Reactions of Platinum Terminal Polyynyl Complexes trans-(C6F5)(p-tol3P)2Pt(C≡C)nH (n = 2-4) and n-BuLi, Generation of Functional Equivalents of Pt(C≡C)nLi Species, and Derivatization with Organic and Inorganic Electrophiles.

Reactions of the title complexes and n-BuLi (1.5 equiv, -45 °C) afford functional equivalents of the deprotonated species trans-(C6F5)(p-tol3P)2Pt(C≡C)nLi (n = 2-4), as assayed by subsequent additions of MeI or Me3SiCl to give trans-(C6F5)(p-tol3P)2Pt(C≡C)nMe (66-52%) or trans-(C6F5)(p-tol3P)2Pt(C≡C)nSiMe3 (63-49%). However, 31P NMR data suggest more complicated mechanistic scenarios, and small amounts of the hydride complex trans-(C6F5)(p-tol3P)2PtH (independently synthesized from the chloride complex, AgClO4, and NaBH4) are detected in most cases. Analogous sequences involving trans-(C6F5)(p-tol3P)2Pt(C≡C)2H and benzyl bromide, D2O, or W(CO)6/Me3O+ BF4- similarly afford products with Pt(C≡C)2Bn, Pt(C≡C)2D, or Pt(C≡C)2C(OCH3)=W(CO)5 linkages. The crystal structures of the tungsten and corresponding SiMe3 adduct, the three Pt(C≡C)nMe species, and hydride complex are determined.

Molecules that Turn Themselves Inside-Out: Tuning in/out Equilibria and Homeomorphic Isomerization in Macrobicyclic Dibridgehead Diphosphines P((CH2 )n )3 P Newly Accessible by Earth-Abundant-Metal Templates.

Photolyses of trans-Fe(CO)3 (P((CH2 )n )3 P) (n=10 (a), 12 (b), 14 (c), 16 (d), 18 (e)) in the presence of PMe3 provide the first economical and scalable route to macrobicyclic dibridgehead diphosphines P((CH2 )n )3 P (1). These are isolated as mixtures of in,in/out,out isomers that equilibrate with degenerate in,out/out,in isomers at 150 °C via pyramidal inversion at phosphorus. For the entire series, VT 31 P NMR data establish or bound Keq , rates, and activation parameters for a variety of phenomena, many of which involve homeomorphic isomerizations, topological processes by which certain molecules can turn themselves inside out (e. g., in,in⇌out,out). This provides the first detailed mapping of such trends in homologous series of aliphatic bicyclic compounds XE((CH2 )n )3 EX with any type of bridgehead. Isomeric diborane adducts 1 a,d ⋅ 2BH3 are also characterized. Crystal structures of out,out-1 a and in,in-1 a ⋅ 2BH3 aid isomer assignments and reveal unusual cage conformations.

Shortwave Infrared Fluorofluorophores for Multicolor In Vivo Imaging.

Developing chemical tools to detect and influence biological processes is a cornerstone of chemical biology. Here we combine two tools which rely on orthogonality- perfluorocarbons and multiplexed shortwave infrared (SWIR) fluorescence imaging- to visualize nanoemulsions in real time in living mice. Drawing inspiration from fluorous and SWIR fluorophore development, we prepared two SWIR-emissive, fluorous-soluble chromenylium polymethine dyes. These are the most red-shifted fluorous fluorophores- "fluorofluorophores"-to date. After characterizing the dyes, their utility was demonstrated by tracking perfluorocarbon nanoemulsion biodistribution in vivo. Using an excitation-multiplexed approach to image two variables simultaneously, we gained insight into the importance of size and surfactant identity on biodistribution.

Monodisperse Molecular Models for the sp Carbon Allotrope Carbyne; Syntheses, Structures, and Properties of Diplatinum Polyynediyl Complexes with PtC20Pt to PtC52Pt Linkages.

