Electrospun nanofibers: building blocks for the repair of bone tissue

• Tuğrul Mert Serim,
• Gülin Amasya,
• Tuğba Eren-Böncü,
• Ceyda Tuba Şengel-Türk and
• Ayşe Nurten Özdemir

Beilstein J. Nanotechnol. 2024, 15, 941–953, doi:10.3762/bjnano.15.77

• observed. Pore size and porosity percentage are also related to the molecular weight of the polymer [57][66]. Solvent or solvent mixture The solvent, or the solvent mixture, used is critical for the stable formation of a Taylor cone. It affects the intermolecular interaction in the polymer–solvent system

Metal-organic framework-based nanomaterials as opto-electrochemical sensors for the detection of antibiotics and hormones: A review

• Akeem Adeyemi Oladipo,
• Saba Derakhshan Oskouei and
• Mustafa Gazi

Beilstein J. Nanotechnol. 2023, 14, 631–673, doi:10.3762/bjnano.14.52

• simpler and more versatile than FRET since it does not require covalent bonding between the analyte and the fluorophore or intermolecular interaction [44][48][49]. Although energy transfer occurs in both IFE and FRET, the process can be distinguished by the fluorescence lifetime. In contrast to FRET

Nanoporous and nonporous conjugated donor–acceptor polymer semiconductors for photocatalytic hydrogen production

• Zhao-Qi Sheng,
• Yu-Qin Xing,
• Yan Chen,
• Guang Zhang,
• Shi-Yong Liu and
• Long Chen

Beilstein J. Nanotechnol. 2021, 12, 607–623, doi:10.3762/bjnano.12.50

• at the meta position intensified the intermolecular interaction, which, however, was weakened by F substitution at the meta position. Consequently, the linear P39 (Figure 5) with both methoxy group and F on BT afforded the highest HER of 399 μmol·h−1 (30 mg). This suggests that selectively

Adsorption and self-assembly of porphyrins on ultrathin CoO films on Ir(100)

• Feifei Xiang,
• Tobias Schmitt,
• Marco Raschmann and
• M. Alexander Schneider

Beilstein J. Nanotechnol. 2020, 11, 1516–1524, doi:10.3762/bjnano.11.134

• , an effective electronic decoupling from the metal substrate is achieved. However, on the 1BL film, Co-DPP molecules are sufficiently mobile at 300 K and coalesce to self-assembled molecular islands when cooled to 80 K despite their rather weak intermolecular interaction. In contrast, on the 2BL film

• through its central metal atom and provides rather weak intermolecular interaction via its phenyl substituents, 2H-TCNPP may use its cyanophenyl groups for either coupling to the substrate or for providing relatively strong molecule–molecule interactions. The two molecules have been investigated on metal

• landscape provided by the ultrathin film, which supports the self-assembly despite the rather weak intermolecular interaction mediated by the phenyl groups. The surface influence is absent or considerably weaker when two bilayer films are deposited. Here, the Co-DPP rotate at temperatures of 80 K and higher

Nontoxic pyrite iron sulfide nanocrystals as second electron acceptor in PTB7:PC₇₁BM-based organic photovoltaic cells

• Olivia Amargós-Reyes,
• José-Luis Maldonado,
• Omar Martínez-Alvarez,
• María-Elena Nicho,
• José Santos-Cruz,
• Juan Nicasio-Collazo,
• Irving Caballero-Quintana and
• Concepción Arenas-Arrocena

Beilstein J. Nanotechnol. 2019, 10, 2238–2250, doi:10.3762/bjnano.10.216

• . This band intensity increase could suggest some intermolecular interaction between the O atom of the carbonyl groups of PTB7 and PC71BM with the Fe atoms of the FeS2 NCs. In addition, upon the incorporation of FeS2 into the PTB7:PC71BM mixture, the 1603 cm−1 band was observed to shift red by ≈4 cm−1 to

Polymorphic self-assembly of pyrazine-based tectons at the solution–solid interface

• Achintya Jana,
• Puneet Mishra and
• Neeladri Das

Beilstein J. Nanotechnol. 2019, 10, 494–499, doi:10.3762/bjnano.10.50

• recent density functional theory calculations indicated that for molecules with pyridine pendants on HOPG substrates, the molecule–substrate interaction energy can become comparable or even exceed the intermolecular interaction energy [24]. Although the molecular surface densities for the two polymorphs

Electro-optical interfacial effects on a graphene/π-conjugated organic semiconductor hybrid system

• Karolline A. S. Araujo,
• Luiz A. Cury,
• Matheus J. S. Matos,
• Thales F. D. Fernandes,
• Luiz G. Cançado and
• Bernardo R. A. Neves

