N-donor Ligands Research Articles

Comparative Analysis of Tetravalent Actinide Schiff Base Complexes: Influence of Donor and Ligand Backbone on Molecular Geometry and Metal Binding.

A series of isostructural early actinide AnIV complexes was synthesized in order to investigate the influence of a conjugated framework in the ligand backbone on An bonding. Therefore, the AnIV complexes [An(pyrophen)2] (An = Th, U, Np, and Pu) with the pure N-donor ligand bis(2-pyrrolecarbonylaldehyde)-o-phenylenediamine referred to as pyrophen, were synthesized and characterized. Solid state analysis via single-crystal X-ray diffraction (SC-XRD) reveals two sets of ligands binding in an almost orthogonal arrangement to the actinide center. For the larger actinides Th and U, the coordination sphere allows for additional coordination by a solvent molecule. Nuclear magnetic resonance spectroscopy (NMR) studies show the presence of highly symmetrical complexes in solution in good agreement with the solvent-free solid structures. While SC-XRD suggests mainly ionic binding, an analysis of paramagnetic NMR contributions and quantum chemical bond analysis hint towards significant covalency in the U, Np, and Pu compounds. This series of An complexes allowed for a thorough structural and theoretical comparison of a conjugated system to a closely related N-donor ligand (pyren)[1] as well as to the mixed N,O Schiff base ligands salophen (conjugated) and salen (non-conjugated).

Bridge-Dependent Donor-Metal-Acceptor-Metal-Donor (D-M-A-M-D) Systems: From Charge Transfer to Electron Transfer in Dioxolene-Ge-Diimine Complexes.

Synthesis and structural characterization of a family of germanium-dioxolene complexes with ditopic N-donor ligands (L1-L5) (L1=1,2-bis(pyridin-2-ylmethylene)hydrazine L2=1,6-bis-(pyridin-2-yl)-2,5-diaza-1,5-hexadiene, L3=N,N-bis(pyridin-2-ylmethylene)-1,4-benzenediamine, L4=N,N-bis(pyridin-2-ylmethylene)-(biphenyl)-4,4-diamine, L5=2,2'-azopyridine) is reported. The reaction of germanium bis-catecholate with bridging ligands L1 - L4, differing by the nature of the linker between pyridine sites gives rise to dinuclear digermanium complexes (36Cat2Ge)2L1-4 (36Cat=dianion of 3,6-di-tert-butylcatechol) 1-4 of DMAMD type (donor-metal-acceptor-metal-donor) with a charge transfer in the UV-Vis region. In opposite, the interaction of the 36Cat2Ge with 2,2'-azopyridine (L5) results in the two-electron transfer from the donor 36Cat2- ligands to the azopyridine bridge forming stable open-shell complex 5 [(36SQ)(36CatGe)]2(L5)2- (36SQ=radical-anionic semiquinonate ligand). Molecular structures of compounds 3 and 5 were determined by single crystal X-ray diffraction analysis. Electronic structures of complexes 1-5 were studied by means of DFT calculations.

Synthesis and Characterization of Solvated Lanthanide(II) Bis(triisopropylsilyl)phosphide Complexes.

Lanthanide (Ln) silylamide chemistry is well-developed, but the corresponding silylphosphide chemistry is immature; there are only ten structurally characterized examples of Ln(II) bis(trimethylsilyl)phosphide complexes to date and no reported derivatives with bulkier R-groups. Here, we report the synthesis of the first f-block bis(triisopropylsilyl)phosphide complexes, [Ln{P(SiiPr3)2}2(THF)x] (1-Ln; Ln = Sm, Eu, x = 3; Ln = Yb, x = 2), by the respective salt metathesis reactions of parent [LnI2(THF)2] with 2 equiv of [Na{P(SiiPr3)2}]n in toluene. Complexes 1-Ln were characterized by a combination of NMR, EPR, ATR-IR, electronic absorption and emission spectroscopies, elemental analysis, SQUID magnetometry, and single crystal X-ray diffraction. These data contrast with those obtained for related Ln(II) bis(trimethylsilyl)phosphide complexes due to the bulkier ligands in 1-Ln and also with Ln(II) bis(triisopropylsilyl)amide complexes due to a combination of longer Ln-P vs. Ln-N bonds and the softer nature of P- vs. N-donor ligands.

