Smaller Lanthanide Research Articles

Lanthanide conjugate Pr-MPO elicits anti-cancer activity by targeting lysosomal machinery and inducing zinc-dependent cataplerosis.

Acquired drug resistance is a major challenge in the management of cancer, which underscores the need for discovery and development of novel therapeutic strategies. We report here the mechanism of the anti-cancer activity of a small coordinate complex composed of the rare earth metal praseodymium (Pr) and mercaptopyridine oxide (MPO; pyrithione). Exposure of cancer cells to relatively low concentrations of the conjugate Pr-MPO (5 µM) significantly impairs cell survival in a p53-independent manner and irrespective of the drug resistant phenotype. Mechanistically, Pr-MPO-induced cell death is caspase-independent, not inhibitable by necrostatin, but associated with the appearance of autophagy markers. However, further analysis revealed incomplete autophagic flux, thus suggesting altered integrity of lysosomal machinery. Supporting the lysosomal targeting activity are data demonstrating increased lysosomal Ca2+ accumulation and alkalinization, which coincides with cytosolic acidification (drop in pHc from 7.75 to 7.00). In parallel, an increase in lysosomal activity of glycosidase alpha acid (GAA), involved in passive glycogen breakdown, correlates with rapid depletion of glucose stores upon Pr-MPO treatment. This is associated with swift cataplerosis of TCA cycle intermediates, loss of NAD+/NADH and increase in pyruvate dehydrogenase (PDH) activity to compensate for pyruvate loss. Addition of exogenous pyruvate rescued cell survival. Notably, lysosomal impairment and metabolic catastrophe triggered by Pr-MPO are suggestive of Zn2+-mediated cytotoxicity, which is confirmed by the ability of Zn2+ chelator TPEN to block Pr-MPO-mediated anti-tumor activity. Together, these results highlight the ability of the small molecule lanthanide conjugate to target the cells' waste clearing machinery as well as mitochondrial metabolism for Zn2+-mediated execution of cancer cells, which could have therapeutic potential against cancers with high metabolic activity.

Synthesis and physical properties of Sm2PdGe3 in a context of RE2PdGe3 family

In this study, we present the crystallographic and magnetic characterization of a new intermetallic compound Sm2PdGe3, which was synthetized by a two stage method employing an eutectic alloy. The investigations carried out exhibited, that Sm2PdGe3 crystallize in AlB2-type structure with lattice parameters a = 4.2189(1) Å and c = 4.1031(2) Å. This compound can be classified as a cluster-glass with a spin freezing temperature Tf = 10.5 K. Furthermore, there were carried out the analysis of the role of the rare earth (RE) elements on the structural parameters of RE2PdGe3 and draw a correlation between the RE radius and the unit cell parameters. We show that a deviation from the ideal 1:3 Pd:Ge ratio is necessary to synthesize RE2PdGe3 with smaller RE elements.

Chelation of [111In]In3+ with the dual-size-selective macrocycles py-macrodipa and py2-macrodipa.

Indium-111 (111In) is a diagnostic radiometal that is important in nuclear medicine for single-photon emission computed tomography (SPECT). In order to apply this radiometal, it needs to be stably chelated and conjugated to a targeting vector that delivers it to diseased tissue. Identifying effective chelators that are capable of binding and retaining [111In]In3+in vivo is an important research area. In this study, two 18-membered macrocyclic chelators, py-macrodipa and py2-macrodipa, were investigated for their ability to form stable coordination complexes with In3+ and to be effectively radiolabeled with [111In]In3+. The In3+ complexes of these two chelators were characterized by NMR spectroscopy, X-ray crystallography, and density functional theory calculations. These studies show that both py-macrodipa and py2-macrodipa form 8-coordinate In3+ complexes and attain an asymmetric conformation, consistent with prior studies on this ligand class with small rare earth metal ions. Spectrophotometric titrations were carried out to determine the thermodynamic stability constants (log KML) of [In(py-macrodipa)]+ and [In(py2-macrodipa)]+, which were found to be 18.96(6) and 19.53(5), respectively, where the values in parentheses are the errors of the last significant figures obtained from the standard deviation from three independent replicates. Radiolabeling studies showed that py-macrodipa and py2-macrodipa can quantitatively be radiolabeled with [111In]In3+ at 25 °C within 5 min, even at ligand concentrations as low as 1 μM. The in vitro stability of the radiolabeled complexes was investigated in human serum at 37 °C, revealing that ∼90% of [111In][In(py-macrodipa)]+ and [111In][In(py2-macrodipa)]+ remained intact after 7 days. The biodistribution of these radiolabeled complexes in mice was investigated, showing lower uptake in the kidneys, liver, and blood at the 24 h mark compared to [111In]InCl3. These results demonstrate the potential of py-macrodipa and py2-macrodipa as chelators for [111In]In3+, suggesting their value for SPECT radiopharmaceuticals.

