Restricting Conformational Space: A New Blueprint for Electrically Switchable Self-Assembled Monolayers.

Tunnel junctions comprising self-assembled monolayers (SAMs) from liquid crystal-inspired molecules show a pronounced hysteretic current-voltage response, due to electric field-driven dipole reorientation in the SAM. This renders these junctions attractive device candidates for emerging technologies such as in-memory and neuromorphic computing. Here, the novel molecular design, device fabrication, and characterization of such resistive switching devices with a largely improved performance, compared to the previously published work are reported. Those former devices suffer from a stochastic switching behavior limiting reliability, as well as from critically small read-out currents. The present progress is based on replacing Al/AlOx with TiN as a new electrode material and as a key point, on redesigning the active molecular material making up the SAM: a previously present, flexible aliphatic moiety has been replaced by a rigid aromatic linker, thereby introducing a molecular "ratchet". This restricts the possible molecular conformations to only two major states of opposite polarity. The above measures have resulted in an increase of the current density by five orders of magnitude as well as in an ON/OFF conductance ratio which is more than ten times higher than the individual scattering ranges of the high and low resistance states.

Odd-even effects in aryl-substituted alkanethiolate SAMs: nonsymmetrical attachment of aryl unit and its impact on the SAM structure.

Aryl-substituted alkanethiolate (AT) self-assembled monolayers (SAMs) exhibit typically so-called odd-even effects, viz. systematic variations in the film structure, packing density, and molecular inclination depending on the parity of the number of the methylene units in the alkyl linker, n. As an exception to this rule, ATs carrying an anthracen-2-yl group (Ant-n) as tail group were reported to have different behavior due the non-symmetric attachment of the anthracene unit to the AT linker, providing additional degree of freedom for the molecular organization and allowing for partial compensation of the odd-even effects. In this context, the structure of SAMs formed by adsorption of anthracene-substituted ATs (Ant-n; n = 1-6) at room temperature on Au(111) substrate was investigated by high-resolution scanning tunnelling microscopy (STM). Most of these SAMs exhibit a coexistence of two different ordered phases, some of which are common for either n = odd or n = even while other vary over the series, showing a broad variety of different structures. The average packing density of the Ant-n SAMs, derived from the analysis of the STM data, varies by 7.5-10% depending on the parity of n, being, as expected, higher for n = odd. The respective extent of the odd-even effects is noticeably lower than that usually observed for other aryl-substituted monolayers (∼25%), which goes in line with the previous findings and emphasizes the impact of the non-symmetric attachment of the aromatic unit.

Phosphonic acid anchored tripodal molecular films on indium tin oxide.

Whereas monopodal self-assembling monolayers (SAMs) are most frequently used for surface and interface engineering, tripodal SAMs are less popular due to the difficulty in achieving a reliable and homogeneous bonding configuration. In this context, in the present study, the potential of phosphonic acid (PA) decorated triptycene (TripPA) for formation of SAMs on oxide substrates was studied, using indium tin oxide (ITO) as a representative and application-relevant test support. A combination of several complementary experimental techniques was applied and a suitable monopodal reference system, benzylphosphonic acid (PPA), was used. The resulting data consistently show that TripPA forms well-defined, densely packed, and nearly contamination-free tripodal SAMs on ITO, with the similar parameters and properties as the monopodal reference system. Modification of wetting properties and work function of ITO by non-substituted and cyano-decorated TripPA SAMs was demonstrated, showing a potential of this tripodal system for surface engineering of oxide substrates.

Metal-organic Frameworks in Semiconductor Devices.

