Supramolecular porous ionic network based on triazinonide and imidazolium: a template-free synthesis of meso-/macroporous organic materials via a one-pot reaction-assembly procedure

RSC Advances ◽  
2016 ◽  
Vol 6 (95) ◽  
pp. 92443-92448 ◽  
Author(s):  
Ze-Huan Hei ◽  
Gan-Lin Song ◽  
Chen-Yu Zhao ◽  
Wenhao Fan ◽  
Mu-Hua Huang

A supramolecular porous ionic network (SPIN-1) was designed and prepared using a one-pot procedure, involving the quaternization of triimidazole triazine with cyanuric chloride followed by hydrolysis andin situassembly.

2019 ◽  
Vol 7 (37) ◽  
pp. 21096-21105 ◽  
Author(s):  
Jian Chen ◽  
Lunbo Duan ◽  
Tian Shi ◽  
Ruoyu Bian ◽  
Yuxiao Lu ◽  
...  

The preparation of CaO/CuO composites with high performance is essential for combined Ca–Cu looping process, where the exothermic reduction of CuO with methane is used in situ to calcine CaCO3.


Nano Letters ◽  
2013 ◽  
Vol 13 (10) ◽  
pp. 4715-4720 ◽  
Author(s):  
Yi Shi ◽  
Jia-Zhao Wang ◽  
Shu-Lei Chou ◽  
David Wexler ◽  
Hui-Jun Li ◽  
...  

CrystEngComm ◽  
2015 ◽  
Vol 17 (11) ◽  
pp. 2359-2367 ◽  
Author(s):  
Manjodh Kaur ◽  
Nipun Kumar Gupta ◽  
C. M. Nagaraja

A facile, one-pot solvothermal method for the syntheses of template-free ZnS NCs (~3–6 nm) using (C7H7)S2as a newin situsource of S2−ions without and with the use of MCE-capping agent has been demonstrated. Photocatalytic investigation of the NCs revealed very good activity for degradation of MO under UV light irradiation.


RSC Advances ◽  
2016 ◽  
Vol 6 (62) ◽  
pp. 56790-56799 ◽  
Author(s):  
Manjodh Kaur ◽  
C. M. Nagaraja

Template-free PbS microstructures composed of nanocrystals exhibiting time-dependent morphological evolution from cubes to dendrites were synthesised by one-pot solvothermal route using DBDS as a new temperature controlled in situ source of S2− ions.


2020 ◽  
Vol 24 (8) ◽  
pp. 900-908
Author(s):  
Ram Naresh Yadav ◽  
Amrendra K Singh ◽  
Bimal Banik

Numerous O (oxa)- and S (thia)-glycosyl esters and their analogous glycosyl acids have been accomplished through stereoselective glycosylation of various peracetylated bromo sugar with benzyl glycolate using InBr3 as a glycosyl promotor followed by in situ hydrogenolysis of resulting glycosyl ester. A tandem glycosylating and hydrogenolytic activity of InBr3 has been successfully investigated in a one-pot procedure. The resulting synthetically valuable and virtually unexplored class of β-CMGL (glycosyl acids) could serve as an excellent potential chiral auxiliary in the asymmetric synthesis of a wide range of enantiomerically pure medicinally prevalent β-lactams and other bioactive molecules of diverse medicinal interest.


2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Lirong Zhang ◽  
Jingjing Zhang ◽  
Lixia Xu ◽  
Zijian Zhuang ◽  
Jingjin Liu ◽  
...  

Abstract Background Therapeutic tumor vaccine (TTV) that induces tumor-specific immunity has enormous potentials in tumor treatment, but high heterogeneity and poor immunogenicity of tumor seriously impair its clinical efficacy. Herein, a novel NIR responsive tumor vaccine in situ (HA-PDA@IQ/DOX HG) was prepared by integrating hyaluronic acid functionalized polydopamine nanoparticles (HA-PDA NPs) with immune adjuvants (Imiquimod, IQ) and doxorubicin (DOX) into thermal-sensitive hydrogel. Results HA-PDA@IQ NPs with high photothermal conversion efficiency (41.2%) and T1-relaxation efficiency were using HA as stabilizer by the one-pot oxidative polymerization. Then, HA-PDA@IQ loaded DOX via π-π stacking and mixed with thermal-sensitive hydrogel to form the HA-PDA@IQ/DOX HG. The hydrogel-confined delivery mode endowed HA-PDA@IQ/DOX NPs with multiple photothermal ablation performance once injection upon NIR irradiation due to the prolonged retention in tumor site. More importantly, this mode enabled HA-PDA@IQ/DOX NPs to promote the DC maturation, memory T cells in lymphatic node as well as cytotoxic T lymphocytes in spleen. Conclusion Taken together, the HA-PDA@IQ/DOX HG could be served as a theranostic tumor vaccine for complete photothermal ablation to trigger robust antitumor immune responses.


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