Coupling Products Research Articles

Breaking degeneracies in exoplanetary parameters through self-consistent atmosphere--interior modelling

With a new generation of observational instruments largely dedicated to exoplanets (i.e. JWST, ELTs, PLATO, and Ariel) providing atmospheric spectra and mass and radius measurements for large exoplanet populations, the planetary models used to understand the findings are being put to the test. We seek to develop a new planetary model, the Heat Atmosphere Density Evolution Solver (HADES), which is the product of self-consistently coupling an atmosphere model and an interior model, and aim to compare its results to currently available findings. We conducted atmospheric calculations under radiative-convective equilibrium, while the interior is based on the most recent and validated ab initio equations of state. We pay particular attention to the atmosphere--interior link by ensuring a continuous thermal, gravity, and molecular mass profile between the two models. We applied the model to the database of currently known exoplanets to characterise intrinsic thermal properties. In contrast to previous findings, we show that intrinsic temperatures (T$_ int $) of 200-400 K ---increasing with equilibrium temperature--- are required to explain the observed radius inflation of hot Jupiters. In addition, we applied our model to perform `atmosphere--interior' retrievals by Bayesian inference using observed spectra and measured parameters. This allows us to showcase the model using example applications, namely to WASP-39 b and 51 Eridani b. For the former, we show how the use of spectroscopic measurements can break degeneracies in the atmospheric metallicity (Z) and intrinsic temperature. We derive relatively high values of Z = 14.79$_ and int $K, which are necessary to explain the radius inflation and the chemical composition of WASP-39 b. With this example, we show the importance of using a self-consistent model with the radius being a constrained parameter of the model and of using the age of the host star to break radius and mass degeneracies. When applying our model to 51 Eridani b, we derive a planet mass M$_p=3.13_ $ M$_ J $ and a core mass M$_ core $ M$_ E $, suggesting a potential formation by core accretion combined with a `hot start' scenario. We conclude that self-consistent atmosphere--interior models efficiently break degeneracies in the structure of both transiting and directly imaged exoplanets. Such tools have great potential to interpret current and future observations, thereby providing new insights into the formation and evolution of exoplanets.

Cross-Coupling of 1,2,3,4-Tetrachlororodibenzo-p-dioxin with Six Coexisting Polycyclic Aromatic Hydrocarbons during Photodegradation on a Fly Ash Surface.

The adverse conditions of the garbage incineration process can lead to the generation of dioxins and polycyclic aromatic hydrocarbons (PAHs). This study aimed to investigate the removal efficiency and possible cross-coupling effect of 1,2,3,4-tetrachlorodibenzo-p-dioxin (1,2,3,4-TCDD) and six coexisting low-molecular-weight PAHs during photodegradation on the fly ash surface. Due to their higher photoreactivity and light-shielding effect, the six PAHs exhibited inhibitory effects on the photodegradation of 1,2,3,4-TCDD, causing a reduction of 4.1%-21.2% in the removal efficiency. Common degradation products of 1,2,3,4-TCDD and PAHs were identified by LC-MS and GC-MS, and the formation of primary products was verified by theoretical calculations of bond dissociate energies, excitation energy, frontier electron densities, and transition states. In addition, high-molecular-weight coupling products of 1,2,3,4-TCDD and its interaction products with PAHs were observed in the mixed irradiation samples, and two coupling elimination mechanisms were proposed to illustrate their formation through C-O-C bonding and -COO- bonding, respectively. According to toxicity prediction analysis, the developmental toxicity and mutagenicity of most interaction products were higher than 1,2,3,4-TCDD. This study provided some new insights into the transformation, interaction, and related ecological risks of dioxins and PAHs coexisting on the surface of fly ash during the waste incineration process.

Half-Sandwich Cerium and Lanthanum Dialkyl Complexes: Synthesis, Structure, and Reactivity Studies.