Extended conjugated polyynes provide models for the elusive sp carbon polymer carbyne, but progress has been hampered by numerous synthetic challenges. Stabilities appear to be enhanced by bulky, electropositive transition-metal endgroups. Reactions of trans-(C6F5)(p-tol3P)2Pt(C≡C)nSiEt3 (n = 4-6, PtCxSi (x = 2n)) with n-Bu4N+F-/Me3SiCl followed by excess tetrayne H(C≡C)4SiEt3 (HC8Si) and then CuCl/TMEDA and O2 give the heterocoupling products PtCx+8Si, PtCx+16Si, and sometimes higher homologues. The PtCx+16Si species presumably arise via protodesilylation of PtCx+8Si under the reaction conditions. Chromatography allows the separation of PtC16Si, PtC24Si, and PtC32Si (from n = 4), PtC18Si and PtC26Si (n = 5), or PtC20Si and PtC28Si (n = 6). These and previously reported species are applied in similar oxidative homocouplings, affording the family of diplatinum polyynediyl complexes PtCxPt (x = 20, 24, 28, 32, 36, 40 in 96-34% yields and x = 44, 48, 52 in 22-7% yields). These are carefully characterized by 13C NMR, UV-visible, and Raman spectroscopy and other techniques, with particular attention to behavior as the Cx chain approaches the macromolecular limit and endgroup effects diminish. The crystal structures of solvates of PtC20Pt, PtC24Pt, and PtC26Si, which feature the longest sp chains structurally characterized to date, are analyzed in detail. All data support a polyyne electronic structure with a nonzero optical band gap and bond length alternation for carbyne.

Building Blocks for Molecular Polygons Based on Platinum Vertices and Polyynediyl Edges.

Reactions of Cl2P(CH2)3PCl2 and p-MgBrC6H4X (X = a/OMe, b/OtBu, c/tBu, d/SiMe3) give the diphosphines (p-XC6H4)2P(CH2)3P(p-C6H4X)2 (1a-d; 47-66%). Additions of 1a,d to (COD)PtCl2 yield (CH2(CH2P(p-C6H4X)2)2)PtCl2 (2a,d; 62-88%), which upon reaction with butadiyne (2 equiv; HNEt2/cat. CuI) give (CH2(CH2P(p-C6H4X)2)2)Pt((C≡C)2H)2 (3a,d; 34-76%). Alternatively, 3a-d can be accessed from trans-(p-tol3P)2Pt((C≡C)2H)2 and 1a-d (30-87%). Reactions of (p-tol3P)2PtCl2 and H(C≡C)2SiR3 (2 equiv, HNEt2/cat. CuI; R = Me/Et/iPr) give trans-(p-tol3P)2Pt((C≡C)2SiR3)2 (77-95%), and subsequent additions of 1a,b,d yield the corresponding adducts (CH2(CH2P(p-C6H4X)2)2)Pt((C≡C)2SiR3)2 (R/X = Me/OMe, 5a; iPr/OMe, 6a; iPr/OtBu, 6b; iPr/SiMe3, 6d; 52-95%) and (for 5a) a luminescent diplatinum byproduct with trans Pt((C≡C)2SiMe3)2 units. 5a and 6b hydrolyze in the presence of F- to 3a,b (92-93%). Reaction of 2a and 3a (HNEt2/cat. CuI) affords the Pt4C16 polygon ([(CH2(CH2P(p-C6H4OMe)2)2)Pt(C≡C)2]4 as an H2NEt2+ Cl- adduct (66%). The 13C{1H} NMR spectra of 3a-d, 5a, and 6a,b,d feature complex AMXX' (CPtPP') spin systems, and simulations allow J values to be extracted. The crystal structures of 2a, 3a,b,d, 5a, and 6a are determined and analyzed.

Syntheses, homeomorphic and configurational isomerizations, and structures of macrocyclic aliphatic dibridgehead diphosphines; molecules that turn themselves inside out.

