Molecular nanoarchitectonics: unification of nanotechnology and molecular/materials science

• Katsuhiko Ariga

Beilstein J. Nanotechnol. 2023, 14, 434–453, doi:10.3762/bjnano.14.35

• heterojunction interface (Figure 10) [126]. This synthesis strategy is based on the difference in dissociation energies of C–Br and C–I bonds. The growth order of the block copolymers of graphene nanoribbons can be controlled. Such heterojunctions provide a viable platform that can be used directly for

Nanotechnology – a robust tool for fighting the challenges of drug resistance in non-small cell lung cancer

• Filip Gorachinov,
• Fatima Mraiche,
• Diala Alhaj Moustafa,
• Ola Hishari,
• Yomna Ismail,
• Jensa Joseph,
• Maja Simonoska Crcarevska,
• Marija Glavas Dodov,
• Nikola Geskovski and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2023, 14, 240–261, doi:10.3762/bjnano.14.23

• subcellular targeting, were synthesized by click coupling reactions or arranged by self-assembly and co-assembly of block copolymers. These carriers may challenge different barriers after bioresponsive cleavage of the above functionalities. One recently published example involves a micellar structure composed

• -(dimethylamino)ethyl methacrylate)-b-poly(ε-caprolactone)-b-poly(2-(dimethylamino)ethyl methacrylate (PDMAEMA20(TPP+)-b-PCL70-b-PDMAEMA20(TPP+)) block copolymers. PEO-PCL blocks were linked using acetal groups to enable the cleavage of the PEO blocks from the NP surface in the acidic environment of a tumor and

Comprehensive review on ultrasound-responsive theranostic nanomaterials: mechanisms, structures and medical applications

• Sepand Tehrani Fateh,
• Lida Moradi,
• Elmira Kohan,
• Michael R. Hamblin and
• Amin Shiralizadeh Dezfuli

Beilstein J. Nanotechnol. 2021, 12, 808–862, doi:10.3762/bjnano.12.64

The impact of molecular tumor profiling on the design strategies for targeting myeloid leukemia and EGFR/CD44-positive solid tumors

• Nikola Geskovski,
• Nadica Matevska-Geshkovska,
• Simona Dimchevska Sazdovska,
• Marija Glavas Dodov,
• Kristina Mladenovska and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2021, 12, 375–401, doi:10.3762/bjnano.12.31

A review on the green and sustainable synthesis of silver nanoparticles and one-dimensional silver nanostructures

• Sina Kaabipour and
• Shohreh Hemmati

Beilstein J. Nanotechnol. 2021, 12, 102–136, doi:10.3762/bjnano.12.9

Effect of different silica coatings on the toxicity of upconversion nanoparticles on RAW 264.7 macrophage cells

• Cynthia Kembuan,
• Helena Oliveira and
• Christina Graf

Beilstein J. Nanotechnol. 2021, 12, 35–48, doi:10.3762/bjnano.12.3

• disintegration processes. Several authors have reported the use of protective coatings, such as poly(acrylic acid) and poly(allylamine hydrochloride) [18], multichelating phosphonate [30][32][33], block copolymers [34], amphiphilic polymers [8][21], or polysulfonates [22]. Silica shells can also be used to

Multilayer capsules made of weak polyelectrolytes: a review on the preparation, functionalization and applications in drug delivery

• Varsha Sharma and
• Anandhakumar Sundaramurthy

Beilstein J. Nanotechnol. 2020, 11, 508–532, doi:10.3762/bjnano.11.41

• study. Block copolymers such as PMA and PAAm-dimethyldiallylammonium chloride (PAAm-DMDAAC) were used to combine the electrostatic and hydrogen bonding interactions, making them stable over a broader pH range by switching the interactions between the electrostatic and hydrogen binding state [89]. While

Rational design of block copolymer self-assemblies in photodynamic therapy

• Maxime Demazeau,
• Laure Gibot,
• Anne-Françoise Mingotaud,
• Patricia Vicendo,
• Clément Roux and
• Barbara Lonetti