Cerium and lanthanum dialkyl complexes [η5-1,2,4-(Me3C)3C5H2]Ln(CH2C6H4-o-NMe2)2 (Ln = Ce 1 and La 2), supported by a tri-tert-butylcyclopentadienyl ligand, have been successfully synthesized. Studies demonstrate that these complexes possess diverse reactivity toward various small molecules. For example, the reaction of complexes 1 and 2 with diphenyl dichalcogenides PhEEPh (E = S, Se) results in the formation of lanthanide thiolates [(η5-1,2,4-(Me3C)3C5H2)Ln(SPh)(μ-SPh)]2 (Ln = Ce 3 and La 4) and selenolates [(η5-1,2,4-(Me3C)3C5H2)Ln(SePh)(μ-SePh)]2 (Ln = Ce 5 and La 6), concomitantly releasing PhE(CH2C6H4-o-NMe2). Furthermore, complexes 1 and 2, upon reaction with dibenzyl disulfide, yield tetranuclear rare-earth metallomacrocyclic compounds {[(η5-1,2,4-(Me3C)3C5H2)Ln(μ-SCH2C6H5)]2(μ-η3:η3-SCHC6H5)}2 (Ln = Ce 7 and La 8). This reaction may involve a process of σ-bond metathesis and C-H activation. While the reaction of 1 and 2 with dibenzyl diselenide in the presence of LiCH2C6H4-o-NMe2 leads to the formation of lanthanide-lithium selenido clusters [(η5-1,2,4-(Me3C)3C5H2)La(μ-SeCH2C6H5)]3(μ3-Se)[μ3-SeLi(THF)3] (Ln = Ce 9 and La 10). Meanwhile, lanthanide selenido clusters [(η5-1,2,4-(Me3C)3C5H2)La(μ-SeCH2C6H4-o-NMe2)]4(μ3-Se)2 (Ln = Ce 11 and La 12) can be obtained by treating 1 and 2 with elemental selenium in a 1:2 molar ratio. Additionally, the treatment of 1 and 2 with benzoxazole generates ring-opening/C-C coupling/C-N coupling products {(η5-1,2,4-(Me3C)3C5H2)La[μ-OC6H4-o-N═CHN(CH(CH2C6H4-o-NMe2)2C6H4-o-O]}2 (Ln = Ce 13 and La 14). All new compounds were characterized by various spectroscopic methods, and their solid-state structures were confirmed by single-crystal X-ray diffraction analyses.

Unusually high selectivity (100 %) of photocatalytic C[sbnd]C coupling achieved by instant reverse reduction of byproducts

The photocatalytic CC coupling of benzyl alcohol (BA) into hydrobenzoin (HB), is appealing to obtain high-value chemicals. However, the selectivity of HB is still low due to the inevitable formation of benzaldehyde. Herein, we report In(OH)3-ZnS photocatalyst for CC coupling of BA into HB with very high selectivity (∼100 %). The introduction of In(OH)3 onto ZnS with stable interaction facilitates light harvesting and separation of photo-excited charges. As a result, BA conversion on optimized In(0.1)-ZnS catalyst (73 %) is much higher than ZnS (29 %). Besides, the surface hydroxyl groups derived from In(OH)3 enables the facile desorption of CH(OH)Ph radical. Therefore, the over oxidation of CH(OH)Ph radical into by-product of benzaldehyde can be effectively inhibited. More significantly, in-situ FTIR spectra and reduction of by-product manifest the instant reverse reduction process of benzaldehyde into CH(OH)Ph radical during CC coupling of BA, which is the key to realizing satisfied HB selectivity (100 %). Theoretical simulations reveal that the weak adsorption of CH(OH)Ph radical over catalyst and the high energy barrier of over-oxidation of CH(OH)Ph into benzaldehyde contributes to the formation of highly selective coupling products. This work will inspire new insights to design rational photoredox systems for organic transformations with high selectivity

Development of Reactivity for Organobismuth (III, V) Toward Sulfur-Containing Compounds

Organobismuth compounds have been used in various areas of science, like biology and organic synthesis, because they are normally nontoxic and exhibit unique properties. Bismuth induces metallothionein production and is known to exhibit thiophilicity. However, few reports on the reactions between bismuth and sulfur compounds exist. This article reviews studies on the reactivity of bismuth (III and V) with sulfur compounds. A simple approach for the reaction of azole-2-thiones, which contains a heterocyclic ring, with triaryl bismuthines in the presence of a copper catalyst affords the S-arylated coupling product. When a palladium catalyst is used instead of a copper catalyst, desulfinative C-C bond formation occurs. These reactions indicate that trivalent bismuth compounds can be used as novel aryl sources. Triphenylbismuth dichloride, an organobismuth (V) reagent, successfully promotes the cyclodesulfurization of thioureas within short reaction times under mild conditions. The reaction affords N-substituted benzoxazol-2-amines in excellent yields. Tafamidis, a drug used to treat transthyretin amyloidosis, can be synthesized using this reaction.