The diphosphine complexes cis- or trans-[upper bond 1 start]PtCl2(P((CH2) n )3P[upper bond 1 end]) (n = b/12, c/14, d/16, e/18) are demetalated by MC[triple bond, length as m-dash]X nucleophiles to give the title compounds (P((CH2) n )3)P (3b-e, 91-71%). These "empty cages" react with PdCl2 or PtCl2 sources to afford trans-[upper bond 1 start]MCl2(P((CH2) n )3P[upper bond 1 end]). Low temperature 31P NMR spectra of 3b and c show two rapidly equilibrating species (3b, 86 : 14; 3c, 97 : 3), assigned based upon computational data to in,in (major) and out,out isomers. These interconvert by homeomorphic isomerizations, akin to turning articles of clothing inside out (3b/c: ΔH ‡ 7.3/8.2 kcal mol-1, ΔS ‡ -19.4/-11.8 eu, minor to major). At 150 °C, 3b, c, e epimerize to (60-51) : (40-49) mixtures of (in,in/out,out) : in,out isomers, which are separated via the bis(borane) adducts 3b, c, e·2BH3. The configurational stabilities of in,out-3b, c, e preclude phosphorus inversion in the interconversion of in,in and out,out isomers. Low temperature 31P NMR spectra of in,out-3b, c reveal degenerate in,out/out,in homeomorphic isomerizations (ΔG ‡ Tc 12.1, 8.5 kcal mol-1). When (in,in/out,out)-3b, c, e are crystallized, out,out isomers are obtained, despite the preference for in,in isomers in solution. The lattice structures are analyzed, and the D 3 symmetry of out,out-3c enables a particularly favorable packing motif. Similarly, (in,in/out,out)-3c, e·2BH3 crystallize in out,out conformations, the former with a cycloalkane solvent guest inside.

Rethinking premedical education.

The world needs more physicians. Increasing their numbers alone won't solve the many problems associated with improving health care. But it doesn't help to have a dearth of doctors, who were generally in short supply before COVID-19 struck. The pandemic has only exacerbated doctor shortages everywhere. This doesn't bode well for a world that must prepare for future pandemics and for populations that are both growing and aging. Better health outcomes require more physicians. So, where are the bottlenecks?

A new supramolecular bonding motif involving NH bonds of ammonium salts and macrocycles derived from platinum corners and butadiynediyl linkers.

CuI catalyzes reactions of cis-(R2C(CH2PPh2)2)Pt(CCCCH)2 and cis-(R2C(CH2PPh2)2)PtI2 in secondary amine solvents HNR'2 to give the title adducts [(R2C(CH2PPh2)2)Pt(CCCC)]4·(H2NR'2+I-)n (R/R'/n = Me/Et/1, Me/((CH2CH2)2O)0.5/3, Et/Et/1, Et/CH2CHCH2/1; 92-42%). Crystal structures of these or closely related species establish folded Pt4 cores containing ammonium cation guests, with NH/ and NCH/CC hydrogen bonding. DOSY NMR experiments show that the host/guest relationship can be maintained in solution.

Square-Planar and Octahedral Gyroscope-Like Metal Complexes Consisting of Dipolar Rotators Encased in Dibridgehead Di(triaryl)phosphine Stators: Syntheses, Structures, Dynamic Properties, and Reactivity.

For a variety of purposes, it is of interest to embed metals in cagelike trans-spanning di(triaryl)phosphine ligands. Toward this end, a combination of P(p-C6H4O(CH2)mCH═CH2)3 [3; m = 4 (a), 5 (b), 6 (c), and 7 (d)], [Rh(COD)(µ-Cl)]2, and CO gives square-planar trans-Rh(CO)(Cl)[P(p-C6H4O(CH2)mCH═CH2)3]2 (4a-4d). Reactions of 4b-4d with Grubbs' catalyst (first generation) and then H2 (catalyst PtO2) yield the title compounds trans-Rh(CO)(Cl)[P(p-C6H4O(CH2)nO-p-C6H4)3P] (n = 2m + 2, 6b-6d; 26-41% from 4b-4d). Two are crystallographically characterized. The Cl-Rh-CO moieties rapidly rotate on the NMR time scale at -120 °C, per the ample clearance provided by the (CH2)n segments. Steric interactions with the PC6H4O linkages are analyzed. LiC≡CAr displaces the chloride ligand from 6b to give RhC≡CAr adducts (Ar = C6H5/p-C6H4CH3, 7b/8b). The ArC≡C-Rh-CO rotator of 7b rapidly rotates on the NMR time scale (-70 °C), but with 8b, the longer p-CH3C6H4C≡C group is confined between two (CH2)12 bridges, even at 120 °C. Reactions of Re(CO)5(X) and 3c (140 °C) give octahedral mer,trans-Re(CO)3(X)[P(p-C6H4O(CH2)6CH═CH2)3]2 (X = Cl/Br), and metathesis/hydrogenation sequences yield mer,trans-Re(CO)3(X)[P(p-C6H4O(CH2)14O-p-C6H4)3P]. Reactions of 6c and 6d and excess PMe3 give the free diphosphines P(p-C6H4O(CH2)nO-p-C6H4)3P (14c and 14d, 83-75%). The addition of 14d to [Rh(CO)2(µ-Cl)]2 reconstitutes 6d (87%). Both in,in and out,out isomers of 14c and 14d are possible, but low-temperature NMR spectra show one set of signals, consistent with rapid homeomorphic isomerizations that turn the molecules inside out. Thermolyses (C6D5Br, 140 °C) effect phosphorus inversion to give in,out isomers.

