Abstract Phosphane, PH3—a highly pyrophoric and toxic gas—is frequently contaminated with H2and P2H4, which makes its handling even more dangerous. The inexpensive metal–organic framework (MOF) magnesium formate, α‐[Mg(O2CH)2], can adsorb up to 10 wt % of PH3. The PH3‐loaded MOF, PH3@α‐[Mg(O2CH)2], is a non‐pyrophoric, recoverable material that even allows brief handling in air, thereby minimizing the hazards associated with the handling and transport of phosphane. α‐[Mg(O2CH)2] further plays a critical role in purifying PH3from H2and P2H4: at 25 °C, H2passes through the MOF channels without adsorption, whereas PH3adsorbs readily and only slowly desorbs under a flow of inert gas (complete desorption time≈6 h). Diphosphane, P2H4, is strongly adsorbed and trapped within the MOF for at least 4 months. P2H4@α‐[Mg(O2CH)2] itself is not pyrophoric and is air‐ and light‐stable at room temperature. 
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                            A unique trimeric triphenylene radical cation: stacking aggregation, bonding, and stability
                        
                    
    
            A unique trimeric radical cation with unequal charge distribution is obtained by chemical oxidation of triphenylene with GaCl3. XRD determined structure is combined with computational modeling showing stabilizing pancake bonding in the π-stacks. 
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                            - PAR ID:
- 10546313
- Publisher / Repository:
- RSC
- Date Published:
- Journal Name:
- Chemical Science
- Volume:
- 15
- Issue:
- 37
- ISSN:
- 2041-6520
- Page Range / eLocation ID:
- 15221 to 15231
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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