University of Turku, Turku, FI-20014, Finland. ... Dr. Sergey Kosourov, e-mail: [email protected], tel: ... Dr. Yagut Allahverdiyeva, e-mail: [email protected], tel:.
purchased from Sinopharm Chemical Reagent Co., Ltd., and deionized water was all ... aluminum clear solution (ACS) and the zeolite A synthesis solutions.
As the magnetic field increases, the M vs. ... Page 6 ... S7,S8,S12 these structural features may well consistent with a ferromagnetic coupling between Cu(1).
sodium borohydride, bromine, iodine monochloride, piperidine, copper (I) chloride, sodium chloride .... compound, PT, and a monochlorinated compound.
The black asterisks mark reflections from the silicon grease used for the sample preparation. The green asterisks mark reflections arising from in situ hydrate.
Electronic Supplementary Information. (ESI). Three Cyclic ... Fig. S13. LC-MS analysis for FDAA derivatives of the hydrolysis of 1 and amino acid standards.
Jun-Cheng Zhang,a,e,f,* Yun-Ze Long,a,e Xusheng Wang,b and Chao-Nan Xuc,d,*. aCollege of Physics, Qingdao University, Qingdao 266071, P. R. China.
DMF was recorded on a Perkin-Elmer Lambda 19 UV/Vis spectrophotometer. .... 4S GIXRD patterns for the films of CuMePc, P3HT and P3HT:CuMePc (weight.
were fit using JADE software from JADE Software Corporation, CA. The chemical ... solutions was calculated using Zeta potential measurements. .... 10 Y. Sun , J. H. Seo , C. J. Takacs , J. Seifter , A. J. Heeger, Adv. Mater., 2011, 23, 1679.
were poured into microtitration plates and suspension of the microorganism with concentration of approximately 105 cfu / mL was added. After incubation at 37 ...
Electronic Supplementary Information (ESI) Morphology Effect on Antibacterial Activity of Cuprous Oxide Huan Pang,a Feng Gao*b and Qingyi Lu*a
SI1. Experimental In a typical procedure, the starting solution was prepared by mixing 0.05 g of glycine and 0.08 g of copper acetate in the mixed solvent of 10 mL of H2O and 5 mL of C2H5OH, and the resulting solution was transferred into 50 mL stainless-steel autoclaves lined with poly(tetrafluoroethylene). The autoclave was sealed and maintained at 140 °C for 24 h and then cooled to room temperature. The products obtained at the bottom of the autoclave were collected, washed three times with deionized water, and dried in air. Characterizations: Scanning electron microscopy (SEM) characterization was performed on Hitachi S-4800 at 10 kV. Powder X-ray diffraction (XRD) patterns were collected using a SHIMADZU, XRD-6000 with Cu Kα radiation) (λ = 1.5418 Å). The antibacterial activity of the synthesized crystals was tested against B. subtilis, S. aureus, S. faecalis, P. aeruginosa, and E. cloacae by determining the MICs (minimum inhibitory concentrations,
μg/mL)
through
a
colorimetric
method
using
the
dye
MTT
(3-(4,5)-dimethylthiahiazo (-z-y1)-3,5-di- phenytetrazoliumromide). A stock solution of the Cu2O crystals (50 µg / ml) was prepared in dimethyl sulfoxide (DMSO) and graded quantities of the test crystals were incorporated in specified quantity of sterilized liquid medium. Then the solutions were poured into microtitration plates and suspension of the microorganism with concentration of approximately 105 cfu / mL was added. After incubation at 37
for 24 h, 50μL of PBS
(Phosphate Buffered Saline 0.01 mol / L, pH 7.4: Na2HPO4·12H2O 2.9 g, KH2PO4 0.2 g, NaCl 8.0 g, KCl 0.2 g, distilled water 1000 mL) containing 2 mg / mL of MTT was added to each well. Incubation was continued at room temperature for 4 - 5 h, followed by the addition of 100 μL of isopropanol containing 5% 1 mol/L HCl to extract the dye. At last, the optical density (OD) was measured with a microplate reader at 570 nm to determine the MICs.
SI2:SEM images of a single perfect octahedral Cu2O crystal and a single corner-truncated octahedral Cu2O crystal, from which it can be clearly seen that the perfect octahedral crystal has point angles as shown in Figure SI2a while the corners of the octahedral crystal in Figure SI2b are truncated.
XRD patterns of the octahedral and cubic Cu2O crystals: a) powder XRD pattern of the octahedral Cu2O crystals; b) powder XRD pattern of the cubic Cu2O crystals; c) XRD pattern of a single octahedral Cu2O crystal; d) XRD pattern of a single cubic Cu2O crystal.