Metal-organic frameworks (MOFs) are a specific class of hybrid, crystalline, nano-porous materials made of metal-ion-based 'nodes' and organic linkers. Most of the studies on MOFs largely focused on porosity, chemical and structural diversity, gas sorption, sensing, drug delivery, catalysis, and separation applications. In contrast, much less reports paid attention to understanding and tuning the electrical properties of MOFs. Poor electrical conductivity of MOFs (~10-7-10-10 S cm-1), reported in earlier studies, impeded their applications in electronics, optoelectronics, and renewable energy storage. To overcome this drawback, the MOF community has adopted several intriguing strategies for electronic applications. The present review focuses on creatively designed bulk MOFs and surface-anchored MOFs (SURMOFs) with different metal nodes (from transition metals to lanthanides), ligand functionalities, and doping entities, allowing tuning and enhancement of electrical conductivity. Diverse platforms for MOFs-based electronic device fabrications, conductivity measurements, and underlying charge transport mechanisms are also addressed. Overall, the review highlights the pros and cons of MOFs-based electronics (MOFtronics), followed by an analysis of the future directions of research, including optimization of the MOF compositions, heterostructures, electrical contacts, device stacking, and further relevant options which can be of interest for MOF researchers and result in improved devices performance.

Concept of Embedded Dipoles as a Versatile Tool for Surface Engineering.

Controlling the physical and chemical properties of surfaces and interfaces is of fundamental relevance in various areas of physical chemistry and a key issue of modern nanotechnology. A highly promising strategy for achieving that control is the use of self-assembled monolayers (SAMs), which are ordered arrays of rodlike molecules bound to the substrate by a suitable anchoring group and carrying a functional tail group at the other end of the molecular backbone. Besides various other applications, SAMs are frequently used in organic electronics for the electrostatic engineering of interfaces by controlling the interfacial level alignment. This is usually achieved by introducing a dipolar tail group at the SAM-semiconductor interface. Such an approach, however, also changes the chemical character of that interface, for example, affecting the growth of subsequent layers. A strategy for avoiding this complication is to embed polar groups into the backbones of the SAM-forming molecules. This allows disentangling electronic interface engineering and the nucleation of further layers, such that both can be optimized independently. This novel concept was successfully demonstrated for both aliphatic and aromatic SAMs on different application-relevant substrates, such as gold, silver, and indium tin oxide. Embedding, for example, ester and pyrimidine groups in different orientations into the backbones of the SAM-forming molecules results in significant work-function changes. These can then be fine-tuned over a wide energy range by growing mixed monolayers consisting of molecules with oppositely oriented polar groups. In such systems, the variation of the work function is accompanied by pronounced shifts of the peaks in X-ray photoelectron spectra, which demonstrates that electrostatically triggered core-level shifts can be as important as the well-established chemical shifts. This illustrates the potential of X-ray photoelectron spectroscopy (XPS) as a tool for probing the local electrostatic energy within monolayers and, in systems like the ones studied here, makes XPS a powerful tool for studying the composition and morphology of binary SAMs. All these experimental observations can be rationalized through simulations, which show that the assemblies of embedded dipolar groups introduce a potential discontinuity within the monolayer, shifting the energy levels above and below the dipoles relative to each other. In molecular and monolayer electronics, embedded-dipole SAMs can be used to control transition voltages and current rectification. In devices based on organic and 2D semiconductors, such as MoS2, they can reduce contact resistances by several orders of magnitude without adversely affecting film growth even on flexible substrates. By varying the orientation of the embedded dipolar moieties, it is also possible to build p- and n-type organic transistors using the same electrode materials (Au). The extensions of the embedded-dipole concept from hybrid interfaces to systems such as metal-organic frameworks is currently underway, which further underlines the high potential of this approach.

Exploiting epoxy-rich poly(ethylene glycol) films for highly selective ssDNA sensing via electrochemical impedance spectroscopy.

This study introduces an alternative approach to immobilize thiolated single-stranded DNA (ssDNA) for the DNA sensing. In contrast to the standard, monomolecular assembly of such moieties on gold substrate, over the thiolate-gold anchors, we propose to use bioinert, porous polyethylene glycol (PEG) films as a 3D template for ssDNA immobilization. The latter process relies on the reaction between the thiol group of the respectively decorated ssDNA and the epoxy groups in the epoxy-rich PEG matrix. The immobilization process and subsequent hybridization ability of the resulting sensing assembly were monitored using cyclic voltammetry and electrochemical impedance spectroscopy, with the latter tool proving itself as the most suitable transduction technique. Electrochemical data confirmed the successful immobilization of thiol-decorated ssDNA probes into the PEG matrix over the thiol-epoxy linkage as well as high hybridization efficiency, selectivity, and sensitivity of the resulting DNA sensor. Whereas this sensor was equivalent to the direct ssDNA assembly in terms of the efficiency, it exhibited a better selectivity and bioinert properties in view of the bioinert character of the PEG matrix. The above findings place PEG films as a promising platform for highly selective ssDNA sensing, leveraging their flexible chemistry, 3D character, and bioinert properties.

