2018
DOI: 10.1016/j.inoche.2018.04.007
|View full text |Cite
|
Sign up to set email alerts
|

A 3D homochiral metal–organic framework with high selective adsorption property

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2020
2020
2022
2022

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 50 publications
0
2
0
Order By: Relevance
“…Especially, the different side groups of amino acids embedding in those ligands could delicately adjust the structure and performance of the resulting HMOFs. More importantly and intriguingly, the in situ formation of metal cluster subunits with different structural types was found during the assembly of Zn-, Cd-, or Eu-HMOF. In contrast, metal clusters with specific geometry and more ligation sites may provide more opportunities for the construction of HMOFs with a novel structure and unique properties. Continuing our work in exploring optical materials of HMOFs, ( S )-5-((2-carboxy-5-oxopyrrolidin-1-yl)­methyl)­isophthalic acid (H 3 L), which had been used by us to construct novel 3D porous helical Ln-HMOFs (Ln = Eu 3+ or Tb 3+ ) with interesting optical properties and excellent thermotolerance, was chosen and synthesized as the enantiopure chiral bridge. In this work, d 10 metal ions Zn 2+ and Cd 2+ were used as metal centers to construct H 3 L-based HMOFs because these metal ions are ideal candidates for fabricating HMOFs due to their flexible coordination number and configuration as well as their complexes’ appealing photoelectric properties. Additionally, the crystalline samples of Zn 2+ and Cd 2+ metal–organic frameworks usually display high optical transparency and excellent physicochemical stability, which are conducive to greatly improving NLO performance .…”
Section: Introductionmentioning
confidence: 97%
“…Especially, the different side groups of amino acids embedding in those ligands could delicately adjust the structure and performance of the resulting HMOFs. More importantly and intriguingly, the in situ formation of metal cluster subunits with different structural types was found during the assembly of Zn-, Cd-, or Eu-HMOF. In contrast, metal clusters with specific geometry and more ligation sites may provide more opportunities for the construction of HMOFs with a novel structure and unique properties. Continuing our work in exploring optical materials of HMOFs, ( S )-5-((2-carboxy-5-oxopyrrolidin-1-yl)­methyl)­isophthalic acid (H 3 L), which had been used by us to construct novel 3D porous helical Ln-HMOFs (Ln = Eu 3+ or Tb 3+ ) with interesting optical properties and excellent thermotolerance, was chosen and synthesized as the enantiopure chiral bridge. In this work, d 10 metal ions Zn 2+ and Cd 2+ were used as metal centers to construct H 3 L-based HMOFs because these metal ions are ideal candidates for fabricating HMOFs due to their flexible coordination number and configuration as well as their complexes’ appealing photoelectric properties. Additionally, the crystalline samples of Zn 2+ and Cd 2+ metal–organic frameworks usually display high optical transparency and excellent physicochemical stability, which are conducive to greatly improving NLO performance .…”
Section: Introductionmentioning
confidence: 97%
“…Selection of the MOF should be focussed on its ability to capture a high volume of guest molecules and on the selectivity of the desired guest molecules. Zheng et al [39] stated that the design and synthesis of flexible MOFs, which can interact with certain guest molecules in a switchable way, would be appealing to explore. Furthermore, Abroshan and Kim [40] studied the stability of IRMOF-1 and IRMOF-10 after the incorporation of imidazolium and pyridinium-based ILs by molecular dynamics.…”
Section: Introductionmentioning
confidence: 99%