[{"_id":"42017","user_id":"237","department":[{"_id":"314"}],"keyword":["Materials Chemistry","Inorganic Chemistry","Polymers and Plastics","Organic Chemistry"],"language":[{"iso":"eng"}],"type":"journal_article","publication":"Macromolecules","status":"public","date_updated":"2023-02-10T15:23:52Z","publisher":"American Chemical Society (ACS)","author":[{"last_name":"Kramer","full_name":"Kramer, Thomas","first_name":"Thomas"},{"full_name":"Schweins, Ralf","last_name":"Schweins","first_name":"Ralf"},{"last_name":"Huber","full_name":"Huber, Klaus","id":"237","first_name":"Klaus"}],"date_created":"2023-02-10T15:23:24Z","volume":38,"title":"Silsesquioxane Molecules and Polystyrene Chains as a Model System for Colloid−Polymer Mixtures in the Protein Limit","doi":"10.1021/ma048766x","publication_status":"published","publication_identifier":{"issn":["0024-9297","1520-5835"]},"issue":"1","year":"2005","citation":{"ama":"Kramer T, Schweins R, Huber K. Silsesquioxane Molecules and Polystyrene Chains as a Model System for Colloid−Polymer Mixtures in the Protein Limit. Macromolecules. 2005;38(1):151-159. doi:10.1021/ma048766x","ieee":"T. Kramer, R. Schweins, and K. Huber, “Silsesquioxane Molecules and Polystyrene Chains as a Model System for Colloid−Polymer Mixtures in the Protein Limit,” Macromolecules, vol. 38, no. 1, pp. 151–159, 2005, doi: 10.1021/ma048766x.","chicago":"Kramer, Thomas, Ralf Schweins, and Klaus Huber. “Silsesquioxane Molecules and Polystyrene Chains as a Model System for Colloid−Polymer Mixtures in the Protein Limit.” Macromolecules 38, no. 1 (2005): 151–59. https://doi.org/10.1021/ma048766x.","apa":"Kramer, T., Schweins, R., & Huber, K. (2005). Silsesquioxane Molecules and Polystyrene Chains as a Model System for Colloid−Polymer Mixtures in the Protein Limit. Macromolecules, 38(1), 151–159. https://doi.org/10.1021/ma048766x","short":"T. Kramer, R. Schweins, K. Huber, Macromolecules 38 (2005) 151–159.","mla":"Kramer, Thomas, et al. “Silsesquioxane Molecules and Polystyrene Chains as a Model System for Colloid−Polymer Mixtures in the Protein Limit.” Macromolecules, vol. 38, no. 1, American Chemical Society (ACS), 2005, pp. 151–59, doi:10.1021/ma048766x.","bibtex":"@article{Kramer_Schweins_Huber_2005, title={Silsesquioxane Molecules and Polystyrene Chains as a Model System for Colloid−Polymer Mixtures in the Protein Limit}, volume={38}, DOI={10.1021/ma048766x}, number={1}, journal={Macromolecules}, publisher={American Chemical Society (ACS)}, author={Kramer, Thomas and Schweins, Ralf and Huber, Klaus}, year={2005}, pages={151–159} }"},"intvolume":" 38","page":"151-159"},{"language":[{"iso":"eng"}],"keyword":["Materials Chemistry","Inorganic Chemistry","Polymers and Plastics","Organic Chemistry"],"department":[{"_id":"314"}],"user_id":"237","_id":"42014","status":"public","publication":"Macromolecules","type":"journal_article","doi":"10.1021/ma051308j","title":"Coil Dimensions of Polystyrene Chains in Colloid−Polymer Mixtures at the Protein Limit:  A SANS Study","volume":38,"author":[{"first_name":"Thomas","last_name":"Kramer","full_name":"Kramer, Thomas"},{"first_name":"Ralf","full_name":"Schweins, Ralf","last_name":"Schweins"},{"last_name":"Huber","id":"237","full_name":"Huber, Klaus","first_name":"Klaus"}],"date_created":"2023-02-10T15:20:44Z","publisher":"American Chemical Society (ACS)","date_updated":"2023-02-10T15:21:03Z","intvolume":" 38","page":"9783-9793","citation":{"ama":"Kramer T, Schweins R, Huber K. Coil Dimensions of Polystyrene Chains in Colloid−Polymer Mixtures at the Protein Limit:  A SANS Study. Macromolecules. 