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author | Norbert Preining <norbert@preining.info> | 2019-09-02 13:46:59 +0900 |
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committer | Norbert Preining <norbert@preining.info> | 2019-09-02 13:46:59 +0900 |
commit | e0c6872cf40896c7be36b11dcc744620f10adf1d (patch) | |
tree | 60335e10d2f4354b0674ec22d7b53f0f8abee672 /support/biblio/EXAMPLES/2sorts |
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-rwxr-xr-x | support/biblio/EXAMPLES/2sorts/libtex | 32 | ||||
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diff --git a/support/biblio/EXAMPLES/2sorts/2sorts.tex b/support/biblio/EXAMPLES/2sorts/2sorts.tex new file mode 100644 index 0000000000..c53a0a2b64 --- /dev/null +++ b/support/biblio/EXAMPLES/2sorts/2sorts.tex @@ -0,0 +1,169 @@ +\documentstyle[aps,manuscript]{revtex} + +\title{Comb copolymer brush with chemically different side chains} +\date{\today} +%----------------------------------------------- + +\newcommand{\vA}{v_{AA}} +\newcommand{\vB}{v_{BB}} +\newcommand{\vAB}{v_{AB}} +\newcommand{\vx}{v} +\newcommand{\mnu}{\nu} +\newcommand{\khi}{\chi} +\newcommand{\dd}{\partial} +%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% + +\begin{document} + +\maketitle +%-------------------------------------------------- + +\begin{abstract} +An investigation of side chain microphase separation +within a single comb copolymer molecule containing chemically different +$A$ and $B$ side chains has been carried out. Expressions for the +transition point $\chi_{AB}^*$ in a +good ($\chi_{AB}^* \sim N^{-3/8}$), +marginal ($\chi_{AB}^* \sim N^{-1/2}$), +$\theta$ ($\chi_{AB}^* \sim N^{-2/3}$), +and poor ($\chi_{AB}^* \sim N^{-1}$) +solvent are derived +both by a mean field calculation and by scaling arguments. +Properties of the system below and above the transition point are +described. +Some unusual ``bow-like'' conformations are predicted for a single +molecule in the microphase separated state in a good solvent. +\end{abstract} +%-------------------------------------------------- +\section{Introduction} + +The conformational characteristics of individual comb copolymers with a +high grafting density of side chains in solution has been addressed in a +series of theoretical papers +\cite{Birshtein,WangSafran,Fredrickson,Rouault1,3dFlex,3dRigid,Potemkin,2dComb} +to begin with the original work of +Birshtein et al \cite{Birshtein}. +Irrespective of the solvent quality, be it a good +solvent or a $\theta$-solvent, all theories predict a cylindrical +brush-like structure for sufficiently long side chains. The pertinent +parameters are the side chain grafting density, the side chain length, +the intrinsic stiffness of the backbone and the side chains (the +respective Kuhn segments) and the solvent quality with respect to the +side chains and the backbone. The conformation is characterized by a +number of quantities, the persistence length of the comb copolymer brush +being most important. For sufficiently long side chains the persistence +length is predicted to exceed the backbone length, thus resulting in a +characteristic cylindrical "bottle-brush" structure. Subsequent computer +simulations using a freely jointed hard sphere model essentially +confirmed this picture +\cite{Mika4,BrinkeIkkala,Rouault2,Mika1,Mika3,Mika2}. + +The experimental investigation of comb copolymers with a high grafting +density has assumed large proportions after the successful +polymerization of macromonomers, yielding degrees of polymerization +significantly exceeding the length of the macromonomer itself, by +Tsukahara and coworkers +\cite{Tsukahara2,Tsukahara3,Schmidt,Tsukahara0}. +Besides polymerization of macromonomers +alternative routes have been developed recently using grafting from a +macroinitiator prepared by either atom-transfer radical polymerization +\cite{Beers1} +or