In-situ coordination chemistry within cobalt-containing phthalocyanine nanoporous crystals

CrystEngComm ◽  
2013 ◽  
Vol 15 (8) ◽  
pp. 1545 ◽  
Author(s):  
C. Grazia Bezzu ◽  
Benson M. Kariuki ◽  
Madeleine Helliwell ◽  
Floriana Tuna ◽  
John E. Warren ◽  
...  

Nanoscale ◽  
2021 ◽  
Author(s):  
B. Cirera ◽  
J. M. Gallego ◽  
J. I. Martínez ◽  
R. Miranda ◽  
D. Écija

This work reports the in-situ design of premetallated dysprosium porphyrin complexes (Dy-2H-4FTPP) on Au(111), whose Kondo resonance can be switched off with atomic precision by sequential transformation into partially and fully metallated species.





2014 ◽  
Vol 43 (39) ◽  
pp. 14520-14524 ◽  
Author(s):  
Despina Dermitzaki ◽  
Catherine P. Raptopoulou ◽  
Vassilis Psycharis ◽  
Albert Escuer ◽  
Spyros P. Perlepes ◽  
...  

The bridging potency of the O-rich PO3F2− group in NiII/oximate chemistry has been studied leading to interesting coordination compounds and revealing an unprecedented PO3F2− to P2O5F22−in situ transformation.





RSC Advances ◽  
2021 ◽  
Vol 11 (40) ◽  
pp. 24709-24721
Author(s):  
Chatphorn Theppitak ◽  
Filip Kielar ◽  
Winya Dungkaew ◽  
Mongkol Sukwattanasinitt ◽  
Laongdao Kangkaew ◽  
...  

The influence of synthetic conditions on the solid-state structural formation of lanthanide(iii) complexes based on a hydrazide ligand have been investigated and reported.



RSC Advances ◽  
2015 ◽  
Vol 5 (35) ◽  
pp. 27743-27751 ◽  
Author(s):  
Yan-Jun Ou ◽  
Yu-Jia Ding ◽  
Qin Wei ◽  
Xu-Jia Hong ◽  
Zhi-Peng Zheng ◽  
...  

An efficient method for the synthesis of N-rich heterocycles has been systematically explored through solvothermal in situ generation from ligand (L) mediated by Cd2+. Their in situ formation mechanisms and coordination chemistry are investigated.



2019 ◽  
Vol 7 (14) ◽  
pp. 2320-2329 ◽  
Author(s):  
Ruifeng Zhu ◽  
Yuhua Zhang ◽  
Xian Fang ◽  
Xiaoqing Cui ◽  
Jing Wang ◽  
...  

In this study, in situ sulfur-doped carbon nitride nanosheets (S-g-C3N4 NSs) are used for the sensitive and selective sensing of l-cysteine (l-Cys) based on the competitive coordination chemistry of Cu2+ between l-Cys and S-g-C3N4 NSs.





2019 ◽  
Vol 10 (14) ◽  
pp. 3949-3955 ◽  
Author(s):  
Xiang-Jing Kong ◽  
Tao He ◽  
Yong-Zheng Zhang ◽  
Xue-Qian Wu ◽  
Si-Nan Wang ◽  
...  

A “One-Pot” strategy has been developed to construct new metal–organic frameworks with complicated ligands from simple precursors by integrating organic and coordination chemistry.



2020 ◽  
Vol 92 (1) ◽  
pp. 49-62 ◽  
Author(s):  
Amin Ismael ◽  
Manabu Abe ◽  
Rui Fausto ◽  
Maria L. S. Cristiano

AbstractThe properties and applications of 2-methyl-(2H)-tetrazole-5-amino-saccharinate (2MTS) in catalysis and chelant-based chemotherapy stimulated investigations on its photostability. The photochemistry of monomeric 2MTS in solid argon (15 K) was compared with those of 2-methyl-(2H)-tetrazole-5-amine (2MT) and 1-methyl-(2H)-tetrazole-5-amine (1MT). Compounds were subjected to in situ narrowband UV-irradiation at different wavelengths. Reactions were followed by infrared spectroscopy, supported by B3LYP/6-311++G(d,p) calculations. Photochemical pathways for 2MT and 2MTS proved similar but photodegradation of 2MTS was 20× slower, unraveling the photostabilizing effect of the saccharyl moiety that extends into the nitrilimine formed from 2MTS and its antiaromatic 1H-diazirene isomer, which proved photostable at 290 nm, unlike the 1H-diazirene formed from 2MT. Analysis of the photochemistries of 2MTS/2MT (250 nm) and 1MT (222 nm), including energy trends calculated for the isomeric C2H5N3 species postulated/observed from photolysis and EPR results, enabled a deeper insight into the photodegradation mechanisms of 1,5-substituted and 2,5-substituted tetrazoles. We postulate a pivotal singlet state imidoylnitrene species, sN1, as common intermediate, which undergoes a Wolff-type isomerization to a stable carbodiimide. Photo-extrusion of N2 from 1,5-substituted tetrazoles generates sN1 directly but from 2,5-substituted tetrazoles it originates a nitrilimine, then a diazirene, which finally leads to sN1. Selective formation of cyanamide from 1MT requires photoisomerization between sN1 and sN2, accessible at 222 nm. EPR studies enabled the detection of methyl nitrene, arising from photolysis of 1H-diazirene intermediate.



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