2005;38(23):9783-9793. doi:10.1021/ma051308j","ieee":"T. Kramer, R. Schweins, and K. Huber, “Coil Dimensions of Polystyrene Chains in Colloid−Polymer Mixtures at the Protein Limit:  A SANS Study,” Macromolecules, vol. 38, no. 23, pp. 9783–9793, 2005, doi: 10.1021/ma051308j.","chicago":"Kramer, Thomas, Ralf Schweins, and Klaus Huber. “Coil Dimensions of Polystyrene Chains in Colloid−Polymer Mixtures at the Protein Limit:  A SANS Study.” Macromolecules 38, no. 23 (2005): 9783–93. https://doi.org/10.1021/ma051308j.","apa":"Kramer, T., Schweins, R., & Huber, K. (2005). Coil Dimensions of Polystyrene Chains in Colloid−Polymer Mixtures at the Protein Limit:  A SANS Study. Macromolecules, 38(23), 9783–9793. https://doi.org/10.1021/ma051308j","mla":"Kramer, Thomas, et al. “Coil Dimensions of Polystyrene Chains in Colloid−Polymer Mixtures at the Protein Limit:  A SANS Study.” Macromolecules, vol. 38, no. 23, American Chemical Society (ACS), 2005, pp. 9783–93, doi:10.1021/ma051308j.","short":"T. Kramer, R. Schweins, K. Huber, Macromolecules 38 (2005) 9783–9793.","bibtex":"@article{Kramer_Schweins_Huber_2005, title={Coil Dimensions of Polystyrene Chains in Colloid−Polymer Mixtures at the Protein Limit:  A SANS Study}, volume={38}, DOI={10.1021/ma051308j}, number={23}, journal={Macromolecules}, publisher={American Chemical Society (ACS)}, author={Kramer, Thomas and Schweins, Ralf and Huber, Klaus}, year={2005}, pages={9783–9793} }"},"year":"2005","issue":"23","publication_identifier":{"issn":["0024-9297","1520-5835"]},"publication_status":"published"},{"citation":{"short":"M. Tiemann, Ö. Weiß, J. Hartikainen, F. Marlow, M. Lindén, ChemPhysChem (2005) 2113–2119.","bibtex":"@article{Tiemann_Weiß_Hartikainen_Marlow_Lindén_2005, title={Early Stages of ZnS Nanoparticle Growth Studied by In-Situ Stopped-Flow UV Absorption Spectroscopy}, DOI={10.1002/cphc.200500163}, journal={ChemPhysChem}, author={Tiemann, Michael and Weiß, Özlem and Hartikainen, Juha and Marlow, Frank and Lindén, Mika}, year={2005}, pages={2113–2119} }","mla":"Tiemann, Michael, et al. “Early Stages of ZnS Nanoparticle Growth Studied by In-Situ Stopped-Flow UV Absorption Spectroscopy.” ChemPhysChem, 2005, pp. 2113–19, doi:10.1002/cphc.200500163.","apa":"Tiemann, M., Weiß, Ö., Hartikainen, J., Marlow, F., & Lindén, M. (2005). Early Stages of ZnS Nanoparticle Growth Studied by In-Situ Stopped-Flow UV Absorption Spectroscopy. ChemPhysChem, 2113–2119. https://doi.org/10.1002/cphc.200500163","ieee":"M. Tiemann, Ö. Weiß, J. Hartikainen, F. Marlow, and M. Lindén, “Early Stages of ZnS Nanoparticle Growth Studied by In-Situ Stopped-Flow UV Absorption Spectroscopy,” ChemPhysChem, pp. 2113–2119, 2005, doi: 10.1002/cphc.200500163.","chicago":"Tiemann, Michael, Özlem Weiß, Juha Hartikainen, Frank Marlow, and Mika Lindén. “Early Stages of ZnS Nanoparticle Growth Studied by In-Situ Stopped-Flow UV Absorption Spectroscopy.” ChemPhysChem, 2005, 2113–19. https://doi.org/10.1002/cphc.200500163.","ama":"Tiemann