Polymorphism and Building-Block-Resolved STM Imaging of Self-Assembled Monolayers of 4-Fluorobenzenemethanethiol on Au(111).

Self-assembled monolayers (SAMs) of 4-fluorobenzenemethanethiol (p-FBMT) on Au(111), prepared by immersion procedure (1 mM ethanolic solution; 60 °C; 18 h), were characterized by scanning tunneling microscopy (STM). The data suggest the formation of highly ordered monolayer with a commensurate structure, described by the 2 3 × 13 R 13 ∘ unit cell. The STM appearance of this cell occurs, however, in two different forms, with either well-localized individual spots or splitting of these spots in two components. These components are assigned to the tunneling through the entire molecule or sulfur docking group only. The respective spots correspond then to the terminal fluorine atom and sulfur docking group, manifesting, thus, building-block-resolving STM imaging. The accessibility of the docking group for direct tunneling is most likely related to a specific molecular organization for one of the two possible internal structures of the unit cell. The above results represent a showcase for potential of STM for imaging of upright-arranged and densely packed molecular assemblies, such as SAMs.

Effect of substitution on the charge transport properties of oligophenylenethiolate self-assembled monolayers.

Electrostatic effects in charge transport across the molecular framework, including those imposed by halogen atoms, have recently attracted noticeable attention of the molecular-electronics community. In this context, in the present work, we studied the effect of tail group (R) substitution on the charge transport properties of oligophenylenethiolate self-assembled monolayers (SAMs) on Au(111), with R = H, F, CH3, and CF3. The length of the molecular backbone was varied from one to three rings and the quality, basic parameters, and electrostatic properties of the SAMs were monitored. For a given length of the molecular backbone, the current density showed a strong dependence on R, being the highest for R = CH3, and then successively lower for R = H, R = CF3, and R = F. This tendency correlated neither with the molecular length of the precursors nor with the work function of the SAMs and was, therefore, exclusively ascribed to the identity of the tail group. In contrast to the current density, the tunneling decay coefficient, describing its dependence on the molecular length, was found to be independent of the identity of the tail group. The reasons behind the observed behavior are discussed and rationalized within the available experimental data and reasonable assumptions.

Femtosecond Charge Transfer Dynamics in Monomolecular Films in the Context of Molecular Electronics.

A key issue of molecular electronics (ME) is the correlation between the molecular structure and the charge transport properties of the molecular framework. Accordingly, a variety of model and potentially useful molecular systems are designed, to prove a particular function or correlation or to build a prototype device. These studies usually involve the measurements of the static electric conductance properties of individual molecules and their assembles on solid supports. At the same time, information about the dynamics of the charge transport (CT) and transfer in such systems, complementary in the context of ME and of a scientific value on its own, is quite scarce. Among other means, this drawback can be resolved by resonant Auger electron spectroscopy (RAES) in combination with core hole clock (CHC) approach, as described in this Account. The RAES-CHC scheme was applied to a variety of aliphatic and aromatic self-assembled monolayers (SAMs), adsorbed on Au(111) over the thiolate and selenolate docking groups. Electron transfer (ET) from a suitable terminal tail group to the substrate, across the molecular framework, was monitored, triggered by resonant excitation of this group (nitrile in most cases) by narrow-band X-ray radiation. This resulted in the quantitative data for the characteristic ET time, τET, in the femtosecond domain, with the time window ranging from ∼1 fs to ∼120 fs. The derived τET exhibit an exponential dependence on the molecular length, mimicking the behavior of the static conductance and suggesting a common physical basis behind the static CT and ET dynamics. The dynamic decay factors, ßET, for the alkyl, oligophenyl, and acene molecular "wires" correlate well with the analogous parameters for the static CT. Both τET and ßET values exhibit a distinct dependence on the character of the involved molecular orbital (MO), demonstrating that the efficiency and rate of the CT in molecular assemblies can be controlled by resonant injection of the charge carriers into specific MOs. This dependence as well as a lack of correlation between the molecular tilt and τET represent strong arguments in favor of the generally accepted model of CT across the molecular framework ("through-bond") in contrast to "through-space" tunneling. Comparison of the SAMs with thiolate and selenolate docking groups suggests that the use of selenolate instead of thiolate does not give any gain in terms of ET dynamics or molecular conductance. Whereas a certain difference in the efficiency of the electronic coupling of thiolate and selenolate to the substrate cannot be completely excluded, this difference is certainly too small to affect the performance of the entire molecule to a noticeable extent. The efficient electronic coupling of the thiolate docking group to the substrate was verified and the decoupling of the electronic subsystems of the substrate and π-conjugated segment by introduction of methylene group into the backbone was demonstrated. No correlation between the molecular dipole or fluorine substitution pattern (at the side positions) and the ET efficiency was recorded. Several representative examples for the resonantly addressable tail groups are given, and perspectives for future research in the context of ET dynamics in molecular assemblies are discussed.