A novel defect fluorite type high-entropy (Dy0.2Ho0.2Er0.2Tm0.2Lu0.2)2Hf2O7 ceramic with low thermal conductivity and CTE: a mechanism study

The “seesaw relationship” between thermal conductivity and thermal expansion coefficient (CTE) in most high temperature ceramics has become an obstacle to the design of long-life multilayer thermal/environmental barrier coatings (T/EBC). Due to low thermal conductivity and CTE, defect fluorite type high-entropy rare earth (RE) hafnates have drawn a lot of interest for potential application in T/EBC systems. This work designs and synthesizes the (Dy0.2Ho0.2Er0.2Tm0.2Lu0.2)2Hf2O7 with comprehensive thermal performance and investigates the thermophysical mechanism from the phonon scale. In addition to the lattice distortion effect caused by the point defects of multicomponent substitutional atoms in (Dy0.2Ho0.2Er0.2Tm0.2Lu0.2)2Hf2O7, the oxygen vacancies in the defect fluorite lattice also play a critical role in reducing the thermal conductivity. From microscopic thermal expansion behavior, the low-frequency optic phonons originated from the vibration of RE atoms are the key factors in altering CTE for hafnates. And doping smaller RE ions is beneficial for enhancing the RE–O bond strength and further reducing CTE. The results contribute to the understanding of high-entropy strategic design and suggest that (Dy0.2Ho0.2Er0.2Tm0.2Lu0.2)2Hf2O7 is a promising top layer material in the implementation of T/EBC.

Size-dependent polymeric arrays of heterometallic Cs+–Ln3+ β-diketonates

A series of alkali–lanthanide heterometallic systems such as Cs+–Ln3+ β-diketonate complexes [Ln(TFPB)4Cs]n (Ln = La (1), Pr (2), Eu (3), Y (4), Yb (5), Lu (6) and TFPB = 4,4,4-trifluoro-1-phenyl-1,3-butanedione) were prepared and structurally explored. The complexes exist only in polymeric forms while both monomeric and polymeric structures are found in the previously reported Na+–Ln3+ congeners. Tuning the sizes of the central rare earth ions from La3+ to Lu3+ results in three types of infinite Cs+–Ln3+ chains which are helical, two-step zigzag and single zigzag patterns. Nonetheless, the Na+–La3+ and Na+–Eu3+ complexes (1-Na and 3-Na) are isomorphous polymers. The size variation of the Ln3+ ions can also alter the degree of π interactions of the Cs+ ions with β-diketonate fragments and phenyl rings. Interestingly, multiple interactions are detected in the complexes with small rare earth ions (5 and 6). Photoluminescence measurements reveal much brighter red emission of 3 than that of 3-Na. It is assumed that the Cs+ ions have more appropriate size than the Na+ ions toward the binding with [Eu(TFPB)4]– anions via oxygen and fluorine atoms, alleviating the energy dissipation of the excited states.

Magnetic, Phonon and Optical Properties of Transition Metal and Rare Earth Ion Doped ZnS Nanoparticles.

The surface, size and ion doping effects on the magnetic, phonon and optical properties of ZnS nanoparticles are studied based on the s-d model including spin-phonon and Coulomb interaction, and using a Green's function theory. The changes of the properties are explained on a microscopic level, due to the different radii between the doping and host ions, which cause different strains-compressive or tensile, and change the exchange interaction constants in our model. The magnetization increases with increasing small transition metal (TM) and rare earth (RE) doping concentration. For larger TM dopants the magnetization decreases. The phonon energies increase with increasing TM, whereas they decrease by RE ions. The phonon damping increases for all doping ions. The changes of the band gap energy with different ion doping concentration is also studied. Band gap changes in doped semiconductors could be due as a result of exchange, s-d, Coulomb and electron-phonon interactions. We have tried to clarify the discrepancies which are reported in the literature in the magnetization and the band gap energy.