M, Weiß Ö, Hartikainen J, Marlow F, Lindén M. Early Stages of ZnS Nanoparticle Growth Studied by In-Situ Stopped-Flow UV Absorption Spectroscopy. ChemPhysChem. Published online 2005:2113-2119. doi:10.1002/cphc.200500163"},"page":"2113-2119","year":"2005","publication_status":"published","quality_controlled":"1","publication_identifier":{"issn":["1439-4235","1439-7641"]},"doi":"10.1002/cphc.200500163","title":"Early Stages of ZnS Nanoparticle Growth Studied by In-Situ Stopped-Flow UV Absorption Spectroscopy","date_created":"2021-10-09T09:48:34Z","author":[{"full_name":"Tiemann, Michael","id":"23547","orcid":"0000-0003-1711-2722","last_name":"Tiemann","first_name":"Michael"},{"first_name":"Özlem","full_name":"Weiß, Özlem","last_name":"Weiß"},{"first_name":"Juha","last_name":"Hartikainen","full_name":"Hartikainen, Juha"},{"last_name":"Marlow","full_name":"Marlow, Frank","first_name":"Frank"},{"last_name":"Lindén","full_name":"Lindén, Mika","first_name":"Mika"}],"date_updated":"2023-03-09T08:58:26Z","status":"public","abstract":[{"lang":"eng","text":"The early stages of ZnS nanoparticle growth from supersaturated solution are investigated in situ by stopped-flow UV absorption spectroscopy with a time resolution of 1.28 ms. A model for data analysis is suggested which makes it possible to study both the average particle radius and the concentration. The average radii lie in the sub-nanometer range. During the first 40 ms, growth is predominantly governed by ripening."}],"type":"journal_article","publication":"ChemPhysChem","language":[{"iso":"eng"}],"extern":"1","article_type":"original","user_id":"23547","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"}],"_id":"25995"},{"date_updated":"2023-03-09T08:58:46Z","date_created":"2021-10-09T09:47:51Z","author":[{"first_name":"Jan","last_name":"Roggenbuck","full_name":"Roggenbuck, Jan"},{"first_name":"Michael","last_name":"Tiemann","orcid":"0000-0003-1711-2722","id":"23547","full_name":"Tiemann, Michael"}],"title":"Ordered Mesoporous Magnesium Oxide with High Thermal Stability Synthesized by Exotemplating Using CMK-3 Carbon","doi":"10.1021/ja043605u","publication_identifier":{"issn":["0002-7863","1520-5126"]},"quality_controlled":"1","publication_status":"published","year":"2005","page":"1096-1097","citation":{"short":"J. Roggenbuck, M. Tiemann, Journal of the American Chemical Society (2005) 1096–1097.","bibtex":"@article{Roggenbuck_Tiemann_2005, title={Ordered Mesoporous Magnesium Oxide with High Thermal Stability Synthesized by Exotemplating Using CMK-3 Carbon}, DOI={10.1021/ja043605u}, journal={Journal of the American Chemical Society}, author={Roggenbuck, Jan and Tiemann, Michael}, year={2005}, pages={1096–1097} }","mla":"Roggenbuck, Jan, and Michael Tiemann. “Ordered Mesoporous Magnesium Oxide with High Thermal Stability Synthesized by Exotemplating Using CMK-3 Carbon.” Journal of the American Chemical Society, 2005, pp. 1096–97, doi:10.1021/ja043605u.","apa":"Roggenbuck, J., & Tiemann, M. (2005). Ordered Mesoporous Magnesium Oxide with High Thermal Stability Synthesized by Exotemplating Using CMK-3 Carbon. Journal of the American Chemical Society, 1096–1097. https://doi.org/10.1021/ja043605u","ama":"Roggenbuck J, Tiemann M. Ordered Mesoporous Magnesium Oxide with High Thermal