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1
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0021586266
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Highly branched dendritic macromolecules by a novel divergent approach
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Tomalia D, Baker H, Dewald J, Hall M, Kallos G, Martin S, Roeck J, Ryder J, Smith P: Highly branched dendritic macromolecules by a novel divergent approach. Polym J 1985, 17:117-132.
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Tomalia, D.1
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Hall, M.4
Kallos, G.5
Martin, S.6
Roeck, J.7
Ryder, J.8
Smith, P.9
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0000102188
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Preparation of highly branched cascade molecules
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Newkome G, Yao Z, Baker G, Gupta V: Preparation of highly branched cascade molecules. J Org Chem 1985, 50:2004-2006.
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Newkome, G.1
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Preparation of polymers with controlled molecular architectures. A new convergent approach to dendritic macromolecules
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Hawker C, Fréchet J: Preparation of polymers with controlled molecular architectures. A new convergent approach to dendritic macromolecules. J Am Chem Soc 1990, 112:7638-7647.
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0026929006
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Hyperbranched polyphenylenes, unique unimoleclar micelles
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Kim Y, Webster O: Hyperbranched polyphenylenes, unique unimoleclar micelles. Macromolecules 1992, 25:5561.
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Macromolecules
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21844449921
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4B building block in dendrimer chemistry
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Very highly branched, fully aromatic polyphenylene derivatives are prepared by a novel use of Diels-Alder chemistry. These unique molecules are not only very soluble and easily processible but they can be used to form a variety of other nanoscopic structures
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4B building block in dendrimer chemistry. J Chem Soc Chem Commun 1998, 1139-1140. Very highly branched, fully aromatic polyphenylene derivatives are prepared by a novel use of Diels-Alder chemistry. These unique molecules are not only very soluble and easily processible but they can be used to form a variety of other nanoscopic structures.
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J Chem Soc Chem Commun
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Morgenroth, F.1
Berresheim, A.2
Wagner, M.3
Mullen, K.4
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7
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0001574886
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Synthesis and biological evaluation of α-D-mannopyranoside-containing dendrimers
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A convergent approach to dendrimers containing numerous mannopyranoside groups at the periphery is described and their use as inhibitors for the binding of concanavalin A lectin to purified yeast is described
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Ashton P, Hounsell E, Jayaraman N, Nilsen T, Spencer N, Stoddart F, Young M: Synthesis and biological evaluation of α-D-mannopyranoside-containing dendrimers. J Org Chem 1998, 63:3429-3437. A convergent approach to dendrimers containing numerous mannopyranoside groups at the periphery is described and their use as inhibitors for the binding of concanavalin A lectin to purified yeast is described.
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J Org Chem
, vol.63
, pp. 3429-3437
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Ashton, P.1
Hounsell, E.2
Jayaraman, N.3
Nilsen, T.4
Spencer, N.5
Stoddart, F.6
Young, M.7
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8
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0032097013
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Hyperbranched polymers prepared via the core-dilution/slow addition technique: Computer simulation of molecular weight distribution and degree of branching
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Hanselmann R, Holter D, Frey H: Hyperbranched polymers prepared via the core-dilution/slow addition technique: computer simulation of molecular weight distribution and degree of branching. Macromolecules 1998, 31:3790-3801.
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Macromolecules
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Hanselmann, R.1
Holter, D.2
Frey, H.3
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9
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0031671958
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Effect of core-forming molecules on molecular weight distribution and degree of branching in the synthesis of hyperbranched polymers
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Radke W, Litvinenko G, Muller A: Effect of core-forming molecules on molecular weight distribution and degree of branching in the synthesis of hyperbranched polymers. Macromolecules 1998, 31:239-248.
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Macromolecules
, vol.31
, pp. 239-248
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Radke, W.1
Litvinenko, G.2
Muller, A.3
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10
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0032474398
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New hyperbranched poly(siloxysilanes): variation of the branching pattern and end-functionalization
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6 monomers and lead to materials with novel properties such as ultra-low viscosity. The use of monomers containing pre-formed dendritic segments leads to macromolecules isomers which differ only in their degree of branching, an emerging and interesting topic in polymer chemistry
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6 monomers and lead to materials with novel properties such as ultra-low viscosity. The use of monomers containing pre-formed dendritic segments leads to macromolecules isomers which differ only in their degree of branching, an emerging and interesting topic in polymer chemistry.
