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Article

Synthesis, Crystal Structure and Hirshfeld Topology Analysis of Polymeric Silver(I) Complex with s-Triazine-Type Ligand

by
Saied M. Soliman
1,2,* and
Ayman El-Faham
1,3,*
1
Department of Chemistry, Faculty of Science, Alexandria University, P.O. Box 426 Ibrahimia, 21321 Alexandria, Egypt
2
Department of Chemistry, Rabigh College of Science and Art, King Abdulaziz University, P.O. Box 80200, Jeddah 21589, Saudi Arabia
3
Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
*
Authors to whom correspondence should be addressed.
Crystals 2017, 7(6), 160; https://doi.org/10.3390/cryst7060160
Submission received: 16 May 2017 / Revised: 25 May 2017 / Accepted: 31 May 2017 / Published: 2 June 2017
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Abstract

:
The synthesis, single crystal X-ray diffraction (SC-XRD) characterization and Hirshfeld topology analysis of molecular packing of the coordination polymer [Ag2L(H2O)2(ClO4)2]n, where L = 2,4,6-trimorpholino-1,3,5-triazine were discussed. The asymmetric unit comprises one Ag2L(H2O)2(ClO4)2 unit. The coordination geometries around the two silver atoms are different where Ag(1) is hexa-coordinated with one L, two bridged water, and two bridged perchlorate augmented with one strong Ag-O interaction from the morpholine O-atom of another ligand (L) unit. The coordination environment is more like to a distorted octahedral arrangement according to the criteria of continuous shape measurements. Ag(2) is coordinated to one L, one terminal water and one terminal perchlorate leading to a distorted trigonal planar arrangement around Ag(2). Hirshfeld analysis of molecular packing indicated that the most important intermolecular contacts affect the molecular packing of the studied complex are the H...H and the O...H interactions. Atoms in molecules (AIM) and natural bond orbital (NBO) analyses were used to describe the strength and nature of the Ag-O and Ag-N interactions.

Graphical Abstract

1. Introduction

Silver(I) complexes attracted the attention of many research groups due to their fascinating structure aspects as well as their interesting biological activity as antimicrobial and antifungal agents [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19]. The complexation between the organic ligand and silver(I) is considered an improvement for the ligand biological activity [20]. Silver sulfadiazine [21] is used as an antibacterial topical cream for burn wounds. From structural point of view, the coordination environment of silver is unpredictable and is found surprising for a d10 metal ion. It could accommodate different coordination geometries, such as linear/bent, trigonal planar or tetrahedral which are the most common. Square planar and hexa-coordinated silver(I) complexes are less common in the literature [22]. In addition, it often serves as a connector (L-Ag-L) between ligands leading to fascinating supramolecular structures. The structure topology of the Ag-complexes depends mainly on the nature of the polydentate ligand and anion [23]. Recently, we presented the X-ray structure combined with topology analysis of a huge unit cell comprises of 96 [AgL2]+ complex ions in 46,000 Å3 unit Cell [24]. Here, we present the synthesis of a new silver(I) perchlorate complex with s-triazine type-ligand namely, 2,4,6-trimorpholino-1,3,5-triazine (L). The structure aspects of this complex are investigated using single crystal X-ray diffraction (SC-XRD) combined with Hirshfeld and atoms in molecules (AIM) topology analyses.

2. Results

The ligand (L, Figure 1) was prepared using the method reported previously in the literature [25]. The studied silver complex has been synthesized using self-assembly technique by mixing the alcoholic solution of the ligand 2,4,6-trimorpholino-1,3,5-triazine (L; Figure 1) with aqueous solution of silver(I) perchlorate in distilled water. The [Ag2L(H2O)2(ClO4)2]n complex is formed as colorless crystals after few days of slow evaporation of the solvent. The structure of the studied silver(I) complex is characterized using elemental analysis, FTIR spectra and SC-XRD analysis.