Stability Synthesized by Exotemplating Using CMK-3 Carbon. Journal of the American Chemical Society. Published online 2005:1096-1097. doi:10.1021/ja043605u","chicago":"Roggenbuck, Jan, and Michael Tiemann. “Ordered Mesoporous Magnesium Oxide with High Thermal Stability Synthesized by Exotemplating Using CMK-3 Carbon.” Journal of the American Chemical Society, 2005, 1096–97. https://doi.org/10.1021/ja043605u.","ieee":"J. Roggenbuck and M. Tiemann, “Ordered Mesoporous Magnesium Oxide with High Thermal Stability Synthesized by Exotemplating Using CMK-3 Carbon,” Journal of the American Chemical Society, pp. 1096–1097, 2005, doi: 10.1021/ja043605u."},"_id":"25994","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"}],"user_id":"23547","article_type":"original","extern":"1","language":[{"iso":"eng"}],"publication":"Journal of the American Chemical Society","type":"journal_article","abstract":[{"text":"Periodically ordered mesoporous magnesium oxides were synthesized by utilization of mesoporous CMK-3 carbon as exotemplate. The products exhibit high thermal stability and basic properties, which makes them promising for application in heterogeneous basic catalysis.","lang":"eng"}],"status":"public"},{"language":[{"iso":"eng"}],"_id":"58598","user_id":"495","department":[{"_id":"321"},{"_id":"35"},{"_id":"301"}],"abstract":[{"lang":"eng","text":"AbstractA series of bis‐guanidine ligands designed for use in biomimetic coordination chemistry has been extended to a library matrix combining unprecedented substitutional flexibility within the guanidyl residues with a wide range of aliphatic and aromatic spacers connecting these functionalities. The underlying protocol can be used with predefined ureas as well as secondary amines to build up these units by reaction with phosgene if the ureas are otherwise unavailable. In the latter case, the resulting urea intermediates do not have to be isolated as the reaction proceeds further with additional phosgene to yield a chloroformamidinium chloride which is transformed into the bis‐guanidine functionality by subsequent reaction with a suitable primary diamine in the presence of triethylamine as an auxiliary base. This concept has been used to synthesise and characterise more then two dozen different bis‐guanidines based on 12 discrete monoguanidine units and seven different spacers. These spacers have been chosen such that the most important phenotypes have been dealt with and which range from rigid to more flexible scaffolds. In addition to spacers with no metal‐binding capabilities, other species containing further donor functions such as N‐methyldiphenyleneamine or pyridine‐2,6‐diyl have also been used. The substitution patterns of the guanidine residues can be classified into acyclic and cyclic types. Among the cyclic types, one subset is characterised by five‐ or six‐membered heterocycles containing both the amino nitrogen atoms and another one by individual N‐heterocyclic systems for each amino nitrogen. Structurally characterised examples are 2‐{2‐[2‐(tetramethylguanidi­no)ethoxy]ethoxy}‐1‐(tetramethylguanidino)ethane (TMG2doo) in its diprotonated form and 2,2′‐bis[2N‐(1,1′,3,3′‐tetramethylguanidine)]diphenyleneamine (TMG2PA) as wellas N1,N3‐bis(dimorpholinomethylene)propane‐1,3‐diamine (DMorphG2p) as free bases. For the permethylated bis‐guanidine derivatives, the barrier to rotation around the (C=N)guanidine bond has been determined by means of temperature‐dependent EXSY 1H NMR spectroscopy to range between 54 and 79 kJ mol–1 depending on the type of spacer. