RESUMO
Two thiacalix[4]arene-protected silver(I) alkynyl nanoclusters, [Na2(H2O)2][Ag9(TC4A)(tBuCîC)4(CH3OH)2(SbF6)0.5(OH)2.5]·3.5H2O·CH3OH (1, abbreviated as Ag9) and [Ag9(TC4A)(tBuCîC)4(CF3COO)]2·4CH3OH (2, abbreviated as Ag18), were synthesized by the reaction of [tBuCîCAg]n, p-tert-butylthiacalix[4]arene (H4TC4A), NaBH4, and AgSbF6 or CF3COOAg in the mixed solvent of methanol-trichloromethane-toluene under solvothermal conditions, respectively. Driven by SbF6- and CF3COO- with different coordination properties, the structural unit [Ag9(TC4A)(tBuCîC)4]+ in both the compounds migrated in different modes, accompanied by distinct Agâ¯Ag distances. Ag9 and Ag18 exhibit similar UV-Vis absorption and diffuse reflection spectra along with contrary tendency between photocurrent responses and solid-state fluorescence. The solution stability of Ag9 and Ag18 was demonstrated by 1H NMR and MALDI-TOF mass spectrometry. The fluorescence responses of Ag9 and Ag18 towards different organic molecules were also investigated, which indicated that the polarity of solvent has a certain effect on the emission intensities of Ag9 and Ag18. This study provides a positive guide for the controlled synthesis and further study of the structure-activity relationship of thiacalix[4]arene-protected silver alkynyl nanoclusters.
RESUMO
Structural transformation is important for the study of silver cluster compounds, in which controlled synthesis of their shapes and sizes via anion template-driven is one key scientific question. In this work, the CO3 2- anion templates were captured by the [t BuC≡CAg]n system under the stimulation induced by carboxylate ligand CF3 COO- /PhCOO- , and two silver alkynyl clusters [(CO3 2- )@Ag21 (t BuC≡C)16 (CF3 COO)3 (H2 O)]â DMFâ 2CH2 Cl2 (1) and [(CO3 2- )2 @Ag24 (t BuC≡C)16 (PhCOO)4 ]â CH3 OHâ 4DMF (2) have been successfully isolated and charactered. With the increase of the number of CO3 2- templates from single to double, the outer silver atoms from twenty-one to twenty-four, accompanied by the growth of the cluster skeleton from 9.8â Å ×6.9â Å of the (CO3 2- )@Ag21 unit to 10.5â Å ×7.3â Å of the (CO3 2- )2 @Ag24 unit. In addition, the syntheses, structures, photocurrent responses, cyclic voltammetry characteristics, luminescence, and photodegradation of compounds 1 and 2 have been studied.
RESUMO
Compound [Ag44 (W10 O32 )(St Bu)24 (CF3 COO)8 ](CF3 COO)6 â 6H2 O (1) was synthesized through a one-pot method. This is the first case of isolating a new silver thiolate cluster containing a [W10 O32 ]6- template which transforms from WO4 2- polyoxoanion through a self-assembly process. The anionic nature of the reduced [W10 O32 ]6- template and the effective silver-oxygen interaction contribute to the formation of the Ag44 nanowheel in 1. The luminescence, photocatalytic activity and electrochemistry properties of 1 were studied.
Assuntos
Luminescência , Prata , Ânions , Prata/químicaRESUMO
The remarkably reversible thermochromic luminescence behavior and the rare nonlinear optical (NLO) properties of the [Ag55(MoO4)6(C[triple bond, length as m-dash]C t Bu)24(CH3COO)18(CH3COO)]·2H2O ({Ag55Mo6} for short) nanocluster reported were investigated experimentally. The important contributions of Ag+, C[triple bond, length as m-dash]C- ions and MoO4 2- groups to the NLO properties were proved by further density functional theory (DFT) calculations.
RESUMO
A high-yield silver alkynyl assembly [Ag8(C[triple bond, length as m-dash]C t Bu)5(CF3COO)3(CH3CN)] n (1) constructed from [AgC[triple bond, length as m-dash]C t Bu] n ligand, CF3COOAg and CH3CN auxiliary ligands with a one-dimensional infinite chain structure has been obtained in one pot. Compound 1 has been well-defined and characterized. The photocurrent properties and the temperature-sensitive luminescent properties of 1 have been investigated.
RESUMO
Compound [Ag42 S5 (StBu)25 (CF3 COO)4 (CO3 )](CO3 )0.5 â CH2 Cl2 â 4CH3 OHâ 9DMF (1) has been obtained and well defined. It consists of a multi-shell structure involving two Ag centres, one Ag5 S5 pentagram, two Ag5 S5 pentagons and one Ag25 S15 shell. Compound 1 has been characterized by XPS, FT-IR, PXRD, TGA, NMR, MS, UV/Vis spectrum, TEM and cyclic voltammetry. Temperature-sensitive luminescent property of 1 has also been investigated.
RESUMO
Nanogenerators capable of harvesting energy from environmental mechanical energy are attractive for many applications. In this paper, we present a simple, low-cost approach to convert low-frequency mechanical energy into electric power using piezoelectric ZnO nanorods grown on a common paper substrate. This energy conversion device has ultrahigh flexibility and piezoelectric sensitivity and can produce an output voltage of up to 10 mV and an output current of about 10 nA. It is demonstrated that the device's electric output behavior can be optionally changed between four types of mode simply by controlling the straining rate. Furthermore, it is also shown that the electric output can be enhanced by scaling the size of the device. This energy-harvesting technology provides a simple and cost-effective platform to capture low-frequency mechanical energy, such as body movements, for practical applications.