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1 evitably attenuate the reactivity of the M-L multiple bond.
2 e additional two electrons to cleave the N-N multiple bond.
3 acter with some contribution also from a C-P multiple bond.
4 l group is directed trans to the uranium-oxo multiple bond.
5 everal other relevant complexes featuring UN multiple bonds.
6 g involving mostly examples of metal-element multiple bonds.
7 tate and sustaining the formation of uranium multiple bonds.
8 al "primed" contact formed from metal-carbon multiple bonds.
9 t rate k(off) for a single bond and also for multiple bonds.
10 racterized compounds containing metal-ligand multiple bonds.
11 pes of transition metal complexes containing multiple bonds.
12 stochastic model involving dissociation from multiple bonds.
13 butadiene systems with conjugated main-group multiple bonds.
14 s the force to be distributed evenly between multiple bonds.
15 : pi-conjugation through both TM-C and TM-TM multiple bonds.
16 is great interest in studying uranium-ligand multiple bonds.
17 the gold-catalyzed functionalization of C-C multiple bonds.
18 on deficiency, boron is versatile in forming multiple bonds.
19 ends of the DNA to two separate surfaces via multiple bonds.
20 step of Noyori hydrogrogenation reactions of multiple bonds.
21 eophilic addition reactions to carbon-carbon multiple bonds.
22 transformations of unactivated carbon-carbon multiple bonds.
23 design main-group metal-boron complexes with multiple bonding.
24 c structure calculations show some degree of multiple bonding.
25 ations suggested sigma(2)pi(4) polarized U-N multiple bonding.
26 bond lengths, suggestive of actinide-ligand multiple bonding.
27 s ascribed to the cooperation of W-O and W-W multiple bonding.
28 3)C correlations ("INADEQUATE"), single- and multiple-bond (13)C-(1)H correlations, and the conventio
29 terized by their two strong trans-An-element multiple bonds, a consequence of the inverse trans influ
30 ese newly discovered reactions can construct multiple bonds all at once, converting linear starting m
32 spite the burgeoning field of uranium-ligand multiple bonds, analogous complexes involving other acti
33 complex is the first lanthanide(IV)-element multiple bond and involves a twofold bonding interaction
34 nt reactions that enable the construction of multiple bonds and/or stereogenic centres in a single sy
35 tances in 4 and 5, indicative of metal-metal multiple bonding, and an unprecedented trigonal monopyra
38 ly authenticated, terminal lanthanide-ligand multiple bonds are rare and expected to be highly reacti
39 ation of SN2 reactions for substrates with a multiple bond at Cbeta (carbon adjacent to the reacting
40 results in rapid and efficient reduction of multiple bonds, azides, imines, and nitro groups, as wel
42 t complex featuring an unsupported, terminal multiple bond between a Ce(IV) ion and a ligand fragment
43 (h)-C80 is the first metallofullerene with a multiple bond between a metal and the central, non-metal
46 ture, i.e., it requires the establishment of multiple bonds between amino acids of viral glycoprotein
48 tal-metal bonding, the occurrence of stable, multiple bonds between different transition metals is un
51 y of f-orbital participation in metal-ligand multiple bonding but has previously eluded characterizat
53 onally due to the limitations of compressing multiple bonding changes onto a 2-dimensional energy sur
54 resonance structures, some of which possess multiple bond character between tungsten and silicon.
55 onic ground-state calculations indicate a PP multiple bond character in which the terminal phosphorus
56 istance suggest a significant degree of P-Ge multiple bond character that is due to delocalization of
57 s-bent structure indicate the presence Sn-Sn multiple bond character unlike the related singly bonded
60 Fe(0) centers were also carried out, whereby multiple bonding character is detected in all cases (Wib
63 ions revealed for all investigated compounds multiple-bonded character for the M-E(II) linkage, which
65 Despite a major expansion of uranium-ligand multiple bond chemistry in recent years, analogous compl
66 tiple Quantum Coherence and 2D Heteronuclear Multiple Bond Coherence spectroscopic analyses to the li
67 nimum for Si-Si and Ge-Ge, is a diradicaloid multiple-bonding configuration where LP and pi are nomin
68 require the presence of aromatic residues or multiple bond conjugation that characterize conventional
70 GH18(N) and cleaves chitooligosaccharides at multiple bonds, consistent with endochitinolytic activit
71 e-quantum coherence (HMQC) and heteronuclear multiple bond correlation (HMBC) spectra were obtained.
