Joseph Parr
@josephmparr
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Jones group at Monash, PhD with Crimmin Imperial College London.
Joined September 2020
Joe's (@josephmparr) work on the activation of C-C single bonds in biphenylene using Mg(I) and Mg-N2 complexes is out @Orgmet_ACS. https://t.co/WxSohv6drJ.
#ozchem #chemtwitter @ChemistryMonash @AFOSR
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Joe (@josephmpar) and Jeremy's work on complexes of 1st row TM metallocenes with sterically constrained diamido Gp2 metal Lewis acids is out as a preprint @ChemRxiv. #ozchem @ChemistryMonash @AFOSR
https://t.co/xUIgkNELzX
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Matt (@EvansInorganic) and co's work on the first main group metal-P4 complexes, redn of P4 to [P4]2- with a Mg-N2 complex, and hydrolysis of [P4]2- to PH3, has been accepted @Chem_CP. https://t.co/rrzi2q3yFg Free access: https://t.co/pwAyZqm9kR
#ozchem @Monash_Science
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Our work on the room-temperature ring-opening of benzene is now published in @J_A_C_S ! Great teamwork and thanks for the kind comments from the reviewers!
pubs.acs.org
Cleaving a benzene ring under mild conditions requires disrupting its aromaticity, which is a significant challenge in modern chemistry. Although the generation of cyclic products from cleaving...
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Interested in learning more about sustainable approaches in fluorine chemistry? @shannon_esf1 has a new @ChemRxiv out summarising synthetic and catalytic approaches that could underpin a future circular economy for fluorocarbons. https://t.co/ndkCyFVBK6
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New paper out today in @NatureSynthesis from Wenbang Yang (@yangwenbang0310). We describe addition of Zn–Zn bonds to main group carbenes. The system nicely illustrates the continuum between oxidative addition and reductive addition processes. https://t.co/CgSfSB6bje
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Matt (@EvansInorganic) and co's work on the first main group metal-P4 complexes, redn of P4 to [P4]2- with a Mg-N2 complex, and hydrolysis of [P4]2- to PH3,has appeared @ChemRxiv. Neutral diamido Gp2 metal complexes as strong Lewis acids #ozchem
https://t.co/vJlFeUkcyW
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I am glad to share my first publication from PhD which is indeed a great feeling:) Congratulations to all the authors who worked really hard to put all the pieces together! More osmium chemistry yet to come!! Stay tuned;) https://t.co/c1iVz7M2si
@USCChemistry @InorgChem
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Assembly of Functionalized Organic Fragments via Reductive Activation and (Cross)-Coupling of C2H4, CO, CO2 and/or H2 Using a Mg-Dinitrogen Complex (Cameron Jones and co-workers) @Jones_Research @ng_tiendat @EvansInorganic @ChemistryMonash #openaccess 🔓
onlinelibrary.wiley.com
A dimagnesium/dipotassium complex of N2 acts as a “masked” source of a dimagnesium(I) diradical in formal reductive coupling and cross-coupling reactions involving various combinations of the simple...
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Dat (@ng_tiendat) and Rahul's latest pre-print on the "Assembly of Functionalized Organic Fragments via Reductive Activation and Cross-Coupling of C2H4, CO, CO2 and/or H2 using a Mg-N2 Complex" can be found at https://t.co/xz7qyvjteM.
#ozchem @ChemistryMonash
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Potential PhD funding (part of an internal competition) in the group to look at designing new heteromultimetallic catalysts for CO2 reduction: https://t.co/lY9c5T73KA If you’re into the interface between computation and organometallic chemistry please apply!
findaphd.com
PhD Project - Programming Copper–Zinc Heteromultimetallic Complexes for CO2 Reduction at University of Bath, listed on FindAPhD.com
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Counterion Loss from Charged Surface-Bound Complexes Drives the Formation of Loosely Packed Monolayers | Journal of the American Chemical Society @mikeinkpen @USCChemistry @oprezhdo #SurfaceBound #Monolayers #Counterion
pubs.acs.org
The functionality of multicomponent self-assembled monolayers (SAMs) can be severely diminished by the segregation of like components into nanoscale domains, a process that maximizes favorable...
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An updated version of this one has now been accepted by @ChemCommun, and is available at https://t.co/EEmtIXL5AD. Although brief, it required lots of hard work from @dom_chem, @EvansInorganic, @Dafydd_Jones7, @josephmparr and Mike Hill (𝕏-less). #ozchem @ChemistryMonash
pubs.rsc.org
A bulky, unsymmetrical β-diketiminate ligand, [HC{MeCN(Dip)}{MeCN(TCHP)}]− (Dip/TCHPNacnac; Dip = 2,6-diisopropylphenyl, TCHP = 2,4,6-tricyclohexylphenyl), has been utilised in the preparation of a...
More than 4 years in the making, and our 1st Monash/Bath (with Mike Hill) study is out on ChemRxiv. A full series of heavier Gp 2 metal hydride complexes [(Nacnac)M(mu-H)]2 (M=Mg, Ca, Sr or Ba). great work by Dom, Matt and Dafydd. #ozchem @ChemistryMonash
https://t.co/1qVeQWf4fu
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Matt’s @EvansInorganic latest paper on the stabilisation of a stannaimine, and its use for the transformation of CO2 to an isocyanate is out now in @ChemCommun #ozchem @ChemistryMonash
https://t.co/9TrqGgMJiW
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More than 4 years in the making, and our 1st Monash/Bath (with Mike Hill) study is out on ChemRxiv. A full series of heavier Gp 2 metal hydride complexes [(Nacnac)M(mu-H)]2 (M=Mg, Ca, Sr or Ba). great work by Dom, Matt and Dafydd. #ozchem @ChemistryMonash
https://t.co/1qVeQWf4fu
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Gina Rai has a new @ChemRxiv preprint out using automation, kinetics and DFT calculations to gain a detailed understanding of the mechanism of Pd-catalysed formylation of aryl bromides. Here is the link: https://t.co/OqdfMLuMMo
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Also out today is a @ChemRxiv preprint from Wenbang Yang describing the reductive addition of Zn–Zn bonds to main group carbene analogues. The work challenges preconceptions behind addition mechanisms, hinting that these may not always be oxidative. https://t.co/0y8fOkyxPA
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Another most read June article, this one on the ring-opening gem-silylborylation of cyclopropenes with silylboronates. From Ryo Shintani and co. at @osaka_univ
#OpenAccess 🔓 https://t.co/CixVSZtYz7
pubs.rsc.org
A KOtBu-catalyzed ring-opening gem-silylborylation of cyclopropenes with silylboronates has been developed for the synthesis of (1-silyl)allylboronates, a useful class of compounds in organic...
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Big week in the Jones group. Two new arrivals, Sophie Unsworth (PhD start) by way of @VicUniWgtn, and new postdoc, Joe Parr (@josephmparr), who recently completed his PhD in @crimmingroup. Big welcome to both! #ozchem @ChemistryMonash
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Danny Sheldon's and @josephmparr's on defluorination of tetrafluoroethane (HFC-134a) is now out in @DaltonTrans. Here is the link:
The second, from Danny Sheldon on the defluorination of HFCs, including an extremely rare example of a 1,2-defluorination of 1,1,1,2-tetrafluoroethane aka HFC-134a (the biggest use HFC). https://t.co/lxe17ATHAl
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