by living cationic polymerization +\cite{Schappacher}. +Using atom transfer +radical polymerization molecular brushes with block copolymer side +chains have been prepared as well. + +The experimental characterization of the comb copolymer brush +conformation in dilute solution is a highly nontrivial issue. It was +achieved recently by Schmidt and co-workers +\cite{Borner1,Wintermantel1,Wintermantel2,Wintermantel3,DziezokSheiko,Sheiko,GerleRoos,FischerGerleSchmidt} +using a combination +of light scattering experiments and theoretical modeling. Since the high +grafting density is supposed to lead to a stiff molecular structure, the +modeling has been based on the Kratky-Porod worm-like chain model. +For high molar mass polymacromonomers based on methacryloyl +end-functionalized oligo methacrylates ($M_n = 2410~g/mole$) in the good +solvent THF, the Kuhn statistical segment length, which is twice the +persistence length, turned out to be $120~nm$. For polymacromonomers +($M_n = 3624~g/mole$) consisting of polystyrene main and side chains this +value was $190~nm$ in the good solvent toluene and $120~nm$ in the +"$\theta$-solvent" cyclohexane. + +At the same time one of the most challenging problems in +the polymer physics is a description of a microphase +formation in copolymer systems. +Theoretically, self-organization in block copolymer systems has +attracted +a lot of attention during the last decades and a fairly complete picture +has emerged for the +relatively simple diblock copolymers. +\cite{Helfand1,Semenov,Leibler,FredricksonHelfand} +As a consequence, the interest gradually shifts towards more +complicated architectures such as comb or graft copolymers +\cite{Dobrynin1,Cruz1,Foster1,WernerFredrickson,Nap1}. +The discussion of structure formation in comb copolymers using the weak +segregation limit has been presented in some detail. Compared to diblock +copolymers the description is only slightly complicated by the fact that +the single chain correlation functions are more involved. Phase diagrams +of various comb copolymer systems have been published. Although +different in details, the general trends are the same as for diblock +copolymers. Of course, rather than the overall chain length, it is the +length of the "repeat unit" that determines the order-disorder +transition temperature as well as the characteristic length scale of the +ordered structures. + +The application of the weak segregation approach, however, requires a +relatively low +grafting density such that the distance between two +consecutive grafting points along the backbone is at least of the order +of the Flory radius of the side chains. If the grafting density of comb +copolymers is very high, the structure in the melt will usually involve +segregation between individual molecules. Even if the incompatibility +between backbone and side chains is high, the high grafting density may +well prevent segregation of several backbones. Furthermore, a high +grafting density combined with long side chains implies the volume +fraction of the backbone to be of the order of 0.1 or lower, not +necessarily the most interesting part of the melt phase diagram. + +Still, microphase separation may occur provided chemically different +side chains are used. In this case unfavorable interaction between the +side chains may lead to a micro domain +structure within a single molecule. The present paper is devoted to this +subject. +The main objective is to identify conditions for "microphase separation" +of side chains of two +different types within a single comb copolymer molecule under different +solvent conditions. + +The paper is organized as follows. The next section describes the +self-consistent field approach to a molecule with a straight +backbone and chemically different side chains. We show the possibility +of side chain separation +within the molecule