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16th European Workshop on Phosphorus Chemistry 24-26 April 2019

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Page 1: 16th European Workshop on - WordPress.com · Kirill Nikitin Univ. College Dublin P47 Syntheses and structures of new diphosphinoboranes Anna Ordyszewska Gdansk Univ. of Technology

16th European Workshop

on

Phosphorus Chemistry

24-26 April 2019

Page 2: 16th European Workshop on - WordPress.com · Kirill Nikitin Univ. College Dublin P47 Syntheses and structures of new diphosphinoboranes Anna Ordyszewska Gdansk Univ. of Technology

Welcome to EWPC-16 and welcome to Bristol!

The European Workshop on Phosphorus Chemistry has a strong reputation for the fruitful exchange of

ideas and opinions through animated discussions in a convivial atmosphere. The aspects of

phosphorus chemistry covered by EWPC span organic, inorganic, polymer, materials and biological

chemistry.

EWPC gives early stage researchers the opportunity to communicate their work to the leading

European research groups in phosphorus chemistry. The program this year includes 33 oral

contributions from PhD students and 70 posters. The Workshop is preceded by the inaugural IndPhos

symposium which will showcase the P-chemistry that is important in industry today with 6 lectures from

leading industrial researchers. It is hoped that the perspective provided by IndPhos will stimulate

future academic-industrial collaborations.

Hansjörg Grützmacher, whose research has attracted much industrial interest, will present a talk that

will bridge IndPhos and EWPC-16.

I would like to thank the generous sponsors of the meeting, particularly Solvay, LANXESS, Strem,

Magritek, OCP, Glindemann and The Royal Society of Chemistry (Dalton Division).

IndPhos was the idea of Chris Slootweg (Univ. Amsterdam) and he has done the great bulk of the

work to make it happen. My group (pictured below) have been brilliant in injecting ideas and helping

with the administration of EWPC.

I hope you find the science absorbing and you enjoy your stay in Bristol.

Paul G Pringle

Callum Branfoot, Rachel Doyle, Sarah Williams, Ailis Chadwick, Lexy Miles-Hobbs, Dan Wise

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24 April

09:20 Introduction

Paul Pringle (Univ. Bristol)

Chair: Chris Slootweg (Univ. Amsterdam)

09:30 Sustainable Industrial Phosphorus Chemistry

Willem Schipper WS Consulting

10:00 Real World Applications of Organophosphorus Chemistry

Chris Harris Solvay

10:30 Catalysis with P-ligands at BASF and New Developments at CaRLa

Thomas Schaub BASF

11:00 Coffee

11:30 Poly(alkylene phosphates)

Jan-Gerd Hansel LANXESS

12:00 IONQUEST for Solvent Extraction:

Industrial Scale-up of Diverse P-Chemistries

Steven van Zutphen Italmatch

12:30 Acylphosphine Oxide Photoinitiators: Some Recent Developments

Reinhard Sommerlade Independent Process Design Chemist

13:00 Lunch

14:00 Building blocks containing phosphorus for atom efficient syntheses

Hansjörg Grützmacher ETH, Zurich

15:00 Coffee

2

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15:30 Introduction

Paul Pringle (Univ. Bristol)

Chair: Erica Neves de Faria (Univ. Oxford)

15:40 O1: Air-stable dialkylphosphine surrogates from zinc phosphide

Tom Barber

Univ. Nottingham, UK

16:00 O2: On the way to nucleophilic phosphinines

Friedrich Wossidlo

Freie Univ. Berlin, Germany

16:20 O3: Investigating the reactivity and reduction chemistry of cobalt diphosphine complexes

Claire Brodie

Durham Univ., UK

16th European Workshop on

Phosphorus Chemistry

Safe, convenient PH3 precursor

Operationally simple, ‘solvent free' alkylation

3

Wednesday 24 April

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16:40 O4: Phosphaalkenes in organic chemistry

