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Matthew Nava

Researcher at Massachusetts Institute of Technology

Publications -  25
Citations -  658

Matthew Nava is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Anthracene & Peroxide. The author has an hindex of 14, co-authored 24 publications receiving 514 citations. Previous affiliations of Matthew Nava include Harvard University & University of California, Riverside.

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Triethylsilyl Perfluoro-Tetraphenylborate, [Et(3)Si][F(20)-BPh(4)], a widely used Non-Existent Compound.

TL;DR: The commonly used triethylsilyl per-fluoro-tetraphenylborate salt, [Et(3)Si(+)][F(20)-BPh(4) (-)], has been misidentified.
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Mechanism and Scope of Phosphinidene Transfer from Dibenzo-7-phosphanorbornadiene Compounds

TL;DR: The breadth of phosphinidene acceptors is expanded to unsaturated substrates beyond 1,3-dienes to include olefins and alkynes; this provides a new synthetic route to valuable amino-substituted phosphiranes and phosphirenes, respectively.
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Spontaneous and Selective Formation of HSNO, a Crucial Intermediate Linking H2S and Nitroso Chemistries

TL;DR: It is established that HSNO is spontaneously formed in high concentration when NO and H2S gases are mixed at room temperature in the presence of metallic surfaces and the length of the S-N bond is found to be unusually long: 1.84 Å.
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A retro Diels-Alder route to diphosphorus chemistry: molecular precursor synthesis, kinetics of P2 transfer to 1,3-dienes, and detection of P2 by molecular beam mass spectrometry.

TL;DR: A molecular beam mass spectrometry study on the thermolysis of solid P2A2 reveals the direct detection of molecular fragments of only P2 and anthracene, thus establishing a link between solution-phase P2-transfer chemistry and production of gas- phase P2 by mild thermal activation of a molecular precursor.
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The Strongest Brønsted Acid: Protonation of Alkanes by H(CHB11F11) at Room Temperature

TL;DR: By protonating alkanes at room temperature, the reactivity of H(CHB11 F11 ) opens up new opportunities for the easier study of acid-catalyzed hydrocarbon reforming.