z−1/2; (iv) x−1/2, −y+1/2, z+1/2.

References

Amrhein, F., Lippe, J. & Mazik, M. (2016). Org. Biomol. Chem.14, 10648–10659. [DOI] [PubMed]
Amrhein, F. & Mazik, M. (2021). Eur. J. Org. Chem. pp. 6282–6303.
Bernstein, J., Davis, R. E., Shimoni, L. & Chang, N.-L. (1995). Angew. Chem. Int. Ed. Engl.34, 1555–1573.
Britton, D. (2003). Acta Cryst. E59, o1089–o1091.
Carrero, P., Ardá, A., Alvarez, M., Doyagüez, E. G., Rivero-Buceta, E., Quesada, E., Prieto, A., Solís, D., Camarasa, M. J., Peréz-Pérez, M. J., Jiménez-Barbero, J. & San-Félix, A. (2013). Eur. J. Org. Chem. pp. 65–76.
Das, D. & Barbour, L. J. (2009). Cryst. Growth Des.9, 1599–1604.
Davis, A. P. & Wareham, R. S. (1999). Angew. Chem. Int. Ed.38, 2978–2996. [PubMed]
Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K. & Puschmann, H. (2009). J. Appl. Cryst.42, 339–341.
Etter, M. C. (1991). J. Phys. Chem.95, 4601–4610.
Groom, C. R., Bruno, I. J., Lightfoot, M. P. & Ward, S. C. (2016). Acta Cryst. B72, 171–179. [DOI] [PMC free article] [PubMed]
Infantes, L., Chisholm, J. & Motherwell, S. (2003). CrystEngComm5, 480–486.
Infantes, L. & Motherwell, S. (2002). CrystEngComm4, 454–461.
Koch, N., Seichter, W. & Mazik, M. (2017). CrystEngComm19, 3817–3833.
Manick, A.-D., Dutasta, J.-P. & Martinez, A. (2023). ChemPlusChem88, e202300291. [DOI] [PubMed]
Mazik, M. (2012). RSC Adv.2, 2630–2642.
Mazik, M. & Buthe, A. C. (2008). Org. Biomol. Chem.6, 1558–1568. [DOI] [PubMed]
Mazik, M. & Hartmann, A. (2008). J. Org. Chem.73, 7444–7450. [DOI] [PubMed]
Mazik, M., Hartmann, A. & Jones, P. G. (2009). Chem. Eur. J.15, 9147–9159. [DOI] [PubMed]
Mazik, M. & Kuschel, M. (2008). Eur. J. Org. Chem. pp. 1517–1526.
Naismith, J. H. & Field, R. A. (1996). J. Biol. Chem.271, 972–976. [DOI] [PubMed]
Nishio, M., Umezawa, Y., Hirota, M. & Takeuchi, Y. (1995). Tetrahedron51, 8665–8701.
Rothenberger, A. & Ponikiewski, L. (2007). Acta Cryst. E63, o2636–o2637.
Sauter, N. K., Glick, G. D., Crowther, R. L., Park, S.-J., Eisen, M. B., Skehel, J. J., Knowles, J. R. & Wiley, D. C. (1992). Proc. Natl Acad. Sci. USA89, 324–328. [DOI] [PMC free article] [PubMed]
Schulze, M., Schwarzer, A. & Mazik, M. (2017). CrystEngComm19, 4003–4016.
Sharon, N. & Lis, H. (2007). In Lectins. Dordrecht: Springer.
Sheldrick, G. M. (2015a). Acta Cryst. A71, 3–8.
Sheldrick, G. M. (2015b). Acta Cryst. C71, 3–8.
Stapf, M. & Mazik, M. (2026). Eur. J. Org. Chem.29, e70593.
Stapf, M., Schmidt, U., Seichter, W. & Mazik, M. (2023). Acta Cryst. E79, 1067–1071. [DOI] [PMC free article] [PubMed]
Stapf, M., Seichter, W. & Mazik, M. (2015). Chem. Eur. J.21, 6350–6354. [DOI] [PubMed]
Stoe (2024). X-RED and X-AREA. Stoe & Cie, Darmstadt, Germany.
Sluis, P. van der & Spek, A. L. (1990). Acta Cryst. A46, 194–201.

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Crystal structure: contains datablock(s) I. DOI: 10.1107/S2056989026008856/jp2032sup1.cif

e-82-01149-sup1.cif^{(2.3MB, cif)}

Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989026008856/jp2032Isup2.hkl

e-82-01149-Isup2.hkl^{(1MB, hkl)}

e-82-01149-Isup3.cml^{(10.9KB, cml)}

Supporting information file. DOI: 10.1107/S2056989026008856/jp2032Isup3.cml

CCDC reference: 2583267

Additional supporting information: crystallographic information; 3D view; checkCIF report

[bb1] Amrhein, F., Lippe, J. & Mazik, M. (2016). Org. Biomol. Chem.14, 10648–10659. [DOI] [PubMed]

[bb2] Amrhein, F. & Mazik, M. (2021). Eur. J. Org. Chem. pp. 6282–6303.