and discuss the limits of the theory's +applicability. +The subsequent section is devoted to possible unusual behavior +of comb copolymer molecules with a flexible backbone and +microphase separated side chains. Then all results are summarized and +discussed in the last section. + +%------------------------------------------- +\section{Useful literature (not from the article)} +Very interesting and useful books on this subject (polymers) are +\cite{bookdeGennesScalingConcepts,GrosKhokh,bookCloizeaux} or more specific +books devoted to peculiarities if comb copolymers behavior +\cite{bookPlate,bookMcArdle}. +Still unpublished works, like \cite{FischerSchmidt}, can be very helpful too. + +Thesis \cite{thesisHyvarinen} is a good reading too! +%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% +\begin{references} + + +\end{references} + + + + + +\end{document}
\ No newline at end of file diff --git a/support/biblio/EXAMPLES/2sorts/2sorts_formats.tex b/support/biblio/EXAMPLES/2sorts/2sorts_formats.tex new file mode 100644 index 0000000000..d95505135d --- /dev/null +++ b/support/biblio/EXAMPLES/2sorts/2sorts_formats.tex @@ -0,0 +1,217 @@ +%% This is an example of a TeX file with formats +%% included into the header of the document. +%% To run it you have to do something like: +%% biblio.pl -o 2sorts_formats.1.tex -d refers.db 2sorts_formats.tex +%% or +%% biblio.pl -o 2sorts_formats.1.tex -d refers.db --nobibitem --uselist 2sorts_formats.tex +%% if you want a really well formatted citation list +%% and then +%% latex 2sorts_formats.1.tex +%% to get 2sorts_formats.1.dvi + +%%------------------------------------------------------ + +%% this is copyed from the template for Macromolecules +%% no ordering of the references is needed. Otherwise add line +%% '%ordering= AUTHORL' + +%begin{biblio} + +%cite_format={(%s)} +%ref_format=${^{%s}}$ + +%% normal article: +% ARTICLE [$AUTHOR0P~L,~F~M; $ {\it $JOURNAL$} {\bf $YEAR$}, {\it $VOL$}, $PAGE$.] + +%% article which is submitted or accepted +% ARTICLE0[$AUTHOR0P~L,~F~M; $ {\it $JOURNAL$} $STATE$.] + +%% normal book +% BOOK [$AUTHOR0P~L,~F~M; $ {\it $TITLE$}; $PUBL$: $PLACE$, $YEAR$.] + +%% article in a book AUTHORE, AUTHORG and AUTHORH - last, first +%% and middle names of the editor +% EDBOOK [$AUTHOR0P~L,~F~M; $ in {\it $BOOKTITLE$}, edited by $AUTHOR0I~E,~G~H;$; $PUBL$: $PLACE$, $YEAR$.] + +%% article in a book without editor +% INBOOK [$AUTHOR0P~L,~F~M; $ in {\it $BOOKTITLE$}, p.$PAGE$ $PUBL$: $PLACE$, $YEAR$.] + +% EPRINT [$AUTHOR0P~L,~F~M; $ in {\it $BOOKTITLE$} $INFO$, $YEAR$.] + +%% Thesis +% THESIS [$AUTHOR0P~L,~F~M; $ {\it $SORT$}; $UNIV$: $PLACE$, $YEAR$.] + +%end{biblio} + +%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% +%REAL DOCUMENT STARTS HERE!!!! + +\documentstyle[aps,manuscript]{revtex} + +\title{Comb copolymer brush with chemically different side chains} +\date{\today} +%----------------------------------------------- + +\newcommand{\vA}{v_{AA}} +\newcommand{\vB}{v_{BB}} +\newcommand{\vAB}{v_{AB}} +\newcommand{\vx}{v} +\newcommand{\mnu}{\nu} +\newcommand{\khi}{\chi} +\newcommand{\dd}{\partial} +%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% + +\begin{document} + +\maketitle +%-------------------------------------------------- + +\begin{abstract} +An investigation of side chain microphase separation +within a single comb copolymer molecule containing chemically different +$A$ and $B$ side chains has been carried out. Expressions for the +transition point $\chi_{AB}^*$ in a +good ($\chi_{AB}^* \sim N^{-3/8}$), +marginal ($\chi_{AB}^* \sim N^{-1/2}$), +$\theta$ ($\chi_{AB}^* \sim N^{-2/3}$), +and poor ($\chi_{AB}^* \sim N^{-1}$) +solvent are derived +both by a mean field calculation and by scaling arguments. +Properties of the system below and above the transition point are +described. +Some unusual ``bow-like'' conformations are predicted