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(1998)
Macromolecules
, vol.31
, pp. 3461-3468
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Miravet, J.1
Fréchet, J.2
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11
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0032494388
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Cyclization in hyperbranched polymer syntheses: Characterization by MALDI-TOF mass spectrometry
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The critical question of cyclization during the synthesis of hyperbranched macromolecules has been probed by MALDI-TOF mass spectrometry. Using this versatile technique it was shown that the extent of cyclization depends on a variety of reaction parameters and can predominate in certain systems. This predominance of cyclization can have important implication for the course of the polymerization and the ultimate molecular weight obtained
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Gooden J, Gross M, Mueller A, Stefanescu A, Wooley K: Cyclization in hyperbranched polymer syntheses: characterization by MALDI-TOF mass spectrometry. J Am Chem Soc 1998, 120:10180-10186. The critical question of cyclization during the synthesis of hyperbranched macromolecules has been probed by MALDI-TOF mass spectrometry. Using this versatile technique it was shown that the extent of cyclization depends on a variety of reaction parameters and can predominate in certain systems. This predominance of cyclization can have important implication for the course of the polymerization and the ultimate molecular weight obtained.
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(1998)
J Am Chem Soc
, vol.120
, pp. 10180-10186
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Gooden, J.1
Gross, M.2
Mueller, A.3
Stefanescu, A.4
Wooley, K.5
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12
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0032049935
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Importance of active site reactivity and reaction conditions in the preparation of hyperbranched polymers by self condensing vinyl polymerization: Highly branched vs. linear poly[4-(chloromethyl)styrene] by metal catalyzed 'living' radical polymerization
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In the self condensing polymerization of vinyl monomers, an interesting new field pioneered by Fréchet, the structure of the branched polymer obtained is dramatically influenced by the reaction conditions. For the polymerization of 4-chloromethylstyrene under ATRP conditions the structure goes from essentially linear to hyperbranched by simply increasing the catalyst monomer ratio from 0.01 to 0.30. This has important consequences for other hyperbranched systems
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Weimer M, Fréchet J, Gitsov I: Importance of active site reactivity and reaction conditions in the preparation of hyperbranched polymers by self condensing vinyl polymerization: highly branched vs. linear poly[4-(chloromethyl)styrene] by metal catalyzed 'living' radical polymerization. J Polym Sci Polym Chem 1998, 36:955-970. In the self condensing polymerization of vinyl monomers, an interesting new field pioneered by Fréchet, the structure of the branched polymer obtained is dramatically influenced by the reaction conditions. For the polymerization of 4-chloromethylstyrene under ATRP conditions the structure goes from essentially linear to hyperbranched by simply increasing the catalyst monomer ratio from 0.01 to 0.30. This has important consequences for other hyperbranched systems.
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(1998)
J Polym Sci Polym Chem
, vol.36
, pp. 955-970
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Weimer, M.1
Fréchet, J.2
Gitsov, I.3
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13
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0032497185
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Visualization of dendrimer molecules by transmission electron microscopy (TEM): Staining methods and cryo-TEM of vitrified solutions
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In a series of elegant experiments, the direct visualization of single dendrimer molecules was obtained by using advanced TEM procedures. Interestingly, the size of the dendrimers was approximately the same within the same generation and varied in a systematic way with increasing generation number. To first approximation, the dendrimers also appeared spherical, all of these features were consistent with the assumed structure of dendrimers
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Jackson C, Chanzy H, Booy F, Drake B, Tomalia D, Bauer B, Amis E: Visualization of dendrimer molecules by transmission electron microscopy (TEM): staining methods and cryo-TEM of vitrified solutions. Macromolecules 1998, 31:6259-6265. In a series of elegant experiments, the direct visualization of single dendrimer molecules was obtained by using advanced TEM procedures. Interestingly, the size of the dendrimers was approximately the same within the same generation and varied in a systematic way with increasing generation number. To first approximation, the dendrimers also appeared spherical, all of these features were consistent with the assumed structure of dendrimers.