Beilstein J. Nanotechnol. 2018, 9, 963–974, doi:10.3762/bjnano.9.90

• microscopy; self-assembly; Introduction Organic semiconductors offer a wide range of possible applications, from thin-film transistors to sensors and solar cells [1][2][3][4][5][6]. Their optical and electronic properties are strongly linked to intermolecular interaction parameters associated with molecular

Synthesis and characterization of two new TiO₂-containing benzothiazole-based imine composites for organic device applications

• Anna Różycka,
• Agnieszka Iwan,
• Krzysztof Artur Bogdanowicz,
• Michal Filapek,
• Natalia Górska,
• Damian Pociecha,
• Marek Malinowski,
• Patryk Fryń,
• Agnieszka Hreniak,
• Jakub Rysz,
• Paweł Dąbczyński and
• Monika Marzec

Beilstein J. Nanotechnol. 2018, 9, 721–739, doi:10.3762/bjnano.9.67

• independently from the ratio of compound: TiO2. Moreover, this becomes a two-step process with well-exhibited maxima. This implies that TiO2 provides not only a larger surface area for sensitizer adsorption and good electron transport [50], but can also shift the dye energy levels by intermolecular interaction

• ratio (3:0, 3:1, 3:2, 3:3) showed a lower energy gap and HOMO–LUMO energy levels compared to pure TiO2. This implies that TiO2 provides not only a larger surface area for sensitizer adsorption and good electron collection, but also causes a shift of the imine energy levels resulting from intermolecular

• interaction. Also the temperature of the phase transition was slightly affected with the increase of TiO2 concentration in imine-based composites. The changes observed in the Fourier transform middle-infrared absorption (FT-MIR) spectra confirmed the significant influence of TiO2 on structural properties of

Engineering of oriented carbon nanotubes in composite materials

• Razieh Beigmoradi,
• Abdolreza Samimi and
• Davod Mohebbi-Kalhori

Beilstein J. Nanotechnol. 2018, 9, 415–435, doi:10.3762/bjnano.9.41

• the CNT structure by adding compounds. It is very difficult to get a good FTIR spectrum of CNTs, thus attenuated total reflection (ATR) FTIR can be used (except with carbon crystal, when germanium is more suitable). The investigation of the intermolecular interaction between the polymer chain and CNT

Controlled supramolecular structure of guanosine monophosphate in the interlayer space of layered double hydroxide

• Gyeong-Hyeon Gwak,
• Istvan Kocsis,
• Yves-Marie Legrand,
• Mihail Barboiu and
• Jae-Min Oh

Beilstein J. Nanotechnol. 2016, 7, 1928–1935, doi:10.3762/bjnano.7.184

• occupies 22 Å2 (60 Å2 × 0.37) and 25 Å2 (60 Å2 × 0.42), respectively for GL-S and GL-R. Thus, the GMP moiety in GL-S could exist separately without effective intermolecular interaction by GMP, while GMPs in GL-R packs to form a ribbon-type supramolecular arrangement. Differential scanning calorimetry (DSC

• attributed to breaking intermolecular interaction of interlayer GMP as well as evaporating interlayer water molecules. Interlayer water was evaporated from the DSC of pristine LDH at around 210 °C with an enthalpy change of ≈40 kJ/mol, which was subtracted from the endothermic enthalpy of GL hybrids. The

• resulting intermolecular interaction between GMP was found to be 11.2 kJ/mol GMP and 101.6 kJ/mol GMP for GL-S and GL-R, respectively. The much higher energy for GL-R implied that there might be strong intermolecular interaction such as hydrogen bonding. According to the literature where hydrogen bonding

Phenalenyl-based mononuclear dysprosium complexes

• Yanhua Lan,
• Andrea Magri,
• Olaf Fuhr and
• Mario Ruben

Beilstein J. Nanotechnol. 2016, 7, 995–1009, doi:10.3762/bjnano.7.92

• condensed rings so that the single-ion anisotropy between the two molecules is probably canceled out leading to a zero overall anisotropy so that no out-of-phase signal could be observed under zero dc field. In principle the effect of the intermolecular interaction could be evaluated by preparing a

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

• interplay between crystallinity, composition, and intermolecular interaction between and within single domains. Bivariate histograms, showing the correlations between different signal channels across the entire image region. The arrow in (a) indicates that the correlation is seen to continue towards the

Anticancer efficacy of a supramolecular complex of a 2-diethylaminoethyl–dextran–MMA graft copolymer and paclitaxel used as an artificial enzyme

• Yasuhiko Onishi,
• Yuki Eshita,
• Rui-Cheng Ji,
• Masayasu Onishi,
• Takashi Kobayashi,
• Masaaki Mizuno,
• Jun Yoshida and
• Naoji Kubota

