Xinyu Tian†
Menghe Baiyin- Inner Mongolia University Key Laboratory of Advanced Materials Chemistry and Devices (AMC&DLab), College of Chemistry & Environmental Science, Inner Mongolia Normal University, Hohhot, China
Four selenoarsenates with different transition-metal complexes [Co(tren)2H]AsSe4 [tren = tris(2-aminoethyl)amine] (1); [Ni2(dien)4](As2Se5) (dien = diethylenetriamine) (2); [Zn(tren)]2(As2Se5) (3) and [Mn(tren)]2(As2Se5) (4) were solvothermally synthesized in a mixed solvent of organic amine and alcohol solution. The compounds 1-4 have pyramidal/tetrahedral structures (AsSe3/AsSe4), and contain transition metal (Co2+, Ni2+, Zn2+ and Mn2+) complex that form distinct zero-dimensional (0-D) clusters. Arsenic atoms form a tetrahedron in compounds 1 and 2; 1 consists of discrete tetrahedral (AsSe4) and transition metal complex [Co(tren)2]2+; 2 is composed of an anion [As2Se5]4- cluster and transition metal complex [Ni(dien)2]2+. In compounds 3 and 4, arsenic atom forms a pyramidal AsSe3 and the two pyramidal AsSe3 share a corner connection to form a dimer [As2Se5]4-; 3 is characterized as a cluster consisting of two unsaturated [Zn(tren)]2+ caiton linked by a dimer (As2Se5)4- linkage; in 4, unsaturated [Mn(tren)]2+ caiton is linked to two trigonal-bipyramidal [Mn(tren)]Se via dimer (As2Se5)4- to form [Mn(tren)]4[As4Se10] cluster. To our knowledge, [Zn(tren)]2(As2Se5) (3) is the first zinc selenoarsenate containing the (As2Se5)4- anion type. Furthermore, the Mn2+ ions adopt a trigonal-biyramidal (five-coordinate) and octahedral (six-coordinate) environment. Adding K2CO3/Cs2CO3 to the synthesis system is necessary and may act as a mineralizer. Several properties of compounds 1-4 have been characterized in our studies, in particular their strong photocurrent response characteristics under visible light irradiation.
Introduction
The wide variety of structures and properties of chalcogenidoarsenates have led to great interest in many areas, including semiconductors, photoelectricity, magnetism, ion exchange, and nonlinear optics (Sheldrick and Wachhold, 1998; Zhou et al., 2009; Zhang et al., 2012; Xiong et al., 2013; Yao et al., 2013; Liu et al., 2014; Zhou et al., 2015; Zhou, 2016; An et al., 2017; Wang et al., 2020; Chen et al., 2021; Li et al., 2021; Liu et al., 2021). The chalcogenidoarsenates are formed by corner- or edge-sharing of [AsQ3]3- and [AsQ4]3- (Q = S, Se) units, resulting in a variety of chalcogenidoarsenate aggregates. Such as [As2Q4]2- (Smith et al., 1996; Xu et al., 2021), [As2Se5]4- (Fu et al., 2006; Jia et al., 2006; Chen et al., 2021), [As2Se6]2- (Wendel and Müller, 1995; Smith et al., 1998; Fu et al., 2005b; Jia et al., 2011; Zhao et al., 2011b; Yang et al., 2018), [As3Q6]3- (An et al., 2017; Fu et al., 2005a; Zhou et al., 2017), [As4Q6]2- (Ansari et al., 1992; Smith et al., 1996), [As4S7]2- (Vater and Sheldrick, 1997), [As4Q8]4- (Kromm and Sheldrick, 2008), [As6S10]2- (Vater and Sheldrick, 1997), [As8S13]2- (Sheldrick and Kaub, 1985b; Sheldrick and Kaub, 1985a; Vater and Sheldrick, 1998), [As10Q3]2- (Smith et al., 1996). The thiophilic metal ions (Cu+, Ag+, Cd2+, Hg2+), which have less or little tendency to form complex cations with the strongly chelating amines, usually bond directly to the chalcogen elements. So far, some [MxAsyQz] chalcogenidoarsenates (M = Cu, Ag, Cd, Hg) have been obtained under solvothermal conditions. Such as, two kinds of [Cu2AsS3]n− chains (5-membered Cu2AsS2 rings and 6-membered Cu2AsS3 rings) form the two-dimensional anionic [Cu2AsS3]n− layer (Yao et al., 2013). The one-dimensional [AgAsS4]n2n− chain is a result of corner and edge sharing between AgS4 and AsS4. The [AgAs2Se5]n3- chains consist of ψ-bitetrahedral [As2Se5]4- units and tetrahedral coordinated Ag+ ions (Wachhold and Kanatzidis, 1999). The three-dimensional [Cu8(μ8-Se) (AsSe4)6/2]n3- framework is constructed of icosahedral Cu8Se13 clusters linked by As5+, with counterions located in the cavities (Zhang et al., 2012). The [CdAs2Se4]n2- chain synthesized by our group is made up of a tetrahedral [CdSe4] connected to a dimer As24+ through an As-Se bond, whereas the [HgAs2Se4]n2- chain is formed by of a tetrahedral [HgSe4] connected to a dimer As24+ dimer (Du et al., 2019; Teri et al., 2021b).
