Crossref journal-article
American Chemical Society (ACS)
Journal of the American Chemical Society (316)
Bibliography

Alkordi, M. H., Liu, Y., Larsen, R. W., Eubank, J. F., & Eddaoudi, M. (2008). Zeolite-like Metal−Organic Frameworks as Platforms for Applications: On Metalloporphyrin-Based Catalysts. Journal of the American Chemical Society, 130(38), 12639–12641.

Authors 5
  1. Mohamed H. Alkordi (first)
  2. Yunling Liu (additional)
  3. Randy W. Larsen (additional)
  4. Jarrod F. Eubank (additional)
  5. Mohamed Eddaoudi (additional)
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  33. All chemicals were Aldrich reagent grade and used as received, unless otherwise noted. In a 20 mL vial, a mixture of In(NO3)3·xH2O (0.015 g, 0.0435 mmol), 4,5-H3ImDC (0.014 g, 0.087 mmol), DMF (1 mL), CH3CN (1 mL), and 0.1 mL of 8 mM methanol solution of [H2TMPyP][p-tosyl]4, were mixed; the vial was sealed and heated to 85°C for 12 h, then to 105 °C for 24 h with a heating rate of 1.5°C/min, and then cooled down to room temperature with a cooling rate of 1°C/min. Dark red crystals of1, [H2TMPyP]4+encapsulated insiderho-ZMOF, were then collected, washed with DMF, and then washed with methanol several times, until no residual amount of porphyrin was present in the washing solution, as evident from the UV−vis spectrum of the washing solution.
  34. In an attempt to maximize porphyrin loading intorho-ZMOF, 1.198 mmole of 4,5-H3ImDC, 0.5 mmole of In(NO3)3·xH2O, 30 μmol of [H2TMPyP][p-tosyl]4, DMF, and ethanol (3 mL each) were mixed in a 25 mL scintillation vial. The vial was then heated using the same procedure for the synthesis of1. The resultant crystals,1′, were washed several times with methanol until no residual porphyrin was present. A 10.8 mg portion of1′ was dissolved in 25 mL of concd HNO3, from which 1 mL was diluted to the volume of 10 mL using DI water. Using atomic absorption to determine concentration of In3+ions and UV−vis for porphyrin (ϵ438= 1.9 × 105M−1cm−1), an estimate of 67% loading of porphyrin into the α-cages (each made of 24 In3+ions) was possible. Further increase of the free-base porphyrin concentration in the reaction mixture precludes formation of crystalline material.
  35. Oxidation reaction conditions: 77 μmol TBHP, dried over MgSO4, 100 μmol chlorobenzene as internal standard, 10 mL cyclohexane, and 88 mg of1a(equivalent to 2.9 μmol of Mn-TMPyP) were mixed, under aerobic conditions, in a 25 mL round-bottom flask fitted with a silicone septum. The reaction mixture was then held at 65°C in an isothermal bath for the required amount of time, as determined by analyzing aliquots of the mixture over time using GC-FID.
Dates
Type When
Created 17 years ago (Aug. 29, 2008, 3:01 a.m.)
Deposited 2 years, 5 months ago (March 7, 2023, 5:38 a.m.)
Indexed 1 month ago (July 31, 2025, 11:48 p.m.)
Issued 17 years ago (Aug. 29, 2008)
Published 17 years ago (Aug. 29, 2008)
Published Online 17 years ago (Aug. 29, 2008)
Published Print 16 years, 11 months ago (Sept. 24, 2008)
Funders 0

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@article{Alkordi_2008, title={Zeolite-like Metal−Organic Frameworks as Platforms for Applications: On Metalloporphyrin-Based Catalysts}, volume={130}, ISSN={1520-5126}, url={http://dx.doi.org/10.1021/ja804703w}, DOI={10.1021/ja804703w}, number={38}, journal={Journal of the American Chemical Society}, publisher={American Chemical Society (ACS)}, author={Alkordi, Mohamed H. and Liu, Yunling and Larsen, Randy W. and Eubank, Jarrod F. and Eddaoudi, Mohamed}, year={2008}, month=aug, pages={12639–12641} }