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W.D. Habicher and I. Bauer University of Technology Dresden Institute of Organic Chemistry. Phosphorus Bridgehead Macrobicycles Synthesis, Structures, Isomerism. HAS-Phosphites as Antioxidants for Synthetic Polymers. processing stabilizer.
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W.D. Habicher and I. Bauer University of Technology Dresden Institute of Organic Chemistry Phosphorus Bridgehead MacrobicyclesSynthesis, Structures, Isomerism
HAS-Phosphites as Antioxidants for Synthetic Polymers processing stabilizer light and long term thermo stabilizer long term thermo stabilizer
Oligomeric Hindered Amine Phosphites as Polymer Stabilizers-Phosphorous Amide Method-
Oligomeric Hindered Amine Phosphites as Polymer Stabilizers-Phosphorous Chloride Method- Unexpected Result: Formation of Macrocyclic Byproducts !!!
Phosphorus Containing Macrocycles in Synthetic Organic and Supramolecular Chemistry • Tricoordinated phosphorus containing macrocycles • can function as ligands for transition metal catalyzed reactions • (Heck reaction, hydroformylation, homogenous catalytic hydration, • Suzuki coupling, Sonogashira coupling etc.) • Pentavalent phosphoryl macrocycles • can be used for metal complexation and for molecular recognition of • H donating substrates also of biologically interesting compounds • such as amino acids
Principles of Macrocycle Formation B. Dietrich, P. Viout, J.-M. Lehn, "Macrocyclic Chemistry: Aspects of Organic and Inorganic Supramolecular Chemistry", VCH, Weinheim, New York, Basel, Cambridge, 1992.
X = Cl, NR Y = lone pair, O, S P chloride method P amidite method 2 Synthesis of Macrocycles with P(III) and P(V) Acid Derivatives
P-Containing Macrobicycles - Principles of Formation I - B. Dietrich, P. Viout, J.-M. Lehn, "Macrocyclic Chemistry: Aspects of Organic and Inorganic Supramolecular Chemistry", VCH, Weinheim, New York, Basel, Cambridge, 1992.
flexible arms In,Out-Isomerism diastereomers relatively rigid arms diastereomers R.W. Alder, S.P. East, Chem. Rev.1996, 96, 2097-2111
Oxidation of in,out-PhosphiteMacrobicycle 1 2 3 31P{1H} NMR: = 147.2 (in), 128.0 (out) 31P{1H} NMR: = 147.9 (in), -21.6 (out) 31P{1H} NMR: = -11.2 (in), -21.8 (out) 1 2 3
Double-CappingMethod for Macrobicycle Formation II in,in 31P NMR after rough chroma- tography out,out macropolycycles in,out
X-Ray Structure of out,out-p,p,p-Phenylene Bridged Phosphite-Macrobicycle 10.5 Å view into the cavity view along the P-P-axis
X-Ray Structure of in,in-p,p,p-Phenylene Bridged Phosphite-Macrobicycle 8.5 Å Conformer A view into the cavity 8.3 Å view along P-P-axis Conformer B
Double-CappingMethod for the Formation of p,m,p-Phenylene Bridged Phosphorus Brigdehead Macrobicycles III 31P NMR of the crude product out,out in,in in,out
X-Ray Structure of out,out-p,m,p-Phenylene Bridged Phosphite-Macrobicycle view along P-P-axis view into the cavity
X-Ray Structure of in,in-p,m,p-Phenylene Bridged Phosphite-Macrobicycle Conformer A view into the cavity Conformer B view along P-P-axis
1,2 3 4 5 Extraction of Metal Cations from Aqueous Solution with Macrocyclic P(III)- and P(V) compounds 1 Extractability [%] 2 3 X = lone pair 4 X = S 5 X = O
Acknowledgement Dr. I. Bauer Dr. M. Gruner G. Theumer (TU Dresden) Prof. I. Antipin Dr. I. I. Stoikov Dr. S. Solovieva (Kazan State University) Prof. E. Kazakova Dr. A. Prosvirkin Dr. A. Ziganshina (A.E. Arbuzov Institute Kazan) Prof. R. Schmutzler, Prof. P.G. Jones, Dr. H. Thönnessen (TU Braunschweig) Dr. R. Fröhlich (University Münster) Financial support DFG: Graduiertenkolleg ”Struktur-Eigenschafts-Beziehungen bei Heterocyclen” DFG + RFFI: Projekt 2133/3-1: „Synthese neuer phosphorhaltiger Makrocyclen und Kryptanden“ Fonds der Chemischen Industrie
„Pyrocatechol phosphites“ P.A. Kirpichnikov etal.
