One-dimensional ladder gallium coordination polymer
Chemical Context
Research on coordination polymers (CPs) and metal–organic frameworks (MOFs) remains a topical area in chemistry, particularly the study of their crystal structures (Cui et al., 2016 ▸). These crystalline materials are typically obtained from a combination of metal ions and organic molecules, giving rise to one-, two- or three-dimensional structures (Chaplais et al., 2009 ▸). A wide variety of synthetic methods have been reported for the preparation of CPs/MOFs (Stock & Biswas, 2012 ▸; Yuan et al., 2018 ▸) ranging from ambient-temperature synthesis to conventional [hydrothermal (HT) and one-pot processes (OP)] and microwave (MWAS) synthesis. In addition, other less common techniques such as electrochemistry (EC), mechanochemistry (MC) and ultrasonic (US) synthesis can be used (Rubio-Martinez et al., 2017 ▸; Stock & Biswas, 2012 ▸).
A large number of MOF-containing divalent transition-metal ions have been described (Stock & Biswas, 2012 ▸; Devic & Serre, 2014 ▸). Examples of CPs/MOFs containing main-group elements, such as Al, Ga, or In, remain scarce (Stock, 2014 ▸). A search in the Cambridge Structural Database unveils around 100 Ga-bearing CP/MOF structures, for example. Remarkably, most of these structures were solved using powder X-ray diffraction (PXRD) techniques (Reinsch & De Vos, 2014 ▸; Volkringer et al., 2009 ▸). Such materials exhibit high thermal and chemical stability and are ideal candidates for a wide variety of applications (Silva et al., 2015 ▸; Yuan et al., 2018 ▸; Ajoyan et al., 2018 ▸; Howarth et al., 2016 ▸). As a result of the close similarity of the coordination chemistry of gallium and aluminium, most of the Ga-CP/MOFs published are isotypic with well-known Al-CP/MOFs, and also with the much rarer In-CP/MOFs (Schilling et al., 2016 ▸). This may, in part, explain why most of the studies found in the literature of Ga-CP/MOFs report only their structures. Furthermore, most of the applications that have been studied are related to those that are also found for Al-CP/MOFs (Banerjee et al., 2011 ▸; Zhang et al., 2018 ▸; Reinsch & De Vos, 2014 ▸; Canivet et al., 2014 ▸; Zhou et al., 2012 ▸). For certain applications, Ga-CP/MOFs excel, even surpassing the performance of the Al-CP/MOFs (Coudert et al., 2014 ▸; Ramaswamy et al., 2017 ▸; Weber et al., 2016 ▸; Gao et al., 2014 ▸). Furthermore, gallium materials possess low toxicity and are found in applications such as gas and water adsorption, shock-absorber technology and semiconductors (Ramaswamy et al., 2017 ▸; Coudert et al., 2014 ▸; Schilling et al., 2016 ▸)
Following our interest in CP/MOFs, we have attempted the preparation of MOF-303 (Fathieh et al., 2018 ▸) with Ga. In this crystallographic report we describe these studies, which culminated in the isolation of a compact one-dimensional ladder coordination polymer, [Ga(HPDC)(OH)(H2O)] (I), prepared by the self-assembly of Ga and the organic linker 3,5-pyrazoledicarboxylic acid monohydrate (H3PDC·H2O). Compound I was obtained using a variety of methods (hydrothermal, microwave and a one-pot process) and a survey of the literature revealed that it is isotypic with a compound published in 2008 (Chen et al., 2008 ▸), which is not unprecedented (Volkringer et al., 2009 ▸; Finsy et al., 2009 ▸; Volkringer et al., 2008 ▸).
Crystal Morphology and Characterization
Compound I was prepared by hydrothermal (HT), microwave (MWAS) and one-pot (OP) synthesis. The general experimental conditions were similar (solvent, molar quantities and temperature). The compound is isotypic with [V(HPDC)(OH)(H2O)] (Chen et al., 2008 ▸), which was prepared using harsher conditions. Our attempts to obtain the analogous V-bearing material using the conditions described here were unsuccessful.