Platinum Elimination from Bis(triethylsilylpolyynyl) Complexes (n-Bu2C(CH2PPh2)2)Pt((C≡C)nSiEt3)2 (n=2, 3) and Macrocycles Comprised of Four L2Pt Corners and Four C≡CC≡CC≡C Linkers; An Approach to Cyclo[24]carbon.

The overarching goal of this study is to effect the elimination of platinum from adducts with cis -C≡C-Pt-C≡C- linkages, thereby generating novel conjugated polyynes. Thus, the bis(hexatriynyl) complex trans-(p-tol3P)2Pt((C≡C)3H)2 is treated with 1,3-diphosphines R2C(CH2PPh2)2 to generate (R2C(CH2PPh2)2)2Pt((C≡C)3H)2 (14; R=c, n-Bu; e, p-tolCH2). These condense with the diiodide complexes R2C(CH2PPh2)2PtI2 (9 a,c) in the presence of CuI (cat.) and excess HNEt2 to give the title macrocycles [(R2C(CH2PPh2)2)Pt(C≡C)3]4 (16 c,e) as adducts of the byproduct [H2NEt2]+ I- (30-66 %). DOSY NMR experiments establish that this association is maintained in solution, but NaOAc removes the ammonium salt. The bis(triethylsilylpolyynyl) complexes (n-Bu2C(CH2PPh2)2)Pt((C≡C)nSiEt3)2 (n=2, 3) are synthesized analogously to 14 c. They react with I2 at rt to give mainly the diiodide complex 9 c and the coupling product Et3Si(C≡CC≡C)nSiEt3. The possibility of competing reactions giving IC≡C species is investigated. Analogous reactions of the Pt4C24 macrocycle 16 c also give 9 c, but no sp 13C NMR signals or mass spectrometric Cx z+ ions (x=24-100) could be detected. It is proposed that some cyclo[24]carbon is generated, but then rapidly converts to other forms of elemental carbon. No cyclotetracosane (C24H48) is detected when this sequence is carried out in the presence of PtO2 and H2.

Examining 1,4,2‐Dioxazol‐5‐One as an Alternative Reagent to Acyl Azides in the Staudinger Reaction

AbstractIn this study, we explore 1,4,2‐dioxazol‐5‐one as an alternative reagent to acyl azides in the Staudinger reaction, providing a safe and efficient method for synthesizing N‐acyliminophosphoranes under metal‐free conditions. This approach involves a heat‐promoted nucleophilic attack of phosphines on 1,4,2‐dioxazol‐5‐ones, followed by the extrusion of CO2 gas, resulting in the formation of the P−N coupling product. The synthetic utility of this metal‐free imidization of phosphine was demonstrated through a gram‐scale reaction and its suitability for subsequent transformations. Density functional theory (DFT) calculations were employed to elucidate the overall reaction pathway leading to the formation of N‐acyliminophosphoranes.

Regulating Chlorine and Hydrogen Atom Transfer for Selective Photoelectrochemical C─C Coupling by Cu-coordination Effect at Semiconductor/Electrolyte Interfaces.

Semiconductor-based photoelectrochemical (PEC) organic transformations usually show radical characteristics, in which the reaction selectivity is often difficult to precisely control due to the nonselectivity of radicals. Accordingly, several simple organic reactions (e.g., oxidations of alcohols, aldehydes, and other small molecules) have been widely studied, while more complicated processes like C─C coupling remain challenging. Herein, a synergistic heterogeneous/homogeneous PEC strategy is developed to achieve a controllable radical-induced C─C coupling reaction mediated by the copper-coordination effect at the semiconductor/electrolyte interfaces, which additionally exerts a significant impact on the product regioselectivity. Through experimental studies and theoretical simulations, this study reveals that the copper-chloride complex effectively regulates the formation of chloride radicals, a typical hydrogen atom transfer agent, on semiconductor surfaces and stabilizes the heterogeneous interfaces by suppressing the radical-induced surface passivation. Taking the Minisci reaction (the coupling between 2-phenylquinoline and cyclohexane) as a model, the yield of the target C─C coupling product reaches up to 90% on TiO2 photoanodes with a selectivity of 95% and long-term stability over 100h. Moreover, such a strategy exhibits a broad scope and can be used for the functionalization of various heteroaromatic hydrocarbons.