for a single +molecule in the microphase separated state in a good solvent. +\end{abstract} +%-------------------------------------------------- +\section{Introduction} + +The conformational characteristics of individual comb copolymers with a +high grafting density of side chains in solution has been addressed in a +series of theoretical papers +\cite{Birshtein,WangSafran,Fredrickson,Rouault1,3dFlex,3dRigid,Potemkin,2dComb} +to begin with the original work of +Birshtein et al \cite{Birshtein}. +Irrespective of the solvent quality, be it a good +solvent or a $\theta$-solvent, all theories predict a cylindrical +brush-like structure for sufficiently long side chains. The pertinent +parameters are the side chain grafting density, the side chain length, +the intrinsic stiffness of the backbone and the side chains (the +respective Kuhn segments) and the solvent quality with respect to the +side chains and the backbone. The conformation is characterized by a +number of quantities, the persistence length of the comb copolymer brush +being most important. For sufficiently long side chains the persistence +length is predicted to exceed the backbone length, thus resulting in a +characteristic cylindrical "bottle-brush" structure. Subsequent computer +simulations using a freely jointed hard sphere model essentially +confirmed this picture +\cite{Mika4,BrinkeIkkala,Rouault2,Mika1,Mika3,Mika2}. + +The experimental investigation of comb copolymers with a high grafting +density has assumed large proportions after the successful +polymerization of macromonomers, yielding degrees of polymerization +significantly exceeding the length of the macromonomer itself, by +Tsukahara and coworkers +\cite{Tsukahara2,Tsukahara3,Schmidt,Tsukahara0}. +Besides polymerization of macromonomers +alternative routes have been developed recently using grafting from a +macroinitiator prepared by either atom-transfer radical polymerization +\cite{Beers1} +or by living cationic polymerization +\cite{Schappacher}. +Using atom transfer +radical polymerization molecular brushes with block copolymer side +chains have been prepared as well. + +The experimental characterization of the comb copolymer brush +conformation in dilute solution is a highly nontrivial issue. It was +achieved recently by Schmidt and co-workers +\cite{Borner1,Wintermantel1,Wintermantel2,Wintermantel3,DziezokSheiko,Sheiko,GerleRoos,FischerGerleSchmidt} +using a combination +of light scattering experiments and theoretical modeling. Since the high +grafting density is supposed to lead to a stiff molecular structure, the +modeling has been based on the Kratky-Porod worm-like chain model. +For high molar mass polymacromonomers based on methacryloyl +end-functionalized oligo methacrylates ($M_n = 2410~g/mole$) in the good +solvent THF, the Kuhn statistical segment length, which is twice the +persistence length, turned out to be $120~nm$. For polymacromonomers +($M_n = 3624~g/mole$) consisting of polystyrene main and side chains this +value was $190~nm$ in the good solvent toluene and $120~nm$ in the +"$\theta$-solvent" cyclohexane. + +At the same time one of the most challenging problems in +the polymer physics is a description of a microphase +formation in copolymer systems. +Theoretically, self-organization in block copolymer systems has +attracted +a lot of attention during the last decades and a fairly complete picture +has emerged for the +relatively simple diblock copolymers. +\cite{Helfand1,Semenov,Leibler,FredricksonHelfand} +As a consequence, the interest gradually shifts towards more +complicated architectures such as comb or graft copolymers +\cite{Dobrynin1,Cruz1,Foster1,WernerFredrickson,Nap1}. +The discussion of structure formation in comb copolymers using the weak +segregation limit has been presented in some detail. Compared to diblock +copolymers the description is only