Electrochemical Characterization of Redox Probes Confined in 3D Conducting Polymer Networks.

In this manuscript we present a versatile platform for introducing functional redox species into tailor-made 3D redox polymer networks. Electrochemical characterization based on cyclic voltammetry is applied to verify the immobilization of the redox species within the conducting networks. Ultimately this strategy shall be extended to (photo)electrocatalytic applications which will profit from the conducting polymer matrix. Soluble precursor copolymers are synthesized via radical copolymerization of vinyltriphenylamine (VTPA) with chloromethylstyrene (CMS) in different ratios, whereas CMS is subsequently converted into azidomethylstyrene (AMS) to yield poly(VTPA-co-AMS) copolymers. Spin-coating of poly(VTPA-co-AMS) on gold electrodes yields thin films which are converted into stable polymer network structures by electrochemical crosslinking of the polymer chains via their pendant triphenylamine groups to yield N,N,N',N'-tetraphenylbenzidine (TPB) crosslinking points. Finally, the resulting redox-active, TPB-crosslinked films are functionalized with ethynylferrocene (EFc) as a representative redox probe using a click reaction. Main experimental tools are polarization modulation infrared reflection absorption spectroscopy and scan rate dependent cyclic voltammetry. Especially the latter proves the successful conversion and the immobilization of redox probes in the polymer matrix. The results are compared with the reference system of azide-terminated self-assembled monolayers on gold substrates, allowing to distinguish between free and immobilized EFc species.

A Copper(I) Complex with Two Unpaired Electrons, Synthesised by Oxidation of a Copper(II) Complex with Two Redox-Active Ligands.

Two homoleptic copper(II) complexes [Cu(L1)2 ] and [Cu(L2)2 ] with anionic redox-active ligands were synthesised, one with urea azine (L1) and the other with thio-urea azine (L2) ligands. One-electron oxidation of the complexes initiates an unprecedented redox-induced electron transfer process, leading to monocationic copper(I) complexes [Cu(L1)2 ]+ and [Cu(L2)2 ]+ with two oxidised ligands. While [Cu(L1)2 ]+ is best described as a CuI complex with two neutral radical ligands that couple antiferromagnetically, [Cu(L2)2 ]+ is a CuI complex with two clearly different ligand units in the solid state and with a magnetic susceptibility close to a diamagnetic compound. Further one-electron oxidation of the complex with L1 ligands results in a dication [Cu(L1)2 ]2+ , best described as a CuI complex with a twofold oxidised, monocationic ligand and a neutral radical ligand. The stability in at least three redox states, the accumulation of spin density at the ligands and the facile ligand-metal electron transfer make these complexes highly attractive for a variety of applications; here the catalytic aerobic oxidation of alcohols to aldehydes is tested.

Interaction of water with oligo(ethylene glycol) terminated monolayers: wetting versus hydration.

