Choline Halide-Based Deep Eutectic Solvents as Biocompatible Catalysts for the Alternating Copolymerization of Epoxides and Cyclic Anhydrides.

Aliphatic polyesters have received considerable attention in recent years due to their biodegradability and biocompatible, mechanical, and thermal properties that can make them a suitable alternative to today's commercialized polymers. The ring-opening copolymerization (ROCOP) of epoxides and cyclic anhydrides is a route to synthesize a diverse array of polyesters that could be useful in many applications. However, the catalysts used rarely consider biocompatible catalysts in the case that any are left in the polymer. To the best of our knowledge, we report the first example of using deep eutectic solvents (DESs) as biocompatible catalysts for this target ROCOP with polymerization activity for at least six diverse monomer pairs. Choline halide salts are active for this polymerization, with dried salts showing polymerization slower than that of those conducted in air. Hydrogen bonding with water is hypothesized to enhance the rate-determining step of epoxide ring opening. While the presence of water improves the rate of polymerization, it also acts as a chain transfer agent, leading to smaller molar mass polymers than intended. Combining the choline halide salts with urea or ethylene glycol hydrogen bond donors in air led to DES catalysts that reacted similarly to the salts exposed to air. However, when generating these DESs in air-free conditions, they showed similar rates of polymerization without a drop in polymer molar mass. The hydrogen bonding provided by urea and ethylene glycol seems to promote the rate increase without serving as a chain transfer agent. Results reported herein display the promising potential of biocompatible catalyst systems for this ROCOP process as well as introducing the use of hydrogen bonding to enhance polymerization rates.

Enhanced Control of Isoprene Polymerization with Trialkyl Rare Earth Metal Complexes through Neutral Donor Support.

The development of catalysts for stereospecific polymerization of 1,3-dienes is an area of interest due to the robust nature of poly(1,3-diene)s' physical and mechanical properties, as well as the material's versatility in many applications. Dialkyl rare earth metal complexes supported by a diverse cast of ligand frameworks are selective for the polymerization of 1,3-dienes and are an exciting option for examination. However, development in this area has been hampered by the focus on complex catalyst systems that are costly to make. In this study, we synthesize a series of simple homoleptic trialkyl rare earth metal precatalysts and highlight their efficacy for isoprene polymerization using 1 or 2 equiv of [Ph3C][B(C6F5)4] activator. We investigated the addition of commercially available in situ donors, leading to the identification of triphenylphosphine as an ideal support to enhance the dispersity control and prevent loss of catalyst activity. We demonstrated how the activation and reaction conditions, including the order/time of reagent addition and donor electronics, had a major impact on the rate, control, and selectivity for the polymerization of 1,3-dienes. Further interrogation of the catalyst system signals the crucial role of triphenylphosphine in providing enhanced stability and control in this living catalyst system.

Controlling selectivity for dechlorination of poly(vinyl chloride) with (xantphos)RhCl.

Reaction of poly(vinyl chloride) (PVC) with 5 equiv. of triethyl silane in THF, in the presence of in situ generated (xantphos)RhCl catalyst, results in partial reduction of PVC via hydrodechlorination to yield poly(vinyl chloride-co-ethylene). Increasing catalyst loading or using N,N-dimethylacetamide (DMA) as a solvent both diminished selectivity for hydrodechlorination, promoting competitive dehydrochlorination reactions. Reaction of PVC with 2 equiv. of sodium formate in THF in the presence of (xantphos)RhCl affords excellent selectivity for hydrodechlorination along with complete PVC dechlorination, yielding polyethylene-like polymers. Higher catalyst loadings were necessary to activate PVC towards reduction in this case. In contrast, reaction of PVC with 1 equiv. of NaH in DMA, in the presence of (xantphos)RhCl, exhibited good selectivity for dehydrochlorination, as well as much higher reaction rates. These results combined shed light on the interplay between critical reaction parameters that control PVC's mode of reactivity.

Simple yttrium salts as highly active and controlled catalysts for the atom-efficient synthesis of high molecular weight polyesters.