Construction of Cd(II) Metal–Organic Frameworks Based on a Robust Heterocyclic Phosphazene and Divergent N-Donor Ligands: A Comprehensive Photocatalytic Investigation on Dye Degradation

Construction of Cd(II) Metal–Organic Frameworks Based on a Robust Heterocyclic Phosphazene and Divergent N-Donor Ligands: A Comprehensive Photocatalytic Investigation on Dye Degradation

Synthesis and study of bistriazolyl-pyrazines as new ligands for An/Ln separations

Herein, we present new hydrophilic tridentate ligands, bistriazolyl pyrazines. Their design was inspired by structurally similar and promising bis-triazolyl-pyridines (PyTri) ligands as well as theoretically derived criteria for the design of tridentate ligands for An/Ln separations suggested by theoretical studies. These ligands have been synthesised, characterised and tested as possible extractants for An/Ln nuclear separations. In addition, UV and fluorescence studies, pKa determination, and crystallographic and theoretical studies have been performed to explain their observed behaviour. Although the results of the solvent extraction studies have shown that these ligands do not possess sufficient selectivity for the extraction of Am vs Eu in i-SANEX conditions, this study presents a valuable test of the criteria for the design of tridentate heterocyclic N-donor ligands for advanced nuclear separation as postulated by theoretical studies a decade ago. Our experimental observations and theoretical studies have found that these criteria might not be the best guidance for designing novel hydrophilic ligands for An/Ln separations in i-SANEX conditions.

Synthesis and electrochemical properties of two cobalt(II) and nickel(II) metal-organic frameworks for excellent performance supercapacitors

Two novel metal-organic frameworks, [Co(HNTB)(bif)]·3H2O·DMA (1) and [(Ni2(μ2O)(HNTB)2(bif)2]·2H2O·2H3O·2DMA (2), were obtained with a tripod-type carboxylic ligand (4,4′,4″-Nitrilotrisbenzoic acid, H3NTB) and a rigid N-donor ligand (2,7-bis(1-imidazoly)fluorene, bif) by solvothermal method. Complex 1 exhibits a 2D layered structure and 2 is a 3D microporous structure with an anionic skeleton. Significantly, their electrochemical tests show that both of them own excellent capacitive performance. Complex 1 has a relatively high specific capacitance (301.2 F g−1 at 1 A g−1) with favorable cycling durability (retained 73.2 % over 3000 cycles). Complex 2 presents a high specific capacitance (329.6 F g−1 at 1 A g−1) with a relatively poor cycling durability (retained 58.9 % over 3000 cycles). Additionally, complex 1 // activates carbon (AC) as an asymmetrical ultra-capacitor exhibits a maximum energy density of 20.9 Wh kg−1 at 800.0 W kg−1 and a high cycle stability (retained 89.2 % over 8000 cycles). Complex 2 // AC owns an energy density of 19.3 Wh kg−1 at 750.0 W kg−1 and a satisfactory cycle stability (retained 88.6 % over 8000 cycles).

Dithiodipropionate and Fumarate Ni, Cu, and Zn Mixed Ligand Complexes

Three nickel, copper, and zinc complexes with dicarboxylic acids (3,3′-dithiodipropionic acid (H2dtdp) and fumaric acid (H2fu)) and N-donor ligands (1,10-phenanthroline (phen), N′–methyldipropylenetriamine (mdpta), and N,N,N′,N″,N″-pentamethyldiethylenetriamine (pmdien)) were synthesized. These complexes were characterized using elemental analysis, IR spectroscopy, and single-crystal X-ray diffraction. Interestingly, [Ni(dtdp)(phen)(H2O)3]∙0.5H2O (1) is a mononuclear complex, where the dtdp dianion employs only one carboxylate group for coordination to the central nickel atom. [(ClO4)(mdpta)Cu(μ-dtdp)Cu(mdpta)(H2O)](ClO4) (2) is a dinuclear copper complex with a dtdp bridge and different coordination on the copper center. [{Zn(pmdien)(H2O)}2(μ-fu)](ClO4)2 (3) is a symmetric dimer with a bridging fumarate ligand. These coordination compounds were tested for their antibacterial activities on Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Enterococcus faecalis bacteria strains. All the complexes show moderate activities on the mentioned strains.