Biorepulsivity of oligo(ethylene glycol) (OEG) substituted self-assembled monolayers (SAMs), serving as model systems for analogous polymeric surfaces, is generally ascribed to the hydration effect. In this context, we applied temperature-programmed desorption to study interaction of water (D2O) with a series of OH-terminated, OEG-substituted alkanethiolate SAMs with variable length of the OEG strand, defining their biorepulsion behavior. Along with the ice overlayer (wetting phase), growing also on the surface of the analogous non-substituted films, a hydration phase, corresponding to the adsorption of D2O into the OEG matrix, was observed, with a higher desorption energy (12.4 kcal mol-1vs. 10.4 kcal mol-1) and a weight correlating with the length of the OEG strand and, consequently, with biorepulsivity. The formation of hydration phase was found to occur over an activation barrier, presumably by temperature-promoted diffusion from the wetting phase, with this process being additionally enforced by a pre-desorption annealing.

Binary aromatic self-assembled monolayers: electrostatic properties and charge tunneling rates across the molecular framework.

A series of single-component and binary SAMs composed of non-substituted (H-BPT) and fluorine-substituted (F-BPT) mercaptobiphenyls on Au(111) was studied in the context of their structure, composition, electrostatic properties, and charge tunneling rates in molecular junctions. All SAMs were found to be well-defined and densely packed, with all molecules bound to the substrate by the thiolate anchor and orientated upright with respect to the substrate. The relative composition of the binary SAMs turned out to be close to the relative contents of both molecules in the solutions from which these SAMs were formed. The work function of the binary SAMs can be varied in a gradual and controlled fashion between the ultimate values for the single-component films, viz.∼4.3 eV and ∼5.2 eV. The extent of the electrostatic effects in photoemission is small, affecting predominantly the apparent binding energy of the terminal fluorine atoms, which is explained by the strong spatial confinement of the step in the electrostatic potential at the SAM-ambient interface. The charge tunneling rate across the molecular framework is noticeably (by about an order of magnitude) higher for the H-BPT SAM than for the F-BPT monolayer, in good agreement with the literature data. The tunneling rates for the mixed SAM are intermediate to those of the single-component films, varying in a gradual fashion with the SAM composition between the respective ultimate values.

Annealing effect for self-assembled monolayers formed from terphenylethanethiol on Au(111).

The structure and morphology of self-assembled monolayers (SAMs) prepared on Au(111) from solutions of terphenylethanethiol (TP2) at room temperature and subsequently annealed at temperatures up to 473 K were investigated using scanning tunneling microscopy. This system is of particular interest because of its metastable character, holding potential for its tailored modification. Indeed, the data suggest the formation of several different structural phases, viz. α, ß, γ, and δ, appearing progressively for the as-prepared and annealed samples. The consecutive α → ß â†’ γ → δ phase transitions occurring with increasing annealing temperature involved a continuous reduction of the molecular packing density and significant changes in the substrate morphology. The major morphological changes were the appearance and progressive growth of monoatomic gold islands, on top of which the TP2 phases were formed, representing in all cases a single domain for a particular island and restricted only by the island size. For all the phases, inclined molecular orientation was assumed while a so-called lying-down arrangement, in which the TP2 backbones are orientated parallel to the gold surface, was not observed. A nearly complete desorption of the TP2 molecules was recorded at an annealing temperature of 473 K, accompanied by the drastic change in the surface morphology.

Shape controlled assembly of carboxylic acids: formation of a binary monolayer by intercalation into molecular nanotunnels.

Binary self-assembled monolayers (SAMs) combining a Y-shaped aromatic carboxylic acid (1,3,5-benzenetribenzoic acid, H3BTB) and a cage-type alicyclic carboxylic acid (adamantane carboxylic acid, AdCA) were investigated by scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), and near edge X-ray absorption fine structure (NEXAFS) spectroscopy. The SAMs, prepared by molecular adsorption from solution on Au substrates modified by underpotential deposition of Ag, exhibit a pronounced dependence of their structure on the assembly protocol. Exposing an H3BTB SAM to AdCA, the highly regular row structure of the native H3BTB layer persists and STM imaging does not show signs of AdCA adsorption. This is in striking contrast to the disordered arrangements of H3BTB and the presence of AdCA employing the inverted adsorption sequence or coadsorption of the two molecules. However, spectroscopic analysis of the H3BTB SAM exposed to AdCA reveals the presence also of the latter, suggesting that the AdCA molecules are hidden in the nanotunnels of the H3BTB monolayer. Direct evidence for the intercalation of AdCA is obtained by STM manipulation experiments which lay bare areas of AdCA molecules upon local removal of H3BTB. Surprisingly, these are densely packed and arranged into a highly ordered monolayer. Formation of such a compact AdCA layer is explained by expulsion of AdCA from the H3BTB nanotunnels of the surrounding intact mixed SAM, driven by release of stress in the nanotunnels built up when AdCA is intercalated.

