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

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

• polymers, heterojunctions between CPs and other semiconductors have also been developed to facilitate the intermolecular charge transfer and transport. The interactions between the CPs and various semiconductors in the heterojunctions could involve strong covalent bonds, ionic bonds, or hydrogen bonds [90

Surface-enhanced Raman scattering of water in aqueous dispersions of silver nanoparticles

• Paulina Filipczak,
• Krzysztof Hałagan,
• Jacek Ulański and
• Marcin Kozanecki

Beilstein J. Nanotechnol. 2021, 12, 497–506, doi:10.3762/bjnano.12.40

• of water molecules) and models of water as a mixture of discrete species (water clusters) [5][6][7][8]. It is difficult to choose between them because the spatial network of hydrogen bonds has features of both continuous and discrete models. The broad Raman band of water located in the range of 3000

• . Irrespective of how the spectra are deconvoluted, all models of liquid water agree that the lower the frequency of the band, the stronger the hydrogen bonds and water structuration. The interactions with various solutes [17][18] and the influence of the temperature [13] on the water structure can be analysed

• , which favours the presence of resonance. This indicates that OH oscillators of water molecules can reach the resonant state provided that they are strongly linked to each other via hydrogen bonds. All factors considered destructive to the hydrogen bond structure (e.g., temperature) make the resonance

Cu₂O nanoparticles for the degradation of methyl parathion

• Juan Rizo,
• David Díaz,
• Benito Reyes-Trejo and
• M. Josefina Arellano-Jiménez

Beilstein J. Nanotechnol. 2020, 11, 1546–1555, doi:10.3762/bjnano.11.137

• found on its surface (see XPS results below). These surface hydroxy groups can either be directly involved in the SN2@P mechanism or they can polarize the oxygen–hydrogen bonds of the water molecules and thus facilitate the hydrolysis of MP. Further research regarding the exact mechanism for the

Key for crossing the BBB with nanoparticles: the rational design

• Sonia M. Lombardo,
• Marc Schneider,
• Akif E. Türeli and
• Nazende Günday Türeli

Beilstein J. Nanotechnol. 2020, 11, 866–883, doi:10.3762/bjnano.11.72

• paracellular pathway of hydrophilic molecules. Therefore, most molecules have to go through the transcellular pathway to cross the BBB. However, only small lipophilic molecules, with a molecular weight lower than 400 Da and less than eight hydrogen bonds, or small gas molecules (such as CO2 or O2) can freely

A novel dry-blending method to reduce the coefficient of thermal expansion of polymer templates for OTFT electrodes

• Xiangdong Ye,
• Bo Tian,
• Yuxuan Guo,
• Fan Fan and
• Anjiang Cai

Beilstein J. Nanotechnol. 2020, 11, 671–677, doi:10.3762/bjnano.11.53

• to 96 ppm/°C. This decrease is mainly attributed to two factors. First, the CTE of SiO2 is only 0.54 ppm/°C [12]. The higher content of SiO2 nanoparticles with a low CTE, the greater the influence on the CTE of PDMS. Second, covalent bonds are formed between SiO2 nanoparticles and PDMS and hydrogen

• bonds are formed between SiO2 nanoparticles [14][21]. The higher content of SiO2 nanoparticles, the greater the interaction among the bonds between PDMS and SiO2 nanoparticles. This restricts the thermal deformation of PDMS. Hence, the CTE of the PDMS/SiO2 composite template significantly decreases. To

Identification of physicochemical properties that modulate nanoparticle aggregation in blood

• Ludovica Soddu,
• Duong N. Trinh,
• Eimear Dunne,
• Dermot Kenny,
• Giorgia Bernardini,
• Ida Kokalari,
• Arianna Marucco,
• Marco P. Monopoli and
• Ivana Fenoglio

Beilstein J. Nanotechnol. 2020, 11, 550–567, doi:10.3762/bjnano.11.44

• groups/nm2 [31][32]. Both surfaces exhibit surface sites able to form hydrogen bonds or hydrophobic interaction with proteins. However, such tendency may be different since hydrogen bond formation obeys geometrical constraints due to the directional character of this bond. On the other hand, both silica

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

• approached, the morphological changes in PVP/PMA capsules were seen with the decrease in multilayer thickness due to disruption of hydrogen bonds [50]. When the same was cross-linked by carbodiimide chemistry, the swelling was observed at higher pH, leading to the formation of highly swollen hydrogels. To

• stabilized with a bifunctional azide crosslinker containing disulfide bonds [95]. The exposure of these capsules to pH 7.2 led to the breaking of hydrogen bonds and complete removal of PMA, resulting in stable PVP capsules with intracellularly degradable disulfide linkages. These multilayers were also found

