pyrophosphate and pyridine

Crosslinked high-performance polymers have many industrial applications, but are difficult to recycle or rework. A novel class of recyclable crosslinking Cu(II)-metallo-supramolecular coordination polymers are successfully prepared, which possess outstanding thermal stability and mechanical property. More importantly, the Cu

Topics: Copper; Cross-Linking Reagents; Diphosphates; Magnetic Resonance Spectroscopy; Polymers; Pyridines; Spectroscopy, Fourier Transform Infrared

The terpyridine anthracene ligand was synthesized and characterized. is a ratiometric fluorescent probe for Cd(2+) with a recognition mechanism based on intramolecular charge transfer (ICT). An complex was isolated, and its structure was established using single-crystal XRD. The complex was able to serve as a novel reversible chemosensing ensemble to allow ratiometric response to pyrophosphate (PPi) in aqueous media. Moreover, the fluorescence imaging in living cells from these two emission channels suggested that was a ratiometric probe for Cd(2+), and the in situ generated complex was also a ratiometric ensemble for PPi detection in living cells.

Topics: Animals; Cadmium; Cell Line; Coordination Complexes; Crystallography, X-Ray; Diphosphates; Fluorescent Dyes; Mice; Microscopy, Confocal; Molecular Conformation; Pyridines; Solutions; Spectrometry, Fluorescence

Herein, we report a new pyridine-biquinoline-derivative fluorophore L for effectively sensing pyrophosphate (PPi) and monohydrogen sulfide (HS(-)) in aqueous buffer and in living cells. L could selectively coordinate with metal ions (M(n+)) in Groups IB and IIB to form L-M(n+) complexes with 1:1 stoichiometry, resulting in fluorescence quenching via photoinduced electron transfer (PET) mechanism. L-Zn(2+) complex was applied to competitively coordinate with PPi to form a new "ate"-type complex, turning on the fluorescence by a 21-fold-increase. The limit of detection (LOD) of this assay for PPi detection in aqueous buffer is 0.85 μM. L-Cu(2+) complex was applied for highly selective detection of HS(-) with an excellent sensitivity by 25-fold decomplexation-induced fluorescence increase. LOD of L-Cu(2+) complex for HS(-) detection in aqueous buffer is 2.24 μM. With the in vitro data obtained, we successfully applied these two complexes for sequential imaging Zn(2+) and PPi, Cu(2+) and HS(-) in living cells, respectively. Since PPi and HS(-) occur in vascular calcification in positive correlation, our multifunctional probe L might help doctors to more precisely diagnose this disease in vivo in the future. For example, we could use radioactive tracer L-(64)Cu for qualitative and quantitative positron emission tomography/computed tomography (PET/CT) imaging of HS(-) in vivo.

Topics: Buffers; Coordination Complexes; Copper; Diphosphates; Fluorescent Dyes; Hep G2 Cells; Humans; Hydrogen Sulfide; Limit of Detection; Molecular Structure; Pyridines; Quinolines; Spectrometry, Fluorescence; Water; Zinc

We presented a novel approach for pyrophosphate (PPi) sensing. Two tetraphenylethene (TPE)-functionalised pyridine salts (TPM and TPH) were designed and synthesized. Both of them exhibited weak emission in the solution state that originates from intramolecular charge transfer (ICT) from TPE to the pyridine; the addition of PPi into the TPM aqueous solution would enhance the fluorescence intensity, which eliminates the emission quenching effect of the iodide ion by the formation of PPi-sensor nanoparticles. The detection limit of TPM was determined to be as low as 133 nM. Meanwhile, a thin solid film of TPM that could detect PPi rapidly was conveniently prepared.

Topics: Chemistry Techniques, Analytical; Diphosphates; Fluorescent Dyes; HeLa Cells; Humans; Limit of Detection; Pyridines; Salts; Spectrometry, Fluorescence; Stilbenes

A simple terpyridine-Zn(II) complex is shown to act as an efficient and highly selective fluorescent sensor for pyrophosphate in water at physiological pH. The sensor complex showed an unprecedented fluorescence response (∼500 fold increase) and a record nanomolar sensitivity (detectable fluorescent response at 20 nM and LOD ∼ 0.8 nM). It has successfully been used to stain and record confocal fluorescence microscopy images of HeLa cells. Moreover, the complex was found to self-assemble into a hydrogel which was subsequently used to coat disposable paper strips for easy, low-cost detection of pyrophosphate.

Topics: Diphosphates; Hydrogels; Limit of Detection; Microscopy, Fluorescence; Pyridines; Spectrophotometry, Ultraviolet; Water; Zinc

A poly(ethylene glycol) (PEG) decorated bis(terpyridine) zinc coordination polymer acts as an anion-responsive material in 100% aqueous solution. Depending on the binding and association constants to Zn(II), the addition of different anions leads to increased emission intensity and/or a shift of the emission wavelength. The sensor was addressed with a collection of common salts to survey the selectivity of the emission response. Phosphate and cyanide, representing the strongest anion binding to zinc(II), were detected even in the presence of other ions in tap water. Biologically relevant phosphates such as diphosphates and adenosine-5'-triphosphate (ATP) also produced a strong response. Because the binding constants with Zn(II) are very high, anion concentrations in the range of 10(-6) to 10(-7) M are sufficient.

Topics: Adenosine Triphosphate; Anions; Cyanides; Diphosphates; Fluorometry; Phosphates; Polyethylene Glycols; Pyridines; Water; Zinc

Pyridyl-based triazole-linked calix[4]arene conjugates, viz. L(1) and L(2), were synthesized and characterized. These two conjugates were shown to be selective and sensitive for Zn(2+) among the 12 metal ions studied in HEPES buffer medium by fluorescence, absorption, and visual color change with the detection limit of ~31 and ~112 ppb, respectively, by L(1) and L(2). Moreover, the utility of the conjugates L(1) and L(2) in showing the zinc recognition in live cells has also been demonstrated using HeLa cells as monitored by fluorescence imaging. The zinc complexes of L(1) and L(2) were isolated, and the structure of [ZnL(1)] has been established by single-crystal XRD and that of [ZnL(2)] by DFT calculations. TDDFT calculations were performed in order to demonstrate the electronic properties of receptors and their zinc complexes. The isolated zinc complexes, viz. [ZnL(1)] and [ZnL(2)], have been used as molecular tools for the recognition of anions on the basis of their binding affinities toward Zn(2+). [ZnL(2)] was found to be sensitive and selective toward phosphate-bearing ions and molecules and in particular to pyrophosphate (PPi) and ATP among the other 18 anions studied; however, [ZnL(1)] was not sensitive toward any of the anions studied. The selectivity has been shown on the basis of the changes observed in the emission and absorption spectral studies through the removal of Zn(2+) from [ZnL(2)] by PPi. Thus, [ZnL(2)] has been shown to detect PPi up to 278 ± 10 ppb at pH 7.4 in aqueous methanolic (1/2 v/v) HEPES buffer.

Topics: Absorption; Adenosine Triphosphate; Calixarenes; Chemistry Techniques, Analytical; Diphosphates; HeLa Cells; Humans; Imines; Intracellular Space; Models, Molecular; Molecular Conformation; Organometallic Compounds; Phenols; Pyridines; Quantum Theory; Solutions; Spectrometry, Fluorescence; Zinc