Beilstein J. Nanotechnol. 2020, 11, 180–212, doi:10.3762/bjnano.11.15

• , regarding the block copolymers used as nanovectors for the delivery of the photosensitizer. In particular, we describe the chemical nature and structure of the block copolymers showing a very large range of existing systems, spanning from natural polymers such as proteins or polysaccharides to synthetic

• that could be either hydrophobic or a polyelectrolyte enabled the creation of numerous systems [8]. Depending on their structure, copolymers may also form self-assemblies. This is typically the case for amphiphilic block copolymers, which can form in aqueous solution polymer nanoobjects such as

• focus on the benefits provided by block copolymers in photodynamic therapy (PDT), as described schematically in Figure 1 [15]. Its concept lies in the use of photosensitizing molecules that have the ability to transfer their energy to oxygen upon irradiation, leading to the in situ formation of reactive

Incorporation of doxorubicin in different polymer nanoparticles and their anticancer activity

• Sebastian Pieper,
• Hannah Onafuye,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Martin Michaelis and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 2062–2072, doi:10.3762/bjnano.10.201

• , nanoparticles produced by nanoprecipitation, micelles based on multi-arm star-shaped PLGA–PEG block copolymers, or nanopolymersomes [14][15][16][17][18]. In addition, PLGA nanoparticles prepared at pH 7 displayed a more controlled and sustained doxorubicin release than PLGA nanoparticles prepared without pH

• such as nanoparticles or micelles with doxorubicin covalently bound to the polymer, nanoparticles produced by nanoprecipitation, micelles based on multi-arm star-shaped PLGA–PEG block copolymers, or nanopolymersomes [14][15][16][17][18]. Nanoparticle efficacy in cell culture Finally, the effects of

• preparations, which display more sustained drug release, such as nanoparticles or micelles with doxorubicin covalently bound to the polymer, nanoparticles produced by nanoprecipitation, micelles based on multi-arm star-shaped PLGA–PEG block copolymers, or nanopolymersomes [14][15][16][17][18] may overcome such

Layered double hydroxide/sepiolite hybrid nanoarchitectures for the controlled release of herbicides

• Ediana Paula Rebitski,
• Margarita Darder and
• Pilar Aranda

Beilstein J. Nanotechnol. 2019, 10, 1679–1690, doi:10.3762/bjnano.10.163

• , iii) field-induced material control, iv) new manipulations of atoms and molecules, and v) theoretical modeling and design [1][2]. Based on these premises a large number of nanoarchitectonic materials have been prepared including mesoporous solids, self-organized block-copolymers, supramolecular

Materials nanoarchitectonics at two-dimensional liquid interfaces

• Katsuhiko Ariga,
• Michio Matsumoto,
• Taizo Mori and
• Lok Kumar Shrestha

Beilstein J. Nanotechnol. 2019, 10, 1559–1587, doi:10.3762/bjnano.10.153

• mechanisms of formation and transformation of zero-dimensional structures within two-dimensional media (dot-dispersed monolayers of block copolymers) [200]. Self-assembled monolayers of polystyrene-b-poly(4-vinylpyridine) and its supramolecular complex with 3-n-pentadecylphenol at the air–water interface

• mechanism might be generalized for zero-dimensional dot-dispersed monolayers of block-copolymers. Wen and co-workers reported the drastic modification of two-dimensionally patterned Langmuir–Blodgett (LB) films of polystyrene-b-poly(2-vinylpyridine) transferred from the air–water interface through acetone

Highly ordered mesoporous silica film nanocomposites containing gold nanoparticles for the catalytic reduction of 4-nitrophenol

• Mohamad Azani Jalani,
• Leny Yuliati,
• Siew Ling Lee and
• Hendrik O. Lintang

Beilstein J. Nanotechnol. 2019, 10, 1368–1379, doi:10.3762/bjnano.10.135

• surfactant to form the material Mobil composition of matter (MCM)-41 [15]. Considering their low toxicity, their bio-degradable nature, and the fact that they are inexpensive and highly availability, non-ionic surfactants such as Brij [16] and Pluronic [17] block copolymers have also been employed as

pH-mediated control over the mesostructure of ordered mesoporous materials templated by polyion complex micelles