Nicolas D'Imperio

Uppsala Univ., Sweden

17:00 O5: Synthesis of cationic polypnictogen complexes

Luis Dütsch

Univ. Regensburg, Germany

17:20 O6: Convenient one-pot reaction for the synthesis of α-H-phosphinate and H-HMBPi salts

Jade Dussart

Univ. Paris, France

18:30 – 20:30 Reception on SS Great Britain

Wednesday 24 April 2019

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Chair: Gabriele Hierlmeier (Univ. Regensberg)

09:00 O7: Investigation of optical and electronic properties of phosphole-based π-systems and phosphanylsiloles

Réka Mokrai

Budapest Univ. of Technology and Economics, Hungary

09:20 O8: Cyclic fluorophosphites: ligands that span the bonding space between phosphites and PF3

Lexy Miles-Hobbs

Univ. Bristol, UK

09:40 O9: Lewis base catalysed isomerisation of a phosphaethynolato- to phosphaketenylborane

Daniel Wilson

Univ. Oxford, UK

10:00 O10: Synthesis and characterization of sterically protected,functionalized 2,4-diphosphapentasilanes

Gernot Weinberger

TU Graz, Austria

10:20 O11: Phosphorandiylium (R3P)2+: a three-coordinate phosphorus dication

Tobias Eder

Univ. Münster, Germany

10:40 Coffee

5

Thursday 25 April 2019

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Chair: Philipp Brehm (Univ. Bonn)

11:10 O12: New family of P-stereogenic phosphahelicenes

Julie Febvay

Institut de Chimie des Substances Naturelles, CNRS, France

First helically chiral BrØnsted acids

11:30 O13: Selective nitrile reduction using solid-supported triphos ligands: application in continuous flow

Robert Konrath

Univ. St Andrews, UK

11:50 O14: NHP-Nitrosyl complexes of iron

Christoph Feil

Univ. Stuttgart, Germany

12:10 O15: Investigation of microwave assisted Kabachnik-Fileds and Biginelli reactions

Nóra Tóth

Budapest Univ. of Technology and Economics, Hungary

12:30 O16: Abnormal reactions of N-heterocyclic carbenes with phosphaalkenes

Zeyu Han

Univ. British Columbia, Canada

12:50 Lunch

Thursday 25 April 2019

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Chair: Daniel Buzsáki (Budapest Univ.)

14:20 O17: Synthesis and reactivity of 3H-phospha-allenes

Jonas Tendyck

Univ. Münster, Germany

14:40 O18: Frustrated radical pair formation

Flip Holtrop

Univ. Amsterdam, Netherlands

15:00 O19: Protolysis reaction and P/N–P/P bond metathesis for the synthesis of cationic polyphosphanes

Clemens Taube

Univ. Dresden, Germany

15:20 O20: Anionic N-heterocyclic carbenes for pnictogen complexes

Luong Phong Ho

Univ. Braunschweig, Germany

15:40 O21: Activation of CO2 and CS2 by diphosphane/BPh3 frustrated Lewis pairs

Natalia Szynkiewicz

Gdansk Univ., Poland

16:00 Coffee

Thursday 25 April 2019

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Chair: Thomasine Curzon (Univ. St Andrews)

16:30 O22: Immobilization of P-based organocatalysts by plasma techniques

Yuya Hu

LIKAT Rostock, Germany

16:50 O23: Primary phosphanes with 2,6-bis-(benzhydryl)phenyl backbones

Tim Suhrbier

Univ. Rostock, Germany

17:10 O24: Reactivity of silane compounds with few-layer black phosphorus

Iñigo Iglesias

CNR-ICCOM, Italy

17:30 O25: Effect of aromatic substituents on formation and reactivity of Li/Cl phosphinidenoid complexes

Alexander Schmer

Univ. Bonn, Germany

17:50 O26: 1,2-Dihydrophosphetes: an unexplored P-containing four-membered ring for optoelectronic applications