3. Discussion

3.1. Crystal Structure Description

The crystal structure of the [Ag2L(H2O)2(ClO4)2]n complex crystallizes in the centrosymmetric, triclinic space group P-1. The asymmetric unit consists of two silver(I), one 2,4,6-trimorpholino-1,3,5-triazine (L) ligand, two coordinated water and two coordinated perchlorate anions. The atomic numbering scheme of the asymmetric unit is shown in Figure 2. Tables S1 and S2 (Supplementary Materials) summarize selected interatomic distances and bond angles, respectively.
In the studied silver complex, there are two different silver atoms with different coordination environments. Ag(1) is hexa-coordinated with one N-atom from the triazine ring (Ag1-N1 = 2.325 Å) of the ligand (L), two water molecules (Ag1-O1 = 2.346 and 2.685 Å), two perchlorate units (Ag1-O8 and Ag1-O9 = 2.699 Å) and one O-atom of morpholine (Ag1-O11 = 2.565 Å) from another ligand (L) unit (Figure 3). In this case, two water bridges and two bridged perchlorate units connect two Ag(1) atoms. The Ag(1)...Ag(1) separation is quite large (3.783 Å), indicating negligible argentophilic interaction. The Ag(1) form strong Ag-O interaction (2.565 Å) with the O-atom of morpholine from another complex unit leading to the formation of one-dimensional coordination polymer along the a-direction (Figure 4). On the other hand, Ag(2) is coordinated to one N-atom from the triazine ring, one water and one perchlorate anion. In this case, the water and perchlorate anion acti as terminal ligands. The N2-Ag2-O2, N2-Ag2-O6 and O2-Ag2-O6 bond angles are 156.4°, 101.7° and 101.6°, respectively. From this point of view, the Ag(2) has a distorted trigonal planar geometry (Figure 3). It is worth noting that Ag2-O6(ClO4) and Ag2-O2(H2O) have slightly shorter distances of 2.672 Å and 2.220 Å, respectively, than the bridged ones. The structure of studied complex contains numerous hydrogen bonds between the H atoms of the water molecules with the O-atoms from the perchlorate anion and morpholine ring in the organic ligands (Table 1 and Figure S1; Supplementary Materials). The bridged and terminal water molecules connects the one-dimensional polymer chains via strong intermolecular O13...H1B (2.038 Å), O4...H2B (2.248 Å) and O12...H2A (2.084 Å) hydrogen bonding interactions shown in Figure 5.

3.2. Continuous Shape Measure (CShM)

Continuous shape measure (CShM) [26,27] is the most common method used to determine the extent of distortion in a given polyhedral from an ideal shape. There are two possible ligand arrangements around the central metal ion for a hexa-coordinated metal complex: octahedral and trigonal prism. Using the CShM, the values of shape measurements of the coordination environment around Ag(1) are 4.984 and 9.291 with respect to the ideal octahedron and trigonal prism, respectively. Larger value of shape measurement indicates a more distorted arrangement compared to the ideal case. From this point of view, the geometry around Ag(1) is more like the octahedron than the trigonal prism.