However, the addition of transition metals (Fe, Co, Ni, Zn, and Mn) is the most efficient and attractive way to synthesize new classes of chalcogenidoarsenates because these elements possess certain optical, magnetic, and electronic properties (Smith et al., 1996; Jia et al., 2011; Zhou, 2016). In the presence of strongly chelated amines, above transition metal ions are easily able to form stable transition metal complexes with organic amines due to variable coordinating environments. The addition of transition metal cations to the reaction mixture may increase the structural variability and tailor the electronic properties. Transition metal complexes (TMCs) can also act as structural directing agents or charge compensating ions, as exemplified by [M(dien)2][As2Se6] (M = Co, Ni), [Ni(en)3]2[As2S5] (en = ethylenediamine), [Fe(phen)3][As2Se6], [Zn(phen) (dien)][As2Se6]·2phen, [Ni(phen)3][As2Se2(μ-Se3) (μ-Se5)] (phen = 1,10-phenanthroline) (Jia et al., 2006; Jia et al., 2011; Zhao et al., 2011b). Noteworthy is that Mn2+ ions can not only coordinate with chalcogen atoms, but can also form transition metal complexes, which can connect with the chalcogenidoarsenate framework to generate new organic hybrid chalcogenidoarsenates, and most of these are zero-or one-dimensional, as exemplified by zero-dimensional {[Mn(phen)]2(AsVS4)2}2− (Liu et al., 2012), {[Mn(dien)]2(AsVS4)2}2− (Zhou et al., 2015), [Mn2(AsS4)4]8− (Iyer and Kanatzidis, 2004), and one-dimensional {[Mn(phen)]3(AsVS4) (AsIIIS3)}n (Liu et al., 2011), [Mn(teta) (AsVS4)]n− (Zhou et al., 2015), [Mn(dien) (AsS4)]nn− (Fu et al., 2005b), [Mn(en)2CuAsVS4]n (Zhou et al., 2015).
On the basis of these findings, a variety of transition metal complexes were selected as structure-directing agents for the synthesis of selenoarsenates with different structures: [Co(tren)2H]AsSe4 (tren = tris(2-aminoethyl)amine) (1); [Ni2(dien)4][As2Se5] (dien = diethylenetriamine) (2); [Zn(tren)]2[As2Se5] (3) and [Mn(tren)]2[As2Se5] (4). According to our knowledge, [Zn(tren)]2[As2Se5] (3) is the first [As2Se5]4− anion type of zinc selenoarsenate. There are two ligand environments of Mn2+ ions in [Mn(tren)]2[As2Se5] (4), which provides novel selenoarsenate of the [As2Se5]4− anion type. Adding K2CO3/Cs2CO3 to the synthesis system is necessary and may act as a mineralizer. Meanwhile, the pH of the solution also influences their structure. Additionally, their synthesis, structure, physical properties, photocurrent response, and magnetic are described in detail.
Experimental Section
All raw materials were purchased from the Shanghai Macklin Co., Ltd.: K2CO3 (99.5%), Cs2CO3 (99.5%), CoCl2·6H2O (98.0%), NiCl2·6H2O (99.0%), Zn(Ac)2·2H2O (99.0%), MnCl2·4H2O (99.0%), As2S3 (99.9%), Se (99.0%), tren (tren = tris(2-aminoethyl)amine) (96.0%), dien (dien = diethylenetriamine) (99.5%), CH3OH (99.5%), C2H5OH (99.7%), PEG-400 (poly-(propylene glycol)-400) (99.5%).
Synthesis of [Co(tren)2H]AsSe4 (1)
Cs2CO3 (17.0 mg, 0.052 mmol), CoCl2·6H2O (24.0 mg, 0.077 mmol), As2S3 (12.0 mg, 0.049 mmol) and Se (18.0 mg, 0.228 mmol), and a mixed solvent of tren (500 mg, 3.424 mmol) and C2H5OH (250 mg, 5.434 mmol) were added to Pyrex glass tube. The glass tube was sealed with a 10% filling, placed into a Teflon-lined stainless steel autoclave and heated at 150°C for 7 d. The products were washed with ethanol and deionized water, respectively, and dark yellow blocks crystal were obtained (27% yield based Se). Elemental analysis for 1: C 19.31%, H 4.92%, N 15.05%. Calc.: C 19.38%, H 4.97%, N 15.07%.
Synthesis of [Ni2(dien)4][As2Se5] (2)
NiCl2·6H2O (24.0 mg, 0.101 mmol), As2S3 (12.0 mg, 0.049 mmol), Se (16.0 mg, 0.203 mmol), and a mixed solvent of dien (630 mg, 4.315 mmol) and CH3OH (240 mg, 7.490 mmol) were added to Pyrex glass tube. The glass tube was sealed with a 10% filling, placed into a Teflon-lined stainless steel autoclave and heated at 150°C for 7 d. The products were washed with ethanol and deionized water, respectively, and red blocks crystal were obtained (29% yield based Se). Elemental analysis for 2: C 17.84%, H 4.79%, N 15.58%. Calc.: C 17.90%, H 4.84%, N 15.67%.
Synthesis of [Zn(tren)]2[As2Se5] (3)
Cs2CO3 (17.0 mg, 0.052 mmol), Zn(Ac)2·2H2O (22.0 mg, 0.100 mmol), As2S3 (12.0 mg, 0.049 mmol), Se (16.0 mg, 0.203 mmol), and a mixed solvent of tren (800 mg, 5.479 mmol) and PEG-400 (250 mg, 4.03 mmol) were added to Pyrex glass tube. The glass tube was sealed with a 10% filling, placed into a Teflon-lined stainless steel autoclave and heated at 160°C for 6 d. The products were washed with ethanol and deionized water, respectively, and yellow blocks crystal were obtained (31% yield based Se). Elemental analysis for 3: C 14.81%, H 3.66%, N 11.52%, calc.: C 14.88%, H 3.71%, N 11.57%.
