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The structure of the base t-Bu-P4 and its protonated form. | Download  Scientific Diagram
The structure of the base t-Bu-P4 and its protonated form. | Download Scientific Diagram

Synthesis of end‐functionalized polyethers by phosphazene base‐catalyzed  ring‐opening polymerization of 1,2‐butylene oxide and glycidyl ether -  Misaka - 2012 - Journal of Polymer Science Part A: Polymer Chemistry -  Wiley Online Library
Synthesis of end‐functionalized polyethers by phosphazene base‐catalyzed ring‐opening polymerization of 1,2‐butylene oxide and glycidyl ether - Misaka - 2012 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library

Phosphazene base P2-F | C12H36FN7P2 | ChemSpider
Phosphazene base P2-F | C12H36FN7P2 | ChemSpider

Phosphazene - Wikipedia
Phosphazene - Wikipedia

Phosphazene base promoted anionic polymerization of n-butyraldehyde -  ScienceDirect
Phosphazene base promoted anionic polymerization of n-butyraldehyde - ScienceDirect

31 P { 1 H} NMR spectra of the pure (a) phosphazene base 2d and (b) PIL...  | Download Scientific Diagram
31 P { 1 H} NMR spectra of the pure (a) phosphazene base 2d and (b) PIL... | Download Scientific Diagram

Two-Step Asymmetric Synthesis of Disubstituted N-Tosyl Aziridines Having  98−100% ee: Use of a Phosphazene Base | The Journal of Organic Chemistry
Two-Step Asymmetric Synthesis of Disubstituted N-Tosyl Aziridines Having 98−100% ee: Use of a Phosphazene Base | The Journal of Organic Chemistry

Phosphazene base P2-Et - ATR-IR - Spectrum - SpectraBase
Phosphazene base P2-Et - ATR-IR - Spectrum - SpectraBase

Phosphazene bases
Phosphazene bases

Phosphazene base P4-t-Bu tetrafluoroborate salt ≥97.0% (NMR) | Sigma-Aldrich
Phosphazene base P4-t-Bu tetrafluoroborate salt ≥97.0% (NMR) | Sigma-Aldrich

Phosphazene base P4-t-Oct 1.00M +/- 0.05M n-hexane 153136-05-1
Phosphazene base P4-t-Oct 1.00M +/- 0.05M n-hexane 153136-05-1

Phosphazene base P1-t-Bu = 97.0 GC 81675-81-2
Phosphazene base P1-t-Bu = 97.0 GC 81675-81-2

Phosphazene base P1-t-Bu-tris(tetramethylene) | CAS 161118-67-8 | SCBT -  Santa Cruz Biotechnology
Phosphazene base P1-t-Bu-tris(tetramethylene) | CAS 161118-67-8 | SCBT - Santa Cruz Biotechnology

Phosphazene base P1-t-Oct | C14H35N4P - PubChem
Phosphazene base P1-t-Oct | C14H35N4P - PubChem

Phosphazene Bases
Phosphazene Bases

pK ip values of phosphazene bases 6a,b and several other representative...  | Download Scientific Diagram
pK ip values of phosphazene bases 6a,b and several other representative... | Download Scientific Diagram

Phosphazene base-promoted functionalization of aryltrimethylsilanes -  Chemical Communications (RSC Publishing) DOI:10.1039/B611090H
Phosphazene base-promoted functionalization of aryltrimethylsilanes - Chemical Communications (RSC Publishing) DOI:10.1039/B611090H

Synthesis of linear and star poly(ε-caprolactone) with controlled and high  molecular weights via cyclic trimeric phosphazene base catalyzed ring-openi  ... - Polymer Chemistry (RSC Publishing) DOI:10.1039/C7PY01673E
Synthesis of linear and star poly(ε-caprolactone) with controlled and high molecular weights via cyclic trimeric phosphazene base catalyzed ring-openi ... - Polymer Chemistry (RSC Publishing) DOI:10.1039/C7PY01673E

Structure of a trimeric phosphazene base (CTPB) (adapted with... | Download  Scientific Diagram
Structure of a trimeric phosphazene base (CTPB) (adapted with... | Download Scientific Diagram

Phosphazene Bases: A New Category of Organocatalysts for the Living  Ring-Opening Polymerization of Cyclic Esters | Macromolecules
Phosphazene Bases: A New Category of Organocatalysts for the Living Ring-Opening Polymerization of Cyclic Esters | Macromolecules

Phosphazene base-catalyzed intramolecular cyclization for efficient  synthesis of benzofurans viacarbon–carbon bond formation - Chemical  Communications (RSC Publishing)
Phosphazene base-catalyzed intramolecular cyclization for efficient synthesis of benzofurans viacarbon–carbon bond formation - Chemical Communications (RSC Publishing)

Deprotonation of benzylic ethers using a hindered phosphazene base. A  synthesis of benzofurans from ortho-substituted benzaldehydes. | Semantic  Scholar
Deprotonation of benzylic ethers using a hindered phosphazene base. A synthesis of benzofurans from ortho-substituted benzaldehydes. | Semantic Scholar

Synthesis of Tris-Phosphazene Bases with Triazine as Core and Their  Applications for Efficient Ring-Opening Alternating Copolymerization of  Epoxide and Anhydride: Notable Effect of Basicity and Molecular Size | ACS  Macro Letters
Synthesis of Tris-Phosphazene Bases with Triazine as Core and Their Applications for Efficient Ring-Opening Alternating Copolymerization of Epoxide and Anhydride: Notable Effect of Basicity and Molecular Size | ACS Macro Letters

Phosphazene base P2-Et | C12H35N7P2 | ChemSpider
Phosphazene base P2-Et | C12H35N7P2 | ChemSpider

CAS#:111324-04-0 | Phosphazene base P4-t-Bu solution purum, ~1.0 M in  hexane | Chemsrc
CAS#:111324-04-0 | Phosphazene base P4-t-Bu solution purum, ~1.0 M in hexane | Chemsrc

Using recyclable polystyrene supported cyclic trimeric phosphazene base as  catalyst to directly prepare hypotoxic polyesters via ring-opening  polymerizations - ScienceDirect
Using recyclable polystyrene supported cyclic trimeric phosphazene base as catalyst to directly prepare hypotoxic polyesters via ring-opening polymerizations - ScienceDirect

Phosphazene base P1-t-Bu-tris(tetramethylene) = 97.0 NT 161118-67-8
Phosphazene base P1-t-Bu-tris(tetramethylene) = 97.0 NT 161118-67-8

Phosphazene base | Sigma-Aldrich
Phosphazene base | Sigma-Aldrich

Phosphazene Bases
Phosphazene Bases

Phosphazene base P1-t-Oct = 97.0 161118-69-0
Phosphazene base P1-t-Oct = 97.0 161118-69-0