MWAS produces phase pure coordination polymers much faster than the HT and OP approaches. PXRD studies have confirmed the same structural features (see Figure S1 in the supporting information). The crystal morphology, however, varied depending on the method employed (Fig. 1 ▸). Crystals typically exhibit irregular shapes. MWAS allowed a faster preparation of I when compared to the other methods (a reduction from 24 h to just 1 h) with a significantly smaller average crystal size (ca 3–5 µm) and a more uniform plate-like morphology. The HT method, on the other hand, afforded larger crystals (ca 15–65 µm) with a more block-type morphology, while the OP method resulted mainly in agglomerated particles with a plate-like morphology.
FT–IR spectroscopy supports the structural features revealed by the X-ray diffraction studies (Figure S2 in the supporting information). Compound I exhibits two broad bands centred at 3280 and 3159 cm attributed to the O—H stretching vibrational modes from the coordinated water molecules and to the N—H stretching vibrations of the pyrazole ring. In the central region of the spectrum, between ca 1700 and 1300 cm, it is possible to discern the typical C—O, C—C and C—N stretching vibrational modes arising from the pyrazole rings and the bending vibration of water molecules.
The materials showed similar thermal decomposition profiles between ambient temperature and ca 1000 K (Figure S3 in the supporting information). Between ambient temperature and ca 548 K, there is almost no weight loss, which is indicative of good thermal stability. The weight loss registered between ca 548 and 618 K is 14.9, 14.6 and 14.8% for the OP-, HT- and MWAS-derived materials, respectively, and is attributed to the release of the water of coordination and the decomposition of the hydroxyl group (theoretical weight loss 14.0%). The subsequent weight loss (ca 44.9%) is attributed to the decomposition of the ligand, resulting in the formation of Ga2O3.
Structural Commentary
Compound I was formulated by single-crystal X-ray diffraction as [Ga(HPDC)(OH)(H2O)] from a crystal obtained using hydrothermal synthetic conditions (see Experimental section for further details). This compound crystallizes in the centrosymmetric Pspace group with the asymmetric unit being composed of one Ga metal centre, one HPDC anionic organic linker, one hydroxyl group and one coordinated water molecule, as depicted in Fig. 2 ▸a.
The anionic organic linker HPDC has two distinct coordination modes: forming a N,O-chelate with the crystallographically independent Ga metal centre [bite angle of 78.02 (11)°], and bridging with an adjacent metal centre through a syn interaction involving the carboxylate group, imposing a Ga⋯Ga intermetallic distance of ca 8.52 Å (i.e. the length of the c axis of the unit cell). The octahedral {GaNO5} coordination sphere is completed by one water molecule and two-symmetry related μ2-bridging hydroxyl groups, which are the responsible for the formation of a centrosymmetric dimer, as depicted in Fig. 2 ▸b (intermetallic distance of ca 2.97 Å).
The Ga—O bond lengths range between 1.903 (3) and 1.988 (3) Å and the Ga—N distance is 2.112 (3) Å (Table 1 ▸), in good agreement with those reported for other carboxylate-based materials as witnessed by a search in the Cambridge Structural Database (CSD version of 2019; Groom et al., 2016 ▸): mean value of 1.988 Å for the Ga—O bond (CSD range, 1.832–2.475 Å) and 2.023 Å for the Ga—N bond (CSD range 1.798–3.275 Å).