Formation of Carbon–Carbon Double Bond between Cp Ligand and Alkenyl Carbon of Titanacyclopentenes

AbstractReactions of bis(cyclopentadienyl)titanacyclopentenes with BiI3 gave coupling products of one Cp ligand and the alkenyl carbons in moderate yields. An NMR study of the tetracyanoethylene (TCNE) adduct of the product showed that the coupled Cp ring and the alkenyl carbons were connected by one carbon–carbon double bond. This is in sharp contrast to coupling reactions of one Cp ligand with the diene moiety in bis(cyclopentadienyl)titanacyclopentadienes, where two carbon–carbon single bonds were formed between those two components to give dihydroindenes or spiro compounds.

Equimolar Cross-Coupling Using Reactive Coiled Coils for Covalent Protein Assemblies.

Biocompatible cross-coupling reactions enable the efficient covalent attachment of large biomolecules at near-stoichiometric ratios, ensuring the stability and integrity of the resulting products. We present an affinity-based peptide platform utilizing coiled coils containing reactive side chains for proximity-driven protein cross-coupling in the presence of a cross-linking agent. This platform supports both chemical synthesis and recombinant expression, using canonical amino acids to generate reactive affinity tags. Employing the E3/R3 coiled coil pair as a scaffold, we design four complementary coils with cysteine residues as cross-linking sites, achieving >90% conversion to covalent heterodimeric coupling products using 3,4-dibromomaleimide. Equimolar mixtures of proteins with reactive coils at their termini yield near-quantitative heterodimeric cross-coupling products. The strategic selection of complementary coiled coil pairs and cross-linking agents enables orthogonal assembly of macromolecules with diverse architectures. This method offers a versatile approach for creating covalent fusion proteins, enhancing their stability and functionality for applications in chemical biology, biotechnology, and medicine.

Evidence for the formation of 6PPD-quinone from antioxidant 6PPD by cytochrome P450

N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD) as a rubber antioxidant has attracted global concern, since its ozone-oxidation product 6PPD-quinone (6PPDQ) was found to be the primary toxicant responsible for urban runoff mortality syndrome in coho salmon. However, the biotransformation fate and associated toxicological mechanism of 6PPD have not received much study yet. In this work, the in vitro assays showed 6PPD can be transformed into 6PPDQ by cytochromes P450 (CYP450) in human liver microsomes (HLMs) with 0.98 % production rate, and the adducts of 6PPDQ with calf thymus DNA and the N-N coupling product between 6PPD and 6PPDQ were further identified after 6PPD incubation in HLMs. Further evidence for the 6PPDQ formation can be obtained from the in vivo assays that the 6PPDQ-DNA adducts and 6PPD-N-N-6PPDQ dimer were detected in mice by oral gavage with 6PPD, and the latter dimer species was detected as well in 6PPD exposure to zebrafish larvae. Especially, the bioaccumulation property and high reactivity of 6PPDQ result in the continuous formation of the significant DNA adducts and 6PPD-N-N-6PPDQ dimer even in case of low production rate of biotransformation of 6PPD to 6PPDQ, which may provide potentially effective biomarkers for such process. DFT computations revealed the formation mechanism of 6PPDQ is the (N)H-abstraction of 6PPD by CYP450, followed by amino radical rebound at the nearby ortho-carbon, yielding a quinol intermediate due to spin delocalization, that might readily undergo further oxidation by CYP450 into 6PPDQ.

Preparation and characterization of high performance super activated carbon based on coupled coal/sargassum precursors

High electrochemical performance supercapacitors require activated carbon with high specific surface area, suitable pore size distribution and surface properties, and high electrical conductivity as electrode materials, whereas there exists a trade-off relationship between specific surface area and electrical conductivity, which is not well met by a single type of carbon source. To solve this problem, the coal and sargassum are adopted to obtain the coupling product via co-thermal dissolution, followed by carbonization and KOH activation. The effects of mixing mass ratio and activation temperature on the prepared activated carbon (AC) are investigated using single factor experimental method. The experimental results show that AC1/3-800 has abundant micropore and mesopore content, good pore structure connectivity, high electrical conductivity and good wettability, and superior electrochemical properties compared with other activated carbons prepared in this experiment. Its total specific surface area is up to 2098.5 m2·g–1, the pore volume is up to 1.33 cm3·g–1, the content of mespores with diameter of 6–8 nm is significantly increased, and the pore size distribution is wide and uniform. When the current density increases from 0.1 A·g–1 to 10 A·g–1, the gravimetric capacitance decreases from 219 F·g–1 to 186 F·g–1 with a capacitance retention of 84.9%, the equivalent series resistance is very small, and the rate performance and reversibility of charging and discharging have also been excellent.