Multiferroic nitride perovskites with giant polarizations and large magnetic moments

Multiferroics with coupling between ferroelectricity and magnetism have been pursued for decades. However, their magnetoelectric performances remain limited due to the common trade-off between ferroelectricity and magnetism. Here, a family of nitride perovskites is proposed as multiferroics with prominent physical properties and nontrivial mechanisms. Taking GdWN$_3$ as a prototype, our first-principles calculations found that its perovskite phases own large polarizations (e.g. $111.3$ $\mu$C/cm$^2$ for the $R3c$ phase) and a magnetic moment $7$ $\mu_{\rm B}$/Gd$^{3+}$. More interestingly, its ferroelectric origin is multiple, with significant contributions from both Gd$^{3+}$ and W$^{6+}$ ions, different from its sister member LaWN$_3$ in which the ferroelectricity almost arises from W$^{6+}$ ions only. With decreasing size of rare earth ions, the A site ions would contribute more and more to the ferroelectric instability. Considering that small rare earth ions can be primary origins of both proper ferroelectricity and magnetism in nitride perovskites, our work provides a route to pursuit more multiferroics with unconventional mechanisms and optimal performances.

Hydrazine Energy Storage: Displacing N2 H4 from the Metal Coordination Sphere.

Hydrogen carriers, such as hydrazine (N2 H4 ), may facilitate long duration energy storage, a vital component for resilient grids by enabling more renewable energy generation. Lanthanide coordination chemistry with N2 H4 as well as efforts to displace N2 H4 from the metal coordination sphere to develop an efficient catalytic production cycle were detailed. Modeling the equilibrium of different ligand coordination, it was predicted that strong sigma donor molecules would be required to displace N2 H4 . Monitoring competition experiments with nuclear magnetic resonance confirmed that trimethyl phosphine oxide, dimethylformamide, and dimethyl sulfoxide displaced N2 H4 in large or small lanthanide complexes.

Multiple Ball Magnet Ingestion With Sandwiching of the Uvula

Foreign body ingestion is common among pediatric emergency admissions, and there is increasing awareness that the ingestion of hazardous small high-powered rare earth magnets is rising. A recent United Kingdom (UK)-based study observed a 56% increase in cases of foreign body ingestion in children from 2016 to 2020, with a fivefold increase in the incidence of magnet ingestion (1). A multicenter UK major trauma center survey recently demonstrated that a significant proportion of pediatric patients experienced serious complications from ball magnet ingestion despite early and often asymptomatic presentation, with 51% requiring operative intervention (2).

Non‐Linear Optical Properties of the (RE)3CuGeS7 Family of Compounds

AbstractNon‐linear optical materials must possess a balanced combination of laser‐induced damage threshold (LDT) and second‐harmonic generation (SHG) and be phase matchable. In our previous work, chiral and polar La3CuGeS7 was identified as a promising non‐linear optical material. Herein, we report the optimization of non‐linear optical properties through replacement of La with smaller lanthanides. It is determined that Gd3CuGeS7 exhibits the best combination of SHG (1.6× AgGaS2 at 88–105 μm particle size) and LDT (3× AgGaS2, 89 MW/cm2) and is phase matchable. Based on changes in metal‐sulfur bond lengths and angles, we further propose structural optimization through solid‐solution formation and doping.

Counterintuitive Lanthanide Hydrolysis-Induced Assembly Mechanism.

The understanding of the hydrolysis mechanism of lanthanide ions is limited by their elusive coordination configuration and undeveloped technology. A potential solution by high-resolution mass spectroscopy studies is hindered by the lack of a stable model under electrospray ionization (ESI) conditions and the complexity of the spectra. Herein, it is demonstrated that diketonate ligands can efficiently stabilize the hydrolyzed intermediate cluster of Ln3+ under ESI conditions, and an effective mass difference fingerprint of isomorphism (MDFI) method is proposed, which can allow the determination of the nuclearity-number of the species without depth resolution. Thus, the hydrolysis of Ln3+ into an atomically precise hydroxide cluster is observed at the level of precise formulae. The species evolution upon hydrolysis is along the dominant path of {Eu3}-{Eu4}-{Eu9}-{Eu10}-{Eu11}-{Eu15}-{Eu16} and a nondominant path of {Eu3}-{Eu4}-{Eu8-1}-{Eu8-2} under the investigated conditions. The crystal of the {Eu16} species was obtained via low-temperature crystallization, and single-crystal X-ray diffraction studies show that its structure contains three octahedral {o-Ln6} units. The contradiction between multiple {o-Ln6} units in the structure and the absence in the formation process indicates that the repetitive subunit observed in the structure does not necessarily correspond to the construction units of high-nuclearity clusters. Photophysical measurements indicate that Eu16 cluster has a high total emission quantum efficacy of 12.8% in the solid state. This study provides fundamental insights into the formation, evolution, and assembly of small lanthanide hydroxide units upon hydrolysis, which is vital for the goal of directional synthesis of lanthanide hydroxide clusters.

