synthesis-of-a-water-soluble-metalorganic-complex-array

Synthesis of a Water-soluble Metal&#8211;Organic Complex Array

We demonstrate a method for the synthesis of a water-soluble multimetallic peptidic array containing a predetermined sequence of metal centers such as ...

National Institute for Materials Science

Two thiourea and urea based indole conjugated ligands show selective color changes with fluoride along with an absorbance band at 936 nm and 904 nm respectively.

Visible and near-infrared sensing of fluoride by indole conjugated urea/thiourea ligands.

A series of new symmetrically functionalized guanidinium chlorides (S1-S10) are synthesized in good yields and their sensing ability toward anions is studied in MeCN-DMF (24 : 1) (v/v). The absorption bands of these molecules in the presence of anions are tuned by varying the functional groups attached to the guanidinium moiety (which resembles urea) with respect to (i) aromaticity (S1-S4), (ii) electron induction effect (S1, S5-S9), (iii) positional isomeric effect (S7-S9), (iv) indole functionality (S10) of the conjugated aryl units. Anions that are above Cl(-) in the Hofmeister series (F(-), AcO(-), H(2)PO(4)(-)) are eligible as an analyte in this series of molecules whereas less basic anions than Cl(-) do not cause any interference. Thus, this series of molecules are suitable for the detection of anions in the narrow window of the Hofmeister series. Out of all the anions, only fluoride causes vivid colour changes from yellow to red to reddish orange and finally to blue, irrespective of the increasing aromaticity, induction and positional isomeric effect of the substituent that is attached to the guanidinium moiety. Interestingly, S9 has shown the ability to sense distinctly both F(-) and AcO(-) colourimetrically. Further S10, a sensor attached with indole functionality shows selective sensing of F(-) colourimetrically with a NIR signature at ∼930 nm though both these outputs are very unstable in nature. Stability constants for complex formation of S1-S10 (except S5) with F(-), AcO(-) are calculated by UV-vis titration experiments. Finally single crystal X-ray structural studies on the species 1 formed upon treating S6 with sodium fluoride confirms -NH deprotonation, whereas the reaction of S6 and S2 with sodium benzoate shows 1:1 host:guest binding that results in complexes 2 and 3 respectively.

Functionalized guanidinium chloride based colourimetric sensors for fluoride and acetate: single crystal X-ray structural evidence of -NH deprotonation and complexation.

Tris(2-aminoethyl)amine (tren) based pentafluorophenyl-substituted tripodal L, tris[[(2,3,4,5,6-pentafluorobenzyl)amino]ethyl]amine receptor is synthesized in good yield and characterized by single crystal X-ray diffraction analysis. Detailed structural aspects of binding of different anionic guests toward L in its triprotonated form are examined thoroughly. Crystallographic results show binding of fluoride in the C(3v)-symmetric cavity of [H(3)L](3+) where spherical anion fluoride is in tricoordinated geometry via (N-H)(+)···F interaction in the complex [H(3)L(F)]·[F](2)·2H(2)O, (3). In the case of complexes [H(3)L(OTs)]·[OTs](2), (4) and [H(3)L(OTs)]·[NO(3)]·[OTs], (5), tetrahedral p-toluenesulphonate ion is engulfed in the cavity of [H(3)L](3+) via (N-H)(+)···O interactions. Interestingly, complex [(H(3)L)(2)(SiF(6))]·[BF(4)](4)·CH(3)OH·H(2)O, (6) shows encapsulation of octahedral hexafluorosilicate in the dimeric capsular assembly of two [H(3)L](3+) units, via a number of (N-H)(+)···F interactions. The kinetic parameters of L upon binding with different anions are evaluated using a potentiometric study in solution state. The potentiometric titration experiments in a polar protic methanol/water (1:1 v/v) binary solvent system show high affinity of the receptor toward more basic fluoride and acetate anions, with a lesser affinity for other inorganic anions (e.g., chloride, bromide, nitrate, sulfate, dihydrogenphosphate, and p-toluenesulphonate).

Anion binding in the C3v-symmetric cavity of a protonated tripodal amine receptor: potentiometric and single crystal X-ray studies.

A new series of tris(2-aminoethyl)amine (tren)-based L-alanine amino acid backboned tripodal hexaamide receptors (L1-L5) with various attached moieties based on electron-withdrawing fluoro groups and lipophilicity have been synthesized and characterized. Detailed binding studies of L1-L5 with different anions, such as halides (F(-), Cl(-), Br(-), and I(-)) and oxyanions (AcO(-), BzO(-) (Bz=benzoyl), NO(3)(-), H(2)PO(4)(-), and HSO(4)(-)), have been carried out by isothermal titration calorimetric (ITC) experiments in acetonitrile/dimethylsulfoxide (99.5:0.5 v/v) at 298 K. ITC titration experiments have clearly shown that receptors L1-L4 invariably form 1:1 complexes with Cl(-), AcO(-), BzO(-), and HSO(4)(-), whereas L5 forms a 1:1 complex only with AcO(-). In the case of Br(-), I(-), and NO(3)(-), no appreciable heat change is observed owing to weak interactions between these anions and receptors; this is further confirmed by (1)H NMR spectroscopy. The ITC binding studies of F(-) and H(2) PO(4)(-) do not fit well for a 1:1 binding model. Furthermore, ITC binding studies also revealed slightly higher selectivity of this series of receptors towards AcO(-) over Cl(-), BzO(-), and HSO(4)(-). Solid-state structural evidence for the recognition of Cl(-) by this new category of receptor was confirmed by single-crystal X-ray structural analysis of the complex of tetrabutylammonium chloride (TBACl) and L1. Single-crystal X-ray diffraction clearly showed that the pentafluorophenyl-functionalized amide receptor (L1) encapsulated Cl(-) in its cavity by hydrogen bonds from amides, and the cavity of L1 was capped with a TBA cation through hydrogen bonding and ion-pair interactions to form a capped-cleft orientation. To understand the role of the cationic counterpart in solution-state Cl(-) binding processes with this series of receptors (L1-L4), a detailed Cl(-) binding study was carried out with three different tetraalkylammonium (Me(4) N(+), Et(4) N(+), and Bu(4) N(+)) salts of Cl(-). The binding affinities of these receptors with different tetralkylammonium salts of Cl(-) gave binding constants with the TBA cation in the following order: butyl>ethyl>methyl. This study further supports the role of the TBA countercation in ion-pair recognition by this series of receptors.