Table 1
Ga1—O1 | 1.903 (3) | Ga1—O2 | 1.987 (3) |
Ga1—O5 | 1.932 (3) | Ga1—O1W | 1.988 (3) |
Ga1—O1 | 1.974 (3) | Ga1—N2 | 2.112 (3) |
O1—Ga1—O5 | 101.59 (12) | O1—Ga1—O1W | 178.65 (12) |
O1—Ga1—O1 | 79.94 (13) | O2—Ga1—O1W | 91.00 (11) |
O5—Ga1—O1 | 93.13 (12) | O1—Ga1—N2 | 93.94 (12) |
O1—Ga1—O2 | 166.31 (11) | O5—Ga1—N2 | 164.18 (12) |
O5—Ga1—O2 | 87.28 (11) | O1—Ga1—N2 | 92.49 (12) |
O1—Ga1—O2 | 89.26 (11) | O2—Ga1—N2 | 78.02 (11) |
O1—Ga1—O1W | 99.60 (12) | O1W—Ga1—N2 | 86.27 (12) |
O5—Ga1—O1W | 88.20 (12) |
Symmetry codes: (i) ; (ii) .
The aforementioned connectivity promotes the formation of a one-dimensional ladder-type coordination polymer along the [001] direction (Fig. 3 ▸a), which close pack in a parallel fashion in the ab plane of the unit cell mediated by various supramolecular contacts (see the following section). Although the organic linkers are stacked within these ladders, the inter-centroid distance is 4.442 (3) Å, indicating the absence of significant π–π supramolecular interactions.
Supramolecular Features
Compound I contains several functional groups that can promote the formation of various hydrogen-bonding interactions (Fig. 4 ▸, Table 2 ▸). The coordinated water molecule is engaged in two strong and directional O—H⋯O hydrogen-bonding interactions with neighbouring carboxylate groups from adjacent one-dimensional chains: dD⋯A distances of 2.643 (4) and 2.803 (4) Å and <(DHA) angles in the 164–165° range (Fig. 4 ▸, Table 2 ▸). These interactions may be described by the graph set motifs, (12) and (20). The independent μ2-bridging hydroxyl group also donates a hydrogen atom to a neighbouring carbonyl group (from the N,O-chelated moiety) in a strong interaction: dD⋯A distance of 2.751 (4) Å and <(DHA) angle of 175°. This contact leads to the formation of a supramolecular chain (10) across neighbouring polymers. Like the μ2-bridging hydroxyl group, the pyrazole ring is involved in a N—H⋯O interaction with a N,O-chelated ligand, leading to the formation of a distinct type of supramolecular chain, (6) [dD⋯A distance of 2.773 (4) Å and <(DHA) angle of 152°].
Table 2
D—H⋯A | D—H | H⋯A | D⋯A | D—H⋯A |
---|---|---|---|---|
O1W—H1X⋯O4 | 0.94 | 1.73 | 2.643 (4) | 164 |
O1W—H1Y⋯O2 | 0.94 | 1.89 | 2.803 (4) | 165 |
O1—H1⋯O3 | 0.77 | 1.99 | 2.751 (4) | 175 |
N1—H1N⋯O3 | 0.88 | 1.96 | 2.773 (4) | 152 |
Symmetry codes: (iii) ; (iv) ; (v) ; (vi) .
These supramolecular interactions lead to a close packing of individual polymers and to a compact crystal structure of I, as shown in Fig. 5 ▸.
Synthesis and Crystallization Procedures
Chemicals were purchased from commercial sources (Merck and TCI) and used without any further purification. The methods and molar quantities described here were based on a methodology described by Yaghi and coworkers for the preparation of MOF-303 (Fathieh et al., 2018 ▸).
Compound I was prepared by dissolving 147 mg (0.57 mmol) of gallium nitrate hexahydrate (Ga(NO3)3·6H2O) and 100 mg (0.57 mmol) of 3,5-pyrazoledicarboxylic acid monohydrate (H3PDC·H2O) in 9.6 mL of water in the corresponding vessel (autoclave for hydrothermal synthesis, microwave vial for microwave synthesis and a round-bottom flask equipped with a condenser for the one-pot approach). Subsequently, the vessels were heated at 373 K for 24 h (hydrothermal and one-pot synthesis) or 1 h (microwave synthesis). The resulting white precipitates were separated by filtration, washed three times with water and three times with ethanol, and dried overnight at ambient temperature (yields: 49, 47 and 60% for the one-pot, hydrothermal and microwave-assisted syntheses, respectively).