Synthesis of [Mn(tren)]2[As2Se5] (4)
K2CO3 (14.0 mg, 0.111 mmol), MnCl2·4H2O (12.0 mg, 0.061 mmol), As2S3 (12.0 mg, 0.049 mmol), Se (16.0 mg, 0.203 mmol), and tren of solvent (600 mg, 4.109 mmol) to a Pyrex glass tube. The glass tube was sealed with a 10% filling, placed into a Teflon-lined stainless steel autoclave and heated at 150°C for 7 d. The products were washed with ethanol and deionized water, respectively, and yellow rodlike crystal were obtained (21% yield based Se). Elemental analysis for 4: C 15.16%, H 3.77%, N 11.77%, Calc: C 15.21%, H 3.80%, N 11.83%.
Results and Discussion
Syntheses
It has been widely observed that transition metal complexes are useful as template or structural-directing agents in the synthesis of chalcogenides. In this work, we have synthesized successfully four novel selenoarsenates in amine-alcohol system by solvothermal method, [Co(tren)2H]AsSe4 (1); [Ni2(dien)4][As2Se5] (2); [Zn(tren)]2[As2Se5] (3) and [Mn(tren)]2[As2Se5] (4). When organic amines and second agents (e.g., methanol, ethanol, polyethylene glycol) are used as mixed solvents in the synthesis of compounds 1, 2 and 3, their effects on crystallization are favorable. Conversely, when the second agent was not present, there was a significant loss of yield. In all probability, this is due to the drastic changes in some physical properties of the solvent (e.g., pH, density, viscosity, and diffusion coefficient), which contribute to the increased solubility and diffusivity of the reactants, as well as crystal growth. Furthermore, we found that adding K2CO3/Cs2CO3 was necessary for the synthesis of compounds 1, 3 and 4. If K2CO3/Cs2CO3 is removed from the reaction system, then the target product is not obtained, indicating its role as a mineralizer. The mineralizer may not be involved in the crystal structure but is crucial to the preparation of chalcogenides.
Structural Descriptions
Compound 1 crystallizes in the monoclinic crystal system in space group P21/n, and it consist of discrete tetrahedral AsSe4 and trigonal-bipyramid [Co(tren)2]2+ (Figure 1). The arsenic atoms have the pentavalent state, and they form tetrahedra AsSe4 by bonding with four Se atoms. Co2+ coordinates with four N atoms of one tren ligand and one N atom of another tren ligand to form a trigonal-bipyramid [Co(tren)2]2+ complex cation. In the compound [Co(phen)3][As2Se2(μ-Se3) (μ-Se5)] (Zhao et al., 2011a), however, arsenic atoms adopt a trivalent state. And the [As2Se2(μ-Se3) (μ-Se5)]2− anion contains two crystallographically As3+ centres, and each is coordinated by a terminal Se2− to give AsSe+ units. The AsSe+ units are joined together by μ-Se32− and μ-Se52− bridging ligands to give rise to a one-dimensional chain [As2Se2(μ-Se3) (μ-Se5)]2− (Du et al., 2019). Moreover, in the compound [Co(peha)][Co(As3S3)2] (Han et al., 2016), the arsenic atom binds three S2− ions, forming a typical trigonal pyramid AsS3. The adjacent trigonal pyramid AsS3 unit is connected by an arsenic atom via two S2− ions, forming As3S3 aggregation. Also the two As3S3 aggregates coordinate to the Co2+ ion via two arsenic atoms and an S atom to form [Co(As3S3)2]2 cluster. For compound 1, the As-Se bonds range between 2.2679(13) and 2.2932(11) Å, while Se-As-Se bond angles range from 106.74(5) to 112.48(5) °. The Co-N bond length ranges from 2.057(8) to 2.258(6) Å with N-Co-N bond angles from 79.3(3) to 178.4(2) °. The bond lengths and angles reported here are similar to those reported previously (Zhao et al., 2011a; Han et al., 2016).
FIGURE 1. Crystal structure of compound 1 (hydrogen atoms are omitted for clarity).
Compound 2 crystallizes in the monoclinic crystal system in space group P21/n. Two [AsSe3] trigonal pyramids are joined via corner sharing to form the [As2Se5]4− anion (Figure 2A). The As(1), Se(2) and Se(3) atoms are disordered. As shown in Figure 2B, the Ni2+ ion is coordinated by six N atoms to produce octahedral [Ni(dien)2]2+. Supplementary Figure S1 shows the cluster structure of the compound 2. Unlike the compound 2, [Ni(en)3]2[As2S5] contains arsenic atoms that adopt a pyramidal coordination geometry by bonding with three S atoms to form the [AsS3] pyramid. Two [AsS3] pyramids form dimeric [As2S5]4− anion by corner-sharing, and the two AsS3 pyramids are in cis-conformation (Jia et al., 2006). For compound 2, the As-Se bonds range from 1.8755(18) to 2.4404(19) Å and Se-As-Se bond angles range from 52.91(8) to 133.15(8)°. The Ni-N bond lengths range from 2.081(6) to 2.135(6) Å while the N-Ni-N bond angles range from 82.2(2) to 178.9(2)°. According to literature, bond lengths and angles are consistent (Jia et al., 2006; Du et al., 2019).