3.3. Analysis of Molecular Packing

The Hirshfeld surfaces mapped over dnorm, shape index (SI) and curvedness are shown in Figure 6 and Figure S2 (Supplementary Materials). These properties give information about the intermolecular interactions in the crystal [28,29,30,31]. The shape index and curvedness maps are the most suited to identify the π–π stacking interactions. It is clear from these maps that the packing of the studied complex showed no signs of π–π stacking interactions as a result of the bulky effect of the morpholine rings attached to the aromatic triazine ring. The curvedness map showed no green flat areas and the shape index has no complementary red (negative) and blue (positive) triangles, which are distinct for the identification of π–π stacking. The decomposition of the fingerprint plot gave the frequency of each intermolecular interaction occur in the crystal (Figure 7). Based on this data, the zero percent of C...C contacts confirm the absence of any π–π stacking interactions in the studied system. It is clear that the main intermolecular interactions affecting the molecular packing of the studied complex are the O...H and H...H interactions. The percentages of these interactions are 49.6% and 38.3%, respectively. Different levels of H...H contacts were observed among the C-H bonds of the morpholine rings. Summary of the most important H...H interactions are shown in Figure 8. These H...H contacts appeared as red spots in the dnorm map indicating their significance. The H16B...H19B and H13A...H19A have contact distances of 2.053 and 2.133 Å, respectively. The former is significantly shorter than twice the van der Waal radii of H-atom indicating its importance in the molecular packing of the studied Ag-complex. The hydrophobic C…H interactions contributed by 2.4% from the overall fingerprint and appeared as fad red spots in the dnorm map (Figure S3, Supplementary Materials). The C9...H12A interaction have contact distance of 2.653 Å, which is also shorter than the van der Waal radii sum of the two elements (2.79 Å).
On the other hand, the polar O...H interactions occur between the morpholine and perchlorate O-atoms as proton acceptor with either the coordinated water or morpholine rings as proton donor. Of the O...H interactions the shortest contacts are O13...H1B (1.843 Å) and O12...H2A (1.954 Å) which occur between the protons from the coordinated water molecules and the O-atoms of the neighboring morpholine ring. These O...H contacts have short intermolecular distances as observed from the intense red spots in the dnorm map and the sharp spikes in the fingerprint plot shown in Figure 9. Moreover, weak polar interaction occurs between the triazine N-atom and the morpholine C-H protons with contact distance of 2.660 Å (N3...H12A). This value is slightly longer than the sum of the van der Waal radii of the N and H atoms (2.640 Å). This interaction appeared to be less significant than the O...H interactions. Interestingly, the decomposed fingerprint plot identified the Ag1…O11 interactions (4.0%) which appeared as dark red spots in the dnorm map and sharp spikes in the decomposed FP plot (Figure S4, Supplementary Materials). These results reveal the polymeric nature of the studied complex via the significant Ag1…O11 (2.565 Å) interactions. On the other hand, two weaker Ag2…O7 and Ag2…O12 interactions were detected with contact distances of 2.996 Å and 2.875 Å, respectively. These interactions appeared as fad red spot in the dnorm map compared to the Ag1…O11 one. The decomposed fingerprint plots shown in Figure S5 (Supplementary Materials) indicated the less importance of the C...O, O...O, N...O and Ag...H contacts in the molecular packing of the studied silver complex.

3.4. AIM and NBO Analyses

The natural bond orbital (NBO) calculations were employed to discuss the amount of electron density transferred among the ligand and Ag(I) ion as well as to describe the strength of Ag-O and Ag-N interactions. The natural charge at the Ag(1) is calculated to be 0.5751, 0.6140, 0.5964 e using B97D, wB97XD and B3LYP methods, respectively, while for Ag(2) are 0.6255, 0.6961, and 0.6610 e, respectively. It is clear that, the more donor atoms around the hexa-coordinated Ag(1) decrease its positive charge density compared to the tri-coordinated Ag(2). Hence, the ligands transferred significant amount of electron density in the range of 0.3860–0.4249 e and 0.3039–0.3745 e, respectively, to the Ag-atoms. Moreover, the interaction energies (E(2)) deduced based on the second order perturbation theory were used to assess the strength of the Ag-O and Ag-N interactions [32,33,34]. The detailed donor (NBOi)-acceptor (NBOj) interactions and their E(2) values are given in Table S3 (Supplementary Materials). The net of each of these interactions are summarized in Table 2. The Ag1-N1 (13.29–18.75 kcal/mol) is weaker than the Ag2-N2 (31.48–30.30 kcal/mol) one. Moreover, the Ag1-O1 bonds (12.04–20.36 kcal/mol) of the bridged water are also weaker than the Ag2-O2 (32.22–40.18 kcal/mol) of the terminal water. The two Ag1-O8 and Ag1-O9 have almost the same interaction energies, which are slightly weaker than the Ag2-O6 of the terminal perchlorate unit. All methods predicted very weak LP(Ag1)→LP*(Ag1ii), which confirm that the argentophilic interaction among these Ag-atoms are insignificant.
Moreover, the AIM topological parameters shown in Table S4 (Supplementary Materials) were used to further describe the strength and nature of the Ag-N and Ag-O interactions. The results shown in this table confirmed the stronger Ag2-N2 than Ag1-N1 bond as the former has higher electron density at the corresponding BCP than the latter [35]. Moreover, the interaction energy computed using the relation (Eint = −V(r)/2) [36] is higher for the Ag2-N2 than that for Ag1-N1, which agrees with the X-ray structure. In addition, it is clear that the Ag2-O2 of the terminal water has higher ρ(r) value than any of the two Ag1-O1 bonds from the bridged water. The same is true for the perchlorate unit where in all cases; shorter distances have higher interactions energies than the longer ones. On the basis of the small negative total energy density H(r) and the ratio |V(r)|/G(r) of ~1, we concluded that the Ag-N and Ag-O bonds nature are intermediate between the ionic and covalent character [37,38].