Hortense Lauwick

Univ. Rennes, CNRS, France

18:30 Poster Event

Thursday 25 April 2019

8

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Chair: Matteo Vanni (CNR-ICCOM)

09:00 O27: Exploiting peri-substitution to promote coupling reactions

Bethany Lawson

Univ. St Andrews, UK

C–H coupling via radical mechanism

09:20 O28: Silylation of Na3P assisted by phosphonium salts: A new route towards reactive P species

Grégoire Le Corre

ETH Zurich, Switzerland

09:40 O29: Catalytic transformation of white phosphorus into aryl phosphines and phosphonium salts

Ulrich Lennert

Univ. Regensburg, Germany

10:00 O30: Direct asymmetric Ru-phosphine-catalyzed reductive amination of aryl-alkyl ketones with NH3/H2

Maximilian Menche

BASF Catalysis Research Laboratory, Heidelberg, Germany

10:20 Coffee

Friday 26 April 2019

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Chair: Steven Beijer (Univ. Amsterdam)

10:50 O31: Asymmetrically substituted phospholes: from fynthesis to imprinted structures

Fabian Roesler

Univ. Kassel, Germany

11:10 O32: Phospholes vs. arsoles: one ring to rule them all

Darren Ould

Cardiff Univ., UK

11:30 O33: Synthesis of heterobimetallic complexes from N,P-based heteroditopic ligands

Saral Baweja

Leipzig Univ., Germany

12:00 EWPC-17

12:15 Finale

12:30 Depart

Friday 26 April 2019

10

Page 12: 16th European Workshop on - WordPress.com · Kirill Nikitin Univ. College Dublin P47 Syntheses and structures of new diphosphinoboranes Anna Ordyszewska Gdansk Univ. of Technology

Posters

No. Title Name Affiliation

P1 Dehydrocoupling of phosphines mediated by alkali metal

catalysts

Vincent Annibale Univ. Bristol

P2 From McMurry to Wittig via phospha-alkenes: novel

approach to reductive carbonyl coupling

Anna Arkhypchuk Uppsala Univ.

P3 Reactions of isonitrile-to-phosphinidene complex

adducts

David Becker Univ. Bonn

P4 An organocatalytic Mitsunobu Esterification Reaction Rhydian Beddoe Univ. Nottingham

P5 Circular chemistry: the sustainable use of phosphorus Steven Beijer Univ. Amsterdam

P6 Investigations on the reactivity of N-Heterocyclic

Phosphenium Complexes of Chromium

Nicholas Birchall Univ. Stuttgart

P7 Reactivity of [Cp*Fe(η5-P5)] towards halogenating agents Helena Brake Univ. Regensburg

P8 CO-insertion into an endocyclic P-C bond of a

constrained tricyclic PC3 phosphine

Alexander Brand Univ. Münster

P9 The homometathesis and heterometathesis reactions of

tetra-aryldiphosphanes

Callum Branfoot Univ. Bristol

P10 TEMPO-substituted phosphane–iron(0) complexes:

precursors for phosphanoxyl complexes?

Philipp Brehm Univ. Bonn

P11 Variation on carbenes and pnictanes – a computational

study

Daniel Buzsaki Budapest Univ.

P12 A strong C2-symmetric BINOL derived phosphorus

Brønsted acid catalyst

Andy Caffyn Manchester Met. Univ.

P13 Coordination chemistry of a

1,1’-diphosphacobaltocenium salt

Duncan Carmichael Ecole Polytechnique

CNRS

P14 Novel diphosphine bioconjugate for nuclear imaging Ailis Chadwick Univ. Bristol