Refinement
Crystal data, data collection and structure refinement details are summarized in Table 3 ▸. Hydrogen atoms bound to carbon and nitrogen were placed at idealized positions using the HFIX 43 instruction in SHELXL2018/3 and included in subsequent refinement with C—H = 0.95 Å and N—H = 0.88 Å with the isotropic thermal displacement parameters fixed at 1.2Ueq of the atom to which they are attached.
Table 3
Crystal data | |
Chemical formula | [Ga(C5H2N2O4)(OH)(H2O)] |
Mr | 258.83 |
Crystal system, space group | Triclinic, P |
Temperature (K) | 150 |
a, b, c (Å) | 6.6055 (13), 6.8830 (16), 8.5178 (19) |
α, β, γ (°) | 94.804 (8), 101.306 (7), 108.596 (7) |
V (Å) | 355.44 (14) |
Z | 2 |
Radiation type | Mo Kα |
μ (mm) | 3.88 |
Crystal size (mm) | 0.13 × 0.10 × 0.07 |
Data collection | |
Diffractometer | Bruker D8 QUEST |
Absorption correction | Multi-scan (SADABS; Bruker, 2001 ▸; Krause et al. 2015 ▸) |
No. of measured, independent and observed [I > 2σ(I)] reflections | 5768, 1303, 1182 |
Rint | 0.034 |
(sin θ/λ)max (Å) | 0.603 |
Refinement | |
R[F > 2σ(F)], wR(F), S | 0.031, 0.074, 1.11 |
No. of reflections | 1303 |
No. of parameters | 136 |
No. of restraints | 3 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å) | 0.65, −0.47 |
Hydrogen atoms from the coordinated water molecule and the hydroxyl group were directly located from difference-Fourier maps and included in the final structural models with the O—H and H⋯H distances restrained to 0.95 (1) and 1.55 (1) Å, respectively, in order to ensure a chemically reasonable environment. These hydrogen atoms were modelled with the isotropic thermal displacement parameters fixed at 1.5Ueq(O).
Abstract
A one-dimensional ladder-type coordination polymer, poly[[(μ2-hydroxido)(μ2-1H-pyrazole-3,5-dicarboxylato)gallium(III)] monohydrate], [Ga(C5H2N2O4)(OH)(H2O)]n or [Ga(HPDC)(OH)(H2O)]n, I, isotypic with a V coordination polymer previously reported by Chen et al. [J. Coord. Chem. (2008). 61, 3556–3567] was prepared from Ga and pyrazole-3,5-dicarboxylic acid monohydrate (H3PDC·H2O). Compound I was isolated using three distinct experimental methods: hydrothermal (HT), microwave-assisted (MWAS) and one-pot (OP) and the crystallite size should be fine-tuned according to the method employed. The coordination polymeric structure is based on a dimeric Ga moiety comprising two μ2-bridging hydroxide groups, which are interconnected by HPDC anionic organic linkers. The close packing of individual polymers is strongly directed by the supramolecular interactions, namely several O—H⋯O and N—H⋯O hydrogen-bonding interactions.
