Synthesis of Silver (I) Complexes of Iminoalkyl Functionalised <svg style="vertical-align:-0.0pt;width:21.2125px;" id="M1" height="14.7625" version="1.1" viewBox="0 0 21.2125 14.7625" width="21.2125"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,14.7625)">
		<g transform="translate(72,-60.19)">
			<text transform="matrix(1,0,0,-1,-71.95,60.24)">
				<tspan style="font-size: 17.93px; " x="0" y="0">𝑁</tspan>
			</text>

		</g>
	</g>
</svg>-Heterocyclic Carbenes

<table class="table-group" id="tab1"><tr><td><table class="table"><tr><td class="thead-hr" colspan="4"><hr/></td></tr><tr class="thead"><td align="left"></td><td align="center">R<sup>1</sup></td><td align="center">R<sup>2</sup></td><td align="center">Product  yield</td></tr><tr><td class="thead-hr" colspan="4"><hr/></td></tr><tr><td align="left"><b>1a</b></td><td align="left">H</td><td align="left">Bn</td><td align="left"><b>2a</b>  79%</td></tr><tr><td align="left"><b>1b</b></td><td align="left">Bn</td><td align="left">Bn</td><td align="left"><b>2b</b>  50%</td></tr><tr><td align="left"><b>1c</b></td><td align="left">Me</td><td align="left">Bn</td><td align="left"><b>2c</b>  84%</td></tr><tr><td align="left"><b>1d</b></td><td align="left"><span style="width: 22.8375px;"><svg height="16.0875" id="M42" style="vertical-align:-0.16379pt" version="1.1" viewbox="0 0 22.8375 16.0875" width="22.8375" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
<g transform="matrix(.012,-0,0,-.012,.062,7.662)"><path d="M135 536q-20 0 -35 15.5t-15 35.5q0 22 15 37t36 15t35.5 -15t14.5 -37q0 -21 -15 -36t-36 -15zM252 0h-220v26q48 5 59 17t11 63v206q0 47 -9 58t-54 18v24q78 12 142 39v-345q0 -51 11.5 -63t59.5 -17v-26z" id="x69"></path></g>
<g transform="matrix(.017,-0,0,-.017,3.875,15.825)"><path d="M372 352v-2q176 -27 176 -159q0 -99 -95 -151q-73 -40 -196 -40h-221v28q65 5 78.5 19t13.5 76v404q0 63 -12 77t-72 18v28h257q102 0 150 -34q26 -18 41 -48.5t15 -65.5q0 -111 -135 -150zM213 362h47q80 0 117.5 32t37.5 96q0 56 -33 92t-100 36q-41 0 -56 -10
q-13 -8 -13 -50v-196zM213 328v-203q0 -54 17 -72.5t66 -18.5q67 1 110.5 37t43.5 110q0 147 -192 147h-45z" id="x42"></path></g><g transform="matrix(.017,-0,0,-.017,13.751,15.825)"><path d="M518 50v-26q-32 -4 -77 -16l-37 -11t-33 -9l-6 6v71q-56 -42 -74 -52q-43 -25 -77 -25q-55 0 -89.5 36.5t-34.5 112.5v196q0 38 -6.5 48.5t-26.5 15.5l-28 6v23q19 1 72 7q59 9 71 11q-3 -31 -3 -145v-135q0 -113 88 -113q59 0 108 48v234q0 38 -8 49t-34 15l-36 6v23
q44 2 90 8q37 4 67 10v-334q0 -37 8.5 -47t38.5 -12z" id="x75"></path></g>
</svg></span></td><td align="left">Bn</td><td align="left"><b>2d </b> 68%</td></tr><tr><td align="left"><b>1e</b></td><td align="left">H</td><td align="left">Ph</td><td align="left"><b>2e</b>  78%</td></tr><tr><td align="left"><b>1f</b></td><td align="left">Bn</td><td align="left">Ph</td><td align="left"><b>2f </b> 66%</td></tr><tr><td align="left"><b>1g</b></td><td align="left">Me</td><td align="left">Ph</td><td align="left"><b>2g</b>  91%</td></tr><tr><td align="left"><b>1h</b></td><td align="left"><span style="width: 22.8375px;"><svg height="16.0875" id="M43" style="vertical-align:-0.16379pt" version="1.1" viewbox="0 0 22.8375 16.0875" width="22.8375" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
<g transform="matrix(.012,-0,0,-.012,.062,7.662)"><path d="M135 536q-20 0 -35 15.5t-15 35.5q0 22 15 37t36 15t35.5 -15t14.5 -37q0 -21 -15 -36t-36 -15zM252 0h-220v26q48 5 59 17t11 63v206q0 47 -9 58t-54 18v24q78 12 142 39v-345q0 -51 11.5 -63t59.5 -17v-26z" id="x69"></path></g>
<g transform="matrix(.017,-0,0,-.017,3.875,15.825)"><path d="M372 352v-2q176 -27 176 -159q0 -99 -95 -151q-73 -40 -196 -40h-221v28q65 5 78.5 19t13.5 76v404q0 63 -12 77t-72 18v28h257q102 0 150 -34q26 -18 41 -48.5t15 -65.5q0 -111 -135 -150zM213 362h47q80 0 117.5 32t37.5 96q0 56 -33 92t-100 36q-41 0 -56 -10
q-13 -8 -13 -50v-196zM213 328v-203q0 -54 17 -72.5t66 -18.5q67 1 110.5 37t43.5 110q0 147 -192 147h-45z" id="x42"></path></g><g transform="matrix(.017,-0,0,-.017,13.751,15.825)"><path d="M518 50v-26q-32 -4 -77 -16l-37 -11t-33 -9l-6 6v71q-56 -42 -74 -52q-43 -25 -77 -25q-55 0 -89.5 36.5t-34.5 112.5v196q0 38 -6.5 48.5t-26.5 15.5l-28 6v23q19 1 72 7q59 9 71 11q-3 -31 -3 -145v-135q0 -113 88 -113q59 0 108 48v234q0 38 -8 49t-34 15l-36 6v23
q44 2 90 8q37 4 67 10v-334q0 -37 8.5 -47t38.5 -12z" id="x75"></path></g>
</svg></span></td><td align="left">Ph</td><td align="left"><b>2h</b>  60%</td></tr><tr class="table-tr"><td colspan="4"><hr class="tbody-hr"/></td></tr></table></td></tr></table>

Synthesis of  benzylhydrylideneaminoalkyl imidazol-2-ylidene silver complexes <b>2a</b>-<b>2h</b>.

International Journal of Inorganic Chemistry

tab1

Table 1

Table 1: Synthesis of Silver (I) Complexes of Iminoalkyl Functionalised <svg style="vertical-align:-0.0pt;width:21.2125px;" id="M1" height="14.7625" version="1.1" viewBox="0 0 21.2125 14.7625" width="21.2125"  xmlns="http://www.w3.org/2000/svg">
	<g transform="matrix(1.25,0,0,-1.25,0,14.7625)">
		<g transform="translate(72,-60.19)">
			<text transform="matrix(1,0,0,-1,-71.95,60.24)">
				<tspan style="font-size: 17.93px; " x="0" y="0">𝑁</tspan>
			</text>

		</g>
	</g>
</svg>-Heterocyclic Carbenes 

International Journal of Inorganic Chemistry

Synthesis of Silver (I) Complexes of Iminoalkyl Functionalised 𝑁 -Heterocyclic Carbenes

Table 1

Synthesis of Silver (I) Complexes of Iminoalkyl Functionalised -Heterocyclic Carbenes