Construction of a nano-rectangular Zn-Nd complex with near-infrared luminescent response towards metal ions

Construction of a nano-rectangular Zn-Nd complex with near-infrared luminescent response towards metal ions

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Xia Liu^a, Xiaoping Yang^a^,^b^,^*, Yanan Ma^a, Jieni Liu^a, Dongliang Shi^a, Desmond Schipper^c

Chinese Chemical Letters | 2021, 32(1) : 569 - 572

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Chinese Chemical Letters | 2021, 32(1): 569-572

• Communication •

Construction of a nano-rectangular Zn-Nd complex with near-infrared luminescent response towards metal ions

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Xia Liu^a, Xiaoping Yang^a^,^b^,^*, Yanan Ma^a, Jieni Liu^a, Dongliang Shi^a, Desmond Schipper^c

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^a College of Chemistry and Materials Engineering, Zhejiang Key Laboratory of Carbon Materials, Wenzhou University, Wenzhou 325035, China

^b College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing 314001, China

^c Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin 78712, United States

Published: 2021-01-15 doi: 10.1016/j.cclet.2020.03.016

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Abstract

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One 6-metal Zn-Nd complex [Zn₂Nd₄L₂(OAc)₁₀(OH)₂(CH₃OH)₂] (1) with Schiff base ligand bis(3-methoxysalicylidene)ethylene-1,2-phenylenediamine (H₂L) was constructed, and it has nanoscale rectangular structure (8×11×28 Å). Excited by ligand-centered absorption bands, 1 shows NIR emission of Nd³⁺ ion. Interestingly, 1 exhibits lanthanide luminescent response towards metal ions, especially to alkali metal ions (Li⁺, Na⁺ and K⁺) at ppm level.

Key words

Construction / Zn-Ln complexes / Schiff base ligand / NIR luminescence properties / Luminescent response

Cite this Article

Xia Liu, Xiaoping Yang, Yanan Ma, Jieni Liu, Dongliang Shi, Desmond Schipper. Construction of a nano-rectangular Zn-Nd complex with near-infrared luminescent response towards metal ions[J]. Chinese Chemical Letters, 2021 , 32 (1) : 569 -572 . DOI: 10.1016/j.cclet.2020.03.016

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Construction of heterometallic nanoclusters with d-block metals and lanthanide(Ⅲ) ions has recently gained considerable attention due to their unique optical, electrical and magnetic properties [1, 2]. Fluorescent response towards analytes (i.e., cations, anions and small molecules) are currently of interest because of its potential application in environment, biology and medicine [3-9]. For example, the development of fluorescent molecular sensors for the recognition of alkali metal ions such as lithium (Li⁺), sodium (Na⁺) and potassium (K⁺) is critical for the biomedical diagnosis [10-12]. Luminescent lanthanide complexes display unrivalled spectroscopic properties, including large Stokes shifts, sharp emission bands and long emission lifetimes. Lanthanide complexes with Nd(Ⅲ), Yb(Ⅲ) and Er(Ⅲ) ions may show near-infrared (NIR) luminescence, which can penetrate deep into the tissues because biological systems are almost transparent in the wavelength range from 900 nm to 1600 nm. So far, many visible luminescent Eu(Ⅲ)- and Tb(Ⅲ)-based complexes have been used as sensors for the detection ofmetal ions [13-18]. However, there are veryfew reports on the NIR luminescent lanthanide-based complexes used as metal ion probes, especially to alkali metal ions.

Metal chromophores with d-block transition-metal ions such as Zn(Ⅱ), Cd(Ⅱ), Pt(Ⅱ) and Ru(Ⅱ) may act as efficient sensitizers for the NIR lanthanide luminescence. Compartmental Schiff bases with two dissimilar metal-binding sites have been widely used to synthesize 3d-4f heteronuclear complexes [19, 20]. As part of our current research on the luminescent response of d-4f complexes towards various analytes [21-23], we report here one 6-metal Zn-Nd complex [Zn₂Nd₄L₂(OAc)₁₀(OH)₂(CH₃OH)₂] (1) with Schiff base ligand bis(3-methoxysalicylidene)ethylene-1,2-phenylenediamine (H₂L, Fig. 1). 1 exhibits nanoscale rectangular structure (8 × 11 × 28 Å). Interestingly, 1 shows luminescent response towards metal ions, especially to Li⁺, Na⁺ and K⁺ ions.