• Emilie Molina,
• Mélody Mathonnat,
• Jason Richard,
• Patrick Lacroix-Desmazes,
• Martin In,
• Philippe Dieudonné,
• Thomas Cacciaguerra,
• Corine Gérardin and
• Nathalie Marcotte

Beilstein J. Nanotechnol. 2019, 10, 144–156, doi:10.3762/bjnano.10.14

• , silica-based ordered mesoporous materials (OMMs) have attracted considerable attention in various fields such as adsorption, separation and catalysis. The formation of these mesostructures relies on a supramolecular assembly process between silicic species and surfactants or amphiphilic block copolymers

• conditions, which are much more appropriate for a large-scale material production with controlled environmental, health and safety risks. Among the SDA materials that have been employed, non-ionic block copolymers such as poly(alkylene oxide) triblock copolymers have attracted more attention due to the

• as the material synthesis is conducted under strongly acidic conditions (charge-matching pathway (S0H+)(X−I+)) [4][8]. In contrast, the first attempts to synthesize materials in quasi neutral solution (pH > 2) using non-ionic block copolymers, which involve weaker interactions between the PEO chains

Block copolymers for designing nanostructured porous coatings

• Roberto Nisticò

Beilstein J. Nanotechnol. 2018, 9, 2332–2344, doi:10.3762/bjnano.9.218

• thin coatings, one simple route involves the use of self-assembled amphiphilic block copolymers either as the porogen (acting as sacrificial templating agents for the production of inorganic architectures) or as a source of the porogen (by self-assembly for the production of polymeric substrates

• ). Therefore, an extended discussion around the exploitation of block copolymers is proposed here in this review, using polystyrene-block-polyethylene oxide (PS-b-PEO) as the model substrate, and critical points are highlighted. Keywords: block copolymers; coatings; materials science; porous materials; self

• using different synthetic routes to facilitate the incorporation of multiple chemical functionalities into the porous framework or at the pore surface [33]. The self-assembly of block copolymers is an exceptional strategy for inducing well-ordered and regular porosity in polymers [6][32]. Block

Nanoconjugates of a calixresorcinarene derivative with methoxy poly(ethylene glycol) fragments for drug encapsulation

• Alina M. Ermakova,
• Julia E. Morozova,
• Yana V. Shalaeva,
• Victor V. Syakaev,
• Aidar T. Gubaidullin,
• Alexandra D. Voloshina,
• Vladimir V. Zobov,
• Irek R. Nizameev,
• Olga B. Bazanova,
• Igor S. Antipin and
• Alexander I. Konovalov

Beilstein J. Nanotechnol. 2018, 9, 2057–2070, doi:10.3762/bjnano.9.195

• higher population of ending groups than linear polymers. Earlier, syntheses of amphiphilic derivatives of calixarenes and oligolactic acid [10][11], calixarenes and PEG [12][13][14][15][16][17][18], calixarene and calixresorcinarene polylactides [19] and polycaprolactones [20][21], as well as block

• copolymers on the base of calixresorcinarene [22] were described. However, the investigations of calixresorcinarene–polymer conjugates involving synthesis, the study of toxicity and the encapsulation of guests are very limited [22]. It is known that PEG is the most commonly used polymer in the production of

Self-assembled quasi-hexagonal arrays of gold nanoparticles with small gaps for surface-enhanced Raman spectroscopy

• Emre Gürdal,
• Simon Dickreuter,
• Fatima Noureddine,
• Pascal Bieschke,
• Dieter P. Kern and
• Monika Fleischer

Beilstein J. Nanotechnol. 2018, 9, 1977–1985, doi:10.3762/bjnano.9.188

• enhanced Raman spectroscopy (SERS) [10]. Ordered arrays of such particles can be fabricated by different methods. Electron-beam lithography for example is a top-down method which provides good control, but is time consuming and costly. In contrast, the self-assembly of block-copolymers is a bottom-up

Facile phase transfer of gold nanorods and nanospheres stabilized with block copolymers