FIGURE 2. (A) [As2Se5]4- anion. (B) Coordination environment of the Ni2+ ion in compound 2 (hydrogen atoms are omitted for clarity).
Compound 3 crystallizes in the monoclinic crystal system in space group C2/c. In contrast to compound 1 and 2, in compound 3 the arsenic atoms are trivalent and they join three Se2− ions to form pyramid AsSe3, followed by two trigonal pyramid AsSe3 units are linked to μ2-Se(3) to form dimers [As2Se5]4−. Figure 3 shows the trigonal-bipyramidal unsaturated [Zn(tren)]2+ caiton formed by the coordination of the Zn2+ ion with four N atoms of the tren ligands and one μ2-Se atom. And two unsaturated [Zn(tren)]2+ caiton forms a cluster structure via dimeric [As2Se5]4− linkage between them. The cluster structure of compound 3 is shown in Supplementary Figure S2. Comparison with only one [As2Se6]2− anion type of zinc selenoarsenate [Zn(phen) (dien)][As2Se6]·2phen is quite different (Jia et al., 2011). In the [Zn(phen) (dien)][As2Se6]·2phen, the AsSe3 pyramids are tied together with two Se-Se bonds, forming the dimeric anion [As2Se6]2−, each [As2Se6]2− anion contains a six-membered ring. With compound 3, As-Se bond lengths range from 2.3181(10) to 2.4685(10) Å; Se-As-Se bond angles are between 86.92(3) and 105.74(4) °; and Zn-N bond lengths are between 2.074(6) and 2.416(6) Å; N-Zn-N bond angles are between 76.8(2) and 171.07(14) °. The bond lengths and angles are consistent with those reported in the literature (Jia et al., 2011; (Teri et al., 2021b). To the best of our knowledge, compound 3 is the first zinc selenoarsenate containing [As2Se5]4- anion type.
FIGURE 3. Trigonal-bipyramidal unsaturated [Zn(tren)]2+ caiton of compound 3 (hydrogen atoms are omitted for clarity).
Compound 4 crystallizes in the triclinic crystal system in space group P
FIGURE 4. Clusters of [Mn(tren)]4[As4Se10] in compound 4 (hydrogen atoms are omitted for clarity).
Compounds 3 and 4 have some special structural features. First, in compounds 3 and 4, it is the dimeric [As2Se5]4− unit that is linked to the transition metal complex. To the best of our knowledge, this type of connection mode has never been done before. It appears that most of them are directly linked to transition metal complexes via the AsSex (x = 3,4) units (Chen et al., 2021; Zhao et al., 2011b). Second, [As2Se6]2− anion type zinc selenoarsenate was synthesized in 2011 by Jia’s group (Jia et al., 2011). In addition, compound 3 is the first [As2Se5]4− anion type of zinc selenoarsenate, which lays a foundation for future work. Lastly, in compound 4, the five- and six-coordinate manganese atoms are linked by dimeric [As2Se5]4− units to form [Mn(tren)]4[As4Se10] clusters. Therefore, compounds 3 and 4 present a new structural pattern.
Powder X-Ray Diffraction and Thermogravimetric-Differential Thermal Analysis
In Supplementary Figure S4, the position of the 2θ diffraction peak obtained by the experiment is consistent with simulation results of the analysis of a single-crystal structure, showing that the products of the compounds are very pure, and all samples can be used for further study. The thermal stability of compounds 1-4 was studied by thermogravimetric and differential thermal analysis (Supplementary Figure S5). During the test, compound 1, the weight loss rate of 14% in the range of 181–286°C, which was consistent with the loss of one molecule of H2Se (theoretical weight loss rate of 10.89%), and at approximately 400–550°C have a significant weight loss rate of 42% (the theoretical weight loss rate of 40.65%), which may be due to the loss of two molecules of tren organic amine, and was accompanied by an endothermic peak at 300 and 578°C in the DTA curve. The weight loss rate of compound 2 is 36% between 346 and 451°C, consistent with the loss of four molecules of dien ligand (theoretical weight loss rate of 38.48%), and the DTA curve shows an endothermic peak at 398°C. Compound 3 has a weight loss of 31% between 252 and 305°C, which is consistent with the loss rate of two molecules of tren ligand (30.22%), and has an endothermic peak at 323°C in the DTA curve. Compound 4 has a weight loss rate of 32% between 200 and 295°C, which is consistent with the loss of a molecule of tren ligand (theoretical weight loss rate of 30.88%). At the same time, the endothermic peak occurs at 249°C on the DTA curve. The appearance of an endothermic peak can be attributed to the formation of amorphous material by structural collapse at a given temperature.
Infrared Spectra
FT-IR spectrum (Supplementary Figure S6) shows that compounds 1, 3, 4 mainly originate from organic solvent tren, and the absorption peaks of compound 2 are mainly due to dien. In the 1, 3, 4, a strong absorption peak between 3,196 cm−1 and 3,092 cm−1 is due to the stretching vibration of the N-H bond; the strong N-H bending vibration appears separately at 1,567, 1,624, 1,601 cm−1; the C-H stretching vibration occurs between 2,968 and 2,838 cm−1; the -CH2- bending vibration peak individually appears at 1,466, 1,466, 1,452 cm−1; C-C, C-N stretching vibration absorption peaks are located in the region of 1,389–1,002 cm−1; weak N-H, C-H bending vibration peaks are located in the region of 994–523 cm−1. In compound 2, the absorption peak at 3,196 cm−1 and 3,104 cm−1 is caused by N-H stretching vibrations. There is a weak C-H stretching vibration absorption peak in the range of 2,911–2,857 cm−1; at 1,452 cm−1, there is a strong -CH2- bending vibration absorption peak; the absorption peaks in the range of 1,384–1,077 cm−1 are the result of C-C and C-N stretching vibrations; there are weak N-H and C-H bending vibration absorption peaks in the range of 951–527 cm−1.
