hrvatski jezikClear Cookie - decide language by browser settings

The Next Generation of Phosphorus Bisylide Superbases – Synthesis, Structures, Basicity and Proton Self‐Exchange

Kögel, Julius F.; Ullrich, Sebastian; Xie, Xiulan; Finger, Lars H.; Kovačević, Borislav; Saame, Jaan; Haljasorg, Tõiv; Leito, Ivo; Sundermeyer, Jörg (2025) The Next Generation of Phosphorus Bisylide Superbases – Synthesis, Structures, Basicity and Proton Self‐Exchange. Chemistry – A European Journal, 31 (19). ISSN 0947-6539

[img] PDF - Published Version - article
Available under License Creative Commons Attribution.

Download (1MB)

Abstract

Herein we present two phosphorus ylide superbases to enhance the basicity of 1,8-bis (methylylidene (hexamethyltriamino) phosphorane) naphthalene (MHPN) – the first superbase with interacting carbon atoms as basicity centers. Its 1-pyrrolidinyl substituted analog 1,8-bis (methylylidene (tris (1-pyrrolidinyl)) phosphorane) naphthalene (MTPN) and MHPN's theoretically predicted higher homologue P2-MHPN exhibit extreme pKaH values of 26.0 and 29.5 (experimental) in THF solution and 33.6 and 37.4 (estimated) in acetonitrile solution. The corresponding calculated gas phase basicity values are 281.4 and 284.6 kcal mol−1, respectively. We prepared the neutral free bases together with the corresponding mono- and bisprotonated species which were characterized by NMR spectroscopy, ESI mass spectrometry, IR spectroscopy, elemental analysis and partly XRD analysis. The monoprotonated forms exhibit a rapid proton self-exchange between the two carbon atoms in peri-position and dynamic NMR spectroscopic methods revealed self-exchange rates of 2298 s−1 and 300 s−1 at 300 K for MTPN and P2-MHPN, respectively. However, computational studies reveal that the proton chelating effect, which typically considerably contributes to the basicity of proton sponges with basicity centers on nitrogen, is negligible in bisylides, as the 1,8-substitution pattern yields almost the same basicity as the corresponding 2,7- or 1,5-substituted analogues.

Item Type: Article
Uncontrolled Keywords: 1,8-bis (methylylidene (hexamethyltriamino) phosphorane) naphthalene; 1,8-bis (methylylidene (tris (1-pyrrolidinyl)) phosphorane) naphthalene; basicity; proton exchange
Subjects: NATURAL SCIENCES
Divisions: Division of Physical Chemistry
Projects:
Project titleProject leaderProject codeProject type
Bis-fosfini kao nemetalni katalizatori za aktivaciju malih molekula - dizajn i sintezaBorislav KovačevićIP-2024-05-7730HrZZ
Depositing User: Lorena Palameta
Date Deposited: 04 Nov 2025 09:14
URI: http://fulir.irb.hr/id/eprint/10129
DOI: 10.1002/chem.202404692

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

Contrast
Increase Font
Decrease Font
Dyslexic Font
Accessibility