Reversible CO 2 Fixation and Release by a Trinuclear Zn(II) Cryptate Complex and Operando Analysis of the Complex Structure
Abstract Metal complexes inspired by carbonic anhydrase (CA), which is a metalloenzyme containing Zn(II), have been investigated as alternatives for CO 2 fixation systems operating under ambient temperature and pressure conditions. In this study, we designed a trinuclear Zn(II) cryptate complex (Zn...
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Published in | ChemSusChem Vol. 16; no. 20 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
20.10.2023
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Online Access | Get full text |
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Abstract | Abstract
Metal complexes inspired by carbonic anhydrase (CA), which is a metalloenzyme containing Zn(II), have been investigated as alternatives for CO
2
fixation systems operating under ambient temperature and pressure conditions. In this study, we designed a trinuclear Zn(II) cryptate complex (Zn
3
L) and demonstrated rapid CO
2
fixation with carbonation of CO
2
using Zn
3
L. The CO
2
fixation performance of Zn
3
L surpassed that of a standard CO
2
absorbent, KOH(aq) solution, under conditions of the same solute concentration. In addition, the reaction achieved operation without support addition of base, which has been often required in systems of CA‐inspired complexes. Fixed CO
2
was released by protonating polyazacryptate ligand (L) and breaking the complex structure, and deprotonation of L induced the reconstruction of Zn
3
L, allowing it to refix CO
2
. This reaction mechanism was proposed based on the analysis of operando extended X‐ray absorption fine structure spectroscopy. Zn
3
L also demonstrated the ability to capture dilute CO
2
from air, and the volume of CO
2
captured by Zn
3
L was approximately 2.6 times that captured by the KOH(aq) solution. Our Zn
3
L exhibited three valuable properties: rapid CO
2
fixation without a base, reversibility, and ability to capture dilute CO
2
; thus Zn
3
L is a promising candidate as CO
2
fixatives. |
---|---|
AbstractList | Abstract
Metal complexes inspired by carbonic anhydrase (CA), which is a metalloenzyme containing Zn(II), have been investigated as alternatives for CO
2
fixation systems operating under ambient temperature and pressure conditions. In this study, we designed a trinuclear Zn(II) cryptate complex (Zn
3
L) and demonstrated rapid CO
2
fixation with carbonation of CO
2
using Zn
3
L. The CO
2
fixation performance of Zn
3
L surpassed that of a standard CO
2
absorbent, KOH(aq) solution, under conditions of the same solute concentration. In addition, the reaction achieved operation without support addition of base, which has been often required in systems of CA‐inspired complexes. Fixed CO
2
was released by protonating polyazacryptate ligand (L) and breaking the complex structure, and deprotonation of L induced the reconstruction of Zn
3
L, allowing it to refix CO
2
. This reaction mechanism was proposed based on the analysis of operando extended X‐ray absorption fine structure spectroscopy. Zn
3
L also demonstrated the ability to capture dilute CO
2
from air, and the volume of CO
2
captured by Zn
3
L was approximately 2.6 times that captured by the KOH(aq) solution. Our Zn
3
L exhibited three valuable properties: rapid CO
2
fixation without a base, reversibility, and ability to capture dilute CO
2
; thus Zn
3
L is a promising candidate as CO
2
fixatives. |
Author | Murase, Masakazu Arai, Takeo Sakamoto, Naonari Ohashi, Masataka Nonaka, Takamasa Maegawa, Yoshifumi Uyama, Takeshi Goto, Yasutomo |
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Metal complexes inspired by carbonic anhydrase (CA), which is a metalloenzyme containing Zn(II), have been investigated as alternatives for CO
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Title | Reversible CO 2 Fixation and Release by a Trinuclear Zn(II) Cryptate Complex and Operando Analysis of the Complex Structure |
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