Mark M. Green - Publications

1980- Chemical and Biomolecular Engineering New York University, New York, NY, United States 
Polymer Chemistry

52 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2011 Jain V, Cheon KS, Tang K, Jha S, Green MM. Chiral cooperativity in helical polymers Israel Journal of Chemistry. 51: 1067-1074. DOI: 10.1002/Ijch.201100050  0.323
2007 Tomar S, Green MM, Day LA. DNA-protein interactions as the source of large-length-scale chirality evident in the liquid crystal behavior of filamentous bacteriophages. Journal of the American Chemical Society. 129: 3367-75. PMID 17316002 DOI: 10.1021/Ja068498D  0.578
2007 Cheon KS, Green MM. Structural deuterium isotope effects reveal the cooperativity of polymers Journal of Labelled Compounds and Radiopharmaceuticals. 50: 961-966. DOI: 10.1002/Jlcr.1401  0.354
2006 Green MM, White JL, Mirau P, Scheinfeld MH. C - H to O hydrogen bonding: The attractive interaction in the blend between polystyrene and poly(vinyl methyl ether) Macromolecules. 39: 5971-5973. DOI: 10.1021/Ma061376L  0.309
2006 Shibaev PV, Chiappetta D, Sanford RL, Palffy-Muhoray P, Moreira M, Cao W, Green MM. Color Changing Cholesteric Polymer Films Sensitive to Amino Acids Macromolecules. 39: 3986-3992. DOI: 10.1021/Ma052046O  0.306
2004 Pearsall SK, Green MM, Morawetz H. Titration of Poly(carboxylic acid)s in Methanol Solution. Polymer Chain Extension, Ionization Equilibria, and Conformational Mobility Macromolecules. 37: 8773-8777. DOI: 10.1021/Ma0491614  0.329
2004 Cheon KS, Selinger JV, Green MM. Counterintuitive influence of microscopic chirality on helical order in polymers Journal of Physical Organic Chemistry. 17: 719-723. DOI: 10.1002/Poc.786  0.332
2003 Tang K, Green MM, Cheon KS, Selinger JV, Garetz BA. Chiral conflict. The effect of temperature on the helical sense of a polymer controlled by the competition between structurally different enantiomers: from dilute solution to the lyotropic liquid crystal state. Journal of the American Chemical Society. 125: 7313-23. PMID 12797806 DOI: 10.1021/Ja030065C  0.347
2003 Guenet J, Poux S, Lopez D, Thierry A, Mathis A, Green MM, Liu W. Encapsulation of magnetic self-assembled systems in thermoreversible gels Macromolecular Symposia. 200: 9-20. DOI: 10.1002/Masy.200351002  0.31
2002 Park JW, Green MM. Atropisomerism as a probe of restrictions to motion above and below the glass transition temperature of Polymers. Chirality. 14: 209-14. PMID 11835567 DOI: 10.1002/Chir.10057  0.588
2001 Green MM, Cheon KS, Yang SY, Park JW, Swansburg S, Liu W. Chiral studies across the spectrum of polymer science Accounts of Chemical Research. 34: 672-680. PMID 11513575 DOI: 10.1021/Ar010009L  0.618
2001 Park JW, Ediger MD, Green MM. Chiral studies in amorphous solids: the effect of the polymeric glassy state on the racemization kinetics of bridged paddled binaphthyls. Journal of the American Chemical Society. 123: 49-56. PMID 11273600 DOI: 10.1021/Ja0023231  0.331
2001 Park J, Green MM, Morawetz H. Racemization Kinetics of Bridged Binaphthyls Do Not Reflect Microviscosities of Rubbery Polymer Matrices Macromolecules. 34: 5719-5722. DOI: 10.1021/Ma010318R  0.318
2001 Muellers BT, Park JW, Brookhart MS, Green MM. Glassy state and secondary structures of chiral macromolecules: Polyisocyanates and polyketones Macromolecules. 34: 572-581. DOI: 10.1021/Ma001102C  0.34
2000 Li J, Schuster GB, Green MM. Investigation of photo-responsive chiral polyisocyanates Molecular Crystals and Liquid Crystals Science and Technology Section a: Molecular Crystals and Liquid Crystals. 344: 7-13. DOI: 10.1080/10587250008023808  0.329
2000 Li J, Schuster GB, Cheon KS, Green MM, Selinger JV. Switching a helical polymer between mirror images using circularly polarized light Journal of the American Chemical Society. 122: 2603-2612. DOI: 10.1021/Ja993290W  0.34
1999 Green MM, Park JW, Sato T, Teramoto A, Lifson S, Selinger RL, Selinger JV. The Macromolecular Route to Chiral Amplification. Angewandte Chemie (International Ed. in English). 38: 3138-3154. PMID 10556885 DOI: 10.1002/(Sici)1521-3773(19991102)38:21<3138::Aid-Anie3138>3.0.Co;2-C  0.324