Mechanism of Coupling of Methylidene to Ethylene Ligands in Dimetallic Assemblies; Computational Investigation of a Model for a Key Step in Catalytic C1 Chemistry.

Methylidene complexes often couple to ethylene complexes, but the mechanistic insight is scant. The path by which two cations [(η5-C5H5)Re(NO)(PPh3)(═CH2)]+ (5+) transform (CH2Cl2/acetonitrile) to [(η5-C5H5)Re(NO)(PPh3)(H2C═CH2)]+ (6+) and [(η5-C5H5)Re(NO)(PPh3)(NCCH3)]+ is studied by density functional theory. Experiments provide a number of constraints such as the second-order rate in 5+; no prior ligand dissociation/exchange; a faster reaction of (S)-5+ with (S)-5+ than with (R)-5+ ("enantiomer self-recognition"). Although dirhenium dications with Re(µ-CH2)2Re cores represent energy minima, they are not accessible by 2 + 2 cycloadditions of 5+. Transition states leading to ReCH2CH2Re linkages are prohibitively high in energy. However, 5+ can give non-covalent SRe/SRe or SRe/RRe dimers with π interactions between the PPh3 ligands but long ReCH2···H2CRe and H2CRe···H2CRe distances (3.073-3.095 Å and 3.878-4.529 Å, respectively). In rate-determining steps, these afford [(η5-C5H5)Re(NO)(PPh3)(µ-η2:η2-H2C···CH2)(Ph3P)(ON)Re(η5-C5H5)]2+ (132+), in which one rhenium binds the bridging ethylene more tightly than the other (2.115-2.098 vs 2.431-2.486 Å to the centroid). In the SRe/RRe adduct, Dewar-Chatt-Duncanson optimization leads to unfavorable PPh3/PPh3 contacts. Ligand interactions are further dissected in the preceding transition states via component analyses, and ΔΔG‡ (1.2 kcal/mol, CH2Cl2) favors the SRe/SRe pathway, in accordance with the experiment. Acetonitrile then displaces 6+ from the more weakly bound rhenium of 132+. The formation of similar µ-H2C···CH2 intermediates is found to be rate-determining for varied coordinatively saturated M═CH2 species [M = Fe(d6)/Re(d4)/Ta(d2)], establishing generality and enhancing relevancy to catalytic CH4 and CO/H2 chemistry.

Tracking Energy Transfer across a Platinum Center.

Rigid, conjugated alkyne bridges serve as important components in various transition-metal complexes used for energy conversion, charge separation, sensing, and molecular electronics. Alkyne stretching modes have potential for modulating charge separation in donor-bridge-acceptor compounds. Understanding the rules of energy relaxation and energy transfer across the metal center in such compounds can help optimize their electron transfer switching properties. We used relaxation-assisted two-dimensional infrared spectroscopy to track energy transfer across metal centers in platinum complexes featuring a triazole-terminated alkyne ligand of two or six carbons, a perfluorophenyl ligand, and two tri(p-tolyl)phosphine ligands. Comprehensive analyses of waiting-time dynamics for numerous cross and diagonal peaks were performed, focusing on coherent oscillation, energy transfer, and cooling parameters. These observables augmented with density functional theory computations of vibrational frequencies and anharmonic force constants enabled identification of different functional groups of the compounds. Computations of vibrational relaxation pathways and mode couplings were performed, and two regimes of intramolecular energy redistribution are described. One involves energy transfer between ligands via high-frequency modes; the transfer is efficient only if the modes involved are delocalized over both ligands. The energy transport pathways between the ligands are identified. Another regime involves redistribution via low-frequency delocalized modes, which does not lead to interligand energy transport.