The Schiff-base ligand H₂L was prepared according to the literature report [24]. Reaction of H₂L with Zn(OAc)₂·2H₂O and NdCl₃·6H₂O in refluxing MeOH gave the Zn-Nd complex 1. The yellow crystalline product of 1 was obtained by the slow diffusion of diethyl ether into the reaction solution, and zinc chloride ([ZnCl₂(H₂O)CH₃OH] was found in the crystalline solid of the product CCDC No. 1971956. As shown in Fig. 1, the X-ray structure of 1 reveals a centrosymmetric core with 2 equiv. ZnLn₂L moieties, which are linked together by two OAc^- anions. In the ZnLn₂L moiety, Zn²⁺ ion is bound in the O₂N₂ cavity of the Schiff base ligand, and shows a square pyramidal geometry. For the two Nd³⁺ ions, one is bound by the O₂O₂ set of the Schiff base ligand and another one is coordinated with five OAc^- and one OH- anions. The Zn²⁺ ion is linked with the former Nd³⁺ ion by the Schiff base ligand and two OAc^- anions, with a separation of 3.402 Å. Both Nd³⁺ ions are nine-coordinated and exhibit a single cap square antiprism geometry. In 1, all Nd³⁺ ions are linked together by ten OAc^- anions and the average Nd(Ⅲ)···Nd(Ⅲ) distance is 4.088 Å. The OAc^- anions exhibit μ₂ and μ₃ coordination modes with the Nd³⁺ ions. The Schiff base ligand is bound to metal ions through its N and O atoms. In 1, there are two methanol molecules coordinated with the Nd(Ⅲ) ions. The metric dimensions of 1 measure approximately 8 × 11 × 28 Å. The Zn—N, Zn—O and Nd—O bond lengths range from 2.036 Å–2.047 Å, 1.994 Å–2.012 Å, and 2.314 Å– 2.679 Å, respectively.

The panoramic scanning electron microscopy (SEM) image and energy dispersive X-ray spectroscopy (EDX) spectrum of 1 are shown in Fig. 2. The molar ratio of Zn/Nd in the EDX spectrum of 1 is found to be about 1:1, consistent with its crystal structure. Thermogravimetric analysis exhibits that 1 loses about 5% of the weight when it is heated at 100 ℃ (Fig. S2 in Supporting information), due to the escaping of solvent molecules in the product. It is found that, when the crystalline product of 1 is separated from its mother solution, it rapidly loses crystallinity. The powder XRD pattern of 1 shows many weak diffraction peaks with large background peaks (Fig. S3 in Supporting information), confirming its amorphous nature. The Zn-Nd complex starts to discompose when it is heated at 200 ℃ (Fig. S2).

The luminescence properties of 1 was studied in CH₃CN and the solid state. As shown in Fig. S4 (Supporting information), compared with the absorption bands of the free H₂L, those of 1 are red-shifted. Excited by ligand-centered absorption bands, 1 shows typical NIR luminescence of Nd³⁺ (⁴F_3/2→⁴I_j/2 transitions, j = 9, 11 and 13) (Fig. S5 in Supporting information). For the lanthanide luminescence of 1, the most intense line is at 1054 nm (⁴F_3/2→⁴I_11/2). The complex shows similar luminescence spectra in the solution and the solid state.

For the lanthanide luminescence, 1 exhibits broad excitation bands, in agreement with their absorption spectra. This confirms that the energy transfer from Zn/L centers to Nd³⁺ ions occurs in 1. The Nd³⁺ ion has many excitation energy levels lying above the emissive ⁴F_3/2 state at 11,300 cm^-1 [25], which helps to accept energy from the Zn/L center. The NIR emission lifetime (τ) of 1 in CH₃CN is 6.2 ms (Fig. S5). Thus, the intrinsic quantum yield (Φ_Ln) of Nd³⁺ in 1 is calculated to be 2.5% (Φ_Ln = τ/τ₀, τ₀ = 250 μs, the natural lifetime of Nd³⁺ ion) [26]. The overall NIR emission quantum yield (Φ_em) of 1 is 0.8%. The energy transfer efficiency (η_sens = Φ_em/Φ_Ln) from Zn/L centers to lanthanide ions in 1 is estimated to be 32% [27]. Solvent molecules such as H₂O can efficiently quench the lanthanide luminescence through nonradiative energy exchange from Ln3⁺ to the solvent molecules [28]. The overall NIR emission quantum yield of 1 in DMF/H₂O (1:1) is found to be 0.5%, which is lower than that in CH₃CN.