Understanding the Role of Parallel Pathways via In-Situ Switching of Quantum Interference in Molecular Tunneling Junctions.

This study describes the modulation of tunneling probabilities in molecular junctions by switching one of two parallel intramolecular pathways. A linearly conjugated molecular wire provides a rigid framework that allows a second, cross-conjugated pathway to be effectively switched on and off by protonation, affecting the total conductance of the junction. This approach works because a traversing electron interacts with the entire quantum-mechanical circuit simultaneously; Kirchhoff's rules do not apply. We confirm this concept by comparing the conductances of a series of compounds with single or parallel pathways in large-area junctions using EGaIn contacts and single-molecule break junctions using gold contacts. We affect switching selectively in one of two parallel pathways by converting a cross-conjugated carbonyl carbon into a trivalent carbocation, which replaces destructive quantum interference with a symmetrical resonance, causing an increase in transmission in the bias window.

Triptycene Tripods for the Formation of Highly Uniform and Densely Packed Self-Assembled Monolayers with Controlled Molecular Orientation.

When employing self-assembled monolayers (SAMs) for tuning surface and interface properties, organic molecules that enable strong binding to the substrate, large-area structural uniformity, precise alignment of functional groups, and control of their density are highly desirable. To achieve these goals, tripod systems bearing multiple bonding sites have been developed as an alternative to conventional monodentate systems. Bonding of all three sites has, however, hardly been achieved, with the consequence that structural uniformity and orientational order in tripodal SAMs are usually quite poor. To overcome that problem, we designed 1,8,13-trimercaptomethyltriptycene (T1) and 1,8,13-trimercaptotriptycene (T2) as potential tripodal SAM precursors and investigated their adsorption behavior on Au(111) combining several advanced experimental techniques and state-of-the-art theoretical simulations. Both SAMs adopt dense, nested hexagonal structures but differ in their adsorption configurations and structural uniformity. While the T2-based SAM exhibits a low degree of order and noticeable deviation from the desired tripodal anchoring, all three anchoring groups of T1 are equally bonded to the surface as thiolates, resulting in an almost upright orientation of the benzene rings and large-area structural uniformity. These superior properties are attributed to the effect of conformationally flexible methylene linkers at the anchoring groups, absent in the case of T2. Both SAMs display interesting electronic properties, and, bearing in mind that the triptycene framework can be functionalized by tail groups in various positions and with high degree of alignment, especially T1 appears as an ideal docking platform for complex and highly functional molecular films.

A dithiocarbamate anchoring group as a flexible platform for interface engineering.

The molecular organization and electronic properties of dithiocarbamate (DTC) anchored self-assembled monolayers (SAMs) linked to Au(111) substrates are studied by a combination of X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorption fine structure (NEXAFS) spectroscopy, and state-of-the-art density functional theory calculations. For that, several piperidine/piperazine precursors with different architecture and substitution patterns are selected. The presented data show that the DTC anchor provides a useful building block for monomolecular self-assembly on coinage metals with both sulfur atoms bonded to the substrate in a way similar to what is usually observed for the more commonly applied thiolate docking group. The combination of the DTC group with the quite flexible piperidine/piperazine cyclic linkers results in a dense molecular packing with an upright orientation of the terminal moieties. The latter comprise phenyl rings bearing various substituents, which enables tuning the interfacial dipole over a wide range. Simulations on two prototypical DTC-docked SAMs help to better understand the experimental observations and provide insight into the local origin of the SAM-induced shifts in the electrostatic energy. In particular, a comparison of measured and simulated XP spectra reveals the significant contribution of the DTC group to the interfacial dipole.