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(1998)
Macromolecules
, vol.31
, pp. 6259-6265
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Jackson, C.1
Chanzy, H.2
Booy, F.3
Drake, B.4
Tomalia, D.5
Bauer, B.6
Amis, E.7
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14
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0032475430
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Visualizable cyclindrical macromolecules with controlled stiffness from backbones containing libraries of self-assembled dendritic side groups
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By controlling the size of dendritic side groups attached to a random coil polymer backbone, the overall flexibility of the chain can be readily controlled. Visualization of these nanoscopic structures by a variety of different techniques provides the first comparative study of these novel materials in different environments
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Percec V, Ahn C, Cho W, Jamieson A, Kim J, Schmidt M, Gerle M, Moller M, Prokhorova S, Sheiko S, Cheng S, Zhang A, Ungar G, Yeardley D: Visualizable cyclindrical macromolecules with controlled stiffness from backbones containing libraries of self-assembled dendritic side groups. J Am Chem Soc 1998, 120:8619-8631. By controlling the size of dendritic side groups attached to a random coil polymer backbone, the overall flexibility of the chain can be readily controlled. Visualization of these nanoscopic structures by a variety of different techniques provides the first comparative study of these novel materials in different environments.
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(1998)
J Am Chem Soc
, vol.120
, pp. 8619-8631
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Percec, V.1
Ahn, C.2
Cho, W.3
Jamieson, A.4
Kim, J.5
Schmidt, M.6
Gerle, M.7
Moller, M.8
Prokhorova, S.9
Sheiko, S.10
Cheng, S.11
Zhang, A.12
Ungar, G.13
Yeardley, D.14
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15
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0020749157
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Structure of highly branched macromolecules
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deGennes P, Hervet H: Structure of highly branched macromolecules. J Phys Lett 1983, 351-360.
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(1983)
J Phys Lett
, pp. 351-360
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Degennes, P.1
Hervet, H.2
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17
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0032000750
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Use of a paramagnetic core to affect longitudinal nuclear relaxation in dendrimers - A tool for probing dendrimer conformation
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By comparing two similar series of dendrimers, which differ only in the nature of the core moiety, the conformational mobility of polyether dendrimers was probed by NMR techniques. Interestingly, these materials were shown to be have a high degree of conformational mobility with the chain end groups having the highest degree of freedom
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Gorman C, Hager M, Parkhurst B, Smith J: Use of a paramagnetic core to affect longitudinal nuclear relaxation in dendrimers - a tool for probing dendrimer conformation. Macromolecules 1998, 31:815-822. By comparing two similar series of dendrimers, which differ only in the nature of the core moiety, the conformational mobility of polyether dendrimers was probed by NMR techniques. Interestingly, these materials were shown to be have a high degree of conformational mobility with the chain end groups having the highest degree of freedom.
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(1998)
Macromolecules
, vol.31
, pp. 815-822
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Gorman, C.1
Hager, M.2
Parkhurst, B.3
Smith, J.4
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18
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0032547252
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Amphiphilic dendrimers as building blocks in supramolecular assemblies
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One of the most critical findings in this paper is the self assembly of amphiphilic dendrimers at the air-water interface to form stable Langmuir-Blodgett films. This is contrary to our naïve view of these dendrimers which consists of a hydrophobic shell surrounding a hydrophilic interior. This finding adds substantial support to the conclusion that, depending on dendrimer structure, the conformation of these materials can be extremely dynamic
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Schenning A, Roman C, Weener J, Baars M, van der Gaast S, Meijer E: Amphiphilic dendrimers as building blocks in supramolecular assemblies. J Am Chem Soc 1998, 120:8199-8208. One of the most critical findings in this paper is the self assembly of amphiphilic dendrimers at the air-water interface to form stable Langmuir-Blodgett films. This is contrary to our naïve view of these dendrimers which consists of a hydrophobic shell surrounding a hydrophilic interior. This finding adds substantial support to the conclusion that, depending on dendrimer structure, the conformation of these materials can be extremely dynamic.