The ring-opening copolymerization (ROCOP) of epoxides and cyclic anhydrides is a promising route to sustainable aliphatic polyesters with diverse mechanical and thermal properties. Here, simple yttrium chloride salts (YCl3THF3.5 and YCl3·6H2O), in combination with a bis(triphenylphosphoranylidene)ammonium chloride [PPN]Cl cocatalyst, are used as efficient and controlled catalysts for ten epoxide and anhydride combinations. In comparison to past literature, this simple salt system exhibits competitive turn-over frequencies (TOFs) for most monomer pairs. Despite no supporting ligand framework, these salts provide excellent control of dispersity, with suppression of side reactions. Using these catalysts, the highest molecular weight reported to date (302.2 kDa) has been obtained with a monosubstituted epoxide and tricyclic anhydride. These data indicate that excellent molecular weight control and suppression of side reactions for ROCOP of epoxides and cyclic anhydrides can coincide with high activity using a simple catalytic system, warranting further research in working towards industrial viability.

Controlled, one-pot synthesis of recyclable poly(1,3-diene)-polyester block copolymers, catalyzed by yttrium ß-diketiminate complexes.

The one-pot synthesis of well-defined block copolymers of olefins/1,3-dienes and polar monomers, such as cyclic esters and acrylates has long been the focus of intense research. Cationic alkyl rare earth metal catalysts, activated by organoborates, have shown to be promising for the polymerization of isoprene or styrene and ε-caprolactone. In this study, we synthesize a series of yttrium bis(alkyl) complexes supported by simple ß-diketiminate ancillary ligands. Subtle changes have been made to the ß-diketiminate ligand framework to elucidate the effect of ligand structure on the rate and selectivity of olefin/1,3-diene and cyclic ester polymerization, with small ligand changes having a large impact on the resulting polymerizations. Generation of the active cationic species was easily streamlined by identification of appropriate catalyst : organoborate ratios, allowing for high catalyst efficiencies. Notably, we demonstrate the first cationic rare earth metal alkyl-initiated polymerization of δ-valerolactone and ε-decalactone as well as introduced five new block copolymer morphologies. In addition, selective degradation of the ester block in poly(isoprene-b-caprolactone) enabled recovery of the polyisoprene block with identical spectroscopic and thermal properties. Significantly, recopolymerization of the recovered poly(1,3-diene) with fresh ε-caprolactone reproduced the desired diblocks with nearly identical thermal and physical properties to those of virgin copolymer, illustrating a plausible recycling scheme for these materials.

Perfectly Alternating Copolymerization of Cyclic Anhydrides and Epoxides with Yttrium ß-Diketiminate Complexes.

Monometallic yttrium ß-diketiminate complexes are active and controlled catalysts for perfectly alternating ring-opening copolymerization of 1-butene oxide and phthalic anhydride under mild conditions. ß-Diketiminate ligands with pendant neutral donors were targeted to identify both the impact of donor strength and number of donors on rates of polymerization and the presence of undesirable side reactions. Initiating groups were also varied between alkyls, chlorides, and alkoxides. In the presence of a cocatalyst, the catalysts studied were active for polymerization with minimal side reactions, whereas lack of cocatalysts led to competing homopolymerization of epoxides. While a greater donor strength and a larger number of donors both increase the rate of polymerization, donor strength generally had a bigger impact when a cocatalyst was used. Additionally, alkoxide and chloride initiators proved to be the fastest, with alkyls being more sluggish. These subtle ligand changes significantly impacting polymerization activity lend promise to the facile tunability of rare earth metal complexes to be highly active for the target copolymerization, which renders further research in this area attractive and timely.

A computational study of the mechanism of chloroalkane dechlorination with Rh(I) complexes.

This work utilizes density functional theory and the energetic span model to determine steps constituting the catalytic cycle and turnover frequencies, respectively, for C(sp3)-Cl activation and dechlorination by model Rh(I) complexes containing POP-Pincer ligands with the aid of Na salts. The steps in the catalytic cycle with NaHCO2 as the hydrogen carrier are (i) rotation of the Rh-Cl bond out of the ligand plane, (ii) metal insertion into the C-Cl bond, (iii) formate binding and removal of one Cl as NaCl, (iv) formation and removal of CO2 from formate-bound Rh, and (v) hydrogenation of the alkyl bound to Rh to form an alkane, followed by Rh-Cl rotation to restore the catalyst resting state. We find that the the turnover-determining states and TOFs for monochloropropane (MCP) dechlorination depend strongly on the hydrogen carrier, with significantly higher TOF for NaH than NaHCO2. Therefore, NaH may be a promising salt for alkylchloride dechlorination with Rh(I) complexes.