1999 Jha SK, Cheon KS, Green MM, Selinger JV. Chiral optical properties of a helical polymer synthesized from nearly racemic chiral monomers highly diluted with achiral monomers Journal of the American Chemical Society. 121: 1665-1673. DOI: 10.1021/Ja983202S  0.343
1999 Green M, Park J, Sato T, Teramoto A, Lifson S, Selinger R, Selinger J. Die makromolekulare Route zur Chiralitätsverstärkung Angewandte Chemie. 111: 3328-3345. DOI: 10.1002/(Sici)1521-3757(19991102)111:21<3328::Aid-Ange3328>3.0.Co;2-Z  0.554
1998 Gu H, Nakamura Y, Sato T, Teramoto A, Green MM, Jha SK, Andreola C, Reidy MP. Optical Rotation of Random Copolyisocyanates of Chiral and Achiral Monomers:  Sergeant and Soldier Copolymers† Macromolecules. 31: 6362-6368. DOI: 10.1021/Ma980648K  0.326
1998 Sato T, Nakamura J, Teramoto A, Green MM. Cholesteric Pitch of Lyotropic Polymer Liquid Crystals Macromolecules. 31: 1398-1405. DOI: 10.1021/Ma970968O  0.317
1998 Green MM, Zanella S, Gu H, Sato T, Gottarelli G, Jha SK, Spada GP, Schoevaars AM, Feringa B, Teramoto A. Mechanism of the Transformation of a Stiff Polymer Lyotropic Nematic Liquid Crystal to the Cholesteric State by Dopant-Mediated Chiral Information Transfer Journal of the American Chemical Society. 120: 9810-9817. DOI: 10.1021/Ja981393T  0.313
1998 Selinger JV, Selinger RLB, Jha SK, Green MM. A chiral polymeric analogy to a one-dimensional paramagneti material Chirality. 10: 41-45. DOI: 10.1002/Chir.8  0.333
1997 Gu H, Sato T, Teramoto A, Varichon L, Green MM. Molecular Mechanisms for the Optical Activities of Polyisocyanates Induced by Intramolecular Chiral Perturbations Polymer Journal. 29: 77-84. DOI: 10.1295/Polymj.29.77  0.368
1997 Khatri CA, Pavlova Y, Green MM, Morawetz H. Chiral Solvation as a Means to Quantitatively Characterize Preferential Solvation of a Helical Polymer in Mixed Solvents Journal of the American Chemical Society. 119: 6991-6995. DOI: 10.1021/Ja9709637  0.348
1997 Chen G, Cooks RG, Jha SK, Oupicky D, Green MM. Block microstructural characterization of copolymers formed from fluorinated and non-fluorinated alkyl polyisocyanates using desorption chemical ionization mass spectrometry International Journal of Mass Spectrometry and Ion Processes. 391-404. DOI: 10.1016/S0168-1176(97)00175-4  0.305
1997 Green MM, Jha SK. The road to chiral amplification in polymers originated in Italy Chirality. 9: 424-427. DOI: 10.1002/(Sici)1520-636X(1997)9:5/6<424::Aid-Chir4>3.0.Co;2-5  0.378
1996 Green MM, Sato T, Teramoto A, Lifson S. Following the polyisocyanate helix reversal from dilute solution through the liquid crystal and into the solid state Macromolecular Symposia. 101: 363-370. DOI: 10.1002/Masy.19961010141  0.36
1995 Green MM, Peterson NC, Sato T, Teramoto A, Cook R, Lifson S. A helical polymer with a cooperative response to chiral information. Science (New York, N.Y.). 268: 1860-6. PMID 17797527 DOI: 10.1126/Science.268.5219.1860  0.37
1995 Khatri CA, Vaidya MM, Levon K, Jha SK, Green MM. Synthesis and Molecular Composites of Functionalized Polyisocyanates Macromolecules. 28: 4719-4728. DOI: 10.1021/Ma00117A052  0.328
1995 Hoke SH, Cooks RG, Munoz B, Chang H, Green MM. Microstructure of Alkyl Isocyanate Copolymers Comprised of Enantiomeric Monomers Determined by Desorption Chemical Ionization Mass Spectrometry Macromolecules. 28: 2955-2960. DOI: 10.1021/Ma00112A048  0.324
1994 Green MM, Teramoto A, Sato T. Cholesteric lyotropic liquid crystals and thermally reversible gels from polyisocyanates Progress in Polymer Science. 19: 1083-1087. DOI: 10.1016/0079-6700(94)90025-6  0.344
1994 Green MM, Khatri C, Mark HF. Helix reversals as bad neighbors to liquid crystal organizations in cholesteric states and thermally reversible gels of poly(ALKYL isocyanates) Macromolecular Symposia. 77: 277-282. DOI: 10.1002/Masy.19940770129  0.327
1993 Green MM, Khatri CA, Reidy MP, Levon K. Dilute-solution chiral optical changes signal the thermally reversible gelation of poly(n-hexyl isocyanate) in hydrocarbon solvents Macromolecules. 26: 4723-4725. DOI: 10.1021/Ma00069A050  0.313