Molecular architectonics of DNA for functional nanoarchitectures

• Debasis Ghosh,
• Lakshmi P. Datta and
• Thimmaiah Govindaraju

Beilstein J. Nanotechnol. 2020, 11, 124–140, doi:10.3762/bjnano.11.11

• via canonical and noncanonical hydrogen bonding, and with guanine via noncanonical hydrogen bonding interactions. The PDI was functionalized with adenine, owing to its unique ability to form hydrogen bonds with other complementary and noncomplementary nucleobases. The canonical hydrogen bonding

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

Beilstein J. Nanotechnol. 2020, 11, 101–123, doi:10.3762/bjnano.11.10

• partitioned into lipid phases from the aqueous phase in the presence of phosphatidylglycerol, a behavior of arginine often referred to as “arginine magic”. The guanidine group found on arginine has proven to form bidentate hydrogen bonds and electrostatic interaction with sulfate, phosphate and carboxylate

Recent progress in perovskite solar cells: the perovskite layer

• Xianfeng Dai,
• Ke Xu and
• Fanan Wei

Beilstein J. Nanotechnol. 2020, 11, 51–60, doi:10.3762/bjnano.11.5

• counterpart. Here, the van der Waals gap between the organic layer and the inorganic slab is removed. The organic layers are connected with perovskite layers by strong hydrogen bonds in the 2D Dion–Jacobson (2DDJ) perovskite, which has a reasonably enhanced stability compared to the 2DRP perovskite. Guo et al

Design of a nanostructured mucoadhesive system containing curcumin for buccal application: from physicochemical to biological aspects

• Sabrina Barbosa de Souza Ferreira,
• Gustavo Braga,
• Évelin Lemos Oliveira,
• Jéssica Bassi da Silva,
• Hélen Cássia Rosseto,
• Lidiane Vizioli de Castro Hoshino,
• Mauro Luciano Baesso,
• Wilker Caetano,
• Craig Murdoch,
• Helen Elizabeth Colley and
• Marcos Luciano Bruschi

Beilstein J. Nanotechnol. 2019, 10, 2304–2328, doi:10.3762/bjnano.10.222

• nanometer-sized assembly into three-dimensional micelles with a hydrophobic core of PPO and a hydrophilic shell of PEO that can interact by hydrogen bonds with the hydrophilic acrylic-acid derivative polymer. This results in a binary polymeric system with good viscoelasticity, mucoadhesion, softness and

• influence (p < 0.05) the elasticity and cohesiveness, which could be explained by the influence by hydrogen bonds and water mobility in the sample. As elucidated in location studies, CUR is a hydrophobic molecule that is located in the core of polymeric micelles and thus it should not influence this

Porous silver-coated pNIPAM-co-AAc hydrogel nanocapsules

• William W. Bryan,
• Riddhiman Medhi,
• Maria D. Marquez,
• Supparesk Rittikulsittichai,
• Michael Tran and
• T. Randall Lee

Beilstein J. Nanotechnol. 2019, 10, 1973–1982, doi:10.3762/bjnano.10.194

• well-documented and has been shown to occur due to changes in the hydrogen bonding between water and hydrophilic sites along the hydrogel polymer backbone (e.g., –C=O and –NH) [58][63][83]. The loss of hydrogen bonds between water molecules and the amide groups of a pNIPAM hydrogel above its LCST leads

High-tolerance crystalline hydrogels formed from self-assembling cyclic dipeptide

• Yongcai You,
• Ruirui Xing,
• Qianli Zou,
• Feng Shi and
• Xuehai Yan

Beilstein J. Nanotechnol. 2019, 10, 1894–1901, doi:10.3762/bjnano.10.184

• precipitation formation [47]. Herein, we investigate the self-assembly and application of a CDP, cyclo-(Trp-Tyr) (C-WY) (Scheme 1). C-WY contains a rigid six-member ring as a bridge, which increases the structural rigidity and stability. The abundant hydrogen bonds in C-WY endow a high propensity for self

• 3317 cm−1, indicating the formation of strong hydrogen bonds between C-WY molecules in the hydrogel (Figure 1B). Further characterization by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) was performed to inspect the morphology of the hydrogel (Figure 1C,D). The fibers in

• and heat, may be due to the entangled fiber network and extensive intermolecular hydrogen bonds in the hydrogel. In summary, the C-WY hydrogel was found to exhibit excellent environmental tolerance, including resistance to biopolymers, pH, and heat. Hence, the C-WY hydrogel is promising for

Chiral nanostructures self-assembled from nitrocinnamic amide amphiphiles: substituent and solvent effects