P15 Bonding and reactivity of phosphorus−antimony peri-

substituted acenaphthenes

Thomasine Curzon Univ. St Andrews

P16 Dismantling the hyperconjugation of π–conjugated

phosphorus heterocycles

Abel de Cózar Univ. the Basque

Country

P17 The sweeter side of SPECT imaging Rachel Doyle Univ. Bristol

P18 Reactivity of sodium phosphanide towards imines Doruk Ergöçmen Univ. Oxford

P19 Reactivity of the 2-phospha-ethynolate anion:

a pathway to phosphinecarboxamides

Erica Faria Univ. Oxford

P20 Stabilising Main Group complexes with auxiliary

phosphine groups

Joey Feld Univ. Oxford

P21 Synthesis and coordination chemistry of cyclo-

triphospirane derivatives with a [L-P3]-core derived from

a Ga2Cl4-bridged triphospha-allyl cation (L = NHC)

Julia Frötschel TU Dresden

P22 New way to run the Wittig Olefination Declan Gilheany Univ. College Dublin

P23 Synthesis and new reactions of 1,2σ3λ3-

oxaphosphetanes

Florian Gleim Univ. Bonn

P24 Reactions of imidazolio-phosphanides with organotin

halides

Florian Goerigk Univ. Stuttgart

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P25 Coordination of phosphaalkynes to transition metals:

potential C-CP cleavage in mesitylphospha-acetylene

Tim Görlich Freie Univ. Berlin

P26 Substituting phosphorus – arsoles as air-stable

alternatives to phospholes

Joshua Green Uppsala Univ.

P27 Fluorophosphonium triflate salt catalysed synthesis of N-

sulfonyl formamidines

Chunxiang Guo Technische Univ.

Dresden

P28 Weak pnictogen bond with bismuth: experimental

evidence based on Bi-P through-space coupling

Dominikus Heift Durham Univ.

P29 Deprotonation and transmetalation of alkoxy substituted

phosphine boranes

Thomas Hettich Univ. Stuttgart

P30 Diphosphatetrahedranes - closing the gap in

phospha-alkyne oligomer chemistry

Gabriele Hierlmeier Univ. Regensburg

P31 Selective activation, functionalization and fragmentation

of white phosphorus by an α-diimine cobalt complex

Christian Hoidn Univ. Regensburg

P32 Frustrated radical pair formation Flip Holtrop Univ. Amsterdam

P33 A new biocompatible diphosphine-peptide chelator:

attaching peptides to 99mTc(V) for targeted SPECT

imaging of disease

Ingebjorg Hungnes King's College London

P34 Synthesis and properties of azophosphines Andrew Jupp Univ. Amsterdam

P35 Synthesising and characterisation of UV curable

phosphorus containing flame retardant polymer

Dilek Kacmaz Yildiz Technical Univ.

P36 Novel access to TTF-fused 1,4-dihydro-1,4-

diphosphinines

Shahriar

Kermanshahian

Univ. Bonn

P37 Towards optical tunable phospholes with functionalities Dieter Klintuch Univ. Kassel

P38 Synthesis and reactivity of a low-valent pyridyl-

diphenylphosphinine iron complex

Julia Leitl Univ. Regensburg

P39 Synthesis and reactivity of the first trans-alkyl cyaphide

complex

Madeleine Levis Univ. Sussex

P40 B(C6F5)3 enabled synthesis of a cyclic

cis-arsaphosphene

Meera Mehta Univ. Oxford

P41 The polymerization of C=P bond of 2-

phosphanaphthalenes

Yanbo Mei ETH Zürich

P42 On the aromaticity of the phosphabenzene –

triphosphabenzene series

Antal Mikehazi Budapest Univ.

P43 Going heavy on cyanates: PCS– and PCSe– Stefan Mitzinger Univ. Oxford

P44 Hetero-cyclopentane-1,3-diyls: modification of molecular

switches

Henrik Müller Univ. Rostock

P45 Tri(N-oleyl)phosphane stock-solution as alternative to

tris(trimethylsilyl)phosphane in the synthesis of narrow

size-distributed InP quantum dots

Michael Müller Technische Univ.