Catalytic methods for chemical recycling or upcycling of commercial polymers.

Polymers (plastics) have transformed our lives by providing access to inexpensive and versatile materials with a variety of useful properties. While polymers have improved our lives in many ways, their longevity has created some unintended consequences. The extreme stability and durability of most commercial polymers, combined with the lack of equivalent degradable alternatives and ineffective collection and recycling policies, have led to an accumulation of polymers in landfills and oceans. This problem is reaching a critical threat to the environment, creating a demand for immediate action. Chemical recycling and upcycling involve the conversion of polymer materials into their original monomers, fuels or chemical precursors for value-added products. These approaches are the most promising for value-recovery of post-consumer polymer products; however, they are often cost-prohibitive in comparison to current recycling and disposal methods. Catalysts can be used to accelerate and improve product selectivity for chemical recycling and upcycling of polymers. This review aims to not only highlight and describe the tremendous efforts towards the development of improved catalysts for well-known chemical recycling processes, but also identify new promising methods for catalytic recycling or upcycling of the most abundant commercial polymers.

Dual-catalytic decarbonylation of fatty acid methyl esters to form olefins.

The homogeneous dehydrative decarbonylation of fatty acid methyl esters (FAMEs) to form olefins is reported. In order to facilitate cleavage of the unactivated acyl C-O bond of the alkyl ester, a one pot dual-catalytic directing group strategy was developed through optimization of the individual transesterification and decarbonylation reaction steps.

Metal versus Ligand Reduction in Ln3+ Complexes of a Mesitylene-Anchored Tris(Aryloxide) Ligand.

The synthesis of 4f n Ln3+ complexes of the tris(aryloxide) mesitylene ligand, ((Ad,MeArO)3mes)3-, with Ln = La, Ce, Pr, Sm, and Yb, and their reduction with potassium have revealed that this ligand system can be redox active with some metals. Protonolysis of [Ln(N(SiMe3)2)3] (Ln = La, Ce, Pr, Sm, Yb) with the tris(phenol) (Ad,MeArOH)3mes yielded the Ln3+ complexes [((Ad,MeArO)3mes)Ln] (Ln = La, Ce, Pr, Sm, Yb), 1-Ln. Single electron reduction of each 4f n complex, 1-Ln, using potassium yielded the reduced products, [K(2.2.2-cryptand)][((Ad,MeArO)3mes)Ln] (Ln = La, Ce, Pr, Sm, Yb), 2-Ln. The Sm and Yb complexes have properties consistent with the presence of Ln2+ ions with traditional 4f n+1 electron configurations. However, the La, Ce, and Pr complexes appear to formally contain Ln3+ ions and ((Ad,MeArO)3mes)4- ligands. Structural comparisons of the [((Ad,MeArO)3mes)Ln] and [((Ad,MeOAr)3mes)Ln]1- complexes along with UV-vis absorption and EPR spectroscopy as well as density functional theory calculations support these ground state assignments.

Comparisons of lanthanide/actinide +2 ions in a tris(aryloxide)arene coordination environment.

A new series of Ln3+ and Ln2+ complexes has been synthesized using the tris(aryloxide)arene ligand system, ((Ad,MeArO)3mes)3-, recently used to isolate a complex of U2+. The triphenol precursor, (Ad,MeArOH)3mes, reacts with the Ln3+ amides, Ln(NR2)3 (R = SiMe3), to form a series of [((Ad,MeArO)3mes)Ln] complexes, 1-Ln. Crystallographic characterization was achieved for Ln = Nd, Gd, Dy, and Er. The complexes 1-Ln can be reduced with potassium graphite in the presence of 2.2.2-cryptand (crypt) to form highly absorbing solutions with properties consistent with Ln2+ complexes, [K(crypt)][((Ad,MeArO)3mes)Ln], 2-Ln. The synthesis of the Nd2+ complex [K(crypt)][((Ad,MeArO)3mes)Nd], 2-Nd, was unambiguously confirmed by X-ray crystallography. In the case of the other lanthanides, crystals were found to contain mixtures of 2-Ln co-crystallized with either a Ln3+ hydride complex, [K(crypt)][((Ad,MeArO)3mes)LnH], 3-Ln, for Ln = Gd, Dy, and Er, or a hydroxide complex, [K(crypt)][((Ad,MeArO)3mes)Ln(OH)], 4-Ln, for Ln = Dy. A Dy2+ complex with 18-crown-6 as the potassium chelator, [K(18-crown-6)(THF)2][((Ad,MeArO)3mes)Dy], 5-Dy, was isolated as a co-crystallized mixture with the Dy3+ hydride complex, [K(18-crown-6)(THF)2][((Ad,MeArO)3mes)DyH], 6-Dy. Structural comparisons of 1-Ln and 2-Ln are presented with respect to their uranium analogs and correlated with density functional theory calculations on their electronic structures.