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)"}],"status":"public","type":"journal_article","publication":"European Journal of Organic Chemistry","title":"A Library of Peralkylated Bis‐guanidine Ligands for Use in Biomimetic Coordination Chemistry","doi":"10.1002/ejoc.200500340","date_updated":"2025-02-12T09:30:43Z","publisher":"Wiley","author":[{"first_name":"Sonja","full_name":"Herres‐Pawlis, Sonja","last_name":"Herres‐Pawlis"},{"first_name":"Adam","full_name":"Neuba, Adam","last_name":"Neuba"},{"last_name":"Seewald","full_name":"Seewald, Oliver","id":"495","first_name":"Oliver"},{"full_name":"Seshadri, Tarimala","last_name":"Seshadri","first_name":"Tarimala"},{"first_name":"Hans","last_name":"Egold","full_name":"Egold, Hans"},{"first_name":"Ulrich","full_name":"Flörke, Ulrich","last_name":"Flörke"},{"first_name":"Gerald","full_name":"Henkel, Gerald","last_name":"Henkel"}],"date_created":"2025-02-12T09:27:00Z","volume":2005,"year":"2005","citation":{"apa":"Herres‐Pawlis, S., Neuba, A., Seewald, O., Seshadri, T., Egold, H., Flörke, U., & Henkel, G. (2005). A Library of Peralkylated Bis‐guanidine Ligands for Use in Biomimetic Coordination Chemistry. European Journal of Organic Chemistry, 2005(22), 4879–4890. https://doi.org/10.1002/ejoc.200500340","short":"S. Herres‐Pawlis, A. Neuba, O. Seewald, T. Seshadri, H. Egold, U. Flörke, G. Henkel, European Journal of Organic Chemistry 2005 (2005) 4879–4890.","mla":"Herres‐Pawlis, Sonja, et al. “A Library of Peralkylated Bis‐guanidine Ligands for Use in Biomimetic Coordination Chemistry.” European Journal of Organic Chemistry, vol. 2005, no. 22, Wiley, 2005, pp. 4879–90, doi:10.1002/ejoc.200500340.","bibtex":"@article{Herres‐Pawlis_Neuba_Seewald_Seshadri_Egold_Flörke_Henkel_2005, title={A Library of Peralkylated Bis‐guanidine Ligands for Use in Biomimetic Coordination Chemistry}, volume={2005}, DOI={10.1002/ejoc.200500340}, number={22}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Herres‐Pawlis, Sonja and Neuba, Adam and Seewald, Oliver and Seshadri, Tarimala and Egold, Hans and Flörke, Ulrich and Henkel, Gerald}, year={2005}, pages={4879–4890} }","chicago":"Herres‐Pawlis, Sonja, Adam Neuba, Oliver Seewald, Tarimala Seshadri, Hans Egold, Ulrich Flörke, and Gerald Henkel. “A Library of Peralkylated Bis‐guanidine Ligands for Use in Biomimetic Coordination Chemistry.” European Journal of Organic Chemistry 2005, no. 22 (2005): 4879–90. https://doi.org/10.1002/ejoc.200500340.","ieee":"S. Herres‐Pawlis et al., “A Library of Peralkylated Bis‐guanidine Ligands for Use in Biomimetic Coordination Chemistry,” European Journal of Organic Chemistry, vol. 2005, no. 22, pp. 4879–4890, 2005, doi: 10.1002/ejoc.200500340.","ama":"Herres‐Pawlis S, Neuba A, Seewald O, et al. A Library of Peralkylated Bis‐guanidine Ligands for Use in Biomimetic Coordination Chemistry. European Journal of Organic Chemistry. 