Construction of helical coordination polymers via flexible conformers of bis(3-pyridyl)cyclotetramethylenesilane: metal(ii) and halogen effects on luminescence, thermolysis and catalysisElectronic supplementary information (ESI) available: TGA and DSC curves of the present complexes; SEM images, powder XRD patterns, and SEM-EDX data for zinc(ii) oxide; 1H NMR spectra on the procedure of transesterification of phenyl acetate in methanol using the present complexes as catalysts. CCDC 1047992-10479
Infinite rectangular-tubular helices, [MX 2 L] (M = Zn( ii ), Hg( ii ); X − = Cl − , Br − ; L = bis(3-pyridyl)cyclotetramethylenesilane), have been efficiently constructed via the combined effects of the potential flexible conformers of L and the tetrahedral geometry of M( ii ) ions. This helical mo...
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Zusammenfassung: | Infinite rectangular-tubular helices, [MX
2
L] (M = Zn(
ii
), Hg(
ii
); X
−
= Cl
−
, Br
−
; L = bis(3-pyridyl)cyclotetramethylenesilane), have been efficiently constructed
via
the combined effects of the potential flexible conformers of L and the tetrahedral geometry of M(
ii
) ions. This helical molecular system affords a racemic mixture of
P
- and
M
-helices in a crystal. The helical pitches (7.8934(4)-8.1560(2) Å) that are sensitive to the nature of M(
ii
) ions and halide anions are attributable to subtle change in the flexible dihedral angles between the two pyridyl groups around Si and the M(
ii
) hinges. Their photoluminescence intensities, correspondingly, are in the order [ZnCl
2
L] > [ZnBr
2
L] > [HgCl
2
L] > [HgBr
2
L]. Zinc(
ii
) complexes show recyclable catalytic effects on the transesterification reaction in the order [ZnCl
2
L] > [ZnBr
2
L]. Calcination of [ZnCl
2
L] and [ZnBr
2
L] at 500 °C produces uniform hexagonal tubular spire crystals of 1.2 × 1.2 × 4.0 μm
3
dimensions and spheres, respectively.
Construction and physicochemical properties of rectangular-tubular-helical coordination polymers of [M(
ii
)X
2
L] (M = Zn(
ii
), Hg(
ii
); X
−
= Cl
−
, Br
−
) were investigated. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c5dt00774g |