Photocurrent Responses
Using a 300 W xenon lamp exposed to visible light (λ ≥ 420 nm) for photocurrent measurements, repeatable responses were observed for compounds 1–4. Compounds 1-4 exhibit good photocurrent profiles under visible light illumination as shown in Figure 5. Compounds 2 and 4 have twice the photocurrent density of 1 and 3. A high photocurrent indicates that the compound has a high photoelectron transfer efficiency, which provides evidence for the application of their photocatalytic properties. The photocurrent densities of compound 2 and 4 are much higher than those of other chalcogenides, including [pipH2]2[pipH]2[In2AsIII2AsV2S10.2Se3.1(Se2)0.7] (ca. 47 nA/cm2) (Wang et al., 2020), Rb2Ba3Cu2Sb2S10 (ca. 6 nA/cm2) (Liu et al., 2020), K3Mn2Sb3S8 (ca. 6 nA/cm2) (Xiao et al., 2021), K2HgSnSe4 (ca. 3 μA/cm2) (Teri et al., 2021a), Cs2Ag6As2S7 (ca. 5 μA/cm2) (Li et al., 2021), and [Zn(tren)2H]SbSe4 (ca. 10 μA/cm2) (Shele et al., 2021).
FIGURE 5. The photocurrent responses of 1–4 (a–d).
Magnetic Properties
The variable-temperature magnetic susceptibility data were collected for compounds at an applied dc field of 1,000 Oe in the 2–300 K temperature range. The χMT vs T and χM vs. T plots for 1 and 2 are shown in Figure 6. For compound 1, the χMT value at 300 K is 2.51 cm3 mol−1 K, and after cooling, the χMT value falls to 1.48 cm3 mol−1 K at 2 K. Meanwhile, χM gradually increases from 0.008 cm3 mol−1 at 300 K to a value of 0.739 cm3 mol−1 at about 2 K. This character suggests the dominant antiferromagnetic interaction between the CoII centers in 1. The 1/χM vs T curve above 50 K obeys the Curie-Weiss law with C = 2.54 cm3 mol−1 K and θ = -0.65 K (Figure 6, insert). The negative θ value further confirms the antiferromagnetic coupling among the Co2+ ions. In compound 2, reached a maximum χMT value of 0.66 cm3 mol−1 K at 300 K and a minimum value of 0.40 cm3 mol−1 K at 2 K as temperature decreased. Furthermore, χM gradually increases from 0.002 cm3 mol−1 at 300 K to a value of 0.203 cm3 mol−1 at about 2 K. This character suggests the dominant antiferromagnetic interaction between the NiII centers in 2. The 1/χM vs T curve above 60 K obeys the Curie-Weiss law with C = 0.56 cm3 mol−1 K and θ = -4.45 K. The negative θ value further confirms the antiferromagnetic coupling among the Ni2+ ions.
FIGURE 6. Temperature dependence of χM and χMT for compounds. Insert: the temperature dependence of 1/χM for compounds with the solid line representing the fit of the Curie-Weiss law.
Conclusion
As a summary, we have synthesized four selenoarsenates using different transition metal complexes as structure-directing agents. 1 has discrete tetrahedral AsSe4 in the presence of the transition metal complex [Co(tren)2]2+. 2 contains the transition metal complex [Ni(dien)2]2+ and [As2Se5]4- cluster. In 3, the transition metal complex unsaturated [Zn(tren)]2+ caiton is directly linked to the dimer [As2Se5]4-. Interestingly, the transition metal complexes of two different coordination modes of Mn2+ are connected through the dimer [As2Se5]4- in 4. Thus, different transition metal complexes that act as structure-directing agents have a significant effect on the structure of selenoarsenates, resulting in fundamentally different structures for 1–4. The photoelectrochemical tests show the compounds have good photocurrent response properties. A study of their magnetic properties has been conducted as well. In addition to providing insight into the structure of chalcogenidoarsenates, the work provided potential applications in optoelectronics.
Data Availability Statement
The original contributions presented in the study are publicly available. This data can be found here: https://www.ccdc.cam.ac.uk/, 2062155, 2062157, 2040069, 2062154. CCDC numbers 2062155 for 1, 2062157 for 2, 2040069 for 3 and 2062154 for 4 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html, or from the Cambridge Crystallographic Data Centre, 12 Union Road.
Author Contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
Funding
This work was supported by Scientific research projects in Inner Mongolia colleges and universities (NJZZ22586), the National Natural Science Foundation of China (21461019), and the Graduate Research Innovation Fund of Inner Mongolia Normal University (CXJJS20106).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2022.890496/full#supplementary-material
Supplementary Data Sheets 1–6 | Cluster structures, physical measurements, including powder X-ray diffraction (PXRD), elemental analysis, electrochemical characterizations, Thermogravimetric-Differential thermal analysis (TG-DTA) and infrared (IR), magnetic susceptibility measurement and tables of crystallographic data.