• Yaroslav I. Derikov,
• Georgiy A. Shandryuk,
• Raisa V. Talroze,
• Alexander A. Ezhov and
• Yaroslav V. Kudryavtsev

Beilstein J. Nanotechnol. 2018, 9, 616–627, doi:10.3762/bjnano.9.58

• the use of strong thiol and amine surfactants. Keywords: Au nanorods; block copolymers; optical absorbance spectroscopy; phase transfer; seeded growth method; Introduction The size effects that determine the functional characteristics of nanoparticles are no less important than their precise

• number of interacting pendant groups that provide nanoparticle “wrapping” [31][32][33]. Block copolymers can also be used for the stabilization of Au nanoparticles via grafting-to [34][35], grafting-from [36] and wrapping [29][37] strategies. Since nanoparticles can be driven by laser light [36], they

• enhance sensitivity of amphiphilic dispersions to external stimuli. Block copolymers are effective for the phase transfer of spherical Au nanoparticles up to 30 nm in diameter from aqueous to organic phases [29][35][36]. The tendency for aggregation is increased when the block interacting with the

Identifying the nature of surface chemical modification for directed self-assembly of block copolymers

• Laura Evangelio,
• Federico Gramazio,
• Matteo Lorenzoni,
• Michaela Gorgoi,
• Francisco Miguel Espinosa,
• Ricardo García,
• Francesc Pérez-Murano and
• Jordi Fraxedas

Beilstein J. Nanotechnol. 2017, 8, 1972–1981, doi:10.3762/bjnano.8.198

• the block copolymers. We have chosen hard X-ray high kinetic energy photoelectron spectroscopy as an exploration technique because it provides information on the electronic structure of buried interfaces. The outcome of the characterization sheds light onto key aspects of directed self-assembly

• : grafted brush layer, chemical pattern creation and brush/block co-polymer interface. Keywords: block copolymer; chemical guiding pattern; directed self-assembly; thin film; X-ray photoemission spectroscopy; Introduction Directed self-assembly (DSA) of block copolymers (BCPs) is a chemical-based

• demonstrated that HAXPES using synchrotron radiation is a powerful spectroscopic tool to explore the chemical properties of surfaces and buried interfaces of brush layers for directed self-assembly of block copolymers, since valuable chemical information as a function of probing depth can be obtained. The

Fabrication of carbon nanospheres by the pyrolysis of polyacrylonitrile–poly(methyl methacrylate) core–shell composite nanoparticles

• Dafu Wei,
• Youwei Zhang and
• Jinping Fu

Beilstein J. Nanotechnol. 2017, 8, 1897–1908, doi:10.3762/bjnano.8.190

• treatments, and thus is very crucial to obtain discrete carbon nanospheres after pyrolysis. Jérom et al. [32] obtained discrete carbon nanocapules after pyrolysis of stable PAN-b-PAA micelles with Au-nanoparticle-crosslinked cores. However, the difficulty in synthesis of the block copolymers and the low

Synthesis of [Fe(L_eq)(L_ax)]_n coordination polymer nanoparticles using blockcopolymer micelles

• Christoph Göbel,
• Ottokar Klimm,
• Florian Puchtler,
• Sabine Rosenfeldt,
• Stephan Förster and
• Birgit Weber

Beilstein J. Nanotechnol. 2017, 8, 1318–1327, doi:10.3762/bjnano.8.133

• (mostly magnetite) [12]. For coordination polymers (CP) or networks a limited amount of methods are applicable because of the very demanding reaction conditions and/or incompatible reactants. Recently we demonstrated that the use of block copolymers (BCPs) is a highly promising and easy approach for the

• the iron centres are still in the HS state. Conclusion This work focused on the transfer of the concept for the formation of nanoparticles of coordination polymers in a block copolymer matrix. The central goal was to demonstrate that this concept of block copolymers as microreactors is not restricted

Polystyrene-block-poly(ethylene oxide) copolymers as templates for stacked, spherical large-mesopore silica coatings: dependence of silica pore size on the PS/PEO ratio