1993 Green MM, Peterson NC, Lifson S, Sato T, Teramoto A. Cooperativity and chirality in a wormlike helical macromolecule Macromolecular Symposia. 70: 23-28. DOI: 10.1002/Masy.19930700105  0.326
1992 Lifson S, Felder CE, Green MM. Helical conformations, internal motion, and helix sense reversal in polyisocyanates and the preferred helix sense of an optically active polyisocyanate Macromolecules. 25: 4142-4148. DOI: 10.1021/Ma00042A015  0.311
1991 Majumdar TK, Eberlin MN, Cooks RG, Green MM, Muñoz B, Reidy MP. Structural Studies on Alkylisocyanate Polymers by Thermal Degradation Tandem Mass Spectrometry Journal of the American Society For Mass Spectrometry. 2: 130-148. PMID 24242173 DOI: 10.1016/1044-0305(91)80007-T  0.333
1991 Green MM, Lifson S, Teramoto A. Cooperation in a deep helical energy well Chirality. 3: 285-291. DOI: 10.1002/Chir.530030412  0.368
1990 Green MM, Ringsdorf H, Wagner J, Wüstefeld R. Induction and Variation of Chirality in Discotic Liquid Crystalline Polymers Angewandte Chemie International Edition in English. 29: 1478-1481. DOI: 10.1002/Anie.199014781  0.335
1988 Green MM, Gross RA, Schilling FC, Zero K, Crosby C. Macromolecular stereochemistry: effect of pendant group structure on the conformational properties of polyisocyanides Macromolecules. 21: 1839-1846. DOI: 10.1021/Ma00184A051  0.468
1988 Green MM, Andreola C, Munoz B, Reidy MP, Zero K. Macromolecular stereochemistry: a cooperative deuterium isotope effect leading to a large optical rotation Journal of the American Chemical Society. 110: 4063-4065. DOI: 10.1021/Ja00220A070  0.341
1987 Green MM, Gross RA, Cook R, Schilling FC. Broken worm and wormlike models for polyisocyanates Macromolecules. 20: 2636-2638. DOI: 10.1021/Ma00176A055  0.418
1987 Green MM, Gross RA, Crosby C, Schilling FC. Macromolecular stereochemistry: the effect of pendant group structure on the axial dimension of polyisocyanates Macromolecules. 20: 992-999. DOI: 10.1021/Ma00171A019  0.443
1984 Green MM, Garetz BA. The configurational stereochemistry of atactic vinyl homopolymers Tetrahedron Letters. 25: 2831-2834. DOI: 10.1016/S0040-4039(01)81302-2  0.352
1979 Fenselau C, Green MM, Jardine I. Regiospecificity of intramolecular hydrogen transfer in cyclohexanol following chemical ionization Organic Mass Spectrometry. 14: 326-329. DOI: 10.1002/Oms.1210140608  0.46
1968 Axelrod M, Bickart P, Jacobus J, Green MM, Mislow K. Absolute configuration of sulfoxides and sulfinates Journal of the American Chemical Society. 90: 4835-4842. DOI: 10.1021/Ja01020A016  0.473
1968 Axelrod M, Bickart P, Goldstein ML, Green MM, Kjær A, Mislow K. Absolute configuration and optical rotatory dispersion of methyl alkyl sulfoxides Tetrahedron Letters. 9: 3249-3252. DOI: 10.1016/S0040-4039(00)89539-8  0.487
1967 Green MM, Djerassi C. Mass spectrometry in structural and stereochemical problems. CXXXVII. Examples of interaction of remote functional groups after electron impact Journal of the American Chemical Society. 89: 5190-5198. DOI: 10.1021/Ja00996A020  0.368
1966 Green MM, Weinberg DS, Djerassi C. Mass spectrometry in structural and stereochemical problems. CXIX. Interaction of remote functional groups in mass spectrometry. Journal of the American Chemical Society. 88: 3883-4. PMID 5916381 DOI: 10.1021/Ja00968A053  0.357
1966 Green MM, Axelrod M, Mislow K. Configurational Correlation of Alcohols by Asymmetric Synthesis of Sulfinate Esters1 Journal of the American Chemical Society. 88: 861-862. DOI: 10.1021/Ja00956A059  0.452
1965 Mislow K, Green MM, Raban M. Absolute Configurations of Sulfoxides by Asymmetric Oxidation of Sulfides1 Journal of the American Chemical Society. 87: 2761-2762. DOI: 10.1021/Ja01090A045  0.448
1965 Mislow K, Green MM, Laur P, Chisholm DR. Optical Rotatory Dispersion and Absolute Configuration of Dialkyl Sulfoxides1 Journal of the American Chemical Society. 87: 665-666. DOI: 10.1021/Ja01081A056  0.48
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