References
An, L., Zhou, J., Zou, H.-H., Xiao, H., Zhao, R., and Ding, Q. (2017). Syntheses, Structures and Properties of a Series of New Lanthanide Chalcoarsenates(III) Containing crown-shaped [As3Q6]3− (Q = S, Se) Clusters. J. Alloys Compd. 702, 594–600. doi:10.1016/j.jallcom.2017.01.284
Ansari, M. A., Ibers, J. A., C.O'Neal, S., Pennington, W. T., and Kolis, J. W. (1992). Solution Chemistry of Arsenic Selenides: Synthesis, Spectroscopy and the X-ray Structures of [PPh4]2[AsnSe6], N = 2,4. Polyhedron 11 (15), 1877–1881. doi:10.1016/S0277-5387(00)83735-3
Chen, M.-M., Ma, Z., Li, B.-X., Wei, W.-B., Wu, X.-T., Lin, H., et al. (2021). M2As2Q5 (M = Ba, Pb; Q = S, Se): a Source of Infrared Nonlinear Optical Materials with Excellent Overall Performance Activated by Multiple Discrete Arsenate Anions. J. Mater. Chem. C 9 (4), 1156–1163. doi:10.1039/d0tc05952h
Du, C., Chen, J., and Baiyin, M. (2019). Solvothermal Syntheses and Characterization of Three One-dimension Cadmium Selenidoarsenates [Ni(1,2-dap)3][As2CdSe4], [Zn(1,2-dap)3][As2CdSe4] and [Ni(en)3][As2CdSe4]. Chem. Res. Chin. Univ. 35 (4), 560–563. doi:10.1007/s40242-019-9011-y
Fu, M.-L., Guo, G.-C., Liu, X., Liu, B., Cai, L.-Z., and Huang, J.-S. (2005b). Syntheses, Structures and Properties of Three Selenoarsenates Templated by Transition Metal Complexes. Inorg. Chem. Commun. 8 (1), 18–21. doi:10.1016/j.inoche.2004.10.021
Fu, M.-L., Guo, G. C., Cai, L.-Z., Zhang, Z. J., and Huang, J.-S. (2005a). Incorporating Transition Metal Complexes into Tetrathioarsenates(V): Syntheses, Structures, And Properties Of Two Unprecedented [Mn(dien)2]n[Mn(dien)AsS4]2n.4nH2O And [Mn(en)3]2[Mn(en)2AsS4][As3S6]. Inorg. Chem. 44 (2), 184–186. doi:10.1021/ic048579f
Fu, M.-L., Guo, G. C., Liu, X., Chen, W.-T., Liu, B., and Huang, J.-S. (2006). Incorporation of a New Type of Transition Metal Complex into the Thioarsenate Anion: Syntheses, Structures, and Properties of Two Novel Compounds [Mn3(2,2′-bipy)3(Asvs4)2]n·nH2o And Mn2(2,2′-Bipy)As2IIIS5. Inorg. Chem. 45 (15), 5793–5798. doi:10.1021/ic0600228
Han, J., Liu, Y., Tang, C., Shen, Y., Lu, J., Zhang, Y., et al. (2016). Thioarsenate Anions Acting as Ligands: Solvothermal Syntheses, crystal Structures and Characterizations of Transition Metal Complexes of Thioarsenate and Polyethyleneamine Ligands. Inorg. Chim. Acta 444, 36–42. doi:10.1016/j.ica.2016.01.027
Iyer, R. G., and Kanatzidis, M. G. (2004). [Mn2(AsS4)4]8− and [Cd2(AsS4)2(AsS5)2] 8−: Discrete Clusters with High Negative Charge from Alkali Metal Polythioarsenate Fluxes. Inorg. Chem. 43 (12), 3656–3662. doi:10.1021/ic049905u
Jia, D.-X., Zhao, Q.-X., Dai, J., Zhang, Y., and Zhu, Q.-Y. (2006). New Chalcogenidoarsenates with Transition Metal Complex Cations: [M(en)3]2As2S5 (M=Mn, Ni) and [Mn(en)3]2As2Se5. Z. Anorg. Allg. Chem. 632 (2), 349–353. doi:10.1002/zaac.200500288
Jia, D., Zhao, J., Pan, Y., Tang, W., Wu, B., and Zhang, Y. (2011). Solvothermal Synthesis and Characterization of Polyselenidoarsenate Salts of Transition Metal Complex Cations. Inorg. Chem. 50 (15), 7195–7201. doi:10.1021/ic2007809
Kromm, A., and Sheldrick, W. S. (2008). (Terpyridine)Manganese(II) Coordination Polymers with Thio- and Selenidoarsenate(III) Ligands: Coligand Influence on the Chalcogenidoarsenate(III) Species and Coordination Mode. Z. Anorg. Allg. Chem. 634 (15), 2948–2953. doi:10.1002/zaac.200800344
Li, Y., Song, X., Zhong, Y., Guo, Y., Ji, M., You, Z., et al. (2021). Temperature Controlling Valance Changes of Crystalline Thioarsenates and Thioantimonates. J. Alloys Compd. 872, 159591–159598. doi:10.1016/j.jallcom.2021.159591
Liu, C., Xiao, Y., Wang, H., Chai, W., Liu, X., Yan, D., et al. (2020). One-Dimensional Chains in Pentanary Chalcogenides A2Ba3Cu2Sb2S10 (A = K, Rb, Cs) Displaying a Photocurrent Response. Inorg. Chem. 59 (3), 1577–1581. doi:10.1021/acs.inorgchem.9b03148