Delicate, a study of the structural changes in ten-coordinated La(III), Ce(III), Pr(III), Nd(III), Sm(III) and Eu(III) sulfates.

We recently presented a new method that allows for a direct structural comparison of coordination complexes. The main difference from other methods is that our AlignIt approach uses common scaling and orientation of the complexes when computing the symmetry deviation, σideal, values. Here, six apparently isostructural lanthanide(III) sulfates K6[(Ln)2(SO4)6]/K5Na[(Ln)2(SO4)6] with ten-coordinated lanthanide(III) sites (Ln(O)10) were prepared, and single-crystal structures were determined and compared using the symmetry deviation (σideal) values. The six structures were shown to fall into two groups: Pr(III) and Eu(III) are identical (σideal = 0.04) bar in size. With a maximum σideal of 0.07, the same was found to be true for La(III), Ce(III), Nd(III), Sm(III) structures. The two groups are shown to be significantly different (σideal > 2.7), yet the coordination geometries of all six are best described as bicapped square antiprisms (σideal = 1.15-1.68). The structures differ in more than symmetry as the smaller lanthanides are shown to crystallize with one sodium and five potassium ions, while the larger lanthanides crystallize with six potassium ions. This does not change the structure and we postulate that the structural variation is due to delicate size matching between alkali and lanthanide ions. For the first six lanthanides, this structure is very robust, which is confirmed as seven doped systems readily crystallized. These doped systems were prepared in order to use europium(III) luminescence as a structural probe. Unsurprisingly, only the doped Eu-La and Eu-Ce systems were found to be luminescent. Between these two and all the europium(III) systems, the intricate structural differences were shown to be enough to change both crystal field splitting and luminescence lifetime. We conclude that even in simple dilution experiments, where luminescent lanthanide(III) ions are introduced in 'innocent' hosts materials, the structure can act as a modulator for the observed properties.

Lanthanide rhenium oxide single crystals from hydrothermal fluids: Synthesis and Structures of Ln2ReO5 (Ln = Pr, Nd), Ln3ReO7 (Ln = Gd and Tb) and Ln6ReO12 (Ln = Yb, Lu)

The phase space involving reactions of rare earth oxides and ReO2 was examined under high temperature hydrothermal conditions (650 ​°C/200 ​MPa), focusing on reactions containing either excess (3:1) or equimolar ratios of lanthanide oxides to ReO2. The products were generally isolated as high quality single crystals and characterized by single crystal X-ray diffraction, in many cases for the first time. The systematic variation of the size of the lanthanide ions had a significant effect on the final product distribution, and a wide range of materials was obtained. In particular, the synthesis of new members of the Ln2ReO5 series based on the larger lanthanides Pr and Nd enabled the structural transition point to be pinpointed between structure types having eclipsed and staggered Re2O8 dimers with a Re–Re triple bond. In the moderately sized lanthanides, a new monoclinic polymorph of Ln3ReO7 (Ln ​= ​Gd, Tb) was obtained, featuring alternating long and short Re–Re bonds in edge-sharing rhenium oxide chains. Among the smallest lanthanides, the Ln6ReO12 composition was characterized for Yb and Lu. A variety of rhenium oxidation states were observed and these were supported by XPS characterization.

Lanthanide Identity Governs Guest-Induced Dimerization in LnIII [15-MC N(L-pheHA) -5])3+ Metallacrowns.

Series of lanthanide-containing metallic coordination complexes are frequently presented as structurally analogous, due to the similar chemical and coordinative properties of the lanthanides. In the case of chiral (LnIII [15-MC N(L-pheHA) -5])3+ metallacrowns (MCs), which are well established supramolecular hosts, the formation of dimers templated by a dicarboxylate guest (muconate) in solution of neutral pH is herein shown to have a unique dependence on the identity of the MC's central lanthanide. Calorimetric data and nuclear magnetic resonance diffusion studies demonstrate that MCs containing larger or smaller lanthanides as the central metal only form monomeric host-guest complexes whereas analogues with intermediate lanthanides (for example, Eu, Gd, Dy) participate in formation of dimeric host-guest-host compartments. The driving force for the dimerization event across the series is thought to be a competition between formation of highly stable MCs (larger lanthanides) and optimally linked bridging guests (smaller lanthanides).