2005;2005(22):4879-4890. doi:10.1002/ejoc.200500340"},"intvolume":" 2005","page":"4879-4890","publication_status":"published","publication_identifier":{"issn":["1434-193X","1099-0690"]},"issue":"22"},{"language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"AbstractSyntheses and Structure of Chiral Metallatetrahedron Complexes of the Type [Re2(M1PPh3)(M2PPh3)(μ‐PCy2)(CO)7C≡CPh] (M1 = Ag, Au; M2 = Cu, Ag, Au)From the reaction of Li[Re2(μ‐H)(μ‐PCy2)(CO)7(C(Ph)O)] (1) with Ph3AuC≡CPh both benzaldehyde and the trinuclear complex Li[Re2(AuPPh3)(μ‐PCy2)(CO)7C≡CPh] (2a) were obtained in high yield. The complex anion was isolated as its PPh4‐salt 2b. The latter reacts with coinage metal complexes PPh3M2Cl [M2 = Cu, Ag, Au] to give chiral heterometallatetrahedranes of the general formula [Re2(AuPPh3)(M2PPh3)(μ‐PCy2)(CO)7C≡CPh] (M2 = Cu 3a, Ag 3b, Au 3c). The corresponding complex [Re2(AgPPh3)2(μ‐PCy2)(CO)7C≡CPh] (3d) is obtained from the reaction of [Re2(AgPPh3)2(μ‐PCy2)(CO)7Cl] (4) with LiC≡CPh. 3d undergoes a metathesis reaction in the presence of PPh3CuCl giving [Re2(AgPPh3)(CuPPh3)(μ‐PCy2)(CO)7C≡CPh] (3e) and PPh3AgCl. Analogous metathesis reactions are observed when 3c is reacted with PPh3AgCl or PPh3CuCl giving 3a or 3b, respectively. The reaction of 1 with PPh3AuCl gives benzaldehyde and Li[Re2(AuPPh3)(μ‐PCy2)(CO)7Cl] (5a) which upon reaction with PhLi forms the trinuclear complex Li[Re2(AuPPh3)(μ‐PCy2)(CO)7Ph] (6a). Again this complex was isolated as its PPh4‐salt 6b. In contrast to 2b, 6b reacts with one equivalent of Ph3PAuCl by transmetalation to give Ph3PAuPh and PPh4[Re2(AuPPh3)(μ‐PCy2)(CO)7Cl] (5b). The X‐ray structures of the compounds 3a, 3b, 3e and 4 are reported."}],"publication":"Zeitschrift für anorganische und allgemeine Chemie","title":"Synthese und Struktur chiraler Heterometallatetrahedrane des Typs [Re2(M1PPh3)(M2PPh3)(μ‐PCy2)(CO)7C≡CPh] (M1 = Ag, Au; M2 = Cu, Ag, Au)","publisher":"Wiley","date_created":"2025-02-12T09:26:12Z","year":"2005","issue":"2","_id":"58597","user_id":"495","department":[{"_id":"321"},{"_id":"35"},{"_id":"301"}],"status":"public","type":"journal_article","doi":"10.1002/zaac.200500340","date_updated":"2025-02-12T09:30:52Z","author":[{"first_name":"Oliver","last_name":"Seewald","id":"495","full_name":"Seewald, Oliver"},{"first_name":"Ulrich","full_name":"Flörke, Ulrich","last_name":"Flörke"},{"first_name":"Hans","full_name":"Egold, Hans","last_name":"Egold"},{"last_name":"Haupt","full_name":"Haupt, Hans‐Jürgen","first_name":"Hans‐Jürgen"},{"first_name":"Meinhard","last_name":"Schwefer","full_name":"Schwefer, Meinhard"}],"volume":632,"citation":{"bibtex":"@article{Seewald_Flörke_Egold_Haupt_Schwefer_2005, title={Synthese und Struktur chiraler Heterometallatetrahedrane des Typs [Re2(M1PPh3)(M2PPh3)(μ‐PCy2)(CO)7C≡CPh] (M1 = Ag, Au; M2 = Cu, Ag, Au)}, volume={632}, DOI={10.1002/zaac.200500340}, number={2}, journal={Zeitschrift für anorganische und allgemeine Chemie}, publisher={Wiley}, author={Seewald, Oliver and Flörke, Ulrich and Egold, Hans and Haupt, Hans‐Jürgen and Schwefer, Meinhard}, year={2005}, pages={204–210} }","mla":"Seewald, Oliver, et al. “Synthese Und Struktur Chiraler Heterometallatetrahedrane Des Typs [Re2(M1PPh3)(M2PPh3)(Μ‐PCy2)(CO)7C≡CPh] (M1 = Ag, Au; M2 = Cu, Ag, Au).” Zeitschrift Für Anorganische Und Allgemeine Chemie, vol. 632, no. 2, Wiley, 2005, pp. 