Crystal structure: contains datablock(s) I. DOI: 10.1107/S2056989019013446/sj5578sup1.cif
Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989019013446/sj5578Isup2.hkl
Supporting Information. DOI: 10.1107/S2056989019013446/sj5578sup3.docx
Click here for additional data file.(239K, docx)CCDC references: 1956892, 1956892
Additional supporting information: crystallographic information; 3D view; checkCIF report
supplementary crystallographic information
Crystal data
[Ga(C5H2N2O4)(OH)(H2O)] | Z = 2 |
Mr = 258.83 | F(000) = 256 |
Triclinic, P1 | Dx = 2.418 Mg m3 |
a = 6.6055 (13) Å | Mo Kα radiation, λ = 0.71073 Å |
b = 6.8830 (16) Å | Cell parameters from 3255 reflections |
c = 8.5178 (19) Å | θ = 2.5–25.4° |
α = 94.804 (8)° | µ = 3.88 mm1 |
β = 101.306 (7)° | T = 150 K |
γ = 108.596 (7)° | Block, colourless |
V = 355.44 (14) Å3 | 0.13 × 0.10 × 0.07 mm |
Data collection
Bruker D8 QUEST diffractometer | 1303 independent reflections |
Radiation source: Sealed tube | 1182 reflections with I > 2σ(I) |
Multi-layer X-ray mirror monochromator | Rint = 0.034 |
Detector resolution: 10.4167 pixels mm-1 | θmax = 25.4°, θmin = 3.7° |
ω / φ scans | h = −7→7 |
Absorption correction: multi-scan (SADABS; Bruker, 2001; Krause et al. 2015) | k = −8→8 |
l = −10→10 | |
5768 measured reflections |
Refinement
Refinement on F2 | 3 restraints |
Least-squares matrix: full | Hydrogen site location: mixed |
R[F > 2σ(F)] = 0.031 | H atoms treated by a mixture of independent and constrained refinement |
wR(F) = 0.074 | w = 1/[σ(Fo) + (0.0292P) + 1.2151P] where P = (Fo + 2Fc)/3 |
S = 1.11 | (Δ/σ)max = 0.001 |
1303 reflections | Δρmax = 0.65 e Å3 |
136 parameters | Δρmin = −0.47 e Å3 |
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. |
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å)
x | y | z | Uiso*/Ueq | ||
Ga1 | 0.20874 (7) | 0.17985 (7) | 1.03804 (5) | 0.00844 (15) | |
O1W | 0.5321 (4) | 0.2428 (4) | 1.0908 (3) | 0.0140 (6) | |
H1X | 0.604 (6) | 0.162 (6) | 1.147 (5) | 0.021* | |
H1Y | 0.627 (5) | 0.335 (5) | 1.040 (5) | 0.021* | |
O1 | 0.1126 (4) | −0.1152 (4) | 1.0094 (3) | 0.0100 (6) | |
H1 | 0.142 (8) | −0.167 (7) | 1.082 (6) | 0.015* | |
N1 | 0.2437 (5) | 0.1027 (5) | 0.4128 (4) | 0.0102 (7) | |
H1N | 0.249943 | −0.023469 | 0.404671 | 0.012* | |
N2 | 0.2363 (5) | 0.2116 (5) | 0.2909 (4) | 0.0088 (7) | |
C1 | 0.2537 (6) | 0.1216 (6) | 0.7048 (5) | 0.0103 (8) | |
