scholarly journals Chiral Self-Assembly of Porphyrins Induced by Chiral Carbon Dots

2020 ◽  
Vol 8 ◽  
Author(s):  
Xiaowei Liu ◽  
Jiayi Lu ◽  
Jingqi Chen ◽  
Mengtian Zhang ◽  
Yingying Chen ◽  
...  
e-Polymers ◽  
2020 ◽  
Vol 20 (1) ◽  
pp. 317-327
Author(s):  
Chenliang Shi ◽  
Ling Lin ◽  
Yukun Yang ◽  
Wenjia Luo ◽  
Maoqing Deng ◽  
...  

AbstractThe influence of density of amino groups, nanoparticles dimension and pH on the interaction between end-functionalized polymers and nanoparticles was extensively investigated in this study. PS–NH2 and H2N–PS–NH2 were prepared using reversible addition–fragmentation chain transfer polymerization and atom transfer radical polymerization. Zero-dimensional carbon dots with sulfonate groups, one-dimensional cellulose nanocrystals with sulfate groups and two-dimensional graphene with sulfonate groups in the aqueous phase were added into the toluene phase containing the aminated PS. The results indicate that aminated PS exhibited the strongest interfacial activity after compounding with sulfonated nanoparticles at a pH of 3. PS ended with two amino groups performed better in reducing the water/toluene interfacial tension than PS ended with only one amino group. The dimension of sulfonated nanoparticles also contributed significantly to the reduction in the water/toluene interfacial tension. The minimal interfacial tension was 4.49 mN/m after compounding PS–NH2 with sulfonated zero-dimensional carbon dots.


Nanoscale ◽  
2021 ◽  
Author(s):  
Lorenzo Branzi ◽  
Giacomo Lucchini ◽  
Elti Cattaruzza ◽  
Nicola Pinna ◽  
Alvise Benedetti ◽  
...  

We report on a Cu(II) catalyzed process for the production of cysteine based chiral carbon dots, the process does not require any thermal treatment and the carbon dots formation is...


2020 ◽  
Author(s):  
Amin Reza Zolghadr ◽  
Behnam Rostami

We describe a systematic investigation of carbon dots (C-dots) assemblies fabricated at the liquid/air interface because of the surface tension gradient. This gradient is originally created by capillary action and increased by addition of sodium dodecyl sulfate (SDS) surfactant or 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) phospholipid to the surface of C-dots aqueous mixture. The arrangement of carbon dots in liquid bulk phase (before self-assembly) and at the surface region (after self-assembly) was examined by TEM microscopy. The presence of SDS surfactant and POPC phospholipid at the air/water interface induced the C-dots compression. In addition, molecular dynamics simulation was conducted to obtain the structure of C-dots at liquid/vapor interface. The orientation of C-dots is evaluated quantitatively at water/vapor surface by using bivariate analysis.


Carbon ◽  
2017 ◽  
Vol 118 ◽  
pp. 625-633 ◽  
Author(s):  
Piao-Yang Cao ◽  
Yong-Lin Liu ◽  
Zuan-Tao Lin ◽  
Jian-Fei Huang ◽  
Wen-Zhao Chen ◽  
...  

Author(s):  
Pengli Gao ◽  
Shuang Chen ◽  
Shi Liu ◽  
Hongxin Liu ◽  
Zhigang Xie ◽  
...  

Author(s):  
Pu Xiao-Long ◽  
yang xuechun ◽  
Shan-Shan Liang ◽  
Wenzhong Wang ◽  
Jing-Tai Zhao ◽  
...  

The N-modified carbon dots/graphitic carbon nitride (NCDs/g-C3N4) aerogel was successfully prepared by simple electrostatic self-assembly of NCDs and g-C3N4 nanosheets without any harmful solvents or cross-linking agents. The prepared aerogel...


Nanoscale ◽  
2020 ◽  
Vol 12 (24) ◽  
pp. 12748-12752
Author(s):  
Jiaqi Zhao ◽  
Li Li ◽  
Fei Li ◽  
Huali Liu ◽  
Zhen Li ◽  
...  

Facile formation of chiral nanofibers with excellent electrochemical performance via self-assembly.


RSC Advances ◽  
2020 ◽  
Vol 10 (53) ◽  
pp. 32202-32210
Author(s):  
Florence Victoria ◽  
John Manioudakis ◽  
Liana Zaroubi ◽  
Brandon Findlay ◽  
Rafik Naccache

Chiral carbon dots, prepared from the unnatural d-enantiomer of cysteine, inhibit the growth of Escherichia coli ATCC 25922 and MG1655 at a lower concentration than l-carbon dots, prepared from the l-enantiomer.


2017 ◽  
Vol 172 ◽  
pp. 93-101 ◽  
Author(s):  
Pengfei Lv ◽  
Yixin Yao ◽  
Dawei Li ◽  
Huimin Zhou ◽  
Muhammad Awais Naeem ◽  
...  

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