slightly complicated by the fact that +the single chain correlation functions are more involved. Phase diagrams +of various comb copolymer systems have been published. Although +different in details, the general trends are the same as for diblock +copolymers. Of course, rather than the overall chain length, it is the +length of the "repeat unit" that determines the order-disorder +transition temperature as well as the characteristic length scale of the +ordered structures. + +The application of the weak segregation approach, however, requires a +relatively low +grafting density such that the distance between two +consecutive grafting points along the backbone is at least of the order +of the Flory radius of the side chains. If the grafting density of comb +copolymers is very high, the structure in the melt will usually involve +segregation between individual molecules. Even if the incompatibility +between backbone and side chains is high, the high grafting density may +well prevent segregation of several backbones. Furthermore, a high +grafting density combined with long side chains implies the volume +fraction of the backbone to be of the order of 0.1 or lower, not +necessarily the most interesting part of the melt phase diagram. + +Still, microphase separation may occur provided chemically different +side chains are used. In this case unfavorable interaction between the +side chains may lead to a micro domain +structure within a single molecule. The present paper is devoted to this +subject. +The main objective is to identify conditions for "microphase separation" +of side chains of two +different types within a single comb copolymer molecule under different +solvent conditions. + +The paper is organized as follows. The next section describes the +self-consistent field approach to a molecule with a straight +backbone and chemically different side chains. We show the possibility +of side chain separation +within the molecule and discuss the limits of the theory's +applicability. +The subsequent section is devoted to possible unusual behavior +of comb copolymer molecules with a flexible backbone and +microphase separated side chains. Then all results are summarized and +discussed in the last section. + +%------------------------------------------- +\section{Useful literature (not from the article)} +Very interesting and useful books on this subject (polymers) are +\cite{bookdeGennesScalingConcepts,GrosKhokh,bookCloizeaux} or more specific +books devoted to peculiarities if comb copolymers behavior +\cite{bookPlate,bookMcArdle}. +Still unpublished works, like \cite{FischerSchmidt}, can be very helpful too. + +Thesis \cite{thesisHyvarinen} is a good reading too! +%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% +\begin{references} + + +\end{references} + + + + + +\end{document}
\ No newline at end of file diff --git a/support/biblio/EXAMPLES/2sorts/libtex b/support/biblio/EXAMPLES/2sorts/libtex new file mode 100755 index 0000000000..c33c392115 --- /dev/null +++ b/support/biblio/EXAMPLES/2sorts/libtex @@ -0,0 +1,32 @@ +JOURNAL="physreve" +PREFIX="../../" + +VLEVEL="1" #verbosity level +PROJECT="2sorts" +REFS="refers.db" +FORMATS=$PREFIX"formats/"$JOURNAL + + + +SUFFIX=".1" + +OUTTEX="$PROJECT$SUFFIX.tex" +OUTDVI="$PROJECT$SUFFIX.dvi" +TEXFILE="$PROJECT.tex" +DVIFILE="$PROJECT.dvi" + + +echo $OUTTEX + +if [ $JOURNAL = "physreve" ] +then + "$PREFIX"biblio.pl -v $VLEVEL -o $OUTTEX -d $REFS -f $FORMATS $TEXFILE +else + "$PREFIX"biblio.pl -v $VLEVEL -o $OUTTEX -d $REFS -f $FORMATS --nobibitem --uselist $TEXFILE +fi + + +latex $OUTTEX +latex $OUTTEX +mv $OUTDVI $DVIFILE +#rm *.aux *.log *~