C2 | 0.2405 (6) | 0.2131 (6) | 0.5511 (4) | 0.0089 (8) | |
C3 | 0.2296 (6) | 0.4004 (6) | 0.5154 (5) | 0.0102 (8) | |
H3 | 0.223752 | 0.511146 | 0.586837 | 0.012* | |
C4 | 0.2289 (6) | 0.3927 (6) | 0.3507 (4) | 0.0074 (8) | |
C5 | 0.2388 (6) | 0.5450 (6) | 0.2360 (5) | 0.0087 (8) | |
O2 | 0.2500 (4) | 0.4783 (4) | 0.0937 (3) | 0.0098 (6) | |
O3 | 0.2423 (5) | 0.7207 (4) | 0.2790 (3) | 0.0137 (6) | |
O4 | 0.2886 (5) | −0.0428 (4) | 0.7039 (3) | 0.0149 (6) | |
O5 | 0.2257 (4) | 0.2323 (4) | 0.8208 (3) | 0.0123 (6) |
Atomic displacement parameters (Å)
U11 | U22 | U33 | U12 | U13 | U23 | |
Ga1 | 0.0123 (2) | 0.0088 (2) | 0.0059 (2) | 0.00441 (17) | 0.00399 (16) | 0.00291 (15) |
O1W | 0.0120 (14) | 0.0172 (16) | 0.0176 (15) | 0.0074 (13) | 0.0071 (12) | 0.0109 (12) |
O1 | 0.0142 (14) | 0.0097 (14) | 0.0078 (14) | 0.0050 (12) | 0.0032 (11) | 0.0044 (11) |
N1 | 0.0164 (17) | 0.0109 (16) | 0.0069 (16) | 0.0069 (14) | 0.0057 (13) | 0.0056 (13) |
N2 | 0.0110 (17) | 0.0093 (16) | 0.0061 (15) | 0.0025 (13) | 0.0034 (13) | 0.0029 (12) |
C1 | 0.0076 (19) | 0.014 (2) | 0.0075 (19) | 0.0009 (16) | 0.0010 (15) | 0.0034 (15) |
C2 | 0.0073 (19) | 0.012 (2) | 0.0071 (19) | 0.0018 (16) | 0.0035 (15) | 0.0016 (15) |
C3 | 0.011 (2) | 0.0117 (19) | 0.0100 (19) | 0.0053 (16) | 0.0060 (16) | 0.0018 (15) |
C4 | 0.0066 (18) | 0.0077 (18) | 0.0084 (18) | 0.0020 (15) | 0.0034 (14) | 0.0024 (15) |
C5 | 0.0071 (19) | 0.0087 (19) | 0.0112 (19) | 0.0040 (15) | 0.0015 (15) | 0.0018 (15) |
O2 | 0.0158 (14) | 0.0064 (13) | 0.0086 (13) | 0.0043 (11) | 0.0048 (11) | 0.0022 (10) |
O3 | 0.0205 (16) | 0.0120 (15) | 0.0110 (14) | 0.0084 (12) | 0.0036 (12) | 0.0033 (11) |
O4 | 0.0203 (16) | 0.0171 (16) | 0.0125 (14) | 0.0100 (13) | 0.0076 (12) | 0.0072 (12) |
O5 | 0.0182 (15) | 0.0139 (14) | 0.0052 (13) | 0.0050 (12) | 0.0036 (11) | 0.0028 (11) |
Geometric parameters (Å, º)
Ga1—O1 | 1.903 (3) | N1—H1N | 0.8800 |
Ga1—O5 | 1.932 (3) | N2—C4 | 1.326 (5) |
Ga1—O1i | 1.974 (3) | C1—O4 | 1.224 (5) |
Ga1—O2ii | 1.987 (3) | C1—O5 | 1.276 (5) |
Ga1—O1W | 1.988 (3) | C1—C2 | 1.499 (5) |
Ga1—N2ii | 2.112 (3) | C2—C3 | 1.369 (6) |
Ga1—Ga1i | 2.9716 (10) | C3—C4 | 1.399 (5) |
O1W—H1X | 0.943 (10) | C3—H3 | 0.9500 |
O1W—H1Y | 0.939 (10) | C4—C5 | 1.487 (5) |
O1—H1 | 0.77 (5) | C5—O3 | 1.225 (5) |
N1—N2 | 1.333 (4) | C5—O2 | 1.284 (5) |
N1—C2 | 1.355 (5) | ||