Mechanistic Insights into the Alternating Copolymerization of Epoxides and Cyclic Anhydrides Using a (Salph)AlCl and Iminium Salt Catalytic System.

Mechanistic studies involving synergistic experiment and theory were performed on the perfectly alternating copolymerization of 1-butene oxide and carbic anhydride using a (salph)AlCl/[PPN]Cl catalytic pair. These studies showed a first-order dependence of the polymerization rate on the epoxide, a zero-order dependence on the cyclic anhydride, and a first-order dependence on the catalyst only if the two members of the catalytic pair are treated as a single unit. Studies of model complexes showed that a mixed alkoxide/carboxylate aluminum intermediate preferentially opens cyclic anhydride over epoxide. In addition, ring-opening of epoxide by an intermediate comprising multiple carboxylates was found to be rate-determining. On the basis of the experimental results and analysis by DFT calculations, a mechanism involving two catalytic cycles is proposed wherein the alternating copolymerization proceeds via intermediates that have carboxylate ligation in common, and a secondary cycle involving a bis-alkoxide species is avoided, thus explaining the lack of side reactions until the polymerization is complete.

Evaluating the electronic structure of formal LnII ions in LnII(C5H4SiMe3)31- using XANES spectroscopy and DFT calculations.

The isolation of [K(2.2.2-cryptand)][Ln(C5H4SiMe3)3], formally containing LnII, for all lanthanides (excluding Pm) was surprising given that +2 oxidation states are typically regarded as inaccessible for most 4f-elements. Herein, X-ray absorption near-edge spectroscopy (XANES), ground-state density functional theory (DFT), and transition dipole moment calculations are used to investigate the possibility that Ln(C5H4SiMe3)31- (Ln = Pr, Nd, Sm, Gd, Tb, Dy, Y, Ho, Er, Tm, Yb and Lu) compounds represented molecular LnII complexes. Results from the ground-state DFT calculations were supported by additional calculations that utilized complete-active-space multi-configuration approach with second-order perturbation theoretical correction (CASPT2). Through comparisons with standards, Ln(C5H4SiMe3)31- (Ln = Sm, Tm, Yb, Lu, Y) are determined to contain 4f6 5d0 (SmII), 4f13 5d0 (TmII), 4f14 5d0 (YbII), 4f14 5d1 (LuII), and 4d1 (YII) electronic configurations. Additionally, our results suggest that Ln(C5H4SiMe3)31- (Ln = Pr, Nd, Gd, Tb, Dy, Ho, and Er) also contain LnII ions, but with 4f n 5d1 configurations (not 4f n+1 5d0). In these 4f n 5d1 complexes, the C3h-symmetric ligand environment provides a highly shielded 5d-orbital of a' symmetry that made the 4f n 5d1 electronic configurations lower in energy than the more typical 4f n+1 5d0 configuration.

Raman spectroscopy of the N-N bond in rare earth dinitrogen complexes.