A surprise landing on the terra incognita of macrocyclic dibridgehead diorganoarsines: syntheses, structures, and reactivities.

Reactions of trans-[Fe(CO)2(NO)(As((CH2)n)3As)]+ BF4- (n = 10, 12, 14) and Bu4N+ Cl- afford the title compounds As((CH2)n)3As, which upon reaction (n = 14) with MCl2 (M = Pt, Ni), Rh(CO)(Cl), and Fe(CO)3 sources reconstitute cage like complexes trans-MLn(As((CH2)14)3As). Reactions with H2O2 and BH3 give the corresponding arsine oxides and boranes. Crystal structures of metal-free species reveal out,out isomers, but cage complex formation is proposed to entail homeomorphic isomerization to in,in isomers with endo directed lone pairs.

Syntheses, rearrangements, and structural analyses of unsaturated nitrogen donor ligands derived from diphenyldiazomethane and the chiral rhenium Lewis acid [(η5-C5H5)Re(NO)(PPh3)].

Diphenyldiazomethane and a labile chlorobenzene complex of [(η5-C5H5)Re(NO)(PPh3)]+ BF4- react to give the η1 adduct [(η5-C5H5)Re(NO)(PPh3)(NNCPh2)]+ BF4- (73%). When this is conducted in the presence of copper powder, a 3-phenyl-1H-indazole complex derived from carbon-hydrogen bond activation, [(η5-C5H5)Re(NO)(PPh3)(NC(Ph)CCHCHCHCHCNH)]+ BF4-, is obtained (65%). Subsequent reaction with NaOCH3 gives indazolyl complex (η5-C5H5)Re(NO)(PPh3)(NCCHCHCHCHCC(Ph)N) (85%), derived from NH deprotonation and a 1,2-rhenium shift. Crystal structures of the three new complexes are determined. DFT calculations are used to probe the mechanism of the 1,2-shift and energetics of alternative Re-N rotamers and linkage isomers, and assign bond orders and dominant resonance formulations.

Platinum(II) alkyl complexes of chelating dibridgehead diphosphines P((CH2)n)3P (n = 14, 18, 22); facile cis/trans isomerizations interconverting gyroscope and parachute like adducts.

The gyroscope like dichloride complexes trans-Pt(Cl)2(P((CH2)n)3P) (trans-2; n = c, 14; e, 18; g, 22) and MeLi (2 equiv.) react to yield the parachute like dimethyl complexes cis-Pt(Me)2(P((CH2)n)3P) (cis-4c,e,g, 70-91%). HCl (1 equiv.) and cis-4c react to give cis-Pt(Cl)(Me)(P((CH2)14)3P) (cis-5c, 83%), which upon stirring with silica gel or crystallization affords trans-5c (89%). Similar reactions of HCl and cis-4e,g give cis/trans-5e,g mixtures that upon stirring with silica gel yield trans-5e,g. A parallel sequence with trans-2c/EtLi gives cis-Pt(Et)2(P((CH2)14)3P) (cis-6c, 85%) but subsequent reaction with HCl affords trans-Pt(Cl)(Et)(P((CH2)14)3P) (trans-7c, 45%) directly. When previously reported cis-Pt(Ph)2(P((CH2)14)3P) is treated with HCl (1 equiv.), cis- and trans-Pt(Cl)(Ph)(P((CH2)14)3P) are isolated (44%, 29%), with the former converting to the latter at 100 °C. Reactions of trans-5c and LiBr or NaI afford the halide complexes trans-Pt(X)(Me)(P((CH2)14)3P) (trans-9c, 88%; trans-10c, 87%). Thermolyses and DFT calculations that include acyclic model compounds establish trans > cis stabilities for all except the dialkyl complexes, for which energies can be closely spaced. The σ donor strengths of the non-phosphine ligands are assigned key roles in the trends. The crystal structures of cis-4c, trans-5c, trans-7c, and trans-10c are determined and analyzed together with the computed structures.

Syntheses, Structures, Reactivities, and Basicities of Quinolinyl and Isoquinolinyl Complexes of an Electron Rich Chiral Rhenium Fragment and Their Electrophilic Addition Products.