204–10, doi:10.1002/zaac.200500340.","short":"O. Seewald, U. Flörke, H. Egold, H. Haupt, M. Schwefer, Zeitschrift Für Anorganische Und Allgemeine Chemie 632 (2005) 204–210.","apa":"Seewald, O., Flörke, U., Egold, H., Haupt, H., & Schwefer, M. (2005). Synthese und Struktur chiraler Heterometallatetrahedrane des Typs [Re2(M1PPh3)(M2PPh3)(μ‐PCy2)(CO)7C≡CPh] (M1 = Ag, Au; M2 = Cu, Ag, Au). Zeitschrift Für Anorganische Und Allgemeine Chemie, 632(2), 204–210. https://doi.org/10.1002/zaac.200500340","ama":"Seewald O, Flörke U, Egold H, Haupt H, Schwefer M. Synthese und Struktur chiraler Heterometallatetrahedrane des Typs [Re2(M1PPh3)(M2PPh3)(μ‐PCy2)(CO)7C≡CPh] (M1 = Ag, Au; M2 = Cu, Ag, Au). Zeitschrift für anorganische und allgemeine Chemie. 2005;632(2):204-210. doi:10.1002/zaac.200500340","chicago":"Seewald, Oliver, Ulrich Flörke, Hans Egold, Hans‐Jürgen Haupt, and Meinhard Schwefer. “Synthese Und Struktur Chiraler Heterometallatetrahedrane Des Typs [Re2(M1PPh3)(M2PPh3)(Μ‐PCy2)(CO)7C≡CPh] (M1 = Ag, Au; M2 = Cu, Ag, Au).” Zeitschrift Für Anorganische Und Allgemeine Chemie 632, no. 2 (2005): 204–10. https://doi.org/10.1002/zaac.200500340.","ieee":"O. Seewald, U. Flörke, H. Egold, H. Haupt, and M. Schwefer, “Synthese und Struktur chiraler Heterometallatetrahedrane des Typs [Re2(M1PPh3)(M2PPh3)(μ‐PCy2)(CO)7C≡CPh] (M1 = Ag, Au; M2 = Cu, Ag, Au),” Zeitschrift für anorganische und allgemeine Chemie, vol. 632, no. 2, pp. 204–210, 2005, doi: 10.1002/zaac.200500340."},"page":"204-210","intvolume":" 632","publication_status":"published","publication_identifier":{"issn":["0044-2313","1521-3749"]}},{"issue":"4","quality_controlled":"1","publication_identifier":{"issn":["0148-6055","1520-8516"]},"publication_status":"published","page":"881-894","intvolume":" 48","citation":{"ama":"Cormier RJ, Schmidt C, Callaghan PT. Director reorientation of a side-chain liquid crystalline polymer under extensional flow. Journal of Rheology. 2004;48(4):881-894. doi:10.1122/1.1753278","ieee":"R. J. Cormier, C. Schmidt, and P. T. Callaghan, “Director reorientation of a side-chain liquid crystalline polymer under extensional flow,” Journal of Rheology, vol. 48, no. 4, pp. 881–894, 2004, doi: 10.1122/1.1753278.","chicago":"Cormier, Ryan J., Claudia Schmidt, and Paul T. Callaghan. “Director Reorientation of a Side-Chain Liquid Crystalline Polymer under Extensional Flow.” Journal of Rheology 48, no. 4 (2004): 881–94. https://doi.org/10.1122/1.1753278.","bibtex":"@article{Cormier_Schmidt_Callaghan_2004, title={Director reorientation of a side-chain liquid crystalline polymer under extensional flow}, volume={48}, DOI={10.1122/1.1753278}, number={4}, journal={Journal of Rheology}, publisher={Society of Rheology}, author={Cormier, Ryan J. and Schmidt, Claudia and Callaghan, Paul T.}, year={2004}, pages={881–894} }","short":"R.J. Cormier, C. Schmidt, P.T. Callaghan, Journal of Rheology 48 (2004) 881–894.","mla":"Cormier, Ryan J., et al. “Director Reorientation of a Side-Chain Liquid Crystalline Polymer under Extensional Flow.” Journal of Rheology, vol. 48, no. 4, Society of Rheology, 2004, pp. 881–94, doi:10.1122/1.1753278.","apa":"Cormier, R. J., Schmidt, C., & Callaghan, P. T. (2004). Director reorientation of a side-chain liquid crystalline polymer under extensional flow. 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