Raman spectra have been collected on single crystals of over 20 different rare earth complexes containing reduced dinitrogen ligands to determine if these data will correlate with periodic properties or relative stability. Four types of complexes were examined: [(C5Me5)2Ln]2(µ-η(2):η(2)-N2), 1-Ln, [(C5Me4H)2(THF)Ln]2(µ-η(2):η(2)-N2), 2-Ln, [(C5H4Me)2Ln]2(µ-η(2):η(2)-N2), 3-Ln, and {[(Me3Si)2N]2(THF)Ln}2(µ-η(2):η(2)-N2), 4-Ln. Although each of the complexes contains a side-on bound dinitrogen ligand that is formally (N2)(2-), the N-N bond distances determined by X-ray crystallography range from 1.088(12) to 1.305(6) Å. In the 4-Ln series (Ln = Gd, Tb, Dy, Ho, Er and Tm), the 1.26-1.31 Å N-N distances do not follow any periodic trends, but the Raman stretching frequencies for Gd-Tm were found to decrease regularly with decreasing atomic number and increasing Lewis acidity of the metal. Similar correlations can be seen with the late metals in complexes of the other series, 1-Ln, 2-Ln and 3-Ln, but exceptions exist, particularly for the larger metals. Comparisons between the several types of complexes as a function of ligand were more complicated and variations in stretching frequency as a function of L in the {[(Me3Si)2N]2Y(L)}2(µ-η(2):η(2)-N2) substituted versions of 4-Y did not give trends consistent with bond distances or Gutmann donor numbers.

Expanding Thorium Hydride Chemistry Through Th²âº, Including the Synthesis of a Mixed-Valent Th4⁺/Th³âº Hydride Complex.

The reactivity of the recently discovered Th(2+) complex [K(18-crown-6)(THF)2][Cp″3Th], 1 [Cp'' = C5H3(SiMe3)2-1,3], with hydrogen reagents has been investigated and found to provide syntheses of new classes of thorium hydride compounds. Complex 1 reacts with [Et3NH][BPh4] to form the terminal Th(4+) hydride complex Cp″3ThH, 2, a reaction that formally involves a net two-electron reduction. Complex 1 also reacts in the solid state and in solution with H2 to form a mixed-valent bimetallic product, [K(18-crown-6)(Et2O)][Cp″2ThH2]2, 3, which was analyzed by X-ray crystallography, electron paramagnetic resonance and optical spectroscopy, and density functional theory. The existence of 3, which formally contains Th(3+) and Th(4+), suggested that KC8 could reduce [(C5Me5)2ThH2]2. In the presence of 18-crown-6, this reaction forms an analogous mixed-valent product formulated as [K(18-crown-6)(THF)][(C5Me5)2ThH2]2, 4. A similar complex with (C5Me4H)(1-) ligands was not obtained, but reaction of (C5Me4H)3Th with H2 in the presence of KC8 and 2.2.2-cryptand at -45 °C produced two monometallic hydride products, namely, (C5Me4H)3ThH, 5, and [K(2.2.2-cryptand)]{(C5Me4H)2[η(1):η(5)-C5Me3H(CH2)]ThH]}, 6. Complex 6 contains a metalated tetramethylcyclopentadienyl dianion, [C5Me3H(CH2)](2-), that binds in a tuck-in mode.

Record High Single-Ion Magnetic Moments Through 4f(n)5d(1) Electron Configurations in the Divalent Lanthanide Complexes [(C5H4SiMe3)3Ln]⁻.

The recently reported series of divalent lanthanide complex salts, namely [K(2.2.2-cryptand)][Cp'3Ln] (Ln = Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm; Cp' = C5H4SiMe3) and the analogous trivalent complexes, Cp'3Ln, have been characterized via dc and ac magnetic susceptibility measurements. The salts of the complexes [Cp'3Dy](-) and [Cp'3Ho](-) exhibit magnetic moments of 11.3 and 11.4 µB, respectively, which are the highest moments reported to date for any monometallic molecular species. The magnetic moments measured at room temperature support the assignments of a 4f(n+1) configuration for Ln = Sm, Eu, Tm and a 4f(n)5d(1) configuration for Ln = Y, La, Gd, Tb, Dy, Ho, Er. In the cases of Ln = Ce, Pr, Nd, simple models do not accurately predict the experimental room temperature magnetic moments. Although an LS coupling scheme is a useful starting point, it is not sufficient to describe the complex magnetic behavior and electronic structure of these intriguing molecules. While no slow magnetic relaxation was observed for any member of the series under zero applied dc field, the large moments accessible with such mixed configurations present important case studies in the pursuit of magnetic materials with inherently larger magnetic moments. This is essential for the design of new bulk magnetic materials and for diminishing processes such as quantum tunneling of the magnetization in single-molecule magnets.

Structural, spectroscopic, and theoretical comparison of traditional vs recently discovered Ln(2+) ions in the [K(2.2.2-cryptand)][(C5H4SiMe3)3Ln] complexes: the variable nature of Dy(2+) and Nd(2+).