A series of amino acid functionalized tripodal hexaamide anion receptors: ion-pair-assisted capped-cleft formation by a pentafluorophenyl-functionalized amide.

Simple tris(2-aminoethyl)amine (TREN) based tripodal urea receptors are investigated for the encapsulation of divalent oxalate (C2O4(2-)) in a semi-aqueous medium. A single crystal X-ray diffraction study shows that the receptor with 3-cyanophenyl functionality captures a staggered conformer whereas the 3-fluorophenyl functionalized receptor encapsulates a less stable planar conformer.

Tris(2-aminoethyl)amine based tripodal urea receptors for oxalate: encapsulation of staggered vs. planar conformers.

The environmentally important and toxic arsenate anion (HAsO4(2-)) is trapped in the cavity of a dimeric capsular assembly formed by a tripodal urea receptor. The selective binding of HAsO4(2-) over other anions is observed in a semi-aqueous solvent using a (1)H NMR titration study.

Arsenate recognition in aqueous media by a simple tripodal urea.

Fluorescent and electron-rich polymer threaded into porous framework provides a scaffold for sensing acceptor molecules through noncovalent interactions. Herein, poly(9-vinylcarbazole) (PVK) threaded MIL-101 with confined nanospace was synthesized by vinyl-monomer impregnation, in situ polymerization, and interpenetration. The pore size of the resulted hybrid could be controlled by varying the time of polymerization and interpenetration. The interaction of PVK-threaded MIL-101 with guest molecules showed a charge-transfer progress with an obvious red shift in the optical spectra. Depending on the degree of the interaction, the solution color changed from blue to green or to yellow. In particular, electron-rich PVK-threaded MIL-101 could effectively probe electron-poor nitro compounds, especially 1,3,5-trinitrobenzene (TNP), a highly explosive material. This sensing approach is a colorimetric methodology, which is very simple and convenient for practical analysis and operation.

Macroscopic architecture of charge transfer-induced molecular recognition from electron-rich polymer interpenetrated porous frameworks.

A series of N-heterocyclic quinoxaline derivatives was successfully synthesized and applied as hole transport layers in quantum dot light-emitting diodes (QLEDs). By inducing sp(2) N-atoms into the quinoxaline backbone, the electron affinity of the obtained material was enhanced, and its optical properties and bandgap became tunable. Quinoxaline based N-heteroacenes show a narrow bandgap, high thermal stability, and aligned film morphology. The resulting N-heteroacene polymer based QLED exhibits superior performance to poly(9-vinylcarbazole) based QLED. This study presents a strategy towards the design of novel N-rich molecules for the fabrication of QLEDs with improved performance.

A quinoxaline based N-heteroacene interfacial layer for efficient hole-injection in quantum dot light-emitting diodes.

The bulk heterojunction (BHJ) plays an indispensable role in organic photovoltaics, and thus has been investigated extensively in recent years. While a p-n heterojunction is usually fabricated using two different donor and acceptor materials such as poly(3-hexylthiophene-2,5-diyl) (P3HT) and phenyl-C61-butyric acid methyl ester (PCBM), it is really rare that such a BHJ is constructed by a single entity. Here, we presented a photoirradiation-induced p-n heterojunction in naphthylamine-based organic photovoltaic cells, where naphthylamine as a typical p-type semiconductor could be oxidized under photoirradiation and transformed into a new semiconductor with the n-type character. The p-n heterojunction was realized using both the remaining naphthylamine and its oxidative product, giving rise to the performance improvement in organic photovoltaic devices. The experimental results show that the power conversion efficiency (PCE) of the devices could be achieved up to 1.79% and 0.43% in solution and thin film processes, respectively. Importantly, this technology using naphthylamine does not require classic P3HT and PCBM to realize the p-n heterojunction, thereby simplifying the device fabrication process. The present approach opens up a promising route for the development of novel materials applicable to the p-n heterojunction.

The photoirradiation induced p-n junction in naphthylamine-based organic photovoltaic cells.

Water-soluble metal-organic complex array 1, bearing Ru(II), Pt(II) and Rh(III) complexes at the side residues of the short peptide, exhibits anion and pH-responsive self-assembly behaviours in aqueous media. NaCl-induced aggregation of 1 at neutral pH was suppressed in phosphate buffered saline containing a mixture of Cl(-), HPO4(2-) and H2PO4(-), which is unconventional for a peptide amphiphile.

A water-soluble metal-organic complex array as a multinuclear heterometallic peptide amphiphile that shows unconventional anion dependency in its self-assembly.

Purnandhu Bose

International Center for Materials Nanoarchitectonics

National Institute for Materials Science

Synthesis of a Water-soluble Metal–Organic Complex Array

Purnandhu Bose

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}International Center for Materials Nanoarchitectonics

National Institute for Materials Science

Synthesis of a Water-soluble Metal–Organic Complex Array

International Center for Materials Nanoarchitectonics