Generating globin-like reactivities in [human serum albumin-FeII(heme)] complex through N-donor ligand addition

Human serum albumin (HSA) has a strong binding affinity for heme b, forming a complex in a 1:1 ratio with the co-factor ([HSA-FeIIIheme]). This system displays spectroscopic and functional properties comparable to globins when chemical derivatives mimicking them are incorporated into the protein matrix. The aim of this study is to generate globin-like systems using [HSA-FeIIIheme] as a protein template and binding N-donor ligands (imidazole, Im; and 1-methylimidazole, 1-MeIm) to construct artificial [HSA-Fe(heme)-(N-donor)] complexes. Their electronic structure and binding thermodynamics are investigated using UV–vis and (synchronous) fluorescence spectroscopies, while ligand-protein interactions are visualized using docking simulations. The imidazole derivatives have a strong affinity for [HSA-FeIIIheme] (K ~ 104–106), where the spontaneous binding of Im and 1-MeIm are dominated by entropic and enthalpic effects, respectively. The reduced form of the [HSA-Fe(heme)-(N-donor)] complexes demonstrate nitrite reductase (NiR) activity similar to that observed in globins, but with significant differences in their rates. [HSA-FeIIheme-(1-MeIm)] reduces nitrite ~4× faster than the Im analogue, and ~ 30× faster than myoglobin (Mb). The enhanced NiR activity of [HSA-FeIIheme-(1-MeIm)] is a cumulative effect of several factors including a slightly expanded and more optimal heme binding pocket, nearby residues as possible proton sources, and a H-bonding interaction between 1-MeIm and residues Arg160 and Lys181 that may have a long-distance influence on the heme π electron density.

Two Stable Pillar-Layered Zn-LMOFs for Highly Fluorescence Sensing of Inorganic Pollutants and Nitro Aromatic Compounds in Water.

Luminescent metal-organic frameworks (LMOFs) are a potential class of functional materials for the photoluminescent detection of a wide range of analytes as well as for the detection of pollutants in wastewater. Herein, by using the pillar-layered strategy, two new luminescence Zn-LMOFs (JLU-MOF222 and JLU-MOF223) were successfully solvothermal synthesized. The 2D layers are both consisting of Zn2+ and TPHC [TPHC = (1,1':2',1″-terphenyl)-3,3″,4,4',4″,5'-hexacarboxylic acid] ligands and then pillared by the different N-donor ligands to form the 3D Zn-LMOFs with fsh topology. Benefiting from the uncoordinated carboxylate sites, uncoordinated N atom, or -NH2 group in the pillaring ligands and excellent stability in pH = 2-13 aqueous phase, JLU-MOF222 and JLU-MOF223 not only can sensitively detect trace amounts of inorganic pollutants (Fe3+, Cr2O72-) and nitro aromatic compounds TNP and 2,4-DNP (TNP = 2,4,6- trinitrophenol, 2,4-DNP = 2,4-dinitrophenol) through luminescence quenching but also exhibit high selectivity of other anti-interference competing analytes. The two new Zn-LMOFs can be used as potential luminescent sensors for pollutant detection in water due to their high KSV and low limit of detection (LOD).

Synthesis, Structure, and Properties of Nontrivial Iridium(III) Complexes Based on Anthracene-Decorated Benzimidazole Ligand.

Reactions of iridium trichloride hydrate with bulky 2-(9-anthracenyl)-1-phenyl-benzimidazole (anbi) in the presence of N-donor ligands afforded a number of unique noncyclometalated complexes, while attempts to prepare a common μ-chloro-bridged bis-cyclometalated dimer systematically gave a monocyclometalated complex cis-[Ir(C,N-anbi)(N-anbi)Cl2] instead. The obtained complexes were characterized by 1H NMR, high-resolution mass spectrometry, single-crystal and powder X-ray diffraction, UV-vis spectroscopy, and cyclic voltammetry. The noncyclometalated complexes fac-[Ir(N-anbi)(N^N)Cl3)], where N^N are 4,4'-disubstituted 2,2'-bipyridines, are octahedral and contain the anthracene and 2,2'-bipyridine units in a close cofacial arrangement. These complexes were found to be exceptionally inert to the chloride ligand exchange even in the presence of silver triflate, forming a rare trinuclear Ir-μ-Cl3-Ag-μ-Cl3-Ir structure instead. In the monocyclometalated complex, the Ir(III) ion is pentacoordinated in a rare square-pyramidal geometry, where the bulky anthracene fragment is involved in the steric shielding of the metal center. This is in line with the results of gas-phase density functional theory calculations, demonstrating that the experimentally observed structure is energetically most preferable. The monocyclometalated complex is deeply colored due to intense charge-transfer absorption bands in the range 450-650 nm with ε = 2000-5000 M-1 cm-1, superior to the noncyclometalated complexes. The synthesis, structures, and properties of the new complexes are discussed in the context of the related mono-, bis-, and noncyclometalated iridium(III) compounds.