• Hejin Jiang,
• Huahua Fan,
• Yuqian Jiang,
• Li Zhang and
• Minghua Liu

Beilstein J. Nanotechnol. 2019, 10, 1608–1617, doi:10.3762/bjnano.10.156

• 4NCLG molecules. Both of the molecules are misaligned in their crystal, which indicates that the bottom molecule is not directly below the upper one. Additionally, the length of intermolecular hydrogen bonds of 2NCLG and 4NCLG assemblies were found to be 1.2 Å and 2.0 Å, respectively. While for 3NCLG

• , the bottom molecule is right below the upper one and the length of intermolecular hydrogen bonds is 2.3 Å (i.e., longer than that of 2NCLG and 3NCLG). This result further demonstrated that the hydrogen bonding of the 3NCLG assembly was weaker than for the 2NCLG and 4NCLG assemblies. The difference in

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

• between amphiphilic triimide with three alkyl chains, a monolayer component, and 1,4,7,10-tetraazacyclododecane (cyclen), a subphase template, was used to regulate the formation of hydrogen bonds between the imide functional groups as hydrogen-bond acceptors and the secondary amine moieties of cyclen as

A silver-nanoparticle/cellulose-nanofiber composite as a highly effective substrate for surface-enhanced Raman spectroscopy

• Yongxin Lu,
• Yan Luo,
• Zehao Lin and
• Jianguo Huang

Beilstein J. Nanotechnol. 2019, 10, 1270–1279, doi:10.3762/bjnano.10.126

• detection limit down to the sub-attomolar (1 × 10−16 M) level and an enhancement factor of 3 × 106 were achieved by using Rhodamine 6G as the analyte. Moreover, this substrate was applied to monitor the molecular recognition through multiple hydrogen bonds in between nucleosides of adenosine and thymidine

• ][58][59]. The SERS substrate was also applied to monitor the molecular recognition through multiple hydrogen bonds between adenosine and thymidine. This paper-based SERS substrate could hold potential in the detection of trace amounts of analytes and for the spectroscopic study of biomolecules

• hydrogen bonds between nucleosides to test its potential in monitoring biomolecules. Figure 6 shows the Raman spectra obtained from adenosine and thymidine, measured before and after the molecular recognition between the two nucleosides on the substrate. Compared to the Raman spectra of the powder samples

Pure and mixed ordered monolayers of tetracyano-2,6-naphthoquinodimethane and hexathiapentacene on the Ag(100) surface

• Robert Harbers,
• Timo Heepenstrick,
• Dmitrii F. Perepichka and
• Moritz Sokolowski

Beilstein J. Nanotechnol. 2019, 10, 1188–1199, doi:10.3762/bjnano.10.118

• formation of the mixed structure occurs spontaneously. An important motif for the structure formation is given by hydrogen bonds between the TNAP molecules. Both molecules, TNAP and HTPEN also form well-ordered monolayers on the Ag(100) surface on their own. In all structures, the molecules are adsorbed in

• planar molecules have been investigated [4][5][6][7][8]. As a result, one finds that, on metallic surfaces, indirect intermolecular charge transfer mediated by the surface plays an important role in addition to intermolecular hydrogen bonds [5]. Particularly interesting are π-conjugated molecules with

• distances from [35], and van der Waals radii from [32]. The structure is composed of parallel rows of molecules aligned along their long axes. The major intermolecular interactions are given by hydrogen bonds between the four cyano groups at the corners and hydrogen atoms on the long sides of the molecule

Porous N- and S-doped carbon–carbon composite electrodes by soft-templating for redox flow batteries

• Maike Schnucklake,
• László Eifert,
• Jonathan Schneider,
• Roswitha Zeis and
• Christina Roth

Beilstein J. Nanotechnol. 2019, 10, 1131–1139, doi:10.3762/bjnano.10.113

• interactions between phloroglucinol and the surfactant lead to the formation of hydrogen bonds to the polyethylene chains of the polymer. In this fashion the porogen initiates a porous structure. It will be removed during the subsequent carbonization step [25]. The new composite materials have great potential

Scavenging of reactive oxygen species by phenolic compound-modified maghemite nanoparticles

• Małgorzata Świętek,
• Yi-Chin Lu,
• Rafał Konefał,
• Liliana P. Ferreira,
• M. Margarida Cruz,
• Yunn-Hwa Ma and
• Daniel Horák

Beilstein J. Nanotechnol. 2019, 10, 1073–1088, doi:10.3762/bjnano.10.108

• augment particle internalization compared to heparin modification alone. Previous studies have suggested that electrostatic interactions, oxidation-dependent conjugation, and hydrogen bonds between the phenolic OH groups and polysaccharide moieties and/or amino acid residues of the cell membrane may

