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alexwang0521銀蟲 (初入文壇)
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[求助]
求翻譯部分化學(xué)相關(guān)的英文文獻(xiàn) 能翻譯多少是多少
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In contrast to dialkyl cyanamido complexes, the reactivity of hydrogen cyanamido/cyanoimido complexes reported so far occurs only at the N atom of cyanoimido or hydrogen cyanamido moieties, but not at the C atom. Herein we report the reaction of an osmium(VI) nitrido complex that bears a tridentate Schiff base ligand, [OsVI(N)( L1)(Cl)-(H2O)] (1 ), with CN under various conditions to afford(PPh4) [OsVI(N)( L1)(CN)(Cl)] ( 2 ), (PPh4)2[OsVI(N)( L2)(CN)2]( 3 ), and (PPh4)2[OsIII{N(H)CN}( L3)(CN)3](4 ). Electrophilic attack of 4 on the Nb atom of the hydrogen cyanamideligand by H+ or MeI readily occurs to produce (PPh4) [OsIII-{NCN(R)2}( L3)(CN)3 ](R = H(5 ); R = Me (6 )). More signifi-cantly, 4 readily undergoes nucleophilic attack at the C atom of the hydrogen cyanamide ligand by a variety of amines to produce a series of novel osmium guanidine com-pounds (PPh4) [OIII{N(H)C (NH2 )NR1R2}( L3)(CN)3](R1=R2= H(7 ); R1= H, R2= CH2 CH3( 8 ); R1= R2= CH2CH3 ( 9 )). These compounds have been characterized by different spectroscopic methods. The crystal structures of 1 – 5 and 7 and 8 have been determined by X-ray crystallography. |

木蟲 (正式寫手)
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相比之下,二烷基氰胺絡(luò)合物,至目前報(bào)道的氰胺或氰亞胺氫的反應(yīng)僅發(fā)生在氰亞胺的N原子上或氰胺的氫原子上,而不是在C原子。在此,我們報(bào)告含鋨(VI)的氮絡(luò)合物反應(yīng)中有三齒Schiff堿配體生成。 More signifi-cantly, 4 readily undergoes nucleophilic attack at the C atom of the hydrogen cyanamide ligand by a variety of amines to produce a series of novel osmium guanidine com-pounds 更為顯著,4容易在C原子的氰胺配體的氫原子容易受各種胺的親核攻擊,生成一系列新穎鋨胍化合物。 These compounds have been characterized by different pectroscopic methods. The crystal structures of 1 – 5 and 7 and 8 have been determined by X-ray crystallography. 這些化合物結(jié)構(gòu)已用不同光譜方法證實(shí)了。晶體結(jié)構(gòu)1 - 5、7 和8個(gè)已通過X-射線晶體確定結(jié)構(gòu)。 |

木蟲 (正式寫手)
| 與二烴基氰胺復(fù)合物相反的是,氫氰胺/氰亞胺化合物的反應(yīng)活性在目前的報(bào)告中僅發(fā)生在氰亞胺的或氫氰胺的氮原子上,而不是在碳原子上。在此我們報(bào)告一種具有希夫堿三齒配體的氮化鋨(六)絡(luò)合物的反應(yīng),[OsVI(N)( L1)(Cl)-(H2O)] (1 ),它在不同條件下與CN形成(PPh4) [OsVI(N)( L1)(CN)(Cl)] ( 2 ), (PPh4)2[OsVI(N)( L2)(CN)2]( 3 ), 和(PPh4)2[OsIII{N(H)CN}( L3)(CN)3](4 ).。4親電進(jìn)攻由H+或MeI配位氫氰銨上的鈮原子,容易生成(PPh4) [OsIII-{NCN(R)2}( L3)(CN)3 ](R = H(5 ),R = Me (6 )).更顯著的是,4容易進(jìn)行親核攻擊由不同胺配位氫氰銨上的碳原子,從而產(chǎn)生一系列新穎的鋨胍化合物((PPh4) [OIII{N(H)C (NH2 )NR1R2}( L3)(CN)3](R1=R2= H(7 ); R1= H, R2= CH2 CH3( 8 ); R1= R2= CH2CH3( 9 ))。這些化合物已由不同光譜法表征,1到5、7和8的晶體結(jié)構(gòu)也用X-晶體衍射測(cè)定了。 |

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