Synthesis of Macrocycles with P(III) and P(V) Acid Derivatives
Stereoisomerism of Tetracoordinated P(III)- and P(V)-Macrocycles 2 Phosphorus Centers 3 Phosphorus Centers 4 Phosphorus Centers X = lone pair, O
Different Ring Sizes of P-Macrocycles Dimers + Trimers Dimers Tetramer
P-Containing Macrocycles from Bisphenols and Naphthols by Phosphorous Amide Method – Literature examples Y. I. Blokhin, D. V. Gusev, V. K. Belsky, A. I. Stash, E. E. Nifantev, Phosphorus, Sulfur and Silicon 1995, 102, 143. Y. I. Blokhin, F. M. Galiaskarova, D. V. Gusev, M. Y. Ergashov, V. K. Belsky and E. E. Nifantev, Phosphorus, Sulfur and Silicon 1996,111, 170.
Phosphorous Amide Method I-Asymmetric P-Macrocycles as Unstable Intermediates-- Formation of Symmetric P-Macrocycles and Open Chain Products-
Phosphorous Amide Method II-Asymmetric P-Macrocycles as Unstable Intermediates-- Formation of Symmetric P-Macrocycles and Open Chain Products-
P-Containing Macrobicycles - Principles of Formation II - B. Dietrich, P. Viout, J.-M. Lehn, "Macrocyclic Chemistry: Aspects of Organic and Inorganic Supramolecular Chemistry", VCH, Weinheim, New York, Basel, Cambridge, 1992.
P-Containing Macrobicycles - Principles of Formation III - B. Dietrich, P. Viout, J.-M. Lehn, "Macrocyclic Chemistry: Aspects of Organic and Inorganic Supramolecular Chemistry", VCH, Weinheim, New York, Basel, Cambridge, 1992.
„In-ness“ and “Out-ness“- of Bridgehead Substituents in-CR 0° £ q£ 90° out-CR 90°£ q £ 180° R.W. Alder, S.P. East, Chem. Rev.1996, 96, 2097-2111
Phosphorus Bridgehead Macrobicycles in Literature B.P. Friedrichsen, R.P. Powell, H.W. Whitlock, J. Am. Chem. Soc. 1990, 112, 8931-8941.
Phosphorus Bridgehead Macrobicycles in Literature J. Mitjaville, A.-M. Caminade, J.-P. Majoral, J. Chem. Soc.Chem. Commun.1994, 112, 2161. Ch.B. Allen, L.O. Spreer, J. Org. Chem.1994, 59, 7695-7700. A.A. Chaikovskaja, T.N. Kudrya, R.I. Yurchenko, O.M. Voitsekhovskaya, A.M. Pinchuk, Zh. Obshch. Khim.1988, 58, 1925-1926.
Oxidation of Isomeric Phosphite Cryptands out,out-isomer in,out-isomer in,in-isomer
Natural Products Showing in,out-Isomerism 3a-Acetoxy-15b- hydroxy-7,16-seco- trinervita-7,11-diene Secotrinerviten- 2b,3a-diol Ingenol
X-Ray Structure of a Novel Bisdioxaphospha[3.1.1.]p,m,p-Cyclophane