2010
DOI: 10.1002/chem.201000427
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Electroactive Benzothiazole Hydrazones and Their [Mo6O19]2− Derivatives: Promising Building Blocks for Conducting Molecular Materials

Abstract: The electroactive benzothiazole hydrazone AMBTH-H(2), a new member of the 2,2'-azino-bis(N-alkylbenzothiazole) family, was synthesised in a five-step procedure and characterised by using X-ray diffraction along with two intermediates and the N-methylbenzothiazole hydrazone MBTH-H(2). Both AMBTH-H(2) and MBTH-H(2) were coupled to [Mo(6)O(19)](2-) in acetonitrile in the presence of dicyclohexylcarbodiimide and dimethylaminopyridine to give two new diazoalkane-hexamolybdates, which were isolated as tetrabutylammo… Show more

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Cited by 31 publications
(19 citation statements)
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“…36 Regarding functionalization of the lindqvist structural class, several examples have been isolated through a range of methods. 25,37,38 Typically, these methods involve the use of some form of activating agent such as DCC for the preparation of organo-imido derivatives from organic amine precursors. Notably in 2010, Wei successfully prepared [Mo 6 O 18 NC-(OCH 2 ) 3 MnMo 6 O 18 (OCH 2 ) 3 CNMo 6 O 18 ] 7− which was the first time a Mn-Anderson had been coupled to the hexamolybdate lindqvist polyanion.…”
mentioning
confidence: 99%
“…36 Regarding functionalization of the lindqvist structural class, several examples have been isolated through a range of methods. 25,37,38 Typically, these methods involve the use of some form of activating agent such as DCC for the preparation of organo-imido derivatives from organic amine precursors. Notably in 2010, Wei successfully prepared [Mo 6 O 18 NC-(OCH 2 ) 3 MnMo 6 O 18 (OCH 2 ) 3 CNMo 6 O 18 ] 7− which was the first time a Mn-Anderson had been coupled to the hexamolybdate lindqvist polyanion.…”
mentioning
confidence: 99%
“…(TBA) 3 2 was prepared by a hydrolytic aggregation reaction from (TBA) 2 [Mo 2 O 7 ], (TBA) 4 a-[Mo 8 O 26 ] and Ti(O i Bu) 4 according to eqn (1) as described previously for (TBA) 3 1. 6 The FTIR, 1 H, 13 C and 17 O NMR spectra of (TBA) 3 2 are all consistent with a structure that is analogous to that of 1, although its high solubility has so far prevented the growth of single crystals for single-crystal X-ray crystallography and purification for elemental analysis.…”
Section: Resultsmentioning
confidence: 70%
“…NMR spectra were recorded on a Bruker Avance 300 spectrometer operating at 300.0 MHz ( 1 H) or 75.39 MHz ( 13 C), or a Jeol Lamda 500 spectrometer operating at 500.0 MHz ( 1 H), 125.65 MHz ( 13 C) or 67.63 MHz ( 17 O). Resonances due to n Bu 4 N + cations are not listed below, but appear as multiplets centred at about 1.0, 1.4, 1.7 and 3.2 ppm in 1 H NMR spectra and as singlets at about 13, 19, 24 and 58 ppm in 13 C{ 1 H} NMR spectra. Two-dimensional 1 H EXSY NMR spectra were obtained at 500 MHz using a 90 •t 1 -90 •t mix -90 • -Acq(t 2 ) sequence with appropriate phasecycling to give a phase sensitive spectrum.…”
Section: Methodsmentioning
confidence: 99%
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“…It can however be noted that the coupling of an electroactive organic molecule and a POM was already successfully achieved in the [Mo6O18(AMBTH)] 2and [Mo6O18(MBTH)] 2hybrids where AMBTH and MBTH are benzothiazole hydrazone derivatives. 25 Here, we describe the synthesis and characterization of three new compounds associating via covalent bonds an Anderson POM platform and TTF organic molecules and in one case an additional SP moiety. Their electrochemical and spectroelectrochemical properties have been thoroughly investigated together with their second order non-linear optical properties.…”
Section: Introductionmentioning
confidence: 99%