Photoisomerization of azobenzene-substituted alkanethiolates on Au(111) substrates in the context of work function variation: the effect of structure and packing density.

Photoisomerization of a series of custom-designed, azobenzene-substituted alkanethiolate (AT) self-assembled monolayers (SAMs) on Au(111) substrates was studied in the context of work function variation, using Kelvin probe measurements as a transduction technique. These SAMs featured variable packing density (by ∼14%; due to the odd-even effects) and, as an option, were additionally decorated with the electron donating/withdrawing -CH3 and -CF3 tail group, respectively, which induce additional dipole moments. The efficiency of photoisomerization and the respective extent of work function variation (ΔΦ) were found to be quite low and independent of the packing density in the SAMs, within the given odd-even packing density variation. They could only be increased, up to ca. 40 meV for ΔΦ, by mixing the azobenzene-substituted ATs with shorter "matrix" molecules, which were introduced for a partial release of the sterical constraints. The ΔΦ values for the SAMs decorated with the -CH3 and -CF3 tail groups were found to be lower than those for the monolayers without such a decoration, which correlated well with the theoretical estimates for the change of the dipole moment of the relevant molecules upon the photoisomerization.

Nanometric Assembly of Functional Terpyridyl Complexes on Transparent and Conductive Oxide Substrates: Structure, Properties, and Applications.

Over the last few decades, molecular assemblies on solid substrates have become increasingly popular, challenging the traditional systems and materials in terms of better control over molecular structure and function at the nanoscale. A variety of such assemblies with high complexity and adjustable properties was generated on the basis of organic, inorganic, organometallic, polymeric, and biomolecular building blocks. Particular versatile elements in this context are terpyridyls due to their wide design flexibility, ease of functionalization, and ability to coordinate to a broad variety of transition-metal ions without forming diastereoisomers, which facilitates tuning of their optical and electronic properties. Specifically, metal-terpyridyl complexes are worthy building blocks for generating optoelectronically active assemblies on technologically relevant transparent and conductive oxide substrates. In this context, the present Account summarizes our recent results on the preparation, characterization, and applications of nanometric (2-10 nm) surface-confined molecular assemblies of Cu2+, Fe2+, Ru2+, and Os2+-terpyridyl complexes on SiOx-based substrates (glass, quartz, silicon, and ITO-coated glass). These assemblies rely on covalent bond formation between the iodo-/chloro-terminated functionalized SiOx substrates and the pendant group (mostly pyridyl) hosted on the terpyridyl complexes. Such an anchoring provides excellent thermal, temporal, radiative, and electrochemical stability to the assemblies as needed for technological applications. The functional, covalently assembled monolayers were extended to fabricate molecular dyads (bilayers), triads (trilayers), and oligomers by an established layer-by-layer procedure using suitable metallolinkers such as Cu2+, Ag+, and Pd2+. The chemical, optical, and electrochemical properties of these assemblies could be precisely adjusted by selection of proper metal-terpyridyl complexes and/or metallolinkers, so that the resulting systems served, relying on the specific design, as sensors, catalysts, molecular logic gates, and photochromic devices. For instance, a Cu-terpyridyl-based assembly on a glass substrate showed "turn on" detection of ascorbic acid. In another example, heterometallic molecular triads were exposed to redox-active NO+ for selective oxidation of the metal ions, and the optical readout was utilized for configuring multiple-input-based molecular logic gates. Furthermore, bias-driven (+0.6 to +1.6 V vs Ag/AgCl) optical properties of the heteroleptic Ru2+/Os2+-terpyridyl monolayers were modulated and "read out" by spectro-electrochemical techniques demonstrating high charge/information density (3-4 × 1014 electrons/cm2). Moreover, the manipulation of the M2+/3+ (M = Fe, Ru, and Os) redox wave in the assembly provided the possibility to create mixed-valence redox-states paving the way toward the fabrication of "multi-bit" memory systems. We truly believe that due to these intriguing characteristics and excellent stability, terpyridyl-based molecular assemblies have the potential to become a versatile platform for the next generation of smart optoelectronic devices.