Recent Advances in Heterogeneously Catalyzed Acceptorless Dehydrogenation of Alcohols to Carbonyl Derivatives and N-heterocyclic Compounds

: Oxidation of alcohols in an oxidant-free condition, commonly known as the acceptorless dehydrogenation (AD) reaction, has recently emerged as one of the widely used processes in synthetic organic chemistry. Alcohol acts as an excellent chemical precursor that produces a variety of dehydrogenated value-added products such as carbonyls, acids, acetals, and several coupling products, followed by the concomitant evolution of molecular hydrogen gas. AD reaction of alcohol, therefore, can be considered as a vital reaction for the hydrogen economy using alcohols as a liquid hydrogen carrier. Over the past decade, the growing importance of AD reactions has set the way for the continuous development of various homogeneous and heterogeneous catalytic systems. With the advantage of reusability and recyclability, heterogeneous catalysts have now become more promising and significant in the catalytic domain. This review aims to make an overview of the transition metal-based heterogeneous catalytic system of acceptorless alcohol dehydrogenation reaction reported till December, 2023.

In Situ generated PdNPs immobilized on polystyrene supported DABCO Dicationic ionic liquid: An efficient and reusable catalyst for Suzuki and Heck coupling reactions

A catalyst named PdNPs-DDIL@PS has been synthesized by immobilizing PdNPs on a DABCO Dicationic Ionic Liquid (DDIL) supported on Merrifield Resin (PS). The PdNPs (∼4.16 nm size) generated in situ were fully characterized using different techniques such as SEM, TEM, TGA-DTA, and XPS. It has been found that the catalyst is highly active in the Suzuki coupling reaction of various aryl bromides and aryl boronic acids in 70 % aqueous ethanol at room temperature. The catalyst produced the desired Suzuki coupling products in good to excellent yields. Additionally, the protocol was extended for the Heck coupling reactions in DMF at 80 °C with good to excellent yields. The catalyst attained a good turnover number (TON) of 160.00–189.92 and a turnover frequency (TOF) of 8.493–18.992 min−1 for the Suzuki and TON of 173.33–189.77 and TOF of 3.952–6.325 min−1 for the Heck coupling reactions. The catalyst displayed at least four times recyclability for the Suzuki coupling without a substantial decrease in product yields. Additionally, it boosts impressive environmentally-friendly credentials in Suzuki coupling reactions.

Photochemical coupling reaction of phenacyl benzoate with acetone to form 1,4‐dicarbonyl compound enabled by charge transfer

AbstractPhotolysis of phenacyl benzoates tethered with a phenol or anisole in acetone resulted in the formation of 1,4‐dicarbonyl compounds, coupling products of the phenacyl moiety with acetone. The reaction occurs via electron and/or proton transfer from a triplet exciplex, leading to the formation of a phenacyl radical, which then adds to the enol form of acetone. The reaction also occurs in intermolecular fashion with external electron donors.

Immobilization of laccase on mesoporous metal organic frameworks for efficient cross-coupling of ethyl ferulate.

Laccases act as green catalysts for oxidative cross-coupling of phenolic antioxidnt compounds, but low stability and non-recyclability limit its application. To address that, metal-organic frameworks Cu-BTC and Cr-MOF were synthesized as supports to immobilize the efficient laccase from Cerrena sp. HYB07. The Brunauer-Emmett-Teller surface area of Cu-BTC and Cr-MOF were 1213.2 and 907.1m2/g, respectively. The two carriers respectively presented pore diameters of 1.2-10nm and 1.4-12nm as octahedron, indicating nano-scale mesoporosity. These Cu-BTC and Cr-MOF carriers could adsorb laccase with enzyme loading of 1933.2 and 1564.4U/g carrier, respectively. The stability and organic solvent tolerance of Cu-BTC-laccase and Cr-MOF-laccase were both obviously improved compared to free laccase. Thermal inactivation kinetics showed that both the two immobilized laccases displayed lower thermal inactivation rate constants. Importantly, the Cu-BTC-laccase and Cr-MOF-laccase both showed much higher activity for cross-coupling of ethyl ferulate than free laccase, which had 2.5-fold higher cross-coupling efficiency than that by free laccase. The ethyl ferulate coupling product was also analyzed by mass spectroscopy and the synthesis pathway of ethyl ferulate dimer was proposed. The cross coupling of ethyl ferulate required the formation of radical intermediates of ethyl ferulate generated by laccase mediated oxidation. This work paved the way for MOFs immobilized laccase for cross coupling of antioxidant phenols.