Dresden

P46 Nucleophilic attack @ phosphorus: single and twin

inversion

Kirill Nikitin Univ. College Dublin

P47 Syntheses and structures of new diphosphinoboranes Anna Ordyszewska Gdansk Univ. of

Technology

P48 Steric control in reactions of N-heterocyclic phosphorus

electrophiles with pentacarbonylmanganate(-I)

Marius Papendick Univ. Stuttgart

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P49 Phosphametacyclophanes: from versatile ligands to

tuneable molecular electronics

Kyle Pearce Univ. Sussex

P50 Investigation of the reactivity of [Cp’’’Co(η4-P4)] Martin Piesch Univ. Regensburg

P51 Catalytic dehydropolymerisation of phosphine–boranes

as a route to structurally diverse materials

Diego Resendiz-Lara Univ. Bristol

P52 Post-functionalizations of diphosphahexaarene

derivatives

Carlos Romero-Nieto Univ. Heidelberg

P53 Synthesis of pyridinylidenamino phosphines: One-pot,

scalable access to electron-rich phosphines

Philipp Rotering Univ. Münster

P54 Preparation of a molecular carbon phosphide precursor Moritz Scharnhölz ETH Zürich

P55 Synthesis of synthetic antibacterial polymers and their

applications in bacteria biosensor

Naime Ceren Süer Yildiz Technical Univ.

P56 Experimental and theoretical aspects of Group 15

biradicals [E(µ-NBbp)]2 (E = P, As)

Lilian Sophie Szych Univ. Rostock

P57 The N-cube: a benchtop reactor system for clean and

safe amine alkylation

Edward Thornton Univ. Nottingham

P58 Study of precatalyst degradation leading to the discovery

of a new Ru0 precatalyst for hydrogenation and

dehydrogenation

Daniel Tindall Catalysis Research

Laboratory (CaRLa)

P59 The chemical behaviour of Al/P- and Ga/P-based FLPs

towards strained cyclic compounds

Marten Uebing Univ. Münster

P60 Palladium/black phosphorus nanohybrid: what surface

techniques tell us about the Pd-P interaction

Matteo Vanni CNR-ICCOM

P61 Resolution of P-stereogenic H-phosphinates and

secondary phosphine oxides with TADDOL-derivatives

Bence Varga Budapest Univ.

P62 Pnictaalkene decorated truxene: synthesis and

optoelectronics

Jordann Wells Uppsala Univ.

P63 Synthesis and reactivity of

tris(1,2,5-trimethylpyrrolyl)phosphine

Janina Werra Univ. Münster

P64 Exploring novel phosphonite chemistry and new

bioisosteres

Dean Wheeler Univ. Nottingham

P65 Pt(0)-catalysed hydrophosphination with a triphosphine

substrate

Sarah Williams Univ. Bristol

P66 Luminescent ruthenium-diphosphine complexes as anti-

cancer agents

Dan Wise Univ. Bristol

P67 Oxidation and coordination of peri-substituted

acenaphthenes with phosphorus-selenium functionalities

Lutao Zhang Univ. St Andrews

P68 Synthesis of 4-phosphoryl pyrazolones and their

application in metal recovery

Jianfeng Zhang Technische Univ.

Dresden

P69 Construction of alkyl-substituted pentaphosphido ligands

by P–P condensation

Christoph Ziegler Univ. Regensburg

P70 Tripodal N-centred phosphine ligands: towards a novel

donor set for 99mTc and 186/188Re radiopharmaceutical

formulation

Saul Cooper Imperial College

London

13

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List of Delegates

Delegate Affiliation Email Address

Anne Abels ETH Zürich [email protected]

Vincent Annibale Univ. Bristol P1 [email protected]

Anna Arkhypchuk Uppsala Univ. P2 [email protected]

Peter Bagi Budapest Univ. [email protected]

Thomas Barber Univ. Nottingham O1 [email protected]

Saral Baweja Univ. Leipzig O33 [email protected]

David Becker Univ. Bonn P3 [email protected]

Rhydian Beddoe Univ. Nottingham P4 [email protected]