74 equential quantum correlation, heteronuclear multiple bond correlation) analysis identified the paral
75 ifuga) species as a test case, heteronuclear multiple-bond correlation (HMBC) barcodes were generated
77 ignments for each regioisomer, heteronuclear multiple-bond correlation spectroscopy was used to assig
78 positive and negative cooperativity between multiple bonds depending on whether the antigen was link
81 t in compounds containing functionalized E=E multiple bonds (E=Si, Ge, Sn, Pb) because of their poten
87 New reactions and reagents that allow for multiple bond-forming events per synthetic operation are
90 te Carlo simulations show that this level of multiple bonding has little effect on parameter estimati
91 tion of boron-X sigma bonds to carbon-carbon multiple bonds has been employed in the preparation of o
92 n metal complexes featuring a metal-nitrogen multiple bond have been widely studied due to their impl
95 s on the developing state of the art in both multiple bond heterofunctionalisation and cross coupling
96 atives as pre-catalysts and intermediates in multiple bond hydrogenation, hydrosilylation and hydrobo
97 of the LUMO of the heavier group 13 element multiple bond in comparison with that of a simple alkene
98 rdless of the presence or absence of a Cbeta multiple bond in the SN2 reactant in a series of analogu
99 acute jump in the rolling velocity, proving multiple bonding in the cell surface and the tether surf
103 nyl cations 1d-4d support a degree of Pt-C10 multiple bonding, increasing in the order 3 < 4 < 2 < 1.
105 s exhibit polarized-covalent thorium-arsenic multiple bonding interactions, hitherto restricted to cr
106 nuclear fuels and as probes of metal ligand multiple bonding involving the f-block actinide metals.
109 in the activation of small molecules bearing multiple bonds leading to [2.2.1]bicyclic heterocycles.
111 ily of uranium(VI) dianions bearing four U-N multiple bonds, [M]2[U(NR)4] (M = Li, Na, K, Rb, Cs).
114 ee categories: (1) addition of Fe-H across a multiple bond of the substrate, (2) reductive eliminatio
115 s proposed that it involves direct single or multiple bonding of one or more C atoms to one or more A
116 t is the net activation of the P-C and Si-Si multiple bonds of the precursors affording a heteroatomi
117 A mild and improved method for reducing multiple bonds on various resins with diimide is describ
118 ophiles to add directly to the metal--ligand multiple bond rather than binding to the metal first and
119 smoothly transitions between our single and multiple bond results, we conclusively demonstrate that
120 nds-even stronger than the known gold-carbon multiple bonds, revealing an inverse correlation between
121 of CID experiments enhances the abundance of multiple bond ruptures important for a complete understa
124 ed C2O1 fragments and demonstrating that the multiple bonded terminal Mo identical withC moiety is an
125 phile attacks a gold-activated carbon-carbon multiple bond to give an alkenyl Au intermediate, notwit
126 lts in the unprecedented cleavage of the C-N multiple bond to give, after rearrangement, the carbene-
128 thorium, under ambient conditions only a few multiple bonds to carbon, nitrogen, oxygen, sulfur, sele
129 thorium, under ambient conditions only a few multiple bonds to carbon, nitrogen, phosphorus and chalc
131 selenium and tellurium are reported, and no multiple bonds to phosphorus are known, reflecting a gen
132 es the reactivity of iron-borne metal-ligand multiple bonds to promote the direct amination of alipha
134 ed significantly by increasing the number of multiple bonds to uranium, as demonstrated by a family o
135 loyed repeatedly for the transfer of heavier multiple bonds to yield low-valent group 14 compounds wi
139 ote the addition of apolar sigma-bonds to CC multiple bonds via a 2e redox sequence and draw thereby
141 till contain a considerable number of hidden multiple bonds, which are experimentally indistinguishab
142 nd substantial polarization of the substrate multiple bond with significant positive charge buildup a
143 halides constitute the major part of heavier multiple bonds with a functional group in allylic positi
144 ry, the study of peripherally functionalised multiple bonds with heavier group 14 elements is already
146 about a decade the compatibility of heavier multiple bonds with various functional groups has moved
149 ctants, and may enable nitrogenase to reduce multiple bonds without unreasonably low redox potentials
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