scholarly journals The elusive cyclotriphosphazene molecule and its Dewar benzene–type valence isomer (P3N3)

2020 ◽  
Vol 6 (30) ◽  
pp. eaba6934 ◽  
Author(s):  
Cheng Zhu ◽  
André K. Eckhardt ◽  
Alexandre Bergantini ◽  
Santosh K. Singh ◽  
Peter R. Schreiner ◽  
...  

Although the chemistry of phosphorus and nitrogen has fascinated chemists for more than 350 years, the Hückel aromatic cyclotriphosphazene (P3N3, 2) molecule—a key molecular building block in phosphorus chemistry—has remained elusive. Here, we report a facile, versatile pathway producing cyclotriphosphazene and its Dewar benzene–type isomer (P3N3, 5) in ammonia-phosphine ices at 5 K exposed to ionizing radiation. Both isomers were detected in the gas phase upon sublimation via photoionization reflectron time-of-flight mass spectrometry and discriminated via isomer-selective photochemistry. Our findings provide a fundamental framework to explore the preparation of inorganic, isovalent species of benzene (C6H6) by formally replacing the C─H moieties alternatingly through phosphorus and nitrogen atoms, thus advancing our perception of the chemical bonding of phosphorus systems.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Cheng Zhu ◽  
André K. Eckhardt ◽  
Sankhabrata Chandra ◽  
Andrew M. Turner ◽  
Peter R. Schreiner ◽  
...  

AbstractPolyhedral nitrogen containing molecules such as prismatic P3N3 - a hitherto elusive isovalent species of prismane (C6H6) - have attracted particular attention from the theoretical, physical, and synthetic chemistry communities. Here we report on the preparation of prismatic P3N3 [1,2,3-triaza-4,5,6-triphosphatetracyclo[2.2.0.02,6.03,5]hexane] by exposing phosphine (PH3) and nitrogen (N2) ice mixtures to energetic electrons. Prismatic P3N3 was detected in the gas phase and discriminated from its isomers utilizing isomer selective, tunable soft photoionization reflectron time-of-flight mass spectrometry during sublimation of the ices along with an isomer-selective photochemical processing converting prismatic P3N3 to 1,2,4-triaza-3,5,6-triphosphabicyclo[2.2.0]hexa-2,5-diene (P3N3). In prismatic P3N3, the P–P, P–N, and N–N bonds are lengthened compared to those in, e.g., diphosphine (P2H4), di-anthracene stabilized phosphorus mononitride (PN), and hydrazine (N2H4), by typically 0.03–0.10 Å.  These findings advance our fundamental understanding of the chemical bonding of poly-nitrogen and poly-phosphorus systems and reveal a versatile pathway to produce exotic, ring-strained cage molecules.


1999 ◽  
Vol 70 (8) ◽  
pp. 3259-3264 ◽  
Author(s):  
Christopher Fockenberg ◽  
Herbert J. Bernstein ◽  
Gregory E. Hall ◽  
James T. Muckerman ◽  
Jack M. Preses ◽  
...  

2003 ◽  
Vol 9 (1) ◽  
pp. 61-70 ◽  
Author(s):  
Sajid Bashir ◽  
Peter J. Derrick ◽  
Peter Critchley ◽  
Paul J. Gates ◽  
James Staunton

Application of matrix-assisted laser desorption/ionization (MALDI) to the analysis of dextran and dextrin derivatives, specifically glucose saccharides, by time-of-flight (TOF) mass spectrometry is reported. MALDI-TOF analysis was carried out on alpha-, beta-and gamma-cyclodextrin, two O-methylated beta-cyclodextrins of differing degrees of substitution (DS) and dextrans (a linear glucose saccharide), as pure and doped solutions and as mixtures of two or more of these analytes. Doping was carried out with trace amounts of inorganic salts. The purpose of the analysis of the cyclodextrins was to determine whether they would form inclusion complexes with the various added cations, or whether less specific cation addition/exchange was occurring either prior to desorption or in the gas phase.


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