Reactions of Li+ [(η5 -C5 H5 )Re(NO)(PPh3 )]- with 2- and 4-chloroquinoline or 1-chloroisoquinoline give the corresponding σ quinolinyl and isoquinolinyl complexes 3, 6, and 8. With 3 and 8 there is further protonation to yield HCl adducts, but additions of KH give the free bases. Treatment of 3 with HBF4 ⋅OEt2 or H(OEt2 )2 + BArf - gives the quinolinium salts [(η5 -C5 H5 )Re(NO)(PPh3 )(C(NH)C(CH)4 C(CH)(CH))]+ X- (3-H+ X- ; X- =BF4 - /BArf - , 94-98 %). Addition of CF3 SO3 CH3 to 3, 6, or 8 affords the corresponding N-methyl quinolinium salts. In the case of [(η5 -C5 H5 )Re(NO)(PPh3 )(C(NCH3 )C(CH)4 C(CH)(CH))]+ CF3 SO3 - (3-CH3 + CF3 SO3 - ), addition of CH3 Li gives the dihydroquinolinium complex (SRe RC ,RRe SC )-[(η5 -C5 H5 )Re(NO)(PPh3 )(C(NCH3 )C(CH)4 C(CHCH3 )(CH2 ))]+ CF3 SO3 - ((SRe RC ,RRe SC )-5+ CF3 SO3 - , 76 %) in diastereomerically pure form. Crystal structures of 3-H+ BArf - , 3-CH3 + CF3 SO3 - , (SRe RC , RRe SC )-5+ Cl- , and 6-CH3 + CF3 SO3 - show that the quinolinium ligands adopt Re⋅⋅⋅C conformations that maximize overlap of their acceptor orbitals with the rhenium fragment HOMO, minimize steric interactions with the bulky PPh3 ligand, and promote various π interactions. NMR experiments establish the Brønsted basicity order 3>8>6, with Ka (BH+ ) values >10 orders of magnitude greater than the parent heterocycles, although they remain less active nucleophilic catalysts in the reactions tested. DFT calculations provide additional insights regarding Re⋅⋅⋅C bonding and conformations, basicities, and the stereochemistry of CH3 Li addition.

Macrocyclic Complexes Derived from Four cis-L2 Pt Corners and Four Butadiynediyl Linkers; Syntheses, Electronic Structures, and Square versus Skew Rhombus Geometries.

The dialkyl malonate derived 1,3-diphosphines R2 C(CH2 PPh2 )2 (R=a, Me; b, Et; c, n-Bu; d, n-Dec; e, Bn; f, p-tolCH2 ) are combined with (p-tol3 P)2 PtCl2 or trans-(p-tol3 P)2 Pt((C≡C)2 H)2 to give the chelates cis-(R2 C(CH2 PPh2 )2 )PtCl2 (2 a-f, 94-69 %) or cis-(R2 C(CH2 PPh2 )2 )Pt((C≡C)2 H)2 (3 a-f, 97-54 %). Complexes 3 a-d are also available from 2 a-d and excess 1,3-butadiyne in the presence of CuI (cat.) and excess HNEt2 (87-65 %). Under similar conditions, 2 and 3 react to give the title compounds [(R2 C(CH2 PPh2 )2 )[Pt(C≡C)2 ]4 (4 a-f; 89-14 % (64 % avg)), from which ammonium salts such as the co-product [H2 NEt2 ]+ Cl- are challenging to remove. Crystal structures of 4 a,b show skew rhombus as opposed to square Pt4 geometries. The NMR and IR properties of 4 a-f are similar to those of mono- or diplatinum model compounds. However, cyclic voltammetry gives only irreversible oxidations. As compared to mono-platinum or Pt(C≡C)2 Pt species, the UV-visible spectra show much more intense and red-shifted bands. Time dependent DFT calculations define the transitions and principal orbitals involved. Electrostatic potential surface maps reveal strongly negative Pt4 C16 cores that likely facilitate ammonium cation binding. Analogous electronic properties of Pt3 C12 and Pt5 C20 homologs and selected equilibria are explored computationally.

Trapping of Terminal Platinapolyynes by Copper(I) Catalyzed Click Cycloadditions; Probes of Labile Intermediates in Syntheses of Complexes with Extended sp Carbon Chains, and Crystallographic Studies.