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(1998)
J Am Chem Soc
, vol.120
, pp. 8199-8208
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Schenning, A.1
Roman, C.2
Weener, J.3
Baars, M.4
Van Der Gaast, S.5
Meijer, E.6
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19
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0032114865
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Rheology of dendrimers. I. Newtonian flow behavior of medium and highly concentrated solutions of polyamidoamine (PAMAM) dendrimers in ethylenediamine (EDA) solvent
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The lack of an abrupt change of slope in the zero-shear viscosity vs. molecular weight relationship coupled with Newtonian flow under highly concentrated conditions is fully consistent with the non-entangling model of dendrimers
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Uppuluri S, Keinath S, Tomalia D, Dvornic P: Rheology of dendrimers. I. Newtonian flow behavior of medium and highly concentrated solutions of polyamidoamine (PAMAM) dendrimers in ethylenediamine (EDA) solvent. Macromolecules 1998, 31:4498-4510. The lack of an abrupt change of slope in the zero-shear viscosity vs. molecular weight relationship coupled with Newtonian flow under highly concentrated conditions is fully consistent with the non-entangling model of dendrimers.
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(1998)
Macromolecules
, vol.31
, pp. 4498-4510
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Uppuluri, S.1
Keinath, S.2
Tomalia, D.3
Dvornic, P.4
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20
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0032115839
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The melt viscosity of dendritic poly(benzyl ether) macromolecules
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In concert with the previous paper, the melt viscosity behavior of a different dendrimer family also shows no critical entanglement molecular weight suggesting that the 3-dimensional highly branched structure of these materials only permits interdigitation of the numerous chain ends
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Farrington P, Hawker C, Fréchet J, Mackay M: The melt viscosity of dendritic poly(benzyl ether) macromolecules. Macromolecules 1998, 31:5043-5050. In concert with the previous paper, the melt viscosity behavior of a different dendrimer family also shows no critical entanglement molecular weight suggesting that the 3-dimensional highly branched structure of these materials only permits interdigitation of the numerous chain ends.
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(1998)
Macromolecules
, vol.31
, pp. 5043-5050
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Farrington, P.1
Hawker, C.2
Fréchet, J.3
Mackay, M.4
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21
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0032492565
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Melt rheology of arborescent graft polystyrenes
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A similar finding in the study of the melt viscosity of a different family of highly branched macromolecules, arborescent polymers, in which the branching units are polymeric in nature, strongly suggests that this unique property is characteristic of very highly branched structures in general
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Hempenius M, Zoetelief W, Gauthier M, Moller M: Melt rheology of arborescent graft polystyrenes. Macromolecules 1998, 31:2299-2304. A similar finding in the study of the melt viscosity of a different family of highly branched macromolecules, arborescent polymers, in which the branching units are polymeric in nature, strongly suggests that this unique property is characteristic of very highly branched structures in general.
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(1998)
Macromolecules
, vol.31
, pp. 2299-2304
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Hempenius, M.1
Zoetelief, W.2
Gauthier, M.3
Moller, M.4
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22
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0032513719
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Preparation and characterization of dendrimer monolayers and dendrimer-alkanethiol mixed monolayers adsorbed to gold
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PAMAM dendrimers have been shown to form highly stable and close packed monolayers on gold surfaces. Interestingly the monolayers are still porous and can undergo significant rearrangement on exposure to alkane thiol solutions. The physical and chemical properties of these dendritic monolayers show significant potential for a variety of different applications
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Tokuhisa H, Zhao M, Baker L, Phan V, Dermody D, Garcia M, Peez R, Crooks R, Mayer T: Preparation and characterization of dendrimer monolayers and dendrimer-alkanethiol mixed monolayers adsorbed to gold. J Am Chem Soc 1998, 120:4492-4501. PAMAM dendrimers have been shown to form highly stable and close packed monolayers on gold surfaces. Interestingly the monolayers are still porous and can undergo significant rearrangement on exposure to alkane thiol solutions. The physical and chemical properties of these dendritic monolayers show significant potential for a variety of different applications.