Emergence of A-Site Cation Order in the Small Rare-Earth Melilites SrREGa3O7 (RE = Dy-Lu, Y).

SrREGa3O7 melilite ceramics with large rare-earth elements (RE = La to Y) are famous materials especially known for their luminescence properties. Using an innovative approach, the full and congruent crystallization from glass process, SrREGa3O7 transparent polycrystalline ceramics with small rare earth elements (RE = Dy-Lu and Y) have been successfully synthesized and characterized. Interestingly, compared to the classic tetragonal (P4̅21m) melilite structure composed of mixed Sr/RE cationic sites, these compositions can crystallize in a 3 × 1 × 1 orthorhombic (P21212) superstructure. A detailed study of the superstructure, investigated using different techniques (synchrotron and neutron powder diffraction, STEM-HAADF imaging, and EDS mapping), highlights the existence of a Sr/RE cation ordering favored by a large Sr/RE size mismatch and a sufficiently small RE cation. An appropriate control of the synthesis conditions through glass crystallization enables the formation of the desired polymorphs, either ordered or disordered. The influence of this tailored cationic ordering/disordering on the RE luminescent spectroscopic properties have been investigated. A stronger structuration of the RE emission band is observed in the ordered ceramic compared to the disordered ceramic and the glass, whose band shapes are very similar, indicating that the RE environments in the glass and disordered ceramic are close.

Lanthanide Oxides: From Diatomics to High-Spin, Strongly Correlated Homo- and Heterometallic Clusters.

Small lanthanide (Ln) oxide clusters present both experimental and theoretical challenges because of their partially filled, core-like 4f n orbitals, a feature that results in a plethora of close-lying and fundamentally similar electronic states. These clusters provide a bottom-up approach toward understanding the electronic structure of defective or doped bulk material but also can offer a challenge to the theorists to find a method robust enough to capture electronic structure patterns that emerge from within the 4f n (0 < n < 14) series. In this Feature Article, we explore the electronic structures of small lanthanide oxide clusters that deviate from bulk stoichiometry using anion photoelectron spectroscopy and supporting density functional theory calculations. We will describe the evolution of electronic structure with oxidation and how LnxOy- cluster reactivities can be correlated with specific Ln-local orbital occupancies. These strongly correlated systems offer additional insights into how interactions between electrons and electronically complex neutrals can lead to detachment transitions that lie outside of the sudden one-electron detachment approximation generally assumed in anion photoelectron spectroscopy. With a better understanding of how we can control nominally forbidden transitions to sample an array of spin states, we suggest that more in-depth studies on the magnetic states of these systems can be explored. Extending these studies to other Ln-based materials with hidden magnetic phases, along with sequentially ligated single molecule magnets, could advance current understanding of these systems.

Rietveld Study of the Changes of Phase Composition, Crystal Structure, and Morphology of BiFeO3 by Partial Substitution of Bismuth with Rare-Earth Ions

BiFeO3 is an interesting material due to its multiferroic properties. It attracts attention due to its potential applications in spintronics and in microelectronics for data storage, among others. Single-phase bulk material from BiFeO3 is difficult to synthesize. The kinetics of perovskite phase formation most often leads to the presence of impurity phases. It has been shown that low levels of replacement of Bi with rare earth ions lead to stabilization of the perovskite phase. In the present work, Rietveld refinement of the crystal structure based on powder X-ray diffraction patterns was applied to study the influence of partial substitution of Bi by rare-earth (RE) elements with different ionic radii on structural and morphological properties of the ferrite phase. Substitution by large RE ions was found to preserve the rhombohedral symmetry of BiFeO3, whereas substitution by smaller RE ions led to the coexistence of two polymorphic perovskite phases with rhombohedral R3c and orthorhombic Pnma symmetries. The unit cell parameters as well as the interatomic distances and angles, not only around the A cation but also around the iron ions, were influenced by the substitution. The mean crystallite and particle size decreased with the decrease of ionic radius of substituting RE ion.