There are total 30 electronegative O atoms from Schiff base ligands and anions (OAc^- and OH^-) in the structure of 1, which may help to form intermolecular electrostatic force with added cations. The lanthanide luminescent response of 1 towards metal ions Li⁺, Na⁺, K⁺, Co²⁺, Cd²⁺, Ag⁺, Cr³⁺, Ni²⁺, Al³⁺, Mn²⁺, Zn²⁺ and Mg²⁺ (metal acetates) have been investigated in DMF. Interestingly, the addition of all metal ions decreases the lanthanide luminescence of 1 (Fig. 3 and Fig. S6 in Supporting information). It is noticeable that, the addition of alkali metal ions Li⁺, Na⁺ and K⁺ causes a more rapid decrease of the luminescence intensity than the addition of other metal ions. The emission intensities at 1054 nm of 1 are decreased more than 50% when the concentrations of added Li⁺, Na⁺ and K⁺ ions are 45.7 μmol/L, 47.4 μmol/L and 61.4 μmol/L, respectively. These concentrations are much lower than those of other ions (Fig. S6). For example, the concentrations of added Zn²⁺ and Mg²⁺ ions to reduce the emission intensities of 1 by half are 1762 μmol/L and 1958 μmol/L, respectively. These results indicate that, compared with other metal ions, 1 shows high sensitivity to Li⁺, Na⁺ and K⁺ ions through lanthanide luminescent response.

The Stern-Volmer equation K_SV = (I₀/I - 1)/[A] can be used to calculate the emission quenching efficiencies (K_SV) of 1 to metal ions [29], where [A] is the concentration of added metal ion, and I₀ (or I) is the emission intensity of 1 at 1054 nm before (or after) the addition of metal ion. The K_SV values of 1 towards Li⁺, Na⁺ and K⁺ ions are found to be 2.98 × 10⁴ L/mol, 2.64 × 10⁴ L/mol and 1.77 × 10⁴ L/mol, respectively. These values are much greater than those to other metal ions (Fig. 4). For example, the K_SV values of 1 towards Zn²⁺ and Mg²⁺ ions are 0.06 × 10⁴ L/mol and 0.04 × 10⁴ L/mol, respectively. The limits of detection (LOD) of 1 to metal ions can be estimated by 3σ/K_SV [30], where s is the standard deviation. The LOD data of 1 to Li⁺, Na⁺ and K⁺ ions are calculated to be 0.47 μmol/L, 0.53 μmol/L and 0.79 μmol/L, respectively, which are comparable to those reported in the literature [31-35]. These results indicate that 1 shows NIR lanthanide luminescent response to these alkali metal ions at ppm level. 1 has similar K_SV and LOD data to Li⁺, Na⁺ and K⁺ ions, thus it needs to use other elemental analysis methods to furtherly differentiate them in practical application.