Beilstein J. Nanotechnol. 2014, 5, 2293–2307, doi:10.3762/bjnano.5.238

• compared with DDMC. Since a shift in wavenumber will take place if an intermolecular interaction occurs, an absorption band will generally envelop the individual peaks. The hydrophobic environment of this intermolecular interaction can also be postulated from the broad absorption spectrum of the DDMC/PTX

Spectroscopic mapping and selective electronic tuning of molecular orbitals in phosphorescent organometallic complexes – a new strategy for OLED materials

• Pascal R. Ewen,
• Jan Sanning,
• Tobias Koch,
• Nikos L. Doltsinis,
• Cristian A. Strassert and
• Daniel Wegner

Beilstein J. Nanotechnol. 2014, 5, 2248–2258, doi:10.3762/bjnano.5.234

• ). The adsorption angle relative to the direction differs for each structure (9 ± 3° (Figure 2d), 4 ± 3° (Figure 2e) and 15 ± 3° (Figure 2f)). This is another indication for a weak overall molecule–substrate coupling. Furthermore, the lateral intermolecular interaction also seems to be relatively weak

Influence of the solvent on the stability of bis(terpyridine) structures on graphite

• Daniela Künzel and
• Axel Groß

Beilstein J. Nanotechnol. 2013, 4, 269–277, doi:10.3762/bjnano.4.29

• , they all agree that the adsorption of BTP from the TCB solvent is almost thermoneutral. The substrate simply acts as a template to allow a planar arrangement of the network, which is stabilized by the intermolecular interaction. Using an atomic thermodynamics approach, the order of the stability of

• TCB solution is almost thermoneutral. Hence, it is the intermolecular interaction in the hydrogen-bonded networks on graphite that stabilizes the molecular layers; the surface just acts as a template to allow a planar arrangement of the hydrogen-bonded network. Computational details In this study

• negative, the intermolecular interaction is attractive, whereas for the DP structure the packing is so dense that the intermolecular interaction is already repulsive. The range of adsorption enthalpies is 80 meV larger than the range of adsorption energies of the corresponding structures at the gas/solid

Structural and electronic properties of oligo- and polythiophenes modified by substituents

• Simon P. Rittmeyer and
• Axel Groß

Beilstein J. Nanotechnol. 2012, 3, 909–919, doi:10.3762/bjnano.3.101

• are not concerned with intermolecular interaction or adsorption of the aromatic molecules [30][31]. The ionic cores were represented by projector augmented wave (PAW) potentials [32] as constructed by Kresse and Joubert [33]. The electronic one-particle wave functions were expanded in a plane-wave

• oligo- and polythiophenes As a first step and as a reference, we determined the properties of unsubstituted oligo- and polythiophenes. All oligomers were modeled by using a sufficiently large box in three dimensions to avoid intermolecular interaction due to the use of a periodic DFT code. Note that in

An NC-AFM and KPFM study of the adsorption of a triphenylene derivative on KBr(001)

• Antoine Hinaut,
• Adeline Pujol,
• Florian Chaumeton,
• David Martrou,
• André Gourdon and
• Sébastien Gauthier

Beilstein J. Nanotechnol. 2012, 3, 221–229, doi:10.3762/bjnano.3.25

• strong intermolecular interaction due to π-stacking. Keywords: atomic force microscopy; insulating surfaces; Kelvin force probe microscopy; molecular adsorption; Introduction The study of molecular adsorption on atomically clean, well-defined surfaces of bulk insulators is progressing rapidly due to

• structure. Considering the structure of the molecule, it is seen that only two CN groups can adsorb on K+ ions when the molecule is nearly vertical, contributing approximately 0.4 eV to the adsorption energy. The stabilization of MLv relative to MLh should then result from the intermolecular interaction

Molecular-resolution imaging of pentacene on KCl(001)

• Julia L. Neff,
• Jan Götzen,
• Enhui Li,
• Michael Marz and
• Regina Hoffmann-Vogel

Beilstein J. Nanotechnol. 2012, 3, 186–191, doi:10.3762/bjnano.3.20

• interaction is indeed weak compared to the intermolecular interaction. Figure 1c illustrates the upright ordering of the molecules. For comparison we have added a top-view sketch of the well-known bulk phase, showing the herringbone arrangement that the molecules assume to optimize the π-stacking (Figure 1d

Surface functionalization of aluminosilicate nanotubes with organic molecules

• Wei Ma,
• Weng On Yah,
• Hideyuki Otsuka and
• Atsushi Takahara

Beilstein J. Nanotechnol. 2012, 3, 82–100, doi:10.3762/bjnano.3.10

• arise from two factors: Planarity and intermolecular interaction [64][65][66]. Normally, red-shifting occurs in the solid state when the molecular backbone is more planar compared to the isolated state in solution, due an increase in conjugation length. Thus, the blue-shifting observed in the spectra of

