A dual-switching spin-crossover framework with redox regulation and guest response
Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{...
Ausführliche Beschreibung
Autor*in: |
Wang, Long-Fei [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2023 |
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Anmerkung: |
© Science China Press 2023 |
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Übergeordnetes Werk: |
Enthalten in: Science in China - Asheville, NC : Science in China Press, 1995, 66(2023), 6 vom: 08. Mai, Seite 1744-1749 |
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Übergeordnetes Werk: |
volume:66 ; year:2023 ; number:6 ; day:08 ; month:05 ; pages:1744-1749 |
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DOI / URN: |
10.1007/s11426-023-1573-8 |
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Katalog-ID: |
SPR051826127 |
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520 | |a Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. | ||
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650 | 4 | |a iron(II) |7 (dpeaa)DE-He213 | |
650 | 4 | |a post-synthetic modification |7 (dpeaa)DE-He213 | |
650 | 4 | |a redox |7 (dpeaa)DE-He213 | |
650 | 4 | |a host-guest interaction |7 (dpeaa)DE-He213 | |
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700 | 1 | |a Ni, Zhao-Ping |4 aut | |
700 | 1 | |a Tong, Ming-Liang |4 aut | |
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10.1007/s11426-023-1573-8 doi (DE-627)SPR051826127 (SPR)s11426-023-1573-8-e DE-627 ger DE-627 rakwb eng Wang, Long-Fei verfasserin aut A dual-switching spin-crossover framework with redox regulation and guest response 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Science China Press 2023 Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. spin crossover (dpeaa)DE-He213 iron(II) (dpeaa)DE-He213 post-synthetic modification (dpeaa)DE-He213 redox (dpeaa)DE-He213 host-guest interaction (dpeaa)DE-He213 Wu, Si-Guo aut Ruan, Ze-Yu aut Jian, Ai-Qi aut Cui, Wen aut Ni, Zhao-Ping aut Tong, Ming-Liang aut Enthalten in Science in China Asheville, NC : Science in China Press, 1995 66(2023), 6 vom: 08. Mai, Seite 1744-1749 (DE-627)327310405 (DE-600)2043454-6 1862-2771 nnns volume:66 year:2023 number:6 day:08 month:05 pages:1744-1749 https://dx.doi.org/10.1007/s11426-023-1573-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 66 2023 6 08 05 1744-1749 |
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10.1007/s11426-023-1573-8 doi (DE-627)SPR051826127 (SPR)s11426-023-1573-8-e DE-627 ger DE-627 rakwb eng Wang, Long-Fei verfasserin aut A dual-switching spin-crossover framework with redox regulation and guest response 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Science China Press 2023 Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. spin crossover (dpeaa)DE-He213 iron(II) (dpeaa)DE-He213 post-synthetic modification (dpeaa)DE-He213 redox (dpeaa)DE-He213 host-guest interaction (dpeaa)DE-He213 Wu, Si-Guo aut Ruan, Ze-Yu aut Jian, Ai-Qi aut Cui, Wen aut Ni, Zhao-Ping aut Tong, Ming-Liang aut Enthalten in Science in China Asheville, NC : Science in China Press, 1995 66(2023), 6 vom: 08. Mai, Seite 1744-1749 (DE-627)327310405 (DE-600)2043454-6 1862-2771 nnns volume:66 year:2023 number:6 day:08 month:05 pages:1744-1749 https://dx.doi.org/10.1007/s11426-023-1573-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 66 2023 6 08 05 1744-1749 |
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10.1007/s11426-023-1573-8 doi (DE-627)SPR051826127 (SPR)s11426-023-1573-8-e DE-627 ger DE-627 rakwb eng Wang, Long-Fei verfasserin aut A dual-switching spin-crossover framework with redox regulation and guest response 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Science China Press 2023 Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. spin crossover (dpeaa)DE-He213 iron(II) (dpeaa)DE-He213 post-synthetic modification (dpeaa)DE-He213 redox (dpeaa)DE-He213 host-guest interaction (dpeaa)DE-He213 Wu, Si-Guo aut Ruan, Ze-Yu aut Jian, Ai-Qi aut Cui, Wen aut Ni, Zhao-Ping aut Tong, Ming-Liang aut Enthalten in Science in China Asheville, NC : Science in China Press, 1995 66(2023), 6 vom: 08. Mai, Seite 1744-1749 (DE-627)327310405 (DE-600)2043454-6 1862-2771 nnns volume:66 year:2023 number:6 day:08 month:05 pages:1744-1749 https://dx.doi.org/10.1007/s11426-023-1573-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 66 2023 6 08 05 1744-1749 |