Steven Beijer Univ. Amsterdam P5 [email protected]

Zoltan Benko Budapest Univ. [email protected]

Sebastian Berthold Univ. Rostock [email protected]

Nicholas Birchall Univ. Stuttgart P6 [email protected]

Helena Brake Univ. Regensburg P7 [email protected]

Alexander Brand Univ. Münster P8 [email protected]

Callum Branfoot Univ. Bristol P9 [email protected]

Philipp Brehm Univ. Bonn P10 [email protected]

Jonas Bresien Univ. Rostock [email protected]

Claire Brodie Durham Univ. O3 [email protected]

Daniel Buzsaki Budapest Univ. P11 [email protected]

Jamie Cadge Univ. Bristol [email protected]

Andy Caffyn MMU, Manchester P12 [email protected]

Maria Caporali CNR-ICCOM [email protected]

Duncan Carmichael Ecole Polytechnique CNRS P13 [email protected]

Ailis Chadwick Univ. Bristol P14 [email protected]

Thomasine Curzon Univ. St Andrews P15 [email protected]

Abel de Cózar Univ. del Pais Vasco P16 [email protected]

Bas de Jong Univ. Amsterdam [email protected]

Fabian Dielmann Univ. Münster [email protected]

Nicolas D. D'Imperio Uppsala Univ. O4 [email protected]

Dustin Dittrich Univ. Münster [email protected]

Rachel Doyle Univ. Bristol P17 [email protected]

Natalia Dunal PCC Rokita [email protected]

Jade Dussart Univ. Paris 13 O6 [email protected]

Luis Dütsch Univ. Regensburg O5 [email protected]

Phil Dyer Durham Univ. [email protected]

Tobias Eder Univ. Münster O11 [email protected]

Andreas Ehlers Univ. Amsterdam [email protected]

Doruk Ergöçmen Univ. Oxford P18 [email protected]

Erica Faria Univ. Oxford P19 [email protected]

Julie Febvay ICSN-CNRS O12 [email protected]

Christoph Feil Univ. Stuttgart O14 [email protected]

Joey Feld Univ. Oxford P20 [email protected]

Julia Frötschel TU Dresden P21 [email protected]

Derek Gates Univ. British Columbia [email protected]

Anna Gerdova Magritek UK [email protected]

Declan Gilheany Univ. College Dublin P22 [email protected]

Florian Gleim Univ. Bonn P23 [email protected]

Dietmar Glindemann Glindemann Polymer Tech. [email protected]

Marion Glindemann Glindemann Polymer Tech. [email protected]

Florian Goerigk Univ. Stuttgart P24 [email protected]

Jose Goicoechea Univ. Oxford [email protected]

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Tim Görlich Freie Univ. Berlin P25 [email protected]

Joshua Green Uppsala Univ. P26 [email protected]

Hansjörg Grützmacher ETH Zurich IndP [email protected]

Chunxiang Guo TU Dresden P27 [email protected]

Zeyu Han Univ. British Columbia O16 [email protected]

Jan-Gerd Hansel LANXESS IndP [email protected]

Dominikus Heift Durham Univ. P28 [email protected]

Thomas Hettich Univ. Stuttgart P29 [email protected]

Gabriele Hierlmeier Univ. Regensburg P30 [email protected]

Lee Higham Newcastle Univ. [email protected]

Muriel Hissler CNRS-Univ. Rennes [email protected]

Luong P. Ho TU Braunschweig O20 [email protected]

Christian Hoidn Univ. Regensburg P31 [email protected]

Flip Holtrop Univ. Amsterdam O18 P32 [email protected]

Yuya Hu LIKAT Leibniz O22 [email protected]

Ingebjorg Hungnes King's College London P33 [email protected]

Iñigo Iglesias CNR-ICCOM O24 [email protected]

Sheena Jackson Solvay [email protected]

Andrew Jupp Univ. Amsterdam P34 [email protected]

