A novel terephthalaldehyde based turn-on fluorescent chemosensor for Cu and its application in imaging of living cells.

A new terephthaldehyde-based chemosensor 1 bearing an aminophenol recognition unit has been synthesized and applied to the fluorescent sensing of metal ions. Molecular system 1 acts as a highly selective and sensitive fluorescence turn-on sensor for Cu. The sensing mechanism has been explored.

Highly selective optical and reversible dual-path chemosensor for cyanide detection and its application in live cells imaging.

A new biocompatible fluorescent receptor 1 was synthesized by conjugating diaminomaleonitrile (DMN) with benzothiazole unit, and characterized by single X-ray. In DMF/water (1:1, v/v), the receptor 1 showed a selectivity turn-on fluorescence at 517nm in the presence of CN. Receptor 1 showed a detection limit down to 0.

A novel zinc(II) and hydrogen sulphate selective fluorescent "turn-on" chemosensor based on isonicotiamide: INHIBIT type's logic gate and application in cancer cell imaging.

We have developed a novel isonicotiamide-based fluorescent "turn-on" chemosensor 1 for the selective detection of Zn(2+) and HSO4(-). The sensor 1 can detect Zn(2+) and HSO4(-) with a detection limit down to the nanomolar level by forming a complex in 1 : 1 stoichiometry in the presence of other anions and 2 : 1 in presence of cations in aqueous solution. Density functional theory calculations on 1 and the 1-Zn(2+)/HSO4(-) complexes are consistent with the experimental results.

Synthesis, spectral, and structural studies of porphyrins having sterically hindered [η(5)-CpCo(η(4)-C4Ph4)] cobalt sandwich units at the meso positions.

Synthesis, spectral, and structural studies of the first examples of porphyrins substituted at the meso positions with sterically hindered η(5)-CpCo(η(4)-C4Ph4) cobalt sandwich units are described. The novel dipyrromethane derived cobalt sandwich compound {η(5)-[(C4H4N)2CH]C5H4}Co(η(4)-C4Ph4) 1, as well as its parent aldehyde, η(5)-[C5H4(CHO)]Co(η(4)-C4Ph4), were used in the synthesis of porphyrins having one or two η(5)-CpCo(η(4)-C4Ph4) groups at their meso positions. 1,9-Diformyldipyrromethane derived η(5)-CpCo(η(4)-C4Ph4) 2 was synthesized using dipyrromethane 1 under Vilsmeier conditions.

Ring-closing metathesis reactions of terminal alkene-derived cyclic phosphazenes.

The first examples of ring-closing metathesis (RCM) reactions of a series of terminal alkene-derived cyclic phosphazenes have been carried out. The tetrakis-, hexakis-, and octakis(allyloxy)cyclophosphazenes (NPPh(2))(NP(OCH(2)CH=CH(2))(2))(2) (1), N(3)P(3)(OCH(2)CH=CH(2))(6) (2), and N(4)P(4)(OCH(2)CH=CH(2))(8) (3) and the tetrakis(allyloxy)-S-phenylthionylphosphazene (NS(O)Ph)[NP(OCH(2)CH=CH(2))(2)](2) (4) were prepared by the reactions of CH(2)=CHCH(2)ONa with the cyclophosphazenes (NPPh(2))(NPCl(2))(2), N(3)P(3)Cl(6), and N(4)P(4)Cl(8) and the S-phenylthionylphosphazene (NS(O)Ph)(NPCl(2))(2). The reactions of 1-4 with Grubbs first-generation olefin metathesis catalyst Cl(2)Ru=CHPh(PCy(3))(2) resulted in the selective formation of seven-membered di-, tri-, and tetraspirocyclic phosphazene compounds (NPPh(2))[NP(OCH(2)CH=CHCH(2)O)](2) (5), N(3)P(3)(OCH(2)CH=CHCH(2)O)(3) (6), and N(4)P(4)(OCH(2)CH=CHCH(2)O)(4) (7) and the dispirocyclic S-phenylthionylphosphazene compound (NS(O)Ph)[NP(OCH(2)CH=CHCH(2)O)](2) (8).

Synthesis and reactions of ethynylferrocene-derived fluoro- and chlorocyclotriphosphazenes.

The reactions of lithiated ethynylferrocene, FcC[triple bond]CLi (Fc = ferrocenyl), with fluoro- and chlorocyclotriphosphazenes, N(3)P(3)X(6) (X = F, Cl), resulted in the formation of stable mono-FcC[triple bond]CP(3)N(3)X(5) [X = F (1), Cl (2)] and geminal bis[(FcC[triple bond]C)(2)PN](X(2)PN)(2) [X = F (3), Cl (4)], ethynylferrocene-substituted cyclophosphazenes. The reactions of 1 and 2 with CpCo(COD) were found to differ in the nature of the sandwich compounds (eta(5)-Cp)Co{eta(4)-C(4)[Fc(2)(N(3)P(3)X(5))(2)]} formed. While the fluorophosphazene-derived compound 1 yielded both cis and trans isomers of the cyclobutadiene complexes 5 and 6, the chlorophosphazene-derived compound 2 was found to give only the trans-cyclophosphazene-disubstituted cyclobutadiene compound 7.