Chiral mono- and dinuclear CoII and CuII enantiomeric pairs with distinct enantiopure N-donor ligands: Presenting highly enhanced third-harmonic generation responses

Employing Co(hfac)2(H2O)2 and Cu(hfac)2(H2O)2 to react with enantiopure bidentate (1LR/1LS) and bis-bidentate (2LR/2LS) N-donor ligands, respectively, four chiral mono- and dinuclear CoII and CuII enantiomeric pairs formulated as M(hfac)2(1LR)/M(hfac)2 (1LS) (M = CoII, R-1-Co/S-1-Co and CuII, R-1-Cu/S-1-Cu) and M2(hfac)4(2LR)/M2 (hfac)4(2LS) (M = CoII, R-2-Co/S-2-Co and CuII, R-2-Cu/S-2-Cu) were isolated, where 1LR/1LS = (−)/(+)-4,5-pinene-2,2ʹ-bipyridine, 2LR/2LS = (−)/(+)-2,5-bis(4ʹ,5ʹ-pinene-2ʹ-pyridyl)pyrazine and hfac− = hexafluoroacetylacetonate. A study of their nonlinear optical responses reveals that dinuclear CoII and CuII enantiomers based on the symmetric 2LR/2LS ligands with larger π-conjugated systems only display very strong THG (third-harmonic generation) responses, while mononuclear ones based on the asymmetric 1LR/1LS ligands with smaller π-conjugated systems simultaneously present THG and SHG (second-harmonic generation) responses. More remarkably, THG intensities of dinuclear R-2-Co and R-2-Cu are 406 and 372 × α-SiO2, being 6.5 and 8.1 times those of the corresponding mononuclear R-1-Co and R-1-Cu, respectively. Furthermore, THG intensities of R-1-Co and R-1-Cu are 6.4 and 5.9 times those of their corresponding precursors Co(hfac)2(H2O)2 and Cu(hfac)2(H2O)2, respectively. The results indicate continuous large enhancements of the THG intensities from the precursors Co(hfac)2(H2O)2 and Cu(hfac)2(H2O)2 to their mononuclear enantiomers and further to their dinuclear species as the conjugation degrees of their ligands increase.

Copper Complexes with Protein-Based N-Donor Ligands as cis-Selective Nascent Cyclopropanases.

In this study, we aimed to develop protein-based metal ligands to catalyze cis-selective cyclopropanation using the TM1459 cupin protein superfamily. Copper complexes with TM1459 mutants containing the 3-His metal-binding site exhibited excellent diastereoselectivity in cyclopropanation reactions with styrene and ethyl diazoacetate. Further mutations in the secondary coordination sphere increased the cis-preference with t-butyl diazoacetate as the substrate with up to 80 : 20 (cis:trans ratio) and high enantioselectivity (90 % ee).

Quantum Chemical Stability Analysis of Phthalocyanine Metal One-Dimensional Polymers with Bidentate Ligands.

The combination of metal-phthalocyanine complexes and axially coordinated organic molecules into polymer chains presents a significant challenge in the synthesis of hybrid materials. A calculated structure for one-dimensional coordinate polymers with N-donor ligands using ab initio (PM6) and DFT (LanL2Dz) methods is presented. DFT methods have shown that there is a linear, one-dimensional structure without distorted geometry for the two bipyridine ligands. The components of the proposed polymers consist of square-planar Zn complexes of phthalocyanine (PcZn) connected via bridging ligands (L). Electronic properties of the monomer PcZnL of zinc phthalocyanine with bidentate ligands have been analyzed using calculations based on density functional theory (B3LYP6-31G(d,p)). Molecular orbital calculations show that this connection between the metallomacrocycle and the conjugated ligand results in a small energy gap, promising molecularly active materials as conductors. The crystallographic reports indicate that obtaining this kind of polymer with the participation of Pc Zn and bidentate ligands is possible.