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(1998)
J Am Chem Soc
, vol.120
, pp. 4492-4501
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Tokuhisa, H.1
Zhao, M.2
Baker, L.3
Phan, V.4
Dermody, D.5
Garcia, M.6
Peez, R.7
Crooks, R.8
Mayer, T.9
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23
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0037816096
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Preparation of Cu nanoclusters within dendrimer templates
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The use of dendrimers as templating agents, in this case of Cu nanoclusters is reported. The discrete size and shape of dendrimers of different generation number can be sued to control the physical properties of the final nanocluster
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Zhao M, Sun L, Crooks R: Preparation of Cu nanoclusters within dendrimer templates. J Am Chem Soc 1998, 120:4877-4878. The use of dendrimers as templating agents, in this case of Cu nanoclusters is reported. The discrete size and shape of dendrimers of different generation number can be sued to control the physical properties of the final nanocluster.
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(1998)
J Am Chem Soc
, vol.120
, pp. 4877-4878
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Zhao, M.1
Sun, L.2
Crooks, R.3
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24
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0032499554
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Semipermeable chemisorbed adlayers of focally substituted organothiol dendrimers on gold
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Gorman G, Miller R, Chen K, Bishop A, Haasch R, Nuzzo R: Semipermeable chemisorbed adlayers of focally substituted organothiol dendrimers on gold. Langmuir 1998, 14:3312-3319.
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(1998)
Langmuir
, vol.14
, pp. 3312-3319
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Gorman, G.1
Miller, R.2
Chen, K.3
Bishop, A.4
Haasch, R.5
Nuzzo, R.6
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25
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0032547321
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Dendritic nucleic acid probes for DNA biosensors
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The use of dendritic DNA surface layers and mass-selective piezoelectric transducers permits the detection and monitoring of hybridization. This novel type of biosensor relies on the dendritic structure to increase the level and efficiency of hybridization due to the dendrimer's highly branched structure and large number of chain end functional groups
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Wang J, Jiang M, Nilsen T, Getts R: Dendritic nucleic acid probes for DNA biosensors. J Am Chem Soc 1998, 120:8281-8282. The use of dendritic DNA surface layers and mass-selective piezoelectric transducers permits the detection and monitoring of hybridization. This novel type of biosensor relies on the dendritic structure to increase the level and efficiency of hybridization due to the dendrimer's highly branched structure and large number of chain end functional groups.
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(1998)
J Am Chem Soc
, vol.120
, pp. 8281-8282
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Wang, J.1
Jiang, M.2
Nilsen, T.3
Getts, R.4
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26
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0032050509
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Stable langmuir and Langmuir-Blodgett films of fullerene glycodendron conjugates
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Cardullo F, Diederich F, Echegoyen L, Habicher T, Jayaraman N, Leblanc R, Stoddart F, Wang S: Stable langmuir and Langmuir-Blodgett films of fullerene glycodendron conjugates. Langmuir 1998, 14:1955-1959.
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(1998)
Langmuir
, vol.14
, pp. 1955-1959
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Cardullo, F.1
Diederich, F.2
Echegoyen, L.3
Habicher, T.4
Jayaraman, N.5
Leblanc, R.6
Stoddart, F.7
Wang, S.8
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27
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0032511372
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Ordered dendritic nanorods with a poly(p-phenylene) backbone
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Stocker W, Karakaya B, Schurmann B, Rabe J, Schluter D: Ordered dendritic nanorods with a poly(p-phenylene) backbone. J Am Chem Soc 1998, 120:7691-7695.