O1—Ga1—O5 | 101.59 (12) | Ga1—O1—H1 | 118 (4) |
O1—Ga1—O1i | 79.94 (13) | Ga1—O1—H1 | 107 (4) |
O5—Ga1—O1i | 93.13 (12) | N2—N1—C2 | 110.6 (3) |
O1—Ga1—O2ii | 166.31 (11) | N2—N1—H1N | 124.7 |
O5—Ga1—O2ii | 87.28 (11) | C2—N1—H1N | 124.7 |
O1—Ga1—O2ii | 89.26 (11) | C4—N2—N1 | 106.8 (3) |
O1—Ga1—O1W | 99.60 (12) | C4—N2—Ga1iii | 112.3 (2) |
O5—Ga1—O1W | 88.20 (12) | N1—N2—Ga1iii | 140.7 (3) |
O1—Ga1—O1W | 178.65 (12) | O4—C1—O5 | 129.1 (4) |
O2—Ga1—O1W | 91.00 (11) | O4—C1—C2 | 118.2 (3) |
O1—Ga1—N2ii | 93.94 (12) | O5—C1—C2 | 112.7 (3) |
O5—Ga1—N2ii | 164.18 (12) | N1—C2—C3 | 107.5 (3) |
O1—Ga1—N2ii | 92.49 (12) | N1—C2—C1 | 119.5 (3) |
O2—Ga1—N2ii | 78.02 (11) | C3—C2—C1 | 133.0 (4) |
O1W—Ga1—N2ii | 86.27 (12) | C2—C3—C4 | 104.8 (3) |
O1—Ga1—Ga1i | 40.86 (8) | C2—C3—H3 | 127.6 |
O5—Ga1—Ga1i | 99.50 (8) | C4—C3—H3 | 127.6 |
O1—Ga1—Ga1i | 39.08 (8) | N2—C4—C3 | 110.3 (3) |
O2—Ga1—Ga1i | 127.84 (8) | N2—C4—C5 | 115.1 (3) |
O1W—Ga1—Ga1i | 140.45 (9) | C3—C4—C5 | 134.4 (3) |
N2—Ga1—Ga1i | 94.18 (9) | O3—C5—O2 | 124.3 (4) |
Ga1—O1W—H1X | 124 (2) | O3—C5—C4 | 121.2 (3) |
Ga1—O1W—H1Y | 123 (2) | O2—C5—C4 | 114.5 (3) |
H1X—O1W—H1Y | 110.8 (16) | C5—O2—Ga1iii | 118.6 (2) |
Ga1—O1—Ga1i | 100.06 (13) | C1—O5—Ga1 | 129.9 (3) |
C2—N1—N2—C4 | 0.2 (4) | N1—N2—C4—C5 | 175.1 (3) |
C2—N1—N2—Ga1iii | −173.6 (3) | Ga1—N2—C4—C5 | −9.2 (4) |
N2—N1—C2—C3 | 0.2 (4) | C2—C3—C4—N2 | 0.7 (4) |
N2—N1—C2—C1 | −178.4 (3) | C2—C3—C4—C5 | −173.7 (4) |
O4—C1—C2—N1 | 7.0 (5) | N2—C4—C5—O3 | −177.0 (3) |
O5—C1—C2—N1 | −173.1 (3) | C3—C4—C5—O3 | −2.8 (7) |
O4—C1—C2—C3 | −171.2 (4) | N2—C4—C5—O2 | 1.0 (5) |
O5—C1—C2—C3 | 8.7 (6) | C3—C4—C5—O2 | 175.2 (4) |
N1—C2—C3—C4 | −0.5 (4) | O3—C5—O2—Ga1iii | −173.3 (3) |
C1—C2—C3—C4 | 177.8 (4) | C4—C5—O2—Ga1iii | 8.8 (4) |
N1—N2—C4—C3 | −0.5 (4) | O4—C1—O5—Ga1 | −4.2 (6) |
Ga1—N2—C4—C3 | 175.2 (2) | C2—C1—O5—Ga1 | 175.8 (2) |
Symmetry codes: (i) −x, −y, −z+2; (ii) x, y, z+1; (iii) x, y, z−1.
Hydrogen-bond geometry (Å, º)
D—H···A | D—H | H···A | D···A | D—H···A |
O1W—H1X···O4iv | 0.94 | 1.73 | 2.643 (4) | 164 |
O1W—H1Y···O2v | 0.94 | 1.89 | 2.803 (4) | 165 |
O1—H1···O3vi | 0.77 | 1.99 | 2.751 (4) | 175 |
N1—H1N···O3vii | 0.88 | 1.96 | 2.773 (4) | 152 |
Symmetry codes: (iv) −x+1, −y, −z+2; (v) −x+1, −y+1, −z+1; (vi) x, y−1, z+1; (vii) x, y−1, z.
Funding Statement
This work was funded by Fundação para a Ciência e a Tecnologia grant .