Copper (II) halide compounds with cationic N-donor ligands: Design, synthesis, structure and magnetism

Copper (II) complexes of the cationic ligands 1-(4′-pyridyl)-pyridinium (L1) and 1-(4′-pyridyl)-pyridin-4-ol (L2) have been prepared and characterized by single crystal X-ray diffraction and variable temperature magnetic susceptibility measurements: [Cu(L1)2X2]X2 [where X = Cl (1), Br (2)], and [Cu(L2)2X2]X2 [where X = Cl (3), Br (4)]. The complexes are fundamentally square planar with L2X2 coordination planes and long, semi-coordinate bonds to the additional halide ions. All compounds crystallize in monoclinic systems with 1 and 2 in the P21/n space group and 3 and 4 in the P21/c space group. The crystal structures are stabilized by both non-classical (in the case of 1 and 2) and classical (3 and 4) hydrogen bonds. EPR data for 1–4 support a rhombohedral structure, in good agreement with the local geometry as seen in the crystal structures. Magnetic susceptibility measurements show the presence of very weak antiferromagnetic interactions. In addition, the syntheses and magnetic properties of two neutral complexes, [Cu(L3)2X2]·2H2O [L3 = 1-(4′-pyridino)-4-pyridone; X = Cl (5), Br (6)] are reported. Magnetic susceptibility data indicate the presence of moderate antiferromagnetic exchange interactions [J ∼ 28 K (5), 60 K (6)] which were well modeled by the S = 1/2 Heisenberg uniform chain model.

High-Efficiency Solar Transformation of Sugars via a Heterogenous Gallium(III) Catalyst.

Extremely limited research exploring the photocatalytic potential of main group metals, such as aluminum, gallium, and tin, has been undertaken due to their weak light harvesting properties. This study reports the efficient transformation of sugars to 5-hydroxymethylfurfural (HMF) with high yield employing an original heterogeneous photocatalyst comprising a gallium(III) complex immobilized on an alumina support. Under visible light irradiation, the reaction rate of HMF formation is ~143 times higher than the equivalent thermal reaction performed in the absence of light. The turnover number (TON) of the heterogeneous gallium(III) photocatalyst was as high as 1500, which was ca. two orders of magnitude higher than the TON of the homogeneous gallium(III) system. It is proposed that photoirradiation significantly enhances the Lewis acidity of the catalyst by forming a semi-coordination state between gallium(III) and N-donor ligands, enabling the increased interaction of reactant sugar molecules with gallium(III) active sites. Consistent with this, the photoresponsive coordination of the gallium(III) complex and the abstraction of the hydroxy group by the metal under irradiation with visible light is observed by NMR spectroscopy for the first time. These findings demonstrate that efficient photocatalysts derived from the main group elements can facilitate biomass conversion using visible light.

Synthesis of ω-Hydroxy Fatty Acid Alkyl Esters by Macrocyclic Lactones Alcoholysis Catalyzed by Homoleptic and Heteroleptic Zinc Aryloxides.

A series of zinc aryloxides, [Zn4(sal-Me)8]⋅2.5(C7H8) (1), [Zn4(sal-Me)8]⋅CH2Cl2 (2), [Zn4(μ3-OR)2(sal-R)6] (3) (for R=Me (0.51), Et (0.49)), [Zn4(μ3-OMe)4(sal-Me)4(HOMe)4] (4), [Zn(sal-Me)2(py)2]⋅THF (5), {[Zn(sal-Me)2(tmbpy)] ⋅ 2(C6H5CH3)}n (6), [Zn2(sal-Me)2(THF)2Cl2] ⋅ 0.5(C6H5CH3) (7), and [Zn4(μ3-OMe)2(sal-Me)4Cl2] (8) (Hsal-Me=methyl salicylate, py=pyridine, tmbpy=4,4'-trimethylenedipyridine) were obtained that have different nuclearities and central core topologies and contain ligands of different basicity and coordination abilities.

6-(6-Methyl-1,2,4,5-Tetrazine-3-yl)-2,2'-Bipyridine: A N-Donor Ligand for the Separation of Lanthanides(III) and Actinides(III).

Here, we report the synthesis of the 6-(6-methyl-1,2,4,5-tetrazine-3-yl)-2,2'-bipyridine (MTB) ligand that has been developed for lanthanide/actinide separation. A multimethod study of the complexation of MTB with trivalent actinide and lanthanide ions is presented. Single-crystal X-ray diffraction measurements reveal the formation of [Ce(MTB)2(NO3)3], [Pr(MTB)(NO3)3H2O], and [Ln(MTB)(NO3)3MeCN] (Ln = Nd, Sm, Eu, Gd). In addition, the complexation of Cm(III) with MTB in solution was studied by time-resolved laser fluorescence spectroscopy. The results show the formation of [Cm(MTB)1-3]3+ complexes, which occur in two different isomers. Quantum chemical calculations reveal an energy difference between these isomers of 12 kJ mol-1, clarifying the initial observations made by time-resolved laser fluorescence spectroscopy (TRLFS). Furthermore, quantum theory of atoms in molecules (QTAIM) analysis of the Cm(III) and Ln(III) complexes was performed, indicating a stronger covalent contribution in the Cm-N interaction compared to the respective Ln-N interaction. These findings align well with extraction data showing a preferred extraction of Am and Cm over lanthanides (e.g., max. SFAm/Eu = 8.3) at nitric acid concentrations <0.1 mol L-1 HNO3.