Dilek Kacmaz Yildiz Technical Univ. P35 [email protected]

Paul Kamer LIKAT Rostock [email protected]

Mary Kedward Strem Chemicals UK [email protected]

Zsolt Kelemen Univ. Barcelona [email protected]

Shahriar Kermanshahian Univ. Bonn P36 [email protected]

Petr Kilian Univ. St Andrews [email protected]

Ashley King Univ. Bristol [email protected]

Dieter Klintuch Univ. Kassel P37 [email protected]

Robert Konrath Univ. St Andrews O13 [email protected]

Anas Lahlou OCP Group [email protected]

Hortense Lauwick CNRS-Univ. Rennes O26 [email protected]

Bethany Lawson Univ. St Andrews O27 [email protected]

Grégoire Le Corre ETH Zürich O28 [email protected]

Marc Lecouvey Univ. Paris 13 [email protected]

Julia Leitl Univ. Regensburg P38 [email protected]

Ulrich Lennert Univ. Regensburg O29 [email protected]

Madeleine Levis Univ. Sussex P39 [email protected]

Angela Marinetti CNRS [email protected]

Nigel Matthews Strem Chemicals UK [email protected]

Meera Mehta Univ. Oxford P40 [email protected]

Yanbo Mei ETH Zürich P41 [email protected]

Maximilian Menche Catalysis Research Lab. O30 [email protected]

Antal Mikehazi Budapest Univ. P42 [email protected]

Lexy Miles-Hobbs Univ. Bristol O8 [email protected]

Stefan Mitzinger Univ. Oxford P43 [email protected]

Reka Mokrai Budapest Univ. O7 [email protected]

Christian Mueller FU Berlin [email protected]

Henrik Müller Univ. Rostock P44 [email protected]

Michael Müller TU Dresden P45 [email protected]

Kirill Nikitin UCD Dublin P46 [email protected]

Nick Norman Univ. Bristol [email protected]

Laszlo Nyulaszi Budapest Univ. [email protected]

Anna Ordyszewska Gdansk Univ. P47 [email protected]

Andreas Orthaber Uppsala Univ. [email protected]

Darren Ould Cardiff Univ. O32 [email protected]

Marius Papendick Univ. Stuttgart P48 [email protected]

Kyle Pearce Univ. Sussex P49 [email protected]

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Maurizio Peruzzini CNR-ICCOM [email protected]

Martin Piesch Univ. Regensburg P50 [email protected]

Rudolf Pietschnig Univ. Kassel [email protected]

Paul Pringle Univ. Bristol [email protected]

Diego Resendiz-Lara Univ. Bristol P51 [email protected]

Fabian Roesler Univ. Kassel O31 [email protected]

Carlos Romero-Nieto Univ. Heidelberg P52 [email protected]

Philipp Rotering Univ. Münster P53 [email protected]

Chris Russell Univ. Bristol [email protected]

Anna C. Sale Evonik Industries [email protected]

Moritz Scharnhölz ETH Zürich P54 [email protected]

Thomas Schaub BASF SE IndP [email protected]

Willem Schipper WS Consulting IndP [email protected]

Alexander Schmer Univ. Bonn O25 [email protected]

Axel Schulz Univ. Rostock [email protected]

Daniel Scott Univ. Regensburg [email protected]

Samuel Scott Univ. Bristol [email protected]

Alexandra Slawin Univ. St Andrews [email protected]

J. Chris Slootweg Univ. Amsterdam [email protected]

Reinhard Sommerlade Process Design Chemist IndP [email protected]

N. Ceren Süer Yildiz Technical Univ. P55 [email protected]

Tim Suhrbier Univ. Rostock O23 [email protected]

Agnieszka Swist PCC Rokita [email protected]

Lilian S. Szych Univ. Rostock P56 [email protected]

Natalia Szynkiewicz Gdansk Univ. O21 [email protected]

Clemens Taube TU Dresden O19 [email protected]

Jonas C. Tendyck Univ. Münster O17 [email protected]