The silylated hexatriynyl complex trans-(C6 F5 )(p-tol3 P)2 Pt(C≡C)3 SiEt3 (PtC6 TES) is converted in situ to PtC6 H (wet n-Bu4 N+ F- , THF) and cross coupled with the diyne H(C≡C)2 SiEt3 (HC4 TES; CuCl/TMEDA, O2 ) to give PtC10 TES (71 %). This sequence is repeated twice to afford PtC14 TES (65 %) and then PtC18 TES (27 %). An analogous series of reactions starting with PtC8 TES gives PtC12 TES (60 %), then PtC16 TES (43 %), and then PtC20 TES (17 %). Similar cross couplings with H(C≡C)2 Si(i-Pr)3 (HC4 TIPS) give PtC12 TIPS (68 %), PtC14 TIPS (68 %), and PtC16 TIPS (34 %). The trialkylsilyl species (up to PtC18 TES) are converted to 3+2 "click" cycloadducts or 1,4-disubstituted 1,2,3-triazoles trans-(C6 F5 )(p-tol3 P)2 Pt(C≡C)n-1 C=CHN(CH2 C6 H5 )N=N (29-92 % after workups). The most general procedure involves generating the terminal polyynes PtCx H (wet n-Bu4 N+ F- , THF) in the presence of benzyl azide in DMF and aqueous CuSO4 /ascorbic acid. All of the preceding complexes are crystallographically characterized and the structural and spectroscopic properties analyzed as a function of chain length. Two pseudopolymorphs of PtC20 TES are obtained, both of which feature molecules with parallel sp carbon chains in a pairwise head/tail packing motif with extensive sp/sp van der Waals contacts.

Gyroscopes and the Chemical Literature, 2002-2020: Approaches to a Nascent Family of Molecular Devices.

Research directed toward the goal of molecular gyroscopes since the coverage of a previous review (2002) is described. Such species are a subclass of molecular rotors, which are comprised of rotators and stators. Major categories include (1) systems in which a rotator is embedded in a cage-like stator reminiscent of mechanical toy gyroscopes and (2) molecules that have been engineered to crystallize with parallel rotators and voids or other features that enable the rotator to rotate in the solid state (amphidynamic crystals). Particular attention is given to structural data and strategies for the minimization of rotational barriers. Synthetic routes are also described. Some allied types of molecules and supramolecular assemblies are also treated.

Toward Frameworks with Multiple Aligned and Interactive Fe(CO)3 Rotators: Syntheses and Structures of Diiron Complexes Linked by Two trans-Diaxial α,ω-Diphosphine Ligands Ar2P(CH2)nPAr2.

Reactions of (η4-benzylideneacetone)Fe(CO)3 and the α,ω-diphosphines Ar2P(CH2)nPAr2 afford the trigonal bipyramidal diiron tetraphosphorus complexes trans,trans-(CO)3Fe[Ar2P(CH2)nPAr2]2Fe(CO)3 (n/Ar = 3/Ph 3, 4/Ph 4a, 4/p-tol 4b; 56-19%). Crystal structures establish essentially parallel P-Fe-P axes, iron-iron distances of 5.894(9)-5.782(1) Å (3) and 6.403(1)-6.466(1) Å (4a,b), and van der Waals radii of 4.45 Å for the Fe(CO)3 rotators, the planes of which are offset by 0.029-1.665 Å. Analogous reactions of Ph2P(CH2)6PPh2 yield the square pyramidal monoiron complex trans-(CO)3Fe[Ph2P(CH2)6PPh2] (6', 31%), a rare case where a diphosphine spans trans basal positions (∠P-Fe-P 147.4(2)°). Both 3 and 6' exhibit two CO 13C NMR signals at room temperature, indicating slow exchange on the NMR time scale, which in the former could entail Fe(CO)3/Fe(CO)3 gearing. Under analogous conditions, 4a,b exhibit one signal. Previously reported adducts of Fe(CO)3 and Ph2P(CH2)nPPh2 are surveyed (1:1, n = 1-5; 2:2, n = 5), and the IR νC≡O band patterns and energies of all complexes analyzed with the aid of DFT calculations. The diiron complexes are preferred thermodynamically. Attention is given to limiting types of Fe(CO)3/Fe(CO)3 interactions in the diiron complexes.