4. Materials and Methods

4.1. General

All chemicals were purchased from commercial sources and were used without further purification. Infrared spectra (4000–400 cm−1) were recorded on Nicolet 6700 spectrometer (International Equipment Trading Ltd., Mundelein, IL, USA) in KBr pellets and the wavenumbers are in cm−1. Elemental analyses were performed on Perkin-Elmer 2400 elemental analyzer (Perkin Elmer, Inc., 940 Winter Street, Waltham, MA, USA).

4.2. X-ray Measurements

Data were collected on a Bruker D8 Quest diffractometer with graphite monochromated Mo-Kα radiation, λ = 0.71073 Å at 113 (2) K and a photon detector. Cell refinement and data reduction were carried out using SAINT [39], and a multi-scan absorption correction was made using SADABS [40]. Heavy atom sites were located using direct methods and refined by full-matrix least-squares techniques on F2 including anisotropic displacement parameters for all non-hydrogen atoms using SHELXT [41]. Hydrogen atoms bonded to carbon atoms were refined isotropically using geometrical restraints while the H atoms bonded to oxygen atoms were allowed to vary freely. The crystallographic data of these complexes were summarized in Table 3. The CIF file CCDC-1549763 contains the supplementary crystallographic data for this compound measured. This can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.

4.3. Hirshfeld Surface Analysis

Hirshfeld surface analyses of the silver complex were made using Crystal Explorer 3.1 program [42]. The Hirshfeld surface, shape index, and curvedness plots were drawn using the same software. The Hirshfeld surfaces mapped over dnorm (range of −0.082 to 1.029 Å) together with their 2D fingerprint plots were used to analyze the intermolecular interactions [43] in the studied complex. The Hirshfeld surfaces mapped over shape index (range of −1.0 to 1.0 Å) and curvedness (−4.0 to 4.0 Å) were drawn to investigate the possibility of π–π stacking among molecular units.

4.4. Synthesis of the Silver(I) Complex

To a solution of L; (~0.3364 g, 1 mmol) in 10 mL methanol, aqueous solution of silver(I) perchlorate (~0.2073 g, 1 mmol) was added. The mixture was filtered off and the clear filtrate is left at room temperature for slow evaporation. After 5 days, colorless crystals of [Ag2L(H2O)2(ClO4)2]n complex were obtained. The crystals were collected from solution and were found suitable for X-ray analysis.
Yield: 84%; IR (νmax, cm−1): [Ag2L(H2O)2(ClO4)2]n: 3422 (m), 2994(w), 2970(w), 2918(w), 1541(vs), 1107(vs), 1090(vs), 926(w); Anal. Calcd. C15H28Ag2Cl2N6O13: C, 22.89; H, 3.59; N, 10.68%. Found: C, 22.90; H, 3.60; N, 10.67%.