Liu, G.-N., Guo, G.-C., Chen, F., Wang, S.-H., Sun, J., and Huang, J.-S. (2012). Structural Diversity, Optical and Magnetic Properties of a Series of Manganese Thioarsenates with 1,10-Phenanthroline or 2,2′-Bipyridine Ligands: Using Monodentate Methylamine as an Alkalinity Regulator. Inorg. Chem. 51 (1), 472–482. doi:10.1021/ic201932z
Liu, G.-N., Guo, G.-C., Wang, M.-S., and Huang, J.-S. (2014). Novel Thioarsenates {[Mn(2,2'-Bipy)2(SCN)] [Mn(2,2'-bipy)](Asvs4)}2 And {[Mn(2,2'-Bipy)2(SCN)]2[Asiii2(S2)2S2]: Introducing An Anionic Second Ligand To Modify Mnii Complex Cations Of 2,2'-Bipyridine. Dalton Trans. 43 (10), 3931–3938. doi:10.1039/c3dt53515k
Liu, G.-N., Jiang, X.-M., Wu, M.-F., Wang, G.-E., Guo, G.-C., and Huang, J.-S. (2011). Stabilization Of Noncondensed (Asiiis3)3- Anions By Coordinating To [Mnii(Phen)]2+ Complex Cations: A Mixed-Valent Thioarsenate (III, V) {[Mn(phen)]3(AsVS3)(AsIIIS3)}n·nH2O Showing The Coexistence Of Antiferromagnetic Order, Photoluminescence, And Nonlinear Optical Properties. Inorg. Chem. 50 (12), 5740–5746. doi:10.1021/ic2005562
Liu, X., Zhou, J., Huang, L., Xiao, H.-P., Amarante, T. R., Almeida Paz, F. A., et al. (2021). A Copper(I)-Thioarsenate(III) Inorganic Framework Directed by [Ni(en)3]2+. Inorg. Chem. 60 (9), 6813–6819. doi:10.1021/acs.inorgchem.1c00703
Sheldrick, W. S., and Kaub, J. (1985b). Darstellung und Struktur von Cs2As8S13/Preparation and Structure of Cs2As8S13. Z. Naturforsch. 40, 571–573. doi:10.1515/znb-1985-0501
Sheldrick, W. S., and Kaub, J. (1985a). Darstellung Und Struktur Von Rb2As8S13·H2O Und (NH4)2As8S13·H2O. Preparation And Structure Of Rb2As8S13·H2O Und (NH4)2As8S13·H2O. Z. Naturforsch. 40 (9), 1130–1133. doi:10.1515/znb-1985-0906
Sheldrick, W. S., and Wachhold, M. (1998). Chalcogenidometalates of the Heavier Group 14 and 15 Elements. Coord. Chem. Rev. 176 (1), 211–322. doi:10.1016/S0010-8545(98)00120-9
Shele, M., Tian, X., and Baiyin, M. (2021). Solvothermal Synthesis and Properties of Three Antimony Chalcogenides Containing Transition Metal Zinc. J. Solid State. Chem. 302, 122401–122408. doi:10.1016/j.jssc.2021.122401
Smith, D. M., Park, C.-W., and Ibers, J. A. (1996). Preparation and Structures of the 2.2.2-Cryptand(1+) Salts of the[Sb2Se4]2-, [As2S4]2-, [As10S3]2-, and [As4Se6]2-Anions. Inorg. Chem. 35 (23), 6682–6687. doi:10.1021/ic960602c
Smith, D. M., Pell, M. A., and Ibers, J. A. (1998). Se22-, Se52-, And Se72- Ligands In [Net4]2[As2Se6], [enH][AsSe6]·2.2.2-cryptand, [NEt4][AsSe8], And [(en)2In(SeAs(Se)Se2)]·en. Inorg. Chem. 37 (10), 2340–2343. doi:10.1021/ic971181h
Teri, G., Li, N., Bai, S., E., N., and Baiyin, M. (2021a). Synthesis, crystal Structure, Photocatalysis, Photocurrent Response: One-Dimensional K2HgSnSe4 and Three-Dimensional Na6Cu8Sn3Se13. CrystEngComm 23 (35), 6079–6085. doi:10.1039/D1CE00821H
Teri, G., Ling, L., Li, N., and Baiyin, M. (2021b). Solvothermal syntheses and characterization of three quaternary selenidoarsenates containing mercury [TM(en)3][HgAs2Se4](TM=Mn, Ni, Zn). Inorg. Chem. Commun. 134, 108967–108972. doi:10.1016/j.inoche.2021.108967
Vater, V., and Sheldrick, W. S. (1997). Solvatothermale Darstellung Und Struktur Von [Me4N]2[As6S10] Und [Me4N]2 [As4S7], Demersten Thioarsenat(III) Mit Ψ-AsS4 Trigonalen Bipyramiden./Solvatothermal Synthesis And Structure Of The Thioarsenates(III) [Me4N]2[As6S10] Und [Me4N]2 [As4S7], The First Thioarsenate(III) With Ψ-AsS4 Trigonal Bipyramids. Z. Naturforsch. 52, 1119–1124. doi:10.1515/znb-1997-0917
Vater, V., and Sheldrick, W. S. (1998). Solventothermal Synthesis and Structure of the Polymerie Thioarsenates(III) (Et4N)2As6S10 and (Et4N)2As8S13. Z. Naturforsch. 53 (11), 1259–1264. doi:10.1515/znb-1998-1103
Wachhold, M., and Kanatzidis, M. G. (1999). Condensation Of Pyramidal [AsSe3]3- Anions For The Construction Of Polymeric Networks: Solventothermal Synthesis Of K3AgAs2Se5·0.25MeOH, K2AgAs3Se6, And Rb2AgAs3Se6. Inorg. Chem. 38 (17), 3863–3870. doi:10.1021/ic990274r
