Theoretical investigation on the polyaddition of A2 and CB2 monomers with non-equal reactivity

[1]  D. Yan,et al.  Effect of Multifunctional Initiator on Self-Condensing Vinyl Polymerization with Nonequal Molar Ratio of Stimulus to Monomer , 2009 .

[2]  D. Yan,et al.  Kinetic analysis of self-condensing vinyl polymerization with unequal reactivities , 2008 .

[3]  D. Yan,et al.  A General Model for the Kinetics of Self-Condensing Vinyl Polymerization , 2008 .

[4]  D. Yan,et al.  Distribution function of hyperbranched polymers formed by AB2 type polycondensation with substitution effect , 2006 .

[5]  D. Yan,et al.  Hyperbranched polymers: from synthesis to applications , 2004 .

[6]  D. Yan,et al.  “A2 + CBn” Approach to Hyperbranched Polymers with Alternating Ureido and Urethano Units , 2003 .

[7]  D. Yan,et al.  Hyperbranched Polymers Made from A2- and BB′2 -Type Monomers, 3. Polyaddition ofN-Methyl-1,3-propanediamine to Divinyl Sulfone , 2001 .

[8]  D. Yan,et al.  Preparation of water-soluble hyperbranched poly(sulfone-amine)s by polyaddition of N-ethylethylenediamine to divinyl sulfone , 2001 .

[9]  D. Yan,et al.  Hyperbranched Polymers Made from A2 and BB‘2 Type Monomers. 1. Polyaddition of 1-(2-Aminoethyl)piperazine to Divinyl Sulfone , 2000 .

[10]  D. Yan,et al.  Kinetic analysis of the polycondensation of ABg type monomer with a multifunctional core , 2000 .

[11]  T. Emrick,et al.  An A2 + B3 approach to hyperbranched aliphatic polyethers containing chain end epoxy substituents , 1999 .

[12]  A. Hult,et al.  Synthesis of hyperbranched aliphatic polyethers via cationic ring-opening polymerization of 3-ethyl-3-(hydroxymethyl)oxetane , 1999 .

[13]  M. Kakimoto,et al.  Synthesis of hyperbranched aromatic polyamide from aromatic diamines and trimesic acid , 1999 .

[14]  D. Yan,et al.  Molecular Weight Distribution of Hyperbranched Polymers Generated from Polycondensation of AB2 Type Monomers in the Presence of Multifunctional Core Moieties , 1999 .

[15]  A. Müller,et al.  Molecular Weight Distribution of Hyperbranched Polymers Generated by Self-Condensing Vinyl Polymerization in Presence of a Multifunctional Initiator , 1999 .

[16]  D. Yan,et al.  Molecular Parameters of Hyperbranched Polymers Made by Self-Condensing Vinyl Polymerization. 2. Degree of Branching† , 1997 .

[17]  D. Yan,et al.  Molecular Parameters of Hyperbranched Polymers Made by Self-Condensing Vinyl Polymerization. 1. Molecular Weight Distribution , 1997 .

[18]  R. B. Grubbs,et al.  Self-Condensing Vinyl Polymerization: An Approach to Dendritic Materials , 1995, Science.

[19]  Masato Suzuki,et al.  Multibranching polymerization: palladium-catalyzed ring-opening polymerization of cyclic carbamate to produce hyperbranched dendritic polyamine , 1992 .

[20]  Young Hwan Kim,et al.  Water soluble hyperbranched polyphenylene: "a unimolecular micelle?" , 1990 .

[21]  D. Yan,et al.  Synthesis of hyperbranched polymers from commercially available A2 and BB′2 type monomers , 2001 .

[22]  D. Yan,et al.  Kinetic model of star‐branched polycondensation , 1998 .