2014
DOI: 10.1016/j.cclet.2013.12.023
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Highly ordered arrangement of meso-tetrakis(4-aminophenyl)porphyrin in self-assembled nanoaggregates via hydrogen bonding

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Cited by 19 publications
(11 citation statements)
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“…Hydrogen-bonding is crucial to achieve the ordered arrangement of meso-tetrakis(4-aminophenyl)porphyrin 4 (Figure 3a) in different nanostructures as reported by Yin et al, who generated nanospheres, nanorods, and nanothorns by modifying porphyrin concentration and using the phase-transfer method [34]. Typically, assemblies were made by rapidly adding 1 mL of methanol to 4 mL of the chloroform porphyrin solutions at different concentrations ranging from 5 × 10 − 4 to 1.5 × 10 − 3 M, and stored for three days to have stable nanosystems for morphological analyses by Transmission and Scanning Electron Microscopies (TEM and SEM, respectively).…”
Section: Solvent-driven Aggregation Protocolmentioning
confidence: 98%
“…Hydrogen-bonding is crucial to achieve the ordered arrangement of meso-tetrakis(4-aminophenyl)porphyrin 4 (Figure 3a) in different nanostructures as reported by Yin et al, who generated nanospheres, nanorods, and nanothorns by modifying porphyrin concentration and using the phase-transfer method [34]. Typically, assemblies were made by rapidly adding 1 mL of methanol to 4 mL of the chloroform porphyrin solutions at different concentrations ranging from 5 × 10 − 4 to 1.5 × 10 − 3 M, and stored for three days to have stable nanosystems for morphological analyses by Transmission and Scanning Electron Microscopies (TEM and SEM, respectively).…”
Section: Solvent-driven Aggregation Protocolmentioning
confidence: 98%
“…At last, 30% epoxy resin solution was added to embed the cells. The ultrathin slices were analyzed by high-resolution transmission electron microscopy (HRTEM, H-7650, Hitachi, Tokyo, Japan) [57,58,[62][63][64][65], scanning transmission microscopy (STEM, Tecnai G 2 F20, FEI, Hillsboro, OR, USA) and EDS. The parameters of these instruments are given in articles [66][67][68][69][70].…”
Section: Analysis Of the Ultrathin Slices Of B Licheniformismentioning
confidence: 99%
“…In the process of biomineralization of carbonate minerals, 10 mL of S. epidermidis Y2 bacterial liquid was centrifuged at a speed of 3000 rpm for 5 min, the pellet including the minerals and the bacteria was washed 3 times with phosphate buffer (Na2HPO4•12H2O 20.7472 g L -1 , NaH2PO4•2H2O 3.1167 g L -1 , pH 7.2) to remove the ingredients from the culture medium. The pellet was fixed by glutaraldehyde (2.5%, v : v) for a night, then dehydrated gradually by acetone solution: 30% ( [87,[92][93][94], SAED [86] and STEM (Tecnai G2 F20, FEI, America) [95].…”
Section: Analysis Of the Nano-meter Spheres And Element Distribution mentioning
confidence: 99%