4.5. Computational Details

Single point calculations for the studied complex were performed using Gaussian 09 program [44]. Different DFT methods (B3LYP, B97D, and WB97XD) were used to describe the nature and strength of the Ag-N and Ag-O interactions in the studied complex. Gaussian built in cc-pvtz basis sets for nonmetal atoms (C, H, N, O and Cl) and def2-TZVP for silver is used. The latter is obtained from EMSL basis set exchange [45]. The Cartesian coordinates of the input structure are taken from the crystallographic information file (CIF) of the studied silver(I) complex. The resulting wavefunction files were analyzed using Multwfn [46] program to perform the topology analysis in the framework of the quantum theory of atoms in molecules (QTAIM) [47]. Topological parameters such as total electron density (ρ(r)), local electron kinetic energy density (G(r)), local electron potential energy density (V(r)) and total energy density (H(r)) were used to describe the nature of the Ag-N and Ag-O bonds. Moreover, natural bond orbital (NBO) calculations were made using the NBO 3.1 [48] program to assign the nature of orbitals included in the metal–ligand interactions. Using the same method, the natural atomic charges were obtained.

5. Conclusions

Using self-assembly technique, the [Ag2L(H2O)2(ClO4)2]n complex was synthesized, where L is 2,4,6-trimorpholino-1,3,5-triazine. The X-ray crystal structure analysis revealed that, the ligand (L) connects the complex units via strong Ag-O(morpholine) interactions leading to the formation of one-dimensional coordination polymer. The coordination geometry around Ag(1) and Ag(2) are distorted octahedral and trigonal planar, respectively. The molecular packing of the studied complex is mainly controlled by the polar O…H and nonpolar H…H interactions. The AIM and NBO results were used to describe the nature and strength of the Ag-O and Ag-N interactions. From the obtained results, it is clear that more donor atoms around the hexa-coordinated Ag(1) decrease its positive charge density compared to the tri-coordinated Ag(2). All methods used predicted very weak LP(Ag1)→LP*(Ag1ii), which confirm that the argentophilic interaction among these Ag-atoms are insignificant. Moreover, the interaction energy computed using the relation (Eint = −V(r)/2) is higher for the Ag2-N2 than that for Ag1-N1, which agrees with the X-ray structure.

Supplementary Materials

The following are available online at www.mdpi.com/2073-4352/7/6/160/s1, Figure S1: The hydrogen bonding network along the viewing b-direction in the studied silver(I) complex, Figure S2: The shape index (SI) and curvedness Hirshfeld surfaces of the [Ag2L(H2O)2(ClO4)2]n complex, Figure S3: The decomposed fingerprint plot (upper) and dnorm map (lower) of the C…H interactions, Figure S4: The decomposed FP plot (upper) and the dnorm map (lower) of the Ag...O interactions: (A) Ag1-O11 (2.565 Å); (B) Ag2…O12 (2.879 Å); and (C) Ag2…O7 (2.996 Å). Note the significant variation of the red color intensity, Figure S5: The decomposed fingerprint plot of the less important contacts observed in the crystal of the studied complex, and Figure S6: FTIR spectra of the studied complex. Table S1: Selected Interatomic distances [Å] for studied complex, Table S2: Selected Interatomic angles [°] for studied complex, Table S3: The detailed intramolecular charge transfer interactions included in the Ag-N and Ag-O interactions using different DFT methods and Table S4: The AIM topological parameters calculated using different DFT methods.

Acknowledgments

The authors extend their appreciation to the Deanship of Scientific Research at King Saud University for funding this work through research group No (RGP-234, Saudi Arabia).