• Roberto Nisticò,
• Giuliana Magnacca,
• Sushilkumar A. Jadhav and
• Dominique Scalarone

Beilstein J. Nanotechnol. 2016, 7, 1454–1460, doi:10.3762/bjnano.7.137

• between the hydrophilic/hydrophobic ratio of the two polymer blocks and the size of the final silica pores. The obtained results prove that by tuning the PS/PEO ratio, the pore size of the templated silica films can be easily and finely predicted. Keywords: block copolymers; controlled porosity

• block copolymers, such as polystyrene-block-poly(ethylene oxide) (PS-b-PEO), have been successfully employed to synthetize mesoporous oxides [19][25]. Starting from these previous works, we decided to develop a systematic study to gain better control on the morphological features of templated silica

• copolymer films obtained by spin-coating deposition of block copolymer micellar solutions were transformed into silica nanoporous thin layers by thermal treatment performed in air. This way, the organic templating species (i.e., block copolymers) were degraded and removed, leaving voids which formed the

Reasons and remedies for the agglomeration of multilayered graphene and carbon nanotubes in polymers

• Rasheed Atif and
• Fawad Inam

Beilstein J. Nanotechnol. 2016, 7, 1174–1196, doi:10.3762/bjnano.7.109

• dispersion [139]. Nanoclay also improved the CNT dispersion state in CNT–polyamide nanocomposites. Titania can improve the mechanical properties of polymers. So, titania is a better option to improve the dispersion of CNTs than block copolymers. Also, large amounts of CNTs can be uniformly dispersed using

Reconstitution of the membrane protein OmpF into biomimetic block copolymer–phospholipid hybrid membranes

• Matthias Bieligmeyer,
• Franjo Artukovic,
• Stephan Nussberger,
• Thomas Hirth,
• Thomas Schiestel and
• Michaela Müller

Beilstein J. Nanotechnol. 2016, 7, 881–892, doi:10.3762/bjnano.7.80

• -isoprene-block-ethylene oxide) block copolymers blended with 1,2-diphytanoyl-sn-glycero-3-phosphocholine. By reconstituting the outer membrane protein OmpF from Escherichia coli into these membranes, we demonstrate functionality of this protein in biomimetic lipopolymer membranes, independent of the

• molecular weight of the block copolymers. At low voltages, the channel conductance of OmpF in 1 M KCl was around 2.3 nS. In line with these experiments, integration of OmpF was also revealed by impedance spectroscopy. Our results indicate that blending synthetic polymer membranes with phospholipids allows

• been assessed yet [46][47]. In the present work, we studied the reconstitution of OmpF from Escherichia coli into biomimetic lipopolymer membranes, generated by self-assembly of amphiphilic poly(1,4-isoprene-block-ethylene oxide) block copolymers (PIPEO) and 1,2-diphytanoyl-sn-glycero-3-phosphocholine

High-resolution noncontact AFM and Kelvin probe force microscopy investigations of self-assembled photovoltaic donor–acceptor dyads

• Benjamin Grévin,
• Pierre-Olivier Schwartz,
• Laure Biniek,
• Martin Brinkmann,
• Nicolas Leclerc,
• Elena Zaborova and
• Stéphane Méry

Beilstein J. Nanotechnol. 2016, 7, 799–808, doi:10.3762/bjnano.7.71

• . To establish the resolution limits of SPV imaging by KPFM, there is now a crucial need to investigate model D–A interfaces with better defined structural and electronic properties. In that context, several groups have used the “microphase separation ability” of D–A block copolymers [12] or oligomers

Correlative infrared nanospectroscopic and nanomechanical imaging of block copolymer microdomains

• Benjamin Pollard and
• Markus B. Raschke

Beilstein J. Nanotechnol. 2016, 7, 605–612, doi:10.3762/bjnano.7.53

• channel alone. These variations suggest that regions of multicomponent chemical composition, such as the interfacial mixing regions between microdomains, are correlated with high spatial heterogeneity in nanoscale material properties. Keywords: block copolymers, force–distance nanomechanical spectroscopy