![Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics](https://pubs.acs.org/cms/10.1021/acs.organomet.0c00411/asset/images/large/om0c00411_0003.jpeg)
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics
![Two Verkade's super bases (Vkd_Me and Vkd_iPr) and two guanidine bases... | Download Scientific Diagram Two Verkade's super bases (Vkd_Me and Vkd_iPr) and two guanidine bases... | Download Scientific Diagram](https://www.researchgate.net/publication/324509068/figure/fig1/AS:615674330238976@1523799607354/Two-Verkades-super-bases-Vkd-Me-and-Vkd-iPr-and-two-guanidine-bases-TMG-and-tBuTMG.png)
Two Verkade's super bases (Vkd_Me and Vkd_iPr) and two guanidine bases... | Download Scientific Diagram
![120666-13-9 | 2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane | Proazaphosphatrane; Verkade base | C9H21N4P | TRC 120666-13-9 | 2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane | Proazaphosphatrane; Verkade base | C9H21N4P | TRC](https://www.trc-canada.com/prod-img/T219435.png)
120666-13-9 | 2,8,9-Trimethyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane | Proazaphosphatrane; Verkade base | C9H21N4P | TRC
![Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics](https://pubs.acs.org/cms/10.1021/acs.organomet.0c00411/asset/images/large/om0c00411_0001.jpeg)
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics
![Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry](https://pubs.acs.org/cms/10.1021/acs.inorgchem.7b01719/asset/images/large/ic-2017-01719s_0010.jpeg)
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry
![Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G](https://pubs.rsc.org/image/article/2019/NJ/c8nj04977g/c8nj04977g-s1_hi-res.gif)
Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G
![Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G](https://pubs.rsc.org/image/article/2019/NJ/c8nj04977g/c8nj04977g-s5_hi-res.gif)
Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G
![Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G](https://pubs.rsc.org/image/article/2019/NJ/c8nj04977g/c8nj04977g-s2_hi-res.gif)
Protonation of Verkade bases: a theoretical study - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ04977G
![Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry](https://pubs.acs.org/cms/10.1021/acs.inorgchem.7b01719/asset/images/large/ic-2017-01719s_0008.jpeg)
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry
![Schematic representation of the considered phosphazenes and Verkade's... | Download Scientific Diagram Schematic representation of the considered phosphazenes and Verkade's... | Download Scientific Diagram](https://www.researchgate.net/profile/Boris-Kovacevic-2/publication/255745356/figure/fig1/AS:668987516018697@1536510461819/Schematic-representation-of-the-considered-phosphazenes-and-Verkades-proton-sponge_Q640.jpg)
Schematic representation of the considered phosphazenes and Verkade's... | Download Scientific Diagram
![Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics](https://pubs.acs.org/cms/10.1021/acs.organomet.0c00411/asset/images/large/om0c00411_0006.jpeg)
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics
![Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics](https://pubs.acs.org/cms/10.1021/acs.organomet.0c00411/asset/images/medium/om0c00411_0003.gif)
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics
![Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry](https://pubs.acs.org/cms/10.1021/acs.inorgchem.7b01719/asset/images/large/ic-2017-01719s_0019.jpeg)
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry
![Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry](https://pubs.acs.org/cms/10.1021/acs.inorgchem.7b01719/asset/images/medium/ic-2017-01719s_0022.gif)
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry
![Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry](https://pubs.acs.org/cms/10.1021/acs.inorgchem.7b01719/asset/images/medium/ic-2017-01719s_0004.gif)
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry
![Verkade super base-catalysed transesterification of propylene carbonate with methanol to co-produce dimethyl carbonate and propylene glycol - ScienceDirect Verkade super base-catalysed transesterification of propylene carbonate with methanol to co-produce dimethyl carbonate and propylene glycol - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1381116909000661-fx1.jpg)
Verkade super base-catalysed transesterification of propylene carbonate with methanol to co-produce dimethyl carbonate and propylene glycol - ScienceDirect
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics
![Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry](https://pubs.acs.org/cms/10.1021/acs.inorgchem.7b01719/asset/images/medium/ic-2017-01719s_0018.gif)
Interactions of Verkade's Superbase with Strong Lewis Acids: From Labile Mono- and Binuclear Lewis Acid–Base Complexes to Phosphenium Cations | Inorganic Chemistry
![Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics](https://pubs.acs.org/cms/10.1021/acs.organomet.0c00411/asset/images/large/om0c00411_0008.jpeg)
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics
![Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics](https://pubs.acs.org/cms/10.1021/acs.organomet.0c00411/asset/images/large/om0c00411_0004.jpeg)
Verkade Base in FLP Chemistry–From Stoichiometric C–H Bond Cleavage to the Catalytic Dimerization of Alkynes | Organometallics
![PDF) Basicity of exceedingly strong non-ionic organic bases in acetonitrile —Verkade's superbase and some related phosphazenes PDF) Basicity of exceedingly strong non-ionic organic bases in acetonitrile —Verkade's superbase and some related phosphazenes](https://www.researchgate.net/profile/Boris-Kovacevic-2/publication/255745356/figure/fig3/AS:668987516002316@1536510461872/Some-characteristic-structural-parameters-and-Loe-wdin-atomic-charges-within_Q320.jpg)