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(1998)
J Am Chem Soc
, vol.120
, pp. 7691-7695
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Stocker, W.1
Karakaya, B.2
Schurmann, B.3
Rabe, J.4
Schluter, D.5
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28
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0032166845
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Templating nanoporosity in thin-film dielectric insulators
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The unique features of dendritic macromolecules are used to control the phase separation of inorganic thermosetts and thermally decomposable dendrimers. Nanophase separation can be achieved which leads to inorganic thin films with nm-sized pores and dielectric constants less than 2.0
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Hedrick J, Miller R, Hawker C, Carter K, Volksen W, Yoon D, Trollsas M: Templating nanoporosity in thin-film dielectric insulators. Adv Mater 1998, 10:1049-1054. The unique features of dendritic macromolecules are used to control the phase separation of inorganic thermosetts and thermally decomposable dendrimers. Nanophase separation can be achieved which leads to inorganic thin films with nm-sized pores and dielectric constants less than 2.0.
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(1998)
Adv Mater
, vol.10
, pp. 1049-1054
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Hedrick, J.1
Miller, R.2
Hawker, C.3
Carter, K.4
Volksen, W.5
Yoon, D.6
Trollsas, M.7
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29
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0008682174
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Alert-tab, a novel application for dendritic macromolecules
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Self assembled dendrimer antibody conjugates have been shown to possess significantly enhanced detection capability, again resulting from the unique dendritic architecture. The exploitation of these is real world sensor applications is discussed
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Durst D: Alert-tab, a novel application for dendritic macromolecules. Proc 50th SERMACS Conf. 1998, 50:234-235. Self assembled dendrimer antibody conjugates have been shown to possess significantly enhanced detection capability, again resulting from the unique dendritic architecture. The exploitation of these is real world sensor applications is discussed.
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(1998)
Proc 50th SERMACS Conf.
, vol.50
, pp. 234-235
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Durst, D.1
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30
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0001480032
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Self assembled lanthanide-cored dendrimer complexes: Enhancement of the luminescence properties of lanthanide ions through site isolation and antenna effects
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The steric isolation of lanthanide ions at the core of self assembled dendrimer has been shown to lead to a dramatic increase in the luminescence behavior. Interestingly this behavior is generationally dependent and demonstrates that the isolation of the lanthanide ion increases as the size of the dendrimer increases
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Kawa M, Fréchet J: Self assembled lanthanide-cored dendrimer complexes: enhancement of the luminescence properties of lanthanide ions through site isolation and antenna effects. Chem Mater 1998, 10:286-296. The steric isolation of lanthanide ions at the core of self assembled dendrimer has been shown to lead to a dramatic increase in the luminescence behavior. Interestingly this behavior is generationally dependent and demonstrates that the isolation of the lanthanide ion increases as the size of the dendrimer increases.
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(1998)
Chem Mater
, vol.10
, pp. 286-296
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Kawa, M.1
Fréchet, J.2
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31
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0002068887
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Effects of dendrimer generation on site isolation of core moieties: Electrochemical and fluorescence quenching studies with metalloporphyrin core dendrimers
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Pollak K, Leon J, Fréchet J, Maskus M, Abruna H: Effects of dendrimer generation on site isolation of core moieties: electrochemical and fluorescence quenching studies with metalloporphyrin core dendrimers. Chem Mater 1998, 10:30-38.
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(1998)
Chem Mater
, vol.10
, pp. 30-38
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Pollak, K.1
Leon, J.2
Fréchet, J.3
Maskus, M.4
Abruna, H.5
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32
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0032182824
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A blue-emitting CdS/dendrimer nanocomposite
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Sookal K, Hanus L, Ploehn H, Murphy C: A blue-emitting CdS/dendrimer nanocomposite. Adv Mater 1998, 10:1083-1087.
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(1998)
Adv Mater
, vol.10
, pp. 1083-1087
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Sookal, K.1
Hanus, L.2
Ploehn, H.3
Murphy, C.4
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33
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0032003948
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Hyperbranched polymers for electroluminescence applications
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Tao X, Zhang Y, Wada T, Sasabe H, Suzuki H, Watanabe T, Miyata S: Hyperbranched polymers for electroluminescence applications. Adv Mater 1998, 10:226-230.