Features and advantages of flexible silicon nanowires for SERS applications

• Hrvoje Gebavi,
• Vlatko Gašparić,
• Dubravko Risović,
• Nikola Baran,
• Paweł Henryk Albrycht and
• Mile Ivanda

Beilstein J. Nanotechnol. 2019, 10, 725–734, doi:10.3762/bjnano.10.72

• water has a stronger impact than ethanol on the surface morphology. This can be explained by the higher average number of hydrogen bonds in water (ca. 3.8) than in ethanol (ca. 2) and the, consequently, stronger surface tension, 72.86 and 22.39 mN·m−1 at 20 °C, respectively [38][39]. SiNWs are captured

Topochemical engineering of composite hybrid fibers using layered double hydroxides and abietic acid

• Liji Sobhana,
• Lokesh Kesavan,
• Jan Gustafsson and
• Pedro Fardim

Beilstein J. Nanotechnol. 2019, 10, 589–605, doi:10.3762/bjnano.10.60

• composites by utilizing the intermolecular hydrogen bonds in natural materials. These materials include wood pulp fibers, abietic acid (resin acid) and inexpensive metal salts. In this work, a hybrid composite was created using bleached and unbleached kraft pulp fibers as cellulose platform. In situ co

• renewable material was combined with cellulose via a structure-directing agent, i.e., a layered double hydroxide (LDH). LDHs, inorganic ceramic materials carry symmetrically distributed charge centers/hydrogen bonds. This idea was the extrapolation of our earlier reported work, where introducing

• show their characteristic peaks at 3500–3000 cm−1 and 1640 cm−1, which are due to stretching and bending of –OH bonds in cellulosic –OH groups/intramolecular hydrogen bonds and in adsorbed water, respectively. The peaks at 897 cm−1, 1117 cm−1 and 1163 cm−1 were assigned to the C–O–C stretching in β

Hydrophilicity and carbon chain length effects on the gas sensing properties of chemoresistive, self-assembled monolayer carbon nanotube sensors

• Juan Casanova-Cháfer,
• Carla Bittencourt and
• Eduard Llobet

Beilstein J. Nanotechnol. 2019, 10, 565–577, doi:10.3762/bjnano.10.58

• SAMs. The nature of these interactions is still the subject of debate. While weak intermolecular attractive forces could be responsible for these interactions, some authors maintain that the formation of hydrogen bonds between the methyl groups present in the thiol molecules and the gas species cannot

• hydrophobic ones. Probably the cause of this effect is due to the stronger electrostatic interactions between nitrogen dioxide and hydrophilic thiols, leading to the formation of stronger hydrogen bonds. The effect of ambient moisture on the sensor response was studied. In order to do so, the gas flow was

• nitrogen dioxide for sensors employing hydrophilic thiols [44]. In contrast, the response to nitrogen dioxide remains basically unchanged for sensors employing hydrophobic thiols. Ambient moisture can interact with the sensor surface via hydrogen bonds (see Figure 6c,d). However, the COOH groups (in

Mechanical and thermodynamic properties of Aβ₄₂, Aβ₄₀, and α-synuclein fibrils: a coarse-grained method to complement experimental studies

• Adolfo B. Poma,
• Horacio V. Guzman,
• Mai Suan Li and
• Panagiotis E. Theodorakis

Beilstein J. Nanotechnol. 2019, 10, 500–513, doi:10.3762/bjnano.10.51

• representation for some biological fibrils as well as their native interactions. These native contacts represent hydrogen bonds (HB), and hydrophobic and ionic bridges. Moreover, we consider contacts between amino acids in individual chains with sequential distance |i − j| > 4. The parameters σij are given by

• is very close to the minimum free energy state (native). Here, the number of hydrogen bonds that participate in the deformation as a whole is larger as reported by all-atom simulations [4][5]. In contrast, during in vitro self-assembly of neurodegenerative fibrils the fibrilization process is

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

• alkyl-substituted derivatives, or unavailability of appropriate templates. Alternatively, one can use the directional nature of hydrogen bonds to induce self-assembly of the molecules containing properly positioned electronegative atoms such as N or O. As a result, the H atoms from one molecule can form

• to 0.36 nm. Based on literature reports, these interactions may be termed as “weak hydrogen bonds” since in each case a hydrogen atom bridges two atoms of relatively low electronegativity [20]. These weak H-bonding interactions, present in the crystal lattice of 1, are shown in Figure S1b of

• available. The possibility of additional hydrogen bonds for polymorph II should be reflected in a preferential growth of such domains. However, no such preference for polymorph II was observed in our detailed STM investigation of the surface. The absence of any distortion from the linear shape of 1 observed