Antisite Defect and Magnetic Frustration in Double Perovskite Ln2CuRuO6 (Ln = La, Pr) Compounds

Magnetism in double perovskite oxides of the formula A2BB'O6 has been a subject of great interest and intensive research in condensed matter physics. In this paper, Ln2CuRuO6 (A = La, Pr) samples were synthesized by solid-state reaction method, and we investigated their structural and magnetic properties. The new double perovskite compound Pr2CuRuO6 stabilizes in the monoclinic P21/n structure with an antisite defect fraction of ~ 3% between Cu and Ru sites. Our structural analysis indicates the severe deformation of Cu-O-Ru bond angle, as La3+ is replaced by the smaller rare earth ion Pr3+. For Pr2CuRuO6, the observed ferromagnetic transition temperature (Tc = 32 K) is higher than that of La2CuRuO6 (Tc = 15 K), which may be possibly associated with the enhanced magnetic interaction due to the distorted Cu-O-Ru bond angle. In addition, the anomalous phenomenon of ZFC susceptibility at low temperature suggests a degree of magnetic frustration and can be attributable to the intrinsic antisite defect in Pr2CuRuO6. The first principle calculations confirm a ferromagnetic Cu-Ru exchange interaction in Pr2CuRuO6, which is different from the antiferromagnetic case for La2CuRuO6.

Liquid crystalline behavior and photoluminescence of lanthanide decanoate nanoparticles synthesized by microwave radiation.

Luminescent lanthanide decanoate nanoparticles (LnC10 NPs; Ln = Pr, Nd, Sm, Eu, Gd, Er) with spherical morphology (<100 nm) have been synthesized via a facile microwave (MWV) method using Ln(NO3)3·xH2O, ethanol/water, and decanoic acid. These hybrid nanomaterials adopt a lamellar structure consisting of inorganic Ln3+ layers separated by a decanoate anion bilayer and exhibit liquid crystalline (LC) phases during melting. The particle size, crystalline structure, and LC behavior were characterized using transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and powder X-ray diffraction (ambient and heated). Thermal analysis indicated the formation of Smectic A LC phases by LnC10 nanoparticles, with the smaller lanthanides (Ln = Sm, Gd, Er) displaying additional solid intermediate and Smectic C phases. The formation of LC phases by the smaller Ln3+ suggests that these nanoscale materials have vastly different thermal properties than their bulk counterparts, which do not exhibit LC behavior. Photoluminescence spectroscopy revealed the LnC10 NPs to be highly optically active, producing strong visible emissions that corresponded to expected electronic transitions by the various Ln3+ ions. Under long-wave UV irradiation (λ = 365 nm), bright visible luminescence was observed for colloidal suspensions of Nd, Sm, Eu, Gd, and ErC10 NPs. To the best of the authors' knowledge, this is the first reported synthesis of nanoscale metal alkanoates, the first report of liquid crystalline behavior by any decanoate of lanthanides smaller than Nd, and the first observation of strong visible luminescence by non-vitrified lanthanide alkanoates.

Postmerger Mass Ejection of Low-mass Binary Neutron Stars

Abstract We study the postmerger mass ejection of low-mass binary neutron stars (NSs) with the system mass of 2.5 M ⊙ and subsequent nucleosynthesis by performing general-relativistic, neutrino-radiation viscous-hydrodynamics simulations in axial symmetry. We find that the merger remnants are long-lived massive NSs surviving more than several seconds, irrespective of the nuclear equations of state (EOSs) adopted. The ejecta masses of our fiducial models are ∼0.06–0.1 M ⊙ (depending on the EOS), being ∼30% of the initial disk masses (∼0.15–0.3 M ⊙). Postprocessing nucleosynthesis calculations indicate that the ejecta is composed mainly of light r-process nuclei with small amounts of lanthanides (mass fraction ∼0.002–0.004) and heavier species due to the modest average electron fraction (∼0.32–0.34) for a reasonable value of the viscous coefficient. Such abundance distributions are compatible with those in weak r-process stars such as HD 122563 but not with the solar r-process-like abundance patterns found in all measured r-process-enhanced metal-poor stars. Therefore, low-mass binary NS mergers should be rare. If such low-mass NS mergers occur, their electromagnetic counterparts, kilonovae, will be characterized by an early bright blue emission because of the large ejecta mass as well as the small lanthanide fraction. We also show, however, that if the effective turbulent viscosity is very high, the electron fraction of the ejecta could be low enough that the solar r-process-like abundance pattern is reproduced and the lanthanide fraction becomes so high that the kilonova would be characterized by early bright blue and late bright red emissions.