Regioselective Synthesis of α-Vinyl Boronates via a Pd-Catalyzed Mizoroki-Heck Reaction.

We report a palladium-catalyzed synthesis of α-vinyl boronates via a regioselective Mizoroki-Heck reaction between aryl triflates and vinyl boronates. This selectivity is achieved by the use of a 1,5-diaza-3,7-diphosphacyclooctane (P2N2) ligand, which results in minimal formation of the more commonly observed (linear) β-product. The choice of base, solvent, and presence of water are shown to be critical for controlling this outcome, with organic bases, nonpolar solvents, and anhydrous conditions favoring the Heck product and suppressing the competitive Suzuki-Miyaura coupling product.

Photochemical conversion of CO to C1 and C2 products mediated by porphyrin rhodium(II) metallo-radical complexes

Unimolecular reduction and bimolecular reductive coupling of carbon monoxide (CO) represent important ways to synthesize organic feedstocks. Reductive activation of CO through open-shell pathways, though rare, can help overcome the barriers of many traditional organometallic elementary reactions that are hard to achieve. Herein we successfully achieve the unimolecular reduction of CO to (TPP)RhCH2OSiR1R2R3 (TPP = 5,10,15,20-tetraphenylporphyrin), and the release of products CH3OSiR1R2R3, TEMPO-CH2OSiR1R2R3 and BrCH2OSiR1R2R3 in near-quantitative yield under visible light (420–780 nm), which involves radical formation from Rh-C bond homolysis. Bimolecular CO reductive coupling products, (TPP)RhCOCH2OSiR1R2R3, are then obtained via a radical mechanism. Subsequent treatment with n-propylamine, BrCCl3 or TEMPO under thermal or photochemical conditions afford small-molecule bimolecular reductive coupling products. To the best of our knowledge, homogeneous systems which reductively couple CO under photochemical conditions have not been reported before. Here, the use of an open-shell transition metal complex, that delivers more than one kind of small-molecule CO reductive coupling products bearing different functional groups, provides opportunities for useful CO reductive transformations.

Oxidative N-N Bond Formation Versus the Curtius Rearrangement.

The oxidative formation of N-N bonds from primary amides has been recently reported and then retracted in the journal Nature Communications by Kathiravan, Nicholls, and co-authors, utilizing a hypervalent iodane reagent. Unfortunately, the authors failed to recognize the Curtius reaction taking place under the described reaction conditions. Thus, the claimed N-N coupling products were not formed. Instead, the Curtius rearrangement urea coupling products were obtained. We demonstrate this herein by means of NMR and x-ray analysis, as well as with the support of an alternative synthetic route.

Synthesis, characterization, crystal structures and catalytic activity of hydrogen bond mediated 2D and 3D-copper(II) coordination networks based on 2-aminoterepthalic acid and 5-aminoisopthalic acid

Two new copper(II) compounds [Cu2(2-NH2BDC)2(bipy)2(H2O)4] (1) and [Cu2(µ2OH)2(5-aip)(bipy)2(H2O)].5H2O (2) have been synthesized and characterized by elemental analyses, IR, thermogravimetric analysis, and electronic absorption spectroscopy. Molecular structures of compounds 1 and 2 were determined crystallographically. Single crystal X-ray studies show that the coordination network 1 is a centrosymmetrical dimeric unit with the 2-aminoterephthalate ligand bridging the two copper atoms. Each CuII atom is hexacoordinated, residing in an octahedral environment, surrounded by one oxygen and one nitrogen atoms from 2-aminoterephthalate ligand and two nitrogen atoms from one bipy ligand and two water molecules to give a CuO3N3 segmentand generate the an infinite three-dimensional (3D) supramolecular structure resulting from CH•••O interactions between adjacent dimer molecules running parallel to the a axis. In compound 2, each CuII atom is pentacoordinated, residing in a square pyramidal geometry and generate an infinite two-dimensional (2D) supramolecular structure resulting from CH•••O, NH•••O and OH•••O hydrogen bond interactions. The coordination network 1 and 2, on pyrolyzing, yielded copper oxide nanoparticles, which have been characterized by TEM and powder X-ray diffraction. The catalytic properties of the resulting copper oxide nanoparticles have also been studied for CN cross-coupling reactions with aryl halides. The CN coupling products were obtained in 70–99 % yields.