Structural distinction and highly sensitive fluorescent detection properties of Cd-based multifunctional sensors with three flexible isomers

Many environmental pollutants are found and need to be detected and treated with the rapid development of industry. Three novel Cd (II) coordination polymers (Cd-CPs) (1–3), with the formula of [Cd(2-HDBB)(4,4′-bbpy)](1), [Cd(3-HDBB)(4,4′-bbpy)](2) and [Cd(4-HDBB)(4,4′-bbpy)0.5·2H2O](3) based on three soft organic isomers: n-(3,5-dicarboxylato benzyloxy) benzoic acid (n = 2, 3 or 4-H3DBB), with one linear N-donor ligand 4,4′-bis(imidazolyl) biphenyl (4,4′-bbpy) have been synthesized hydrothermally and characterized in detail. The significant structural differences are both coordination polymers 1 and 2 featuring two-dimensional networks, while 3 with 1D ladder-like chain due to the change of isomers. Despite structural differences, the series of Cd-CPs exhibits similar fluorescence sensing properties. Fluorescent sensing properties exhibit all the Cd-CPs have been discovered to detect Fe3+, Cr2O72−, tetracycline (TET) and nitrobenzene (NB) selectively and sensitively with the low detection limits, respectively. The results of theoretical calculation verified the fluorescence detection mechanism of NB by these cadmium complexes. Therefore, the Cd-CPs might be used as an excellent multi-functional luminescent sensor in the future.

Theoretical study of the ability of symmetric and asymmetric N-donor ligands to separate Am(III) and Eu(III) and the bonding nature

In the reprocessing of spent nuclear fuel, nitrogen-donor extractants are more effective in separating actinides and lanthanides. In this article, a series of heterocyclic N-donor ligands with different backbones and different side chain substituents are systematically investigated to analyze their extraction selectivity and complexation abilities for Am(Ⅲ) and Eu(Ⅲ) by using scalar relativistic density functional theory (DFT). Through the analysis of geometric structures and bond properties of the complexes by means of the NBO and QTAIM methods, it was observed that the coordination ability of the N-donor ligand with Am(Ⅲ) was stronger than with Eu(Ⅲ). Thermodynamic analysis showed that these ligands have good extraction ability and separation performance for Am(III) and Eu(III), the backbone and side chain substituents of the ligands and also the organic solvents have significant influences on the extraction selectivity of the ligands for Am(III) and Eu(III) ions. This work provides some theoretical insights for the design of N-donor extractants with good separation performance for lanthanides and actinides.

Stable Cd(II)-based coordination polymer as a multifunctional fluorescent sensor for ascorbic acid, acetylacetone and nitrofuran antibiotics

The concentrations of hazardous volatile organic compounds (VOCs), pharmaceutical antibiotics and biomolecules in water systems are closely related with public health and ecological security. Thus, the convenient and accurate detection of these harmful items can not only reflect the state of human health but also evaluate the level of homologous contamination in the environment. To this end, a new Cd(II)-CP ({[Cd3L2(bmoe)]·DMF}n) with excellent luminescence properties was designed by employing the semi-rigid tricarboxylic acid 4-(2′,3′-dicarboxylphenoxy) (H3L) and N-donor ligand 1,1′-bis(1H-benzimidazolyl) oxydiethane (bmoe). The as-prepared Cd-CP features the unique uninodal sql topology. Benefiting from its great stability in the aqueous system, Cd-CP serves as a versatile multifunctional fluorescent sensor for different analytes, ascorbic acid (AA), nitrofuran antibiotics nitrofurantoin (NFT) and nitrofurazone (NFZ) and acetylacetone (ACAC). The established methods are characterized with impressive low detection limits, ultrafast response time, high sensitivity, strong anti-interference ability, as well as reliable reproducibility. Experimental and theoretical calculation reveals that the collaborative effects of Förster resonance energy transfer (FRET), inner-filter effect (IFE) and photoinduced electron transfer (PET) are the most probable causes behind the quenching of the CP's fluorescence signal.