The Ln(3+) and Ln(2+) complexes, Cp'3Ln, 1, (Cp' = C5H4SiMe3) and [K(2.2.2-cryptand)][Cp'3Ln], 2, respectively, have been synthesized for the six lanthanides traditionally known in +2 oxidation states, i.e., Ln = Eu, Yb, Sm, Tm, Dy, and Nd, to allow direct structural and spectroscopic comparison with the recently discovered Ln(2+) ions of Ln = Pr, Gd, Tb, Ho, Y, Er, and Lu in 2. 2-La and 2-Ce were also prepared to allow the first comparison of all the lanthanides in the same coordination environment in both +2 and +3 oxidation states. 2-La and 2-Ce show the same unusual structural feature of the recently discovered +2 complexes, that the Ln-(Cp' ring centroid) distances are only about 0.03 Å longer than in the +3 analogs, 1. The Eu, Yb, Sm, Tm, Dy, and Nd complexes were expected to show much larger differences, but this was observed for only four of these traditional six lanthanides. 2-Dy and 2-Nd are like the new nine ions in this tris(cyclopentadienyl) coordination geometry. A DFT-based model explains the results and shows that a 4f (n)5d(1) electron configuration is appropriate not only for the nine recently discovered Ln(2+) ions in 2 but also for Dy(2+) and Nd(2+), which traditionally have 4f (n+1) electron configurations like Eu(2+), Yb(2+), Sm(2+), and Tm(2+). These results indicate that the ground state of a lanthanide ion in a molecule can be changed by the ligand set, a previously unknown option with these metals due to the limited radial extension of the 4f orbitals.

Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1- anion containing thorium in the formal +2 oxidation state.

Reduction of the Th3+ complex Cp''3Th, 1 [Cp'' = C5H3(SiMe3)2], with potassium graphite in THF in the presence of 2.2.2-cryptand generates [K(2.2.2-cryptand)][Cp''3Th], 2, a complex containing thorium in the formal +2 oxidation state. Reaction of 1 with KC8 in the presence of 18-crown-6 generates the analogous Th2+ compound, [K(18-crown-6)(THF)2][Cp''3Th], 3. Complexes 2 and 3 form dark green solutions in THF with ε = 23 000 M-1 cm-1, but crystallize as dichroic dark blue/red crystals. X-ray crystallography revealed that the anions in 2 and 3 have trigonal planar coordination geometries, with 2.521 and 2.525 ŠTh-(Cp'' ring centroid) distances, respectively, equivalent to the 2.520 Šdistance measured in 1. Density functional theory analysis of (Cp''3Th)1- is consistent with a 6d2 ground state, the first example of this transition metal electron configuration. Complex 3 reacts as a two-electron reductant with cyclooctatetraene to make Cp''2Th(C8H8), 4, and [K(18-crown-6)]Cp''.

Isolation of +2 rare earth metal ions with three anionic carbocyclic rings: bimetallic bis(cyclopentadienyl) reduced arene complexes of La2+ and Ce2+ are four electron reductants.

A new option for stabilizing unusual Ln2+ ions has been identified in the reaction of Cp'3Ln, 1-Ln (Ln = La, Ce; Cp' = C5H4SiMe3), with potassium graphite (KC8) in benzene in the presence of 2.2.2-cryptand. This generates [K(2.2.2-cryptand)]2[(Cp'2Ln)2(µ-η6:η6-C6H6)], 2-Ln, complexes that contain La and Ce in the formal +2 oxidation state. These complexes expand the range of coordination environments known for these ions beyond the previously established examples, (Cp''3Ln)1- and (Cp'3Ln)1- (Cp'' = C5H3(SiMe3)2-1,3), and generalize the viability of using three anionic carbocyclic rings to stabilize highly reactive Ln2+ ions. In 2-Ln, a non-planar bridging (C6H6)2- ligand shared between two metals takes the place of a cyclopentadienyl ligand in (Cp'3Ln)1-. The intensely colored (ε = ∼8000 M-1 cm-1) 2-Ln complexes react as four electron reductants with two equiv. of naphthalene to produce two equiv. of the reduced naphthalenide complex, [K(2.2.2-cryptand)][Cp'2Ln(η4-C10H8)].