Wang, F., Yang, D.-D., Liao, Y.-Y., Ma, Z.-J., Hu, B., Wang, Y.-Q., et al. (2020). Synthesizing Crystalline Chalcogenidoarsenates in Thiol-Amine Solvent Mixtures. Inorg. Chem. 59 (4), 2337–2347. doi:10.1021/acs.inorgchem.9b03165
Wendel, K., and Müller, U. (1995). Das Cyclische Thioarsenat(III) (PPh4)2As2S6. Z. Anorg. Allg. Chem. 621 (6), 979–981. doi:10.1002/zaac.19956210614
Xiao, Y., Chen, M.-M., Shen, Y.-Y., Liu, P.-F., Lin, H., and Liu, Y. (2021). A3Mn2Sb3S8 (A=K and Rb): a New Type of Multifunctional Infrared Nonlinear Optical Material Based on Unique Three-Dimensional Open Frameworks. Inorg. Chem. Front. 8 (11), 2835–2843. doi:10.1039/D1QI00214G
Xiong, W.-W., Athresh, E. U., Ng, Y. T., Ding, J., Wu, T., and Zhang, Q. (2013). Growing Crystalline Chalcogenidoarsenates in Surfactants: From Zero-Dimensional Cluster to Three-Dimensional Framework. J. Am. Chem. Soc. 135 (4), 1256–1259. doi:10.1021/ja3116179
Xu, Y., Liu, X., Zhou, J., and Zou, H.-H. (2021). Two Organic Hybrid Manganese Selenoarsenates: The Discovery of One-Dimensional Low-Valent Selenoarsenate(II). Inorg. Chem. 60 (24), 19226–19232. doi:10.1021/acs.inorgchem.1c03008
Yang, D.-D., Song, Y., Zhang, B., Shen, N.-N., Xu, G.-L., Xiong, W.-W., et al. (2018). Exploring the Surfactant-Thermal Synthesis of Crystalline Functional Thioarsenates. Cryst. Growth Des. 18 (5), 3255–3262. doi:10.1021/acs.cgd.8b00495
Yao, H.-G., Ji, M., Ji, S.-H., and An, Y.-L. (2013). Synthesis, Structure and Characterization of Two New Copper(і)-Thioarsenates (ІІІ) Constructed by the [AsS3]3- and CuSx Units. J. Solid State. Chem. 198, 289–294. doi:10.1016/j.jssc.2012.08.039
Zhang, R.-C., Zhang, C., Zhang, D.-J., Wang, J.-J., Zhang, Z.-F., Ji, M., et al. (2012). Copper-Rich Framework Selenoarsenates Based on Icosahedral Cu8Se13 Clusters. Z. Anorg. Allg. Chem. 638 (15), 2503–2507. doi:10.1002/zaac.201200233
Zhao, J., Liang, J., Chen, J., Pan, Y., Zhang, Y., and Jia, D. (2011a). Novel Polyselenidoarsenate And Selenidoarsenate: Solvothermal Synthesis And Characterization Of [Co(phen)3][As2Se2(μ-Se3)(μ-Se5)] And [Co(phen)3]2[As8Se14]. Inorg. Chem. 50 (6), 2288–2293. doi:10.1021/ic1024444
Zhao, J., Liang, J., Pan, Y., Zhang, Y., and Jia, D. (2011b). New Polyselenidoarsenate Salts With Transition Metal Complexes As Counterions: Solvothermal Synthesis, Crystal Structures, And Properties Of [M(dien)2]As2Se6 (M= Co, Ni) and [Mn(dap)3]As2Se6. Monatsh Chem. 142 (12), 1203–1209. doi:10.1007/s00706-011-0561-z
Zhou, J., Dai, J., Bian, G.-Q., and Li, C.-Y. (2009). Solvothermal Synthesis of Group 13-15 Chalcogenidometalates with Chelating Organic Amines. Coord. Chem. Rev. 253 (9-10), 1221–1247. doi:10.1016/j.ccr.2008.08.015
Zhou, J. (2016). Synthesis of Heterometallic Chalcogenides Containing Lanthanide and Group 13-15 Metal Elements. Coord. Chem. Rev. 315, 112–134. doi:10.1016/j.ccr.2016.01.009
Zhou, J., Tan, X.-F., Liu, X., Qing, M., Zhao, R.-Q., and Tang, Q. (2015). A Series of New Manganese Thioarsenates(v) Based on Different Unsaturated [Mn(amine)x]2+complexes. Dalton Trans. 44 (37), 16430–16438. doi:10.1039/c5dt02910d
Keywords: solvothermal method, selenoarsenates, crystal structure, photocurrent responses, transition metal complex
Citation: Tian X, Teri G, Shele M, E N, Qi L, Liu M and Baiyin M (2022) Strong Photocurrent Response of Selenoarsenates With Different Transition Metal Complexes as Structure-Directing Agents. Front. Chem. 10:890496. doi: 10.3389/fchem.2022.890496
Received: 06 March 2022; Accepted: 21 March 2022;
Published: 05 May 2022.
Edited by:
Zhong Jin, Nanjing University, ChinaReviewed by:
Jun-Jie Wang, Anyang Normal University, ChinaJian Zhou, Chongqing Normal University, China
Copyright © 2022 Tian, Teri, Shele, E, Qi, Liu and Baiyin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Menghe Baiyin, baiymh@imnu.edu.cn
†These authors have contributed equally to this work