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(1998)
Adv Mater
, vol.10
, pp. 226-230
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Tao, X.1
Zhang, Y.2
Wada, T.3
Sasabe, H.4
Suzuki, H.5
Watanabe, T.6
Miyata, S.7
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34
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0032001596
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A novel class of p-electron dendrimers for thermally and morphologically stable amorphous molecular materials
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Katsuma K, Shirato Y: A novel class of p-electron dendrimers for thermally and morphologically stable amorphous molecular materials. Adv Mater 1998, 10:223-226.
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(1998)
Adv Mater
, vol.10
, pp. 223-226
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Katsuma, K.1
Shirato, Y.2
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35
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0032500347
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Synthesis of a novel dendritic liquid crystalline polymer showing a ferroelectric SmC* phase
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Busson P, Ihre H, Hult A: Synthesis of a novel dendritic liquid crystalline polymer showing a ferroelectric SmC* phase. J Am Chem Soc 1998, 120:9070-9071.
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(1998)
J Am Chem Soc
, vol.120
, pp. 9070-9071
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Busson, P.1
Ihre, H.2
Hult, A.3
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36
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0032543180
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A dendritic macrocyclic organic polyradical with a very high spin of S=10
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The synthesis of dendritic polyradicals with numerous unpaired electrons is reported and the magnetic properties of these materials discussed
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Rajca A, Wongsriratanakul J, Rajca S, Cerny R: A dendritic macrocyclic organic polyradical with a very high spin of S=10. Angew Chem Int ed Engl 1998, 37:1229-1301. The synthesis of dendritic polyradicals with numerous unpaired electrons is reported and the magnetic properties of these materials discussed.
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(1998)
Angew Chem Int Ed Engl
, vol.37
, pp. 1229-1301
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Rajca, A.1
Wongsriratanakul, J.2
Rajca, S.3
Cerny, R.4
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37
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0001164835
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Vapoconductivity. Sorption of organic vapors causes large increases in the conductivity of a dendrimer
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Polyamido dendrimers with oligiothiphene units at the chain ends have been used a 'molecular sponges' to detect volatile organic compounds. It is found that the conductivity of these novel dendrimers increases dramatically with sorption of these molecules leading to potential sensor applications
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Miller L, Kunugi Y, Canavesi A, Rigaut S, Moorefield C, Newkome G: Vapoconductivity. Sorption of organic vapors causes large increases in the conductivity of a dendrimer. Chem Mater 1998, 10:1751-1754. Polyamido dendrimers with oligiothiphene units at the chain ends have been used a 'molecular sponges' to detect volatile organic compounds. It is found that the conductivity of these novel dendrimers increases dramatically with sorption of these molecules leading to potential sensor applications.
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(1998)
Chem Mater
, vol.10
, pp. 1751-1754
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Miller, L.1
Kunugi, Y.2
Canavesi, A.3
Rigaut, S.4
Moorefield, C.5
Newkome, G.6
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Dendritic rods with a poly(triacetylene) backbone: Insulated molecular wires
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Hybrid dendritic linear block copolymers are used to form nanoscopic materials. In this case rigid rod poly(triacetylene) backbones are encases in a surrounding dendritic sheath leading to multi-nanometer long rods, analogous to insulated molecular wires. Interestingly there is no loss of π-electron character even for the case when large dendrimers are attached to the backbone
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Schenning A, Martin R, Ito M, Diederich F, Boudon C, Gisselbrecht J, Gross M: Dendritic rods with a poly(triacetylene) backbone: insulated molecular wires. J Chem Soc Chem Commun 1998, 1013-1015. Hybrid dendritic linear block copolymers are used to form nanoscopic materials. In this case rigid rod poly(triacetylene) backbones are encases in a surrounding dendritic sheath leading to multi-nanometer long rods, analogous to insulated molecular wires. Interestingly there is no loss of π-electron character even for the case when large dendrimers are attached to the backbone.
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(1998)
J Chem Soc Chem Commun
, pp. 1013-1015
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Schenning, A.1
Martin, R.2
Ito, M.3
Diederich, F.4
Boudon, C.5
Gisselbrecht, J.6
Gross, M.7
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