\ No newline at end of file diff --git a/support/biblio/EXAMPLES/2sorts/refers.db b/support/biblio/EXAMPLES/2sorts/refers.db new file mode 100644 index 0000000000..fb2654ac9e --- /dev/null +++ b/support/biblio/EXAMPLES/2sorts/refers.db @@ -0,0 +1,1186 @@ +LABEL = thesisHyvarinen +TYPE = thesis +AUTHORL = Hyv\"arinen +AUTHORF = S. +SORT = Licentiate Thesis +UNIV = University of Helsinki +PLACE = Helsinki +YEAR = 1997 +TITLE = +URL = +---------- +LABEL = Brinke4 +TYPE = edbook +AUTHORP = |ten +AUTHORL = Ikkala|Brinke +AUTHORF = O.|G. +BOOKTITLE= Handbook of Advanced Electronic and Photonic Materials and Devices, Part 8 Conducting Polymers +AUTHORI = +AUTHORE = Nalwa +AUTHORG = Hari +AUTHORH = Singh +PAGE = 185 +PUBL = Academic Press +PLACE = +YEAR = 2000 +---------- +LABEL = bookMcArdle +TYPE = edbook +AUTHORL = Warner +AUTHORF = M. +AUTHORM = +TITLE = The physical principles of side chain polymer liquid crystals +BOOKTITLE= Side Chain Liquid Crystal Polymers +AUTHORI = +AUTHORE = McArdle +AUTHORG = C. +AUTHORH = B. +PUBL = Blackie +PLACE = Glasgow and London +YEAR = 1989 +PAGE = 7 +EPAGE = 29 +---------- +LABEL = bookdeGennesLiqCryst +TYPE = book +AUTHORP = de +AUTHORL = Gennes +AUTHORF = P.-G. +AUTHORM = +TITLE = The Physics of Liquid Crystals +PUBL = Clarendon Press +PLACE = Oxford +YEAR = 1974 +---------- +LABEL = bookdeGennesScalingConcepts +TYPE = book +AUTHORP = de +AUTHORL = Gennes +AUTHORF = P.-G. +AUTHORM = +TITLE = Scaling Concepts in Polymer Physics +PUBL = Cornell University Press +PLACE = Ithaca +YEAR = 1985 +PAGES = 325 +---------- +LABEL = bookPlate +TYPE = book +AUTHORL = Plate|Shibaev +AUTHORF = N. |V. +AUTHORM = A. |P. +TITLE = Comb-Shaped Polymers and Liquid Crystals +PUBL = Plenum Press +PLACE = New York and London +YEAR = 1987 +PAGES = 415 +---------- +LABEL = GrosKhokh +TYPE = book +AUTHORL = Grosberg|Khokhlov +AUTHORF = A. |A. +AUTHORM = Yu. |R. +TITLE = Statistical Physics of Macromolecules +PUBL = American Institute of Physics +PLACE = New York +YEAR = 1994 +---------- +LABEL = Landau +TYPE = book +AUTHORL = Landau|Lifshits +AUTHORF = L |E. +AUTHORM = D. |M. +TITLE = Statistical Physics +PUBL = Pergamon +PLACE = Oxford +YEAR = 1980 +---------- +LABEL = bookLipatovNesterov +TYPE = book +AUTHORL = Lipatov|Nesterov +AUTHORF = Y. |A. +AUTHORM = S. |E. +TITLE = Thermodynamics of Polymer Blends +PUBL = Technomic +PLACE = Lancaster, Basel +YEAR = 1997 +---------- +LABEL = bookCloizeaux +TYPE = book +AUTHORP = des +AUTHORL = Cloizeaux|Jannink +AUTHORF = J. |G. +TITLE = Polymers in Solutions: Their modelling and Structure +PUBL = Clarendon Press +PLACE = Oxford +YEAR = 1990 +PAGES = 896 +---------- +LABEL = LifshitzGrosbergKhokhlov1 +TYPE = article +AUTHORL = Lifshitz|Grosberg|Khokhlov +AUTHORF = I. |A. |A. +AUTHORM = M. |Yu. |R. +JOURNAL = Rev. Mod. Phys. +VOL = 50 +PAGE = 683 +EPAGE = 713 +YEAR = 1978 +TITLE = Some problems of the statistical physics of polymer chains with volume interaction +URL = RevModPhys_LifshitsGrosbergKhokhlov1978.pdf +---------- +LABEL = Vasilevskaya +TYPE = article +AUTHORP = | | | |ten +AUTHORL = Vasilevskaya|Klochkov|Khalatur|Khokhlov|Brinke +AUTHORF = V. |A. |P. |A. |G. +AUTHORM = V. |A. |G. |R. | +TITLE = Microphase separation within comb-like copolymer with attractive side-chains: computer simulations +JOURNAL = Macromol. Theory and Simul. +VOL = 10 +PAGE = 389 +EPAGE = 394 +YEAR = 2001 +URL = vasilevskaya_attractive.pdf +---------- +LABEL = Helfand1 +TYPE = article +AUTHORL = Helfand|Wasserman +AUTHORF = E. |Z. +AUTHORM = |R. +TITLE = +JOURNAL = Macromolecules +VOL = 9 +PAGE = 879 +YEAR = 1976 +---------- +LABEL = Tsukahara0 +TYPE = edbook +AUTHORL = Tsukahara +AUTHORF = Y. +BOOKTITLE=Macromolecular Design: Concept and Practice +AUTHORI = +AUTHORE = Mishra +AUTHORG = M. +AUTHORH = +PAGE = 161 +EPAGE = 227 +PUBL = Polymer Frontiers International Inc. +PLACE = New York +YEAR = 1993 +---------- +LABEL = Schmidt +TYPE = article +AUTHORL = Tsukahara|Tsutsumi|Yamashita|Shimada +AUTHORF = Y. |K. |S. |S. +TITLE = +JOURNAL = Macromolecules +VOL = 23 +PAGE = 5201 +YEAR = 1990 +---------- +LABEL = Tsukahara2 +TYPE = article +AUTHORL = Tsukahara|Mizuno|Segawa|Yamashita +AUTHORF = Y. |K. |A. |Y. +TITLE = +JOURNAL = Macromolecules +VOL = 22 +PAGE = 1546 +EPAGE = 1552 +YEAR = 1989 +---------- +LABEL = Tsukahara3 +TYPE = article +AUTHORL = Tsukahara|Tsutsumi|Yamashita +AUTHORF = Y. |K. |Y. +TITLE = +JOURNAL = Macromolecules +VOL = 22 +PAGE = 2869 +EPAGE = 2871 +YEAR = 1989 +---------- +LABEL = Ballauff +TYPE = article +AUTHORL = Ballauff +AUTHORF = M. +AUTHORM = +TITLE = +JOURNAL = Angew. Chem. Int. Ed. Engl. +VOL = 28 +PAGE = 253 +YEAR = 1989 +---------- +LABEL = Antonietti +TYPE = article +AUTHORL = Antonietti|Henke|Th\"unemann +AUTHORF = M. |S. |A. +AUTHORM = | |F. +TITLE = Highly Ordered Materials with Ultra-Low Surface Energies. Polyelectrolyte-Surfactant Complexes with Fluorinated Surfactants +JOURNAL = Adv. Mater. +VOL = 8 +PAGE = 45 +YEAR = 1996 +---------- +LABEL = Thunemann +TYPE = article +AUTHORL = Th\"unemann|Lochaas +AUTHORF = A. |K. +AUTHORM = F. |H. +TITLE = PHYSISORPTION, INTERFACIAL FILMS, MEMBRANES - Self-Assembly of Perfluorodecanoic Acid with Cationic Copolymers: Ultra-Low Energy Surfaces and Mesomorphous Structures +JOURNAL = Langmuir +VOL = 14 +PAGE = 4898 +EPAGE = 4903 +YEAR = 1998 +---------- +LABEL = Semenov +TYPE = article +AUTHORL = Semenov +AUTHORF = A. +TITLE = +JOURNAL = Sov. Phys. JETP +PAGE = 733 +YEAR = 1985 +VOL = 61 +---------- +LABEL = LikhtmanSemenov +TYPE = article +AUTHORL = Likhtman|Semenov +AUTHORF = A.|A. +AUTHORM = E.|N. +JOURNAL = Macromolecules +PAGE = 7273 +EPAGE = 7278 +YEAR = 1997 +VOL = 30 +TITLE = Theory of Microphase Separation in Block Copolymer/Homopolymer Mixtures +URL = ma9702713.pdf +---------- +LABEL = RubinsteinSemenov +TYPE = article +AUTHORL = Rubinstein|Semenov +AUTHORF = M.|A. +AUTHORM = |N. +JOURNAL = Macromolecules +PAGE = 1058 +EPAGE = 1068 +YEAR = 2001 +VOL = 34 +TITLE = Dynamics of Entangled Solutions of Associating Polymers +URL = ma0013049.pdf +---------- +LABEL = Floudas +TYPE = article +AUTHORL = Floudas|Hadjichristidis|Stamm|Likhtman|Semenov +AUTHORF = G. |N. |M. |A. |A. +AUTHORM = | | |E. |N. +JOURNAL = J. of Chem. Phys. +PAGE = 3318 +EPAGE = 3328 +YEAR = 1997 +VOL = 106 +TITLE = Microphase separation in block copolymer-homopolymer blends: Theory and experiment +URL = JCP03318.pdf +---------- +LABEL = Leibler +TYPE = article +AUTHORL = Leibler +AUTHORF = L. +TITLE = +JOURNAL = Macromolecules +PAGE = 1602 +YEAR = 1980 +VOL = 13 +---------- +LABEL = FredricksonHelfand +TYPE = article +AUTHORL = Fredrickson|Helfand +AUTHORF = G. |E. +AUTHORM = H. | +TITLE = +JOURNAL = Macromolecules +PAGE = 697 +YEAR = 1987 +VOL = 87 +---------- +LABEL = Dobrynin1 +TYPE = article +AUTHORL = Dobrynin|Erukhimovich +AUTHORF = A.|I. +AUTHORM = V.|Y. +TITLE = Computer-aided comparative investigation of architecture influence of block copolymer phase diagrams +JOURNAL = Macromolecules +PAGE = 276 +EPAGE = 281 +YEAR = 1993 +VOL = 26 +---------- +LABEL = Cruz1 +TYPE = article +AUTHORL = Olvera de la Cruz|Sanchez +AUTHORF = M. |I. +TITLE = +JOURNAL = Macromolecules +PAGE = 2501 +YEAR = 1986 +VOL = 19 +---------- +LABEL = Foster1 +TYPE = article +AUTHORL = Foster|Jasnow|Balazs +AUTHORF = D. |D. |A. +AUTHORM = P. | |C. +TITLE = +JOURNAL = Macromolecules +PAGE = 3450 +YEAR = 1995 +VOL = 28 +---------- +LABEL = WernerFredrickson +TYPE = article +AUTHORL = Werner|Fredrickson +AUTHORF = A.|G. +AUTHORM = |H. +TITLE = Architectural Effects on the Stability Limits of $ABS$ Block Copolymers +JOURNAL = J. Polym. Sci. B: Polym. Phys. +PAGE = 849 +EPAGE = 864 +YEAR = 1997 +VOL = 35 +URL = JPolimSciB_v35p849y1997.pdf +---------- +LABEL = Nap1 +TYPE = article +AUTHORP = | |ten +AUTHORL = Nap|Kok|Brinke|Kuchanov +AUTHORF = R. |C. |G. |S. +AUTHORM = J. | | |I. +TITLE = Microphase separation at two length scales +JOURNAL = Eur. Phys. J. 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