Author Contributions

Saied M Soliman conceived, designed and performed the synthesis of the studied complex. In addition, he carried out the SC-XRD data collection, wrote the X-ray structure studies and performed the computational studies. Ayman El-Faham carried out the synthesis of the organic ligand and contributed reagents, materials, and analysis tools. Both authors contributed to the preparation of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Crystals 07 00160 g001 550
Figure 1. The structure of the ligand L.
Figure 1. The structure of the ligand L.
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Figure 2. The asymmetric unit and atomic numbering scheme of the [Ag2L(H2O)2(ClO4)2]n complex. Note that the Ag1-N1; 2.325(2), Ag1-O1; 2.346(2) and Ag1-O9; 2.699(2) interatomic distances are longer than the corresponding Ag2-N2; 2.232(2), Ag2-O2; 2.220(2), and Ag2-O6; 2.672(3), respectively.
Figure 2. The asymmetric unit and atomic numbering scheme of the [Ag2L(H2O)2(ClO4)2]n complex. Note that the Ag1-N1; 2.325(2), Ag1-O1; 2.346(2) and Ag1-O9; 2.699(2) interatomic distances are longer than the corresponding Ag2-N2; 2.232(2), Ag2-O2; 2.220(2), and Ag2-O6; 2.672(3), respectively.
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Crystals 07 00160 g003 550
Figure 3. The different coordination environments around Ag-atoms in the studied complex.
Figure 3. The different coordination environments around Ag-atoms in the studied complex.
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Crystals 07 00160 g004 550
Figure 4. The one-dimensional coordination polymer formed via the Ag1-O11(morpholine) and Ag1-N1(triazine) interactions. Ag1 acts as connector between the ligand units forming 1D coordination polymer.
Figure 4. The one-dimensional coordination polymer formed via the Ag1-O11(morpholine) and Ag1-N1(triazine) interactions. Ag1 acts as connector between the ligand units forming 1D coordination polymer.
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Crystals 07 00160 g005a 550Crystals 07 00160 g005b 550
Figure 5. The hydrogen bonding interactions formed between the morpholine O-atoms and the protons from the bridged (A) and terminal water molecules and perchlorate anion (B) which connects the octahedral and trigonal planar coordination environments, respectively.
Figure 5. The hydrogen bonding interactions formed between the morpholine O-atoms and the protons from the bridged (A) and terminal water molecules and perchlorate anion (B) which connects the octahedral and trigonal planar coordination environments, respectively.
Crystals 07 00160 g005aCrystals 07 00160 g005b
Crystals 07 00160 g006 550
Figure 6. The dnorm Hirshfeld surface of the [Ag2L(H2O)2(ClO4)2]n complex.
Figure 6. The dnorm Hirshfeld surface of the [Ag2L(H2O)2(ClO4)2]n complex.
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Figure 7. The percentages of all possible intermolecular contacts in the crystal of the studied complex.
Figure 7. The percentages of all possible intermolecular contacts in the crystal of the studied complex.
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Figure 8. The decomposed fingerprint plot of the H...H contacts (a) and the dnorm map (b) showing the most important H...H intermolecular interactions: (A) H16B...H19B (2.053 Å); and (B) H13A...H19A (2.133 Å).
Figure 8. The decomposed fingerprint plot of the H...H contacts (a) and the dnorm map (b) showing the most important H...H intermolecular interactions: (A) H16B...H19B (2.053 Å); and (B) H13A...H19A (2.133 Å).
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Figure 9. The decomposed fingerprint plot (a) and the dnorm map (b) of the possible O...H contacts observed from the Hirshfeld surface analysis of the studied silver(I) complex: (A) O13...H1B (1.843 Å); (B) O6...H12B (2.275 Å); (C) O4...H2B (2.076 Å); (D) O6...H2B (2.342 Å); (E) O12...H2A (1.954 Å); (F) O7...H17B (2.453 Å); (G) O7...H21B (2.375 Å); and (H) O9...H19A (2.541 Å), O9...H13A (2.376 Å).