The added metal ions may affect the ligand-to-metal energy transfer process in 1 due to their perturbation to the electronic structure and excited state of the ligand, resulting in so-called chelation enhancement of the quenching emission (CHEQ) effect [36]. For example, with unfilled d electronic configurations, 3d-block metal ions Co²⁺, Cr³⁺, Ni²⁺ and Mn²⁺ have d-d transitions, which may consume the excitation energy of lanthanide ions through f→d energy transfers and decrease the lanthanide luminescence of 1 [37]. Zn²⁺ and Mg²⁺ ions have d¹⁰ and d⁰ electronic configurations, respectively, which prevent the quenching of lanthanide luminescence through d-d transitions, and 1 has low K_SV values to these two metal ions. The interactions between the added metal ions and 1 play a key role in the lanthanide luminescent response. 1 shows higher K_SV values to alkali metal ions than to other metal ions, probably due to the formation of stronger intermolecular interactions between the alkali metal ions and 1. For example, alkali metal ions may interact with macrocyclic compounds and framework complexes through cation-π interactions due to their suitable ionic size [38-41]. The interactions between the added alkali metal ions and 1 were confirmed by UV– vis spectra [42]. As shown in Fig. S7 (Supporting information), the red-shift of the absorption bands of 1 with the addition of alkali metal ions indicates the formation of interactions between the metal ions and 1. The CHEQ effect of alkali metal ions to 1 was investigated by the measurement of emission lifetimes and quantum yields after the addition of metal ions. For example, when the concentration of the added Li⁺ ion is 45.7 μmol/L, the luminescence lifetime (τ) and the overall emission quantum yield (Φ_em) of 1 are 5.6 ms and 0.3%, respectively. Thus, the intrinsic quantum yield (Φ_Ln) is calculated to be 2.2%, and the efficiency (η_sens) of the energy transfer is estimated to be 13.6%, which is lower than that without the Li⁺ ion. These results indicate that the addition of alkali metal ions may decrease the efficiency of the energy transfer process in 1.

In summary, a nano-rectangular Zn-Nd complex 1 with molecular size of 10 × 14 × 18 Å was successfully synthesized using a Schiff base ligand, and identified with X-ray crystallography. Upon the excitation of absorption bands, 1 exhibits the typical NIR luminescence of Nd³⁺ ion. The addition of Li⁺, Na⁺, K⁺, Co²⁺, Cd²⁺, Ag⁺, Cr³⁺, Ni²⁺, Al³⁺, Mn²⁺, Zn²⁺ and Mg²⁺ ions decreases the lanthanide luminescence of 1. It shows high sensitivity to alkali metal ions (Li⁺, Na⁺ and K⁺) at ppm level. Further studies focused on the luminescent response of d–f complexes to other analytes are in progress.

Conflicts of competing interest

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The authors declare that there are no conflicts of interest.

Acknowledgment

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The work was supported by the National Natural Science Foundation of China (No. 21771141).

Appendix A. Supplementary data

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Supplementary material related to this article canbefound, in the online version, at doi:https://doi.org/10.1016/j.cclet.2020.03.016.

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Year 2021 volume 32 Issue 1

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doi: 10.1016/j.cclet.2020.03.016

Receive Date：2020-02-02
Online Date：2026-01-04
Published：2021-01-15

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Received：2020-02-02
Revised：2020-02-17
Accepted：2020-03-05

Affiliations

^a College of Chemistry and Materials Engineering, Zhejiang Key Laboratory of Carbon Materials, Wenzhou University, Wenzhou 325035, China

^b College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing 314001, China

^c Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin 78712, United States

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表12种不同金属材料的力学参数

科 Family	属数 Number of genus	种数 Number of species	占总种数比例 Percentage of total species (%)	属 Genus	种数 Number of species	占总种数比例 Percentage of total species (%)
鹅膏菌科Amanitaceae	2	11	5.26	鹅膏菌属 Amanita	10	4.78
小菇科 Mycenaceae	2	12	5.74	丝盖伞属 Inocybe	5	2.39
多孔菌科 Polyporaceae	8	14	6.70	蜡蘑属 Laccaria	5	2.39
红菇科 Russulaceae	3	23	11.00	小皮伞属 Marasmius	6	2.87
				小菇属 Mycena	11	5.26
				光柄菇属 Pluteus	5	2.39
				红菇属 Russula	17	8.13
				栓菌属 Trametes	5	2.39

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Fig. 1 A view of the crystal structure of 1 (Nd³⁺: blue; Zn²⁺: green).

Fig. 2 (a) Scanning electron microscopy image and (b) energy dispersive X-ray spectroscopy spectrum of 1.

Fig. 3 Lanthanide luminescent response of 1 (50 μmol/L) to the addition of different concentrations of Li⁺ ion in DMF. λ_ex =395 nm.

Fig. 4 Lanthanide luminescence quenching efficiencies (K_SV) of 1 (50 μmol/L) towards metal cations.

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