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10.1007/s11426-023-1573-8 doi (DE-627)SPR051826127 (SPR)s11426-023-1573-8-e DE-627 ger DE-627 rakwb eng Wang, Long-Fei verfasserin aut A dual-switching spin-crossover framework with redox regulation and guest response 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Science China Press 2023 Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. spin crossover (dpeaa)DE-He213 iron(II) (dpeaa)DE-He213 post-synthetic modification (dpeaa)DE-He213 redox (dpeaa)DE-He213 host-guest interaction (dpeaa)DE-He213 Wu, Si-Guo aut Ruan, Ze-Yu aut Jian, Ai-Qi aut Cui, Wen aut Ni, Zhao-Ping aut Tong, Ming-Liang aut Enthalten in Science in China Asheville, NC : Science in China Press, 1995 66(2023), 6 vom: 08. Mai, Seite 1744-1749 (DE-627)327310405 (DE-600)2043454-6 1862-2771 nnns volume:66 year:2023 number:6 day:08 month:05 pages:1744-1749 https://dx.doi.org/10.1007/s11426-023-1573-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 66 2023 6 08 05 1744-1749 |
allfieldsSound |
10.1007/s11426-023-1573-8 doi (DE-627)SPR051826127 (SPR)s11426-023-1573-8-e DE-627 ger DE-627 rakwb eng Wang, Long-Fei verfasserin aut A dual-switching spin-crossover framework with redox regulation and guest response 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Science China Press 2023 Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. spin crossover (dpeaa)DE-He213 iron(II) (dpeaa)DE-He213 post-synthetic modification (dpeaa)DE-He213 redox (dpeaa)DE-He213 host-guest interaction (dpeaa)DE-He213 Wu, Si-Guo aut Ruan, Ze-Yu aut Jian, Ai-Qi aut Cui, Wen aut Ni, Zhao-Ping aut Tong, Ming-Liang aut Enthalten in Science in China Asheville, NC : Science in China Press, 1995 66(2023), 6 vom: 08. Mai, Seite 1744-1749 (DE-627)327310405 (DE-600)2043454-6 1862-2771 nnns volume:66 year:2023 number:6 day:08 month:05 pages:1744-1749 https://dx.doi.org/10.1007/s11426-023-1573-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 66 2023 6 08 05 1744-1749 |
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The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. 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Wang, Long-Fei |
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Wang, Long-Fei misc spin crossover misc iron(II) misc post-synthetic modification misc redox misc host-guest interaction A dual-switching spin-crossover framework with redox regulation and guest response |
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A dual-switching spin-crossover framework with redox regulation and guest response spin crossover (dpeaa)DE-He213 iron(II) (dpeaa)DE-He213 post-synthetic modification (dpeaa)DE-He213 redox (dpeaa)DE-He213 host-guest interaction (dpeaa)DE-He213 |
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dual-switching spin-crossover framework with redox regulation and guest response |
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A dual-switching spin-crossover framework with redox regulation and guest response |
abstract |
Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. © Science China Press 2023 |
abstractGer |
Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. © Science China Press 2023 |
abstract_unstemmed |
Abstract A dual-switching spin crossover metal-organic framework (SCO-MOF) [Fe(TPB){$ Pt^{II} $(CN)4}]·3iPrOH·$ 4H_{2} $O (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) is developed via the combination of redox-active framework and tunable guests. The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. Therefore, the combination of electronic bistability, redox reaction and guest recognition in a homogeneous lattice provides a utility platform for designing multi-responsive molecule-based materials. © Science China Press 2023 |
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A dual-switching spin-crossover framework with redox regulation and guest response |
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The reversible structural transformation between [$ Pt^{II} $(CN)4]2− and [$ Pt^{IV} %$ Br_{2} $(CN)4]2− moieties can be manipulated by redox post-synthetic modification (PSM), which results in the change of SCO behaviors from step-wise to one-step. The influences of the oxidative addition of bromides on the ligand field splitting of Fe side are further explored by density functional theory calculations. Besides, the modulation of hysteretic four-/three-step, one-step and four-step SCO behaviors can be achieved by tuning the composition of guest molecules. 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