Figure 9. The decomposed fingerprint plot (a) and the dnorm map (b) of the possible O...H contacts observed from the Hirshfeld surface analysis of the studied silver(I) complex: (A) O13...H1B (1.843 Å); (B) O6...H12B (2.275 Å); (C) O4...H2B (2.076 Å); (D) O6...H2B (2.342 Å); (E) O12...H2A (1.954 Å); (F) O7...H17B (2.453 Å); (G) O7...H21B (2.375 Å); and (H) O9...H19A (2.541 Å), O9...H13A (2.376 Å).
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Table
Table 1. The important hydrogen bonds in the crystal structure of the studied complex [Å and °].
Table 1. The important hydrogen bonds in the crystal structure of the studied complex [Å and °].
D-H...Ad(D-H)d(H...A)d(D...A)<(DHA)
O1-H1A...O100.802.172.870145.4
O1-H1B...O13#10.782.042.801165.7
O2#2-H2B#2...O4#30.782.252.965152.7
O2#4-H2A#4...O120.852.082.893159.9
Symmetry transformations used to generate equivalent atoms: #1 1 − x, −y, 1 − z; #2 + x, 1 + y, +z; #3 − x, 1 − y, 2 − z; #4 1 + x, 1 + y, +z.
Table
Table 2. Summary of the net intramolecular charge transfer interactions and their E(2) values (kcal/mol) included in the Ag-N and Ag-O bonds using different DFT methods.
Table 2. Summary of the net intramolecular charge transfer interactions and their E(2) values (kcal/mol) included in the Ag-N and Ag-O bonds using different DFT methods.
NBOiNBOjB97DWB97XDB3LYPNBOiNBOjB97DWB97XDB3LYP
LP(N1)LP*(Ag1)13.2918.5714.63LP(1)N2LP*(Ag2)31.4840.3033.75
LP(O1)LP*(Ag1)12.0415.5612.85LP(O2)LP*(Ag2)32.2240.1834.08
LP(O1)LP*(Ag1ii)15.7820.3617.43LP(O6)LP*(Ag2)24.4730.2826.15
LP(O8)LP*(Ag1)23.0329.3425.17
LP(O9)LP*(Ag1)22.8729.5924.88
LP(O11)LP*(Ag1)16.6122.1118.16
LP(Ag1)LP*(Ag1)0.820.971.08
Table
Table 3. Crystallographic data and processing parameters for the studied complex.
Table 3. Crystallographic data and processing parameters for the studied complex.
Empirical formulaC15H28Ag2Cl2N6O13
Formula weight787.07 g/mol
Temperature115(2)
Wavelength0.71073 Å
Crystal systemTriclinic
Space groupP-1
Unit cell dimensionsa = 10.0030(15) Åα = 100.928(5)°
b = 10.1143(18) Åβ = 92.299(5)°
c = 13.191(2) Åγ = 108.348(5)°
Cell volume1236.6(4) Å3
Z2
Density (calculated)2.114 g/cm3
Absorption coefficient1.877 mm−1
F(000)784
Crystal size (mm)0.412 × 0.211 × 0.200
θ range for data collection2.17° to 25.31°
Index ranges−11 ≤ h ≤ 12, −12 ≤ k ≤ 12, −15 ≤ l ≤ 15
Reflections collected19888
Independent reflections4486 [R(int) = 0.0260]
Completeness to theta = 25°99.7%
Refinement methodFull-matrix least-squares on F2
Data/restraints/parameters4486/0/356
Goodness-of-fit on F21.069
Final R indices [I > 2sigma(I)]R1 = 0.0189, wR2 = 0.0408
R indices (all data)R1 = 0.0220, wR2 = 0.0420
Extinction coefficient0.0062(2)
Largest diff. peak and hole0.675 and −0.710 eÅ−3

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Soliman, S.M.; El-Faham, A. Synthesis, Crystal Structure and Hirshfeld Topology Analysis of Polymeric Silver(I) Complex with s-Triazine-Type Ligand. Crystals 2017, 7, 160. https://doi.org/10.3390/cryst7060160

AMA Style

Soliman SM, El-Faham A. Synthesis, Crystal Structure and Hirshfeld Topology Analysis of Polymeric Silver(I) Complex with s-Triazine-Type Ligand. Crystals. 2017; 7(6):160. https://doi.org/10.3390/cryst7060160

Chicago/Turabian Style

Soliman, Saied M., and Ayman El-Faham. 2017. "Synthesis, Crystal Structure and Hirshfeld Topology Analysis of Polymeric Silver(I) Complex with s-Triazine-Type Ligand" Crystals 7, no. 6: 160. https://doi.org/10.3390/cryst7060160

APA Style

Soliman, S. M., & El-Faham, A. (2017). Synthesis, Crystal Structure and Hirshfeld Topology Analysis of Polymeric Silver(I) Complex with s-Triazine-Type Ligand. Crystals, 7(6), 160. https://doi.org/10.3390/cryst7060160

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