[bb3] Bernstein, J., Davis, R. E., Shimoni, L. & Chang, N.-L. (1995). Angew. Chem. Int. Ed. Engl.34, 1555–1573.

[bb4] Britton, D. (2003). Acta Cryst. E59, o1089–o1091.

[bb5] Carrero, P., Ardá, A., Alvarez, M., Doyagüez, E. G., Rivero-Buceta, E., Quesada, E., Prieto, A., Solís, D., Camarasa, M. J., Peréz-Pérez, M. J., Jiménez-Barbero, J. & San-Félix, A. (2013). Eur. J. Org. Chem. pp. 65–76.

[bb6] Das, D. & Barbour, L. J. (2009). Cryst. Growth Des.9, 1599–1604.

[bb7] Davis, A. P. & Wareham, R. S. (1999). Angew. Chem. Int. Ed.38, 2978–2996. [PubMed]

[bb8] Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K. & Puschmann, H. (2009). J. Appl. Cryst.42, 339–341.

[bb9] Etter, M. C. (1991). J. Phys. Chem.95, 4601–4610.

[bb10] Groom, C. R., Bruno, I. J., Lightfoot, M. P. & Ward, S. C. (2016). Acta Cryst. B72, 171–179. [DOI] [PMC free article] [PubMed]

[bb11] Infantes, L., Chisholm, J. & Motherwell, S. (2003). CrystEngComm5, 480–486.

[bb12] Infantes, L. & Motherwell, S. (2002). CrystEngComm4, 454–461.

[bb13] Koch, N., Seichter, W. & Mazik, M. (2017). CrystEngComm19, 3817–3833.

[bb14] Manick, A.-D., Dutasta, J.-P. & Martinez, A. (2023). ChemPlusChem88, e202300291. [DOI] [PubMed]

[bb15] Mazik, M. (2012). RSC Adv.2, 2630–2642.

[bb16] Mazik, M. & Buthe, A. C. (2008). Org. Biomol. Chem.6, 1558–1568. [DOI] [PubMed]

[bb17] Mazik, M. & Hartmann, A. (2008). J. Org. Chem.73, 7444–7450. [DOI] [PubMed]

[bb18] Mazik, M., Hartmann, A. & Jones, P. G. (2009). Chem. Eur. J.15, 9147–9159. [DOI] [PubMed]

[bb19] Mazik, M. & Kuschel, M. (2008). Eur. J. Org. Chem. pp. 1517–1526.

[bb20] Naismith, J. H. & Field, R. A. (1996). J. Biol. Chem.271, 972–976. [DOI] [PubMed]

[bb21] Nishio, M., Umezawa, Y., Hirota, M. & Takeuchi, Y. (1995). Tetrahedron51, 8665–8701.

[bb22] Rothenberger, A. & Ponikiewski, L. (2007). Acta Cryst. E63, o2636–o2637.

[bb23] Sauter, N. K., Glick, G. D., Crowther, R. L., Park, S.-J., Eisen, M. B., Skehel, J. J., Knowles, J. R. & Wiley, D. C. (1992). Proc. Natl Acad. Sci. USA89, 324–328. [DOI] [PMC free article] [PubMed]

[bb24] Schulze, M., Schwarzer, A. & Mazik, M. (2017). CrystEngComm19, 4003–4016.

[bb25] Sharon, N. & Lis, H. (2007). In Lectins. Dordrecht: Springer.

[bb26] Sheldrick, G. M. (2015a). Acta Cryst. A71, 3–8.

[bb27] Sheldrick, G. M. (2015b). Acta Cryst. C71, 3–8.

[bb28] Stapf, M. & Mazik, M. (2026). Eur. J. Org. Chem.29, e70593.

[bb29] Stapf, M., Schmidt, U., Seichter, W. & Mazik, M. (2023). Acta Cryst. E79, 1067–1071. [DOI] [PMC free article] [PubMed]

[bb30] Stapf, M., Seichter, W. & Mazik, M. (2015). Chem. Eur. J.21, 6350–6354. [DOI] [PubMed]

[bb31] Stoe (2024). X-RED and X-AREA. Stoe & Cie, Darmstadt, Germany.

[bb32] Sluis, P. van der & Spek, A. L. (1990). Acta Cryst. A46, 194–201.

PERMALINK

Crystal structure of a hydrate of 1,3,5-substituted 2,4,6-trialkylbenzene bearing hydroxymethyl and pyridinylamino groups

Manuel Stapf

Wilhelm Seichter

Monika Mazik

Roles

Abstract

1. Chemical context

2. Structural Commentary

Figure 1.