Edward Thornton Univ. Nottingham P57 [email protected]

Daniel J. Tindall Catalysis Research Lab. P58 [email protected]

Nóra Tóth Budapest Univ. O15 [email protected]

Oliver Townrow Univ. Oxford [email protected]

Marten Uebing WWU Münster P59 [email protected]

Werner Uhl Univ. Münster [email protected]

Steven van Zutphen Italmatch Chemicals IndP [email protected]

Matteo Vanni CNR-ICCOM P60 [email protected]

Bence Varga Budapest Univ. P61 [email protected]

Norbert Weferling WefConsult [email protected]

Gernot Weinberger TU Graz O10 [email protected]

Jordann Wells Uppsala Univ. P62 [email protected]

Janina A. Werra Univ. Münster P63 [email protected]

Dean Wheeler Univ. Nottingham P64 [email protected]

Sarah Williams Univ. Bristol P65 [email protected]

Daniel Wilson Univ. Oxford O9 [email protected]

Dan Wise Univ. Bristol P66 [email protected]

Robert Wolf Univ. Regensburg [email protected]

Gary Woodward Solvay IndP [email protected]

Derek Woollins Univ. St Andrews [email protected]

Friedrich Wossidlo FU Berlin O2 [email protected]

Lutao Zhang Univ. St Andrews P67 [email protected]

Jianfeng Zhang TU Dresden P68 [email protected]

Christoph Ziegler Univ. Regensburg P69 [email protected]

Saul Cooper Imperial College London P70 [email protected]

Chris Harris Solvay IndP [email protected]

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PTFE (“TEFLON”) Sealing Ring for hermetic greaseless Glass Joints

Glindemann D.1,*

1 Glindemann Polymer Technologies,

Goettinger Bogen 15, 06126 Halle, Germany *[email protected]

There is a prejudice that PTFE (often called “Teflon”) is too inelastic to be a hermetic sealant for greaseless conical joints. Therefore, teaching books recommend threaded or flanged “O-ring joints” for hermetic manipulation of air- and moisture sensitive chemicals if joint grease is no option. Here we show (Figure 1) that the common ground conical glass joint can be sealed relatively hermetic and at low cost with a narrow flat PTFE sealing ring (less than 1 mm wide and 0.1 mm thick, weight only 5 mg PTFE). The sealing ring is high-vacuum tight (air leakage rate 10-8… 10-6 mBar*Liter/sec), solvent tight (loss of ethyl acetate out of containers < 0.1 mg/day) and resistant to fluctuation of temperature (freezing-thawing-heating cycles). The reusable PTFE sealing ring prevents stuck joints, is thin enough to be used with all joint clamps and is fixed elastically (without groove) on the glass joint. We demonstrate also a new all-glass-syringe ((Figure 1, 1 - 100 mL) that is gastight at fluctuating temperatures (freezing-thawing-cycles) by a similar exchangeable sealing ring (PTFE) in a groove of the glass piston.

Fig.1. Left: PTFE-sealing ring fixed elastic (no groove necessary). Middle: Sealing ring intransparent without pressure. Right: Sealing ring transparent under sealing pressure. Far right: A similar PTFE ring and a piston groove

make an all-glass-syringe gastight.

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SoC

SSGB

Park Street

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European Workshops on Phosphorus Chemistry

1 2004 Kaiserslautern Deutschland

2 2005 Bonn Deutschland

3 2006 Leipzig Deutschland

4 2007 Zandvoort Nederland

5 2008 Regensburg Deutschland

6 2009 Firenze Italia

7 2010 Budapest Magyarország

8 2011 Münster Deutschland

9 2012 Rennes France

10 2013 Regensburg Deutschland

11 2014 Со́фия България

12 2015 Kassel Deutschland

13 2016 Berlin Deutschland

14 2017 Cluj-Napoca România

15 2018 Uppsala Sverige

16 2019 Bristol United Kingdom