• thiophene/imogolite films compared to solution indicates that additional an intermolecular interaction was present that plays a role in controlling the solid-state optical properties [65]. Fluorescence spectroscopy is a suitable analytical tool for monitoring the intermolecular interactions of terthiophene

• before and after chemisorption on imogolite. The absorption peak of the HT3P/imogolite hybrid at 322 nm, shifted from that of the HT3P in THF solution (λmax 367 nm), provides additional proof for the formation of an H-type intermolecular interaction of terthiophene on the imogolite surface (Figure 18

STM study on the self-assembly of oligothiophene-based organic semiconductors

• Elena Mena-Osteritz,
• Marta Urdanpilleta,
• Erwaa El-Hosseiny,
• Berndt Koslowski,
• Paul Ziemann and
• Peter Bäuerle

Beilstein J. Nanotechnol. 2011, 2, 802–808, doi:10.3762/bjnano.2.88

• ordering on the substrate. Keywords: 2-D crystals; functionalized oligothiophenes; H-bonding; intermolecular interaction; scanning tunneling microscopy; Introduction In the last few decades conjugated organic polymers and oligomers have attracted a broad interest due to their excellent electronic and

Self-organizing bioinspired oligothiophene–oligopeptide hybrids

• Alexey K. Shaytan,
• Eva-Kathrin Schillinger,
• Elena Mena-Osteritz,
• Sylvia Schmid,
• Pavel G. Khalatur,
• Peter Bäuerle and
• Alexei R. Khokhlov

Beilstein J. Nanotechnol. 2011, 2, 525–544, doi:10.3762/bjnano.2.57

• dipole moments of the single molecules in addition to a favorable intermolecular interaction of hydrophilic (peptide–PEO) and hydrophobic (quaterthiophene) parts of the molecules. Furthermore, the model revealed a separation of 8 Å between the quaterthiophene backbones of two adjacent dimers of 6', due

• to the antiparallel intermolecular interaction of their peptide arms, similar to the case of 1' (Figure 8). In the case of the postulated formation of dimers of 6', however, favorable van der Waals interactions of the alkyl side chains are also involved (Figure 10d) [29]. Eventually, the voids in

Intermolecular vs molecule–substrate interactions: A combined STM and theoretical study of supramolecular phases on graphene/Ru(0001)

• Michael Roos,
• Benedikt Uhl,
• Daniela Künzel,
• Harry E. Hoster,
• Axel Groß and
• R. Jürgen Behm

Beilstein J. Nanotechnol. 2011, 2, 365–373, doi:10.3762/bjnano.2.42

• different behavior of the PTCDA molecules, we again compare the corrugation of the adsorption energy with the intermolecular interaction between adjacent molecules in the herringbone configuration of PTCDA. Recent DFT calculations by Mura et al. [26] have shown that the stabilization energy per molecule is

• exclusively populated the areas between the maxima of the moiré structure of the buckled graphene layer. The consequences for the competing intermolecular interactions and corrugation in the adsorption potential are discussed and compared with the theoretical results. Keywords: graphene film; intermolecular

• interaction; large organic molecules; substrate–adsorbate interaction; supramolecular structure; Introduction It is well known that the formation of highly ordered 2D supramolecular networks on smooth surfaces, such as metal substrates or highly oriented pyrolytic graphite (HOPG), is mainly governed by the

Manipulation of gold colloidal nanoparticles with atomic force microscopy in dynamic mode: influence of particle–substrate chemistry and morphology, and of operating conditions

• Samer Darwich,
• Karine Mougin,
• Akshata Rao,
• Enrico Gnecco,
• Shrisudersan Jayaraman and
• Hamidou Haidara

Beilstein J. Nanotechnol. 2011, 2, 85–98, doi:10.3762/bjnano.2.10

• the particles, we did not find any differences when manipulating ordered vs random distributed particles. Keywords: atomic force microscopy; intermolecular interaction; manipulation; nanoparticles; precise positioning; self-assembled monolayers; Introduction Nanotechnology, which aims at the ideal

Oriented growth of porphyrin-based molecular wires on ionic crystals analysed by nc-AFM

• Thilo Glatzel,
• Lars Zimmerli,
• Shigeki Kawai,
• Ernst Meyer,
• Leslie-Anne Fendt and
• Francois Diederich

Beilstein J. Nanotechnol. 2011, 2, 34–39, doi:10.3762/bjnano.2.4

• moment of the molecules was sufficient to bind them to the surface; while a stabilization of the molecular assemblies was reached due to the intermolecular interaction by π–π